Abstract is: John L. Hopper is an Australian genetic epidemiologist and professor at the University of Melbourne, where he is a Professorial Fellow and Director of the Centre for Epidemiology and Biostatistics in the School of Population Global Health. He is also a National Health and Medical Research Council (NHMRC) Senior Principal Research Fellow, and was one of the first nine Australia Fellows chosen by the NHMRC in 2007. Since 1990, he has been the director of Twins Research Australia (formerly the Australian Twin Registry).
| human | Q5 |
| P2671 | Google Knowledge Graph ID | /g/11gr6vtmpm |
| P1960 | Google Scholar author ID | i9GTRzQAAAAJ |
| P496 | ORCID iD | 0000-0002-8567-173X |
| P1153 | Scopus author ID | 7201924128 |
| P8207 | The Conversation author ID | 1429 |
| P1556 | zbMATH author ID | hopper.john-llewelyn |
| P27 | country of citizenship | Australia | Q408 |
| P69 | educated at | Monash University | Q598841 |
| La Trobe University | Q1478723 | ||
| P108 | employer | University of Melbourne | Q319078 |
| P734 | family name | Hopper | Q21501617 |
| Hopper | Q21501617 | ||
| Hopper | Q21501617 | ||
| P101 | field of work | genetic epidemiology | Q5532897 |
| P735 | given name | John | Q4925477 |
| John | Q4925477 | ||
| Llewelyn | Q21503586 | ||
| Llewelyn | Q21503586 | ||
| P106 | occupation | researcher | Q1650915 |
| statistician | Q2732142 | ||
| geneticist | Q3126128 | ||
| epidemiologist | Q13416803 | ||
| P21 | sex or gender | male | Q6581097 |
| Q64115284 | 10-year performance of four models of breast cancer risk: a validation study |
| Q36016386 | 11q13 is a susceptibility locus for hormone receptor positive breast cancer |
| Q35785911 | 14th Annual Meeting of the Collaborative Group of the Americas on Inherited Colorectal Cancer Dallas, TX, USA. 12-13 October 2010. Abstracts |
| Q35871567 | 19p13.1 is a triple-negative-specific breast cancer susceptibility locus |
| Q40052964 | 20/20--Alcohol and age-related macular degeneration: the Melbourne Collaborative Cohort Study |
| Q33848895 | 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy |
| Q57945242 | 350 HFE C282Y HOMOZYGOSITY IS ASSOCIATED WITH AN INCREASED RISK OF TOTAL HIP REPLACEMENT FOR OSTEOARTHRITIS IN MEN BUT NOT WOMEN |
| Q54569428 | 5alpha-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia. |
| Q36021406 | 7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium |
| Q37169873 | 9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium |
| Q47953281 | A 12-month prospective study of the relationship between stress fractures and bone turnover in athletes |
| Q51569689 | A BRCA1 promoter variant (rs11655505) and breast cancer risk. |
| Q57100437 | A Comparison of Adiposity Measures as Predictors of All-cause Mortality: The Melbourne Collaborative Cohort Study* |
| Q53283615 | A Mixed-Effects Model for Powerful Association Tests in Integrative Functional Genomics. |
| Q34613667 | A PALB2 mutation associated with high risk of breast cancer |
| Q57265744 | A Systematic Approach to Analysing Gene-Gene Interactions: Polymorphisms at the Microsomal Epoxide Hydrolase EPHX and Glutathione S-transferase GSTM1, GSTT1, and GSTP1 Loci and Breast Cancer Risk |
| Q34175965 | A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk |
| Q61132431 | A co-twin study of the effect of calcium supplementation on bone density during adolescence |
| Q34015399 | A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics |
| Q104471089 | A combined proteomics and Mendelian randomization approach to investigate the effects of aspirin-targeted proteins on colorectal cancer |
| Q57250674 | A common coding variant in CASP8 is associated with breast cancer risk |
| Q57100446 | A comparison of different methods for including 'age at menopause' in analyses of the association between hormone replacement therapy use and breast cancer |
| Q45399914 | A comparison of self-reported and record-linked blood donation history in an Australian cohort |
| Q35957063 | A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density |
| Q28384136 | A discrete choice experiment of preferences for genetic counselling among Jewish women seeking cancer genetics services |
| Q41455686 | A family study of panic disorder |
| Q41982877 | A family study of panic disorder: reanalysis using a regressive logistic model that incorporates a sibship environment |
| Q42667209 | A genetic and environmental analysis of a twin family study of alcohol use, anxiety, and depression |
| Q37272982 | A genome wide linkage search for breast cancer susceptibility genes |
| Q36395306 | A genome-wide association study for colorectal cancer identifies a risk locus in 14q23.1. |
| Q56436562 | A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 |
| Q29417036 | A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. |
| Q35889669 | A genome-wide linkage study of mammographic density, a risk factor for breast cancer |
| Q37619303 | A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium |
| Q35089479 | A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population |
| Q36435849 | A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. |
| Q36477652 | A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease |
| Q36512734 | A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry |
| Q92711687 | A network analysis to identify mediators of germline-driven differences in breast cancer prognosis |
| Q35626744 | A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer |
| Q37399509 | A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis |
| Q34737151 | A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study |
| Q39680659 | A novel polymorphism in a forkhead box A1 (FOXA1) binding site of the human UDP glucuronosyltransferase 2B17 gene modulates promoter activity and is associated with altered levels of circulating androstane-3α,17β-diol glucuronide |
| Q35699278 | A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma |
| Q49056658 | A prospective longitudinal study of serum testosterone, dehydroepiandrosterone sulfate, and sex hormone-binding globulin levels through the menopause transition. |
| Q48715331 | A prospective population-based study of menopausal symptoms. |
| Q44012585 | A prospective study of bone loss in menopausal Australian-born women |
| Q57265807 | A protein-truncating mutation inCYP17A1 in three sisters with early-onset breast cancer |
| Q31109774 | A range of simple summary genome-wide statistics for detecting genetic linkage using high density marker data |
| Q37632049 | A risk prediction algorithm based on family history and common genetic variants: application to prostate cancer with potential clinical impact |
| Q37599352 | A role for XRCC2 gene polymorphisms in breast cancer risk and survival |
| Q34998516 | A three-protein biomarker panel assessed in diagnostic tissue predicts death from prostate cancer for men with localized disease |
| Q57305942 | A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer |
| Q42598301 | A twin study of genetic influences on epilepsy outcome |
| Q29417157 | A variant in FTO shows association with melanoma risk not due to BMI |
| Q36043159 | ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry |
| Q56438288 | AT-tributable risks? |
| Q57188445 | AVERAGE VOLUME OF ALCOHOL CONSUMED, TYPE OF BEVERAGE, DRINKING PATTERN AND THE RISK OF DEATH FROM ALL CAUSES |
| Q34172196 | Abdominal obesity and age-related macular degeneration |
| Q51582208 | Abridged adapter primers increase the target scope of Hi-Plex. |
| Q61782514 | Abstract 32: Lynch syndrome-associated breast cancers: Clinicopathological characteristics of a case series from the Colon CFR |
| Q58047207 | Abstract 4831: Additive and multiplicative gene-environment interactions for colorectal cancer risk |
| Q57785674 | Abstract LB-282: Transethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A |
| Q57637098 | Acceptability and Usability of iPrevent�, a Web-Based Tool for Assessment and Management of Breast Cancer Risk. (Preprint) |
| Q92102602 | Accuracy of Risk Estimates from the iPrevent Breast Cancer Risk Assessment and Management Tool |
| Q36422294 | Accuracy of self-reported nevus and pigmentation phenotype compared with clinical assessment in a population-based study of young Australian adults |
| Q68117480 | Acute stroke outcome: effects of stroke type and risk factors |
| Q33912818 | Adaptive evolution of the tumour suppressor BRCA1 in humans and chimpanzees. Australian Breast Cancer Family Study |
| Q35219159 | Adequacy of risk-reducing gynaecologic surgery in BRCA1 or BRCA2 mutation carriers and other women at high risk of pelvic serous cancer |
| Q50977654 | Adult serum cytokine concentrations and the persistence of asthma. |
| Q24535695 | After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer |
| Q56437837 | AfterhMSH2 andhMLH1?what next? Analysis of three-generational, population-based, early-onset colorectal cancer families |
| Q39437211 | Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers |
| Q34644094 | Age-dependent associations between androgenetic alopecia and prostate cancer risk |
| Q53021229 | Age-related macular degeneration in ethnically diverse Australia: Melbourne Collaborative Cohort Study. |
| Q58613780 | Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC) |
| Q51028293 | Age-specific norms and determinants of anxiety and depression in 731 women with breast cancer recruited through a population-based cancer registry. |
| Q46455507 | Agreement between self-reported breast cancer treatment and medical records in a population-based Breast Cancer Family Registry |
| Q39218432 | Alcohol Consumption and the Risk of Colorectal Cancer for Mismatch Repair Gene Mutation Carriers |
| Q52291866 | Alcohol consumption and cardiovascular mortality accounting for possible misclassification of intake: 11-year follow-up of the Melbourne Collaborative Cohort Study. |
| Q57265769 | Alcohol consumption and prostate cancer risk: Results from the Melbourne collaborative cohort study |
| Q44143065 | Alcohol consumption and risk of glioblastoma; evidence from the Melbourne Collaborative Cohort Study |
| Q30779634 | Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases |
| Q44640070 | Alcohol consumption for different periods in life, intake pattern over time and all-cause mortality |
| Q41088489 | Alcohol use, smoking habits and the Adult Eysenck Personality Questionnaire in adolescent Australian twins [corrected] |
| Q30747351 | Alcohol, tobacco and breast cancer--collaborative reanalysis of individual data from 53 epidemiological studies, including 58,515 women with breast cancer and 95,067 women without the disease |
| Q33636690 | Alpha-1-antitrypsin deficiency and smoking as risk factors for mismatch repair deficient colorectal cancer: a study from the colon cancer family registry |
| Q46011428 | Ambient wood smoke exposure and respiratory symptoms in Tasmania, Australia. |
| Q39428233 | Ambient wood smoke, traffic pollution and adult asthma prevalence and severity |
| Q36073563 | An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression |
| Q46063050 | An inverse association between ovarian cysts and breast cancer in the breast cancer family registry |
| Q52585935 | An open-source, integrated pedigree data management and visualization tool for genetic epidemiology. |
| Q34308746 | Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families |
| Q34480599 | Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource |
| Q44204316 | Analysis of dynamic computed tomography scan brain images |
| Q38378456 | Analysis of the breast cancer methylome using formalin-fixed paraffin-embedded tumour |
| Q70568011 | Analysis of variation in blood lead levels in Melbourne families |
| Q42653120 | Analytical and graphical methods to model the association between family history and disease from a case-control study |
| Q45980590 | Analyzing the etiology of benign rolandic epilepsy: a multicenter twin collaboration. |
| Q57269082 | Androgen receptor exon 1 cag repeat length and risk of ovarian cancer |
| Q34523806 | Androgenetic alopecia and prostate cancer: findings from an Australian case-control study |
| Q28191418 | Androgenetic alopecia in men aged 40-69 years: prevalence and risk factors |
| Q61442784 | Anti-Müllerian Hormone Serum Concentrations of Women With Germline BRCA1 or BRCA2 Mutations |
| Q57100196 | Apolipoprotein E Gene Associations in Age-related Macular Degeneration: The Melbourne Collaborative Cohort Study |
| Q36008157 | Application of genetics to the prevention of colorectal cancer. |
| Q45763447 | Architecture of cortical bone determines in part its remodelling and structural decay |
| Q57305998 | Are PALB2 mutations associated with increased risk of male breast cancer? |
| Q57265609 | Are genetic and environmental components of variance in mammographic density measures that predict breast cancer risk independent of within-twin pair differences in body mass index? |
| Q41661586 | Are obesity and body fat distribution associated with low back pain in women? A population-based study of 1128 Spanish twins |
| Q100387828 | Are the Relationships of Lean Mass and Fat Mass With Bone Microarchitecture Causal or Due to Familial Confounders? A Novel Study of Adult Female Twin Pairs |
| Q36763034 | Are the common genetic variants associated with colorectal cancer risk for DNA mismatch repair gene mutation carriers? |
| Q36787357 | Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories? |
| Q36294966 | Aspirin, Ibuprofen, and the Risk of Colorectal Cancer in Lynch Syndrome |
| Q39164029 | Assessing and managing breast cancer risk: clinicians' current practice and future needs |
| Q34613673 | Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study |
| Q64940233 | Assessing patient readiness for personalized genomic medicine. |
| Q56893420 | Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies |
| Q88159791 | Assessing the ProMCol classifier as a prognostic marker for non-metastatic colorectal cancer within the Melbourne Collaborative Cohort Study |
| Q64056497 | Association analyses identify 31 new risk loci for colorectal cancer susceptibility |
| Q45979098 | Association analysis identifies 65 new breast cancer risk loci. |
| Q37623732 | Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease |
| Q51399486 | Association analysis of oestrogen receptor beta gene (ESR2) polymorphisms with female pattern hair loss. |
| Q40317688 | Association between DNA methylation at SOCS3 gene and body mass index might be due to familial confounding |
| Q58298117 | Association between birth weight and educational attainment: an individual-based pooled analysis of nine twin cohorts |
| Q38860166 | Association between birthweight and later body mass index: an individual-based pooled analysis of 27 twin cohorts participating in the CODATwins project |
| Q35920915 | Association between body mass index and mortality for colorectal cancer survivors: overall and by tumor molecular phenotype |
| Q37192664 | Association between hypermethylation of DNA repetitive elements in white blood cell DNA and early-onset colorectal cancer |
| Q39791494 | Association between selected dietary scores and the risk of urothelial cell carcinoma: A prospective cohort study |
| Q47903752 | Association of DNA Methylation-Based Biological Age with Health Risk Factors, and Overall and Cause-Specific Mortality |
| Q37292963 | Association of ESR1 gene tagging SNPs with breast cancer risk |
| Q46707380 | Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis |
| Q35246178 | Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants |
| Q47191928 | Association of birth weight and current body size to blood pressure in female twins |
| Q37684672 | Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21. |
| Q57543292 | Association of current and former smoking with body mass index: A study of smoking discordant twin pairs from 21 twin cohorts |
| Q37268494 | Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry |
| Q114182713 | Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment |
| Q52587998 | Associations between birth size and later height from infancy through adulthood: An individual based pooled analysis of 28 twin cohorts participating in the CODATwins project. |
| Q37382206 | Associations between smoking, alcohol consumption, and colorectal cancer, overall and by tumor microsatellite instability status |
| Q47232610 | Associations between weight in early adulthood, change in weight, and breast cancer risk in postmenopausal women |
| Q47690269 | Associations of alcohol intake, smoking, physical activity and obesity with survival following colorectal cancer diagnosis by stage, anatomic site and tumor molecular subtype |
| Q35022847 | Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies |
| Q35532898 | Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium |
| Q54679615 | Associations of mammographic dense and nondense areas and body mass index with risk of breast cancer. |
| Q57056093 | Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis |
| Q57265673 | Asthma, Asthma Medications, and Prostate Cancer Risk |
| Q30485831 | Australian Twin Registry: 30 years of progress |
| Q57297338 | Australian Twin Registry: A Nationally Funded Resource for Medical and Scientific Research, Incorporating match and WATCH |
| Q53242830 | Australian Twin Registry: a nationally funded resource for medical and scientific research, incorporating match and WATCH. |
| Q37204722 | Australian clinicians and chemoprevention for women at high familial risk for breast cancer |
| Q44953939 | Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics |
| Q24531993 | Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies |
| Q34782265 | BRAFV600E immunohistochemistry facilitates universal screening of colorectal cancers for Lynch syndrome |
| Q37416050 | BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: an open resource for collaborative research |
| Q34571646 | BRCA1 and BRCA2 mutation carriers, oral contraceptive use, and breast cancer before age 50. |
| Q36420531 | BRCA1 promoter deletions in young women with breast cancer and a strong family history: a population-based study |
| Q38914005 | BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer |
| Q37002955 | BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers |
| Q57306056 | BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk |
| Q42506232 | BRCA2 mutation-associated breast cancers exhibit a distinguishing phenotype based on morphology and molecular profiles from tissue microarrays |
| Q56995151 | Background, rationale and protocol for a case-control-family study of breast cancer |
| Q44357049 | Biological markers that predict clinical recurrence in ductal carcinoma in situ of the breast |
| Q52576402 | Birth size and gestational age in opposite-sex twins as compared to same-sex twins: An individual-based pooled analysis of 21 cohorts. |
| Q38864714 | Blood pressure and risk of breast cancer, overall and by subtypes: a prospective cohort study |
| Q41066127 | Blood pressure in subjects from rural Greece, comparing individuals migrating to Melbourne, Australia with non-migrant relatives |
| Q46115524 | Body mass index and breast cancer survival: a Mendelian randomization analysis |
| Q30502502 | Body mass index in early adulthood and colorectal cancer risk for carriers and non-carriers of germline mutations in DNA mismatch repair genes |
| Q34883523 | Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers |
| Q47367583 | Body size and composition and colon cancer risk in women |
| Q47313556 | Body size and composition and risk of rectal cancer (Australia). |
| Q47357608 | Body size and composition and the risk of gastric and oesophageal adenocarcinoma |
| Q47373087 | Body size and composition and the risk of lymphohematopoietic malignancies |
| Q38403904 | Body size and risk for colorectal cancers showing BRAF mutations or microsatellite instability: a pooled analysis |
| Q47412578 | Body size, weight change, and risk of colon cancer |
| Q36794730 | Bone density determinants in elderly women: a twin study |
| Q71665300 | Bone mineral density and hormone levels in menopausal Australian women |
| Q71477234 | Bone turnover markers and bone density across the menopausal transition |
| Q57265621 | Breast Cancer Prognosis inBRCA1andBRCA2Mutation Carriers: An International Prospective Breast Cancer Family Registry Population-Based Cohort Study |
| Q48175282 | Breast Cancer Risk Associations with Digital Mammographic Density by Pixel Brightness Threshold and Mammographic System. |
| Q36619329 | Breast Cancer Risk Prediction Using Clinical Models and 77 Independent Risk-Associated SNPs for Women Aged Under 50 Years: Australian Breast Cancer Family Registry |
| Q43073201 | Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies |
| Q57265906 | Breast cancer in Australian women under the age of 40 |
| Q34327945 | Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 |
| Q51003387 | Breast cancer risk for Korean women with germline mutations in BRCA1 and BRCA2. |
| Q35609710 | Breast cancer risk for noncarriers of family-specific BRCA1 and BRCA2 mutations: findings from the Breast Cancer Family Registry |
| Q37410693 | Breast cancer risk prediction using a polygenic risk score in the familial setting: a prospective study from the Breast Cancer Family Registry and kConFab |
| Q35940158 | Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. |
| Q44937823 | Breast cancer risks for BRCA1/2 carriers |
| Q57305977 | Breast-Cancer Risk in Families With Mutations in PALB2 |
| Q34148873 | Breast-cancer risk in families with mutations in PALB2 |
| Q40044786 | Bronchial hyperresponsiveness and obesity in middle age: insights from an Australian cohort |
| Q41004860 | CFTR deltaF508 carrier status, risk of breast cancer before the age of 40 and histological grading in a population-based case-control study |
| Q36449203 | CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer |
| Q24810733 | CYP17 genetic polymorphism, breast cancer, and breast cancer risk factors: Australian Breast Cancer Family Study |
| Q73088381 | CYP17 promoter polymorphism and breast cancer in Australian women under age forty years |
| Q36419325 | CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer |
| Q36750746 | CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk |
| Q44793797 | Can genetic associations change with age? CFH and age-related macular degeneration |
| Q92005489 | Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families |
| Q57265774 | Cancer Risks For Mismatch Repair Gene Mutation Carriers: A Population-Based Early Onset Case-Family Study |
| Q51726517 | Cancer risk management practices of noncarriers within BRCA1/2 mutation positive families in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer. |
| Q30563768 | Cancer risks for MLH1 and MSH2 mutation carriers |
| Q30461804 | Cancer risks for monoallelic MUTYH mutation carriers with a family history of colorectal cancer |
| Q37700797 | Cancer risks for relatives of children with cancer |
| Q36369233 | Cancer risks for relatives of patients with serrated polyposis |
| Q28385765 | Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk |
| Q33736763 | Case-control study of overweight, obesity, and colorectal cancer risk, overall and by tumor microsatellite instability status |
| Q49874632 | Causal effect of smoking on DNA methylation in peripheral blood: a twin and family study. |
| Q57305951 | Causes of blood methylomic variation for middle-aged women measured by the HumanMethylation450 array |
| Q72595861 | Cerebral hypoperfusion in stroke prognosis and brain recovery |
| Q38533169 | Changes in axial bone density with age: a twin study |
| Q50677600 | Changes in body composition as determinants of longitudinal changes in bone mineral measures in 8 to 26-year-old female twins. |
| Q44228291 | Changes in physical activity and health outcomes in a population-based cohort of mid-life Australian-born women |
| Q58104811 | Childhood allergic rhinitis predicts asthma incidence and persistence to middle age: A longitudinal study |
| Q40892499 | Childhood body mass index and adult mammographic density measures that predict breast cancer risk |
| Q36244800 | Childhood cancers in families with and without Lynch syndrome |
| Q57599233 | Childhood eczema and asthma incidence and persistence: A cohort study from childhood to middle age |
| Q40371861 | Childhood immunization and atopic disease into middle-age--a prospective cohort study |
| Q37078547 | Childhood infections and adult height in monozygotic twin pairs |
| Q47968216 | Childhood infections and the risk of asthma: a longitudinal study over 37 years |
| Q51761040 | Childhood measles contributes to post-bronchodilator airflow obstruction in middle-aged adults: A cohort study. |
| Q52599973 | Childhood predictors of lung function trajectories and future COPD risk: a prospective cohort study from the first to the sixth decade of life. |
| Q51725781 | Childhood wheeze phenotypes show less than expected growth in FEV1 across adolescence. |
| Q40707751 | Cholecystectomy and the risk of colorectal cancer by tumor mismatch repair deficiency status. |
| Q36599631 | Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG |
| Q56994835 | Circulating Insulin-Like Growth Factor-I and Binding Protein-3 and Risk of Prostate Cancer |
| Q57265750 | Circulating Insulin-Like Growth Factor-I and Binding Protein-3 and the Risk of Breast Cancer |
| Q35287715 | Circulating sex hormones and breast cancer risk factors in postmenopausal women: reanalysis of 13 studies |
| Q46569800 | Circulating steroid hormone concentrations in postmenopausal women in relation to body size and composition |
| Q43189592 | Circulating steroid hormone levels and risk of breast cancer for postmenopausal women |
| Q46910105 | Circulating steroid hormones and the risk of prostate cancer |
| Q37254403 | Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics |
| Q57306048 | Clinical Classification ofBRCA1andBRCA2DNA Sequence Variants: The Value of Cytokeratin Profiles and Evolutionary Analysis—A Report From the kConFab Investigators |
| Q39683513 | Clinical and functional differences between early-onset and late-onset adult asthma: a population-based Tasmanian Longitudinal Health Study |
| Q40706266 | Cohort Profile: Melbourne Atopy Cohort study (MACS). |
| Q37219731 | Cohort Profile: The Breast Cancer Prospective Family Study Cohort (ProF-SC) |
| Q56379999 | Cohort Profile: The Colon Cancer Family Registry Cohort (CCFRC) |
| Q40149181 | Cohort Profile: The Melbourne Collaborative Cohort Study (Health 2020). |
| Q40641928 | Cohort Profile: The Tasmanian Longitudinal Health STUDY (TAHS). |
| Q53226230 | Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer. |
| Q35925149 | Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study |
| Q36000794 | Colorectal cancer linkage on chromosomes 4q21, 8q13, 12q24, and 15q22. |
| Q28284149 | Colorectal carcinomas with KRAS mutation are associated with distinctive morphological and molecular features |
| Q55520252 | Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance. |
| Q94486442 | Combined associations of a polygenic risk score and classical risk factors with breast cancer risk |
| Q40594667 | Commentary: Case-control-family designs: a paradigm for future epidemiology research? |
| Q47322321 | Common Pediatric Pain Disorders and Their Clinical Associations |
| Q36839777 | Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers |
| Q34394665 | Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction |
| Q35889575 | Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. |
| Q36600605 | Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk |
| Q33742096 | Common genetic variants and modification of penetrance of BRCA2-associated breast cancer |
| Q43166839 | Common genetic variants associated with breast cancer and mammographic density measures that predict disease |
| Q35794653 | Common germline polymorphisms associated with breast cancer-specific survival |
| Q34379032 | Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium |
| Q37371151 | Common sequence variants on 20q11.22 confer melanoma susceptibility |
| Q36393232 | Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers |
| Q35870067 | Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers |
| Q37434133 | Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers |
| Q34792833 | Common variants in ZNF365 are associated with both mammographic density and breast cancer risk |
| Q29417133 | Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk |
| Q33679480 | Comparing the frequency of common genetic variants and haplotypes between carriers and non-carriers of BRCA1 and BRCA2 deleterious mutations in Australian women diagnosed with breast cancer before 40 years of age. |
| Q31082788 | Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
| Q40718941 | Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations |
| Q36315747 | Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer |
| Q37121925 | Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics |
| Q36026731 | Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer |
| Q34181322 | Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer |
| Q33959070 | Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. |
| Q33700463 | Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity |
| Q33646285 | Constitutional methylation of the BRCA1 promoter is specifically associated with BRCA1 mutation-associated pathology in early-onset breast cancer |
| Q43244689 | Consumption of animal products, their nutrient components and postmenopausal circulating steroid hormone concentrations |
| Q37577739 | Contralateral risk-reducing mastectomy in BRCA1 and BRCA2 mutation carriers and other high-risk women in the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab). |
| Q35029565 | Contribution of large genomic BRCA1 alterations to early-onset breast cancer selected for family history and tumour morphology: a report from The Breast Cancer Family Registry |
| Q34102586 | Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer |
| Q55257640 | Correction: Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22. |
| Q57266620 | Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer |
| Q57278898 | Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC) |
| Q45812067 | Correlations between cerebral arterial velocities, blood flow, and delayed ischemia after subarachnoid hemorrhage |
| Q49498050 | Corrigendum: Risk of colorectal cancer for carriers of a germ-line mutation in POLE or POLD1. |
| Q50240714 | Corrigendum: genome-wide association study of colorectal cancer identifies six new susceptibility loci. |
| Q48526678 | Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women. |
| Q38687607 | Cost-effectiveness of population based BRCA testing with varying Ashkenazi Jewish ancestry |
| Q67910152 | Costs and benefits of the use of commercial market research approaches in large scale surveys |
| Q28388475 | Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations |
| Q72486756 | Crossed cerebellar diaschisis and brain recovery after stroke |
| Q37409157 | Cumulative impact of common genetic variants and other risk factors on colorectal cancer risk in 42,103 individuals |
| Q37194155 | Current asthma contributes as much as smoking to chronic bronchitis in middle age: a prospective population-based study |
| Q36694276 | Cytomegalovirus, Epstein-Barr virus and risk of breast cancer before age 40 years: a case-control study |
| Q21144874 | DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers |
| Q90858079 | DNA methylation-based biological age, genome-wide average DNA methylation, and conventional breast cancer risk factors |
| Q48192088 | DNA methylation-based biological aging and cancer risk and survival: Pooled analysis of seven prospective studies |
| Q37685729 | DNA mismatch repair gene MSH6 implicated in determining age at natural menopause |
| Q92831013 | DNA repair and cancer in colon and rectum: Novel players in genetic susceptibility |
| Q43218563 | De novo BRCA1 mutation in a patient with breast cancer and an inherited BRCA2 mutation |
| Q37332239 | Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer |
| Q40270211 | Dependence of cancer risk from environmental exposures on underlying genetic susceptibility: an illustration with polycyclic aromatic hydrocarbons and breast cancer |
| Q35587019 | Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes |
| Q40760869 | Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS). |
| Q36803796 | Detection of large scale 3' deletions in the PMS2 gene amongst Colon-CFR participants: have we been missing anything? |
| Q44581219 | Determinants of bone density in 30- to 65-year-old women: a co-twin study |
| Q36687318 | Determinants of bone mass in 10- to 26-year-old females: A twin study |
| Q61132491 | Determinants of hip axis length in women aged 10–89 years: A twin study |
| Q51802404 | Determinants of preferences for genetic counselling in Jewish women. |
| Q49846654 | Determining Risk of Colorectal Cancer and Starting Age of Screening Based on Lifestyle, Environmental, and Genetic Factors. |
| Q35872667 | Determining the familial risk distribution of colorectal cancer: a data mining approach. |
| Q36217478 | Determining the frequency of de novo germline mutations in DNA mismatch repair genes |
| Q40712359 | Development and External Validation of a Melanoma Risk Prediction Model Based on Self-assessed Risk Factors |
| Q44609956 | Diabetes, hyperinsulinemia, and hyperlipidemia in small aboriginal community in northern Australia |
| Q33588213 | Diagnostic chest X-rays and breast cancer risk before age 50 years for BRCA1 and BRCA2 mutation carriers |
| Q31155090 | Diet and exercise during growth have site-specific skeletal effects: a co-twin control study |
| Q57265592 | Dietary Intake of B Vitamins and Methionine and Colorectal Cancer Risk |
| Q46516453 | Dietary carbohydrate, fibre, glycaemic index, glycaemic load and the risk of postmenopausal breast cancer |
| Q43498594 | Dietary intake of B vitamins and methionine and breast cancer risk |
| Q57265625 | Dietary intake of B vitamins and methionine and prostate cancer incidence and mortality |
| Q57265626 | Dietary intake of B vitamins and methionine and risk of lung cancer |
| Q49990651 | Dietary intake of nutrients involved in one-carbon metabolism and risk of urothelial cell carcinoma: A prospective cohort study. |
| Q50594346 | Dietary patterns and prostate cancer risk. |
| Q34627774 | Dietary patterns and risk of breast cancer |
| Q44643595 | Dietary patterns and their associations with age-related macular degeneration: the Melbourne collaborative cohort study |
| Q34115013 | Differences in drinking patterns associated with migration from a Greek island to Melbourne, Australia: a study of sibships |
| Q38692419 | Differences in genetic and environmental variation in adult BMI by sex, age, time period, and region: an individual-based pooled analysis of 40 twin cohorts |
| Q46763107 | Disclosing genetic research results: experiences of the Colon Cancer Family Registry |
| Q60472142 | Discovery of common and rare genetic risk variants for colorectal cancer |
| Q34662485 | Disease-specific prospective family study cohorts enriched for familial risk |
| Q43642380 | Do BRCA1 and BRCA2 mutation carriers have earlier natural menopause than their noncarrier relatives? Results from the Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer |
| Q34069646 | Does dietary folate intake modify effect of alcohol consumption on breast cancer risk? Prospective cohort study |
| Q30571269 | Does eczema in infancy cause hay fever, asthma, or both in childhood? Insights from a novel regression model of sibling data |
| Q33593851 | Does risk of endometrial cancer for women without a germline mutation in a DNA mismatch repair gene depend on family history of endometrial cancer or colorectal cancer? |
| Q36615581 | Does smoking among friends explain apparent genetic effects on current smoking in adolescence and young adulthood? |
| Q33612493 | Does the sex of one's co-twin affect height and BMI in adulthood? A study of dizygotic adult twins from 31 cohorts |
| Q45171190 | Domestic airborne pollutants and asthma and respiratory symptoms in middle age. |
| Q45207103 | Dynamic CT brain scanning in the haemodynamic evaluation of cerebral arterial occlusive disease |
| Q28208394 | ELAC2/HPC2 polymorphisms, prostate-specific antigen levels, and prostate cancer |
| Q46853263 | Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots |
| Q47175049 | Early growth, adult body size and prostate cancer risk |
| Q43605844 | Early seizures after acute stroke. Risk of late seizures |
| Q57265659 | Early-life sun exposure and risk of melanoma before age 40 years |
| Q50012629 | Early-onset baldness and the risk of aggressive prostate cancer: findings from a case-control study. |
| Q45069217 | Education in Twins and Their Parents Across Birth Cohorts Over 100 years: An Individual-Level Pooled Analysis of 42-Twin Cohorts |
| Q68461392 | Effect of early menopause on bone mass in normal women and patients with osteoporosis |
| Q53408150 | Effects of Tamoxifen and oestrogen on histology and radiographic density in high and low mammographic density human breast tissues maintained in murine tissue engineering chambers. |
| Q39443485 | Efficacy of a Sleep Quality Intervention in People With Low Back Pain: Protocol for a Feasibility Randomized Co-Twin Controlled Trial |
| Q40266305 | Ejaculatory frequency and the risk of aggressive prostate cancer: Findings from a case-control study |
| Q45073555 | Enrichment of colorectal cancer associations in functional regions: Insight for using epigenomics data in the analysis of whole genome sequence-imputed GWAS data |
| Q47196130 | Epigenetic supersimilarity of monozygotic twin pairs |
| Q57265567 | Epigenome-wide methylation in DNA from peripheral blood as a marker of risk for breast cancer |
| Q50895975 | Epilepsies in twins: genetics of the major epilepsy syndromes. |
| Q55481904 | Epilepsy and primary cerebral tumours. |
| Q30920805 | Epilepsy in twins: insights from unique historical data of William Lennox |
| Q43545423 | Epileptic seizures in acute stroke |
| Q55208680 | Erratum to: Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study. |
| Q42412214 | Erratum: A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer |
| Q57250672 | Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk |
| Q57202568 | Erratum: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk |
| Q57265517 | Erratum: Current asthma contributes as much as smoking to chronic bronchitis in middle age: a prospective population-based study [Corrigendum] |
| Q53075668 | Estimates of familial risks from family data are biased when ascertainment of families is not independent of family history. |
| Q36990074 | Estimating cumulative risks for breast cancer for carriers of variants in uncommon genes |
| Q33763770 | Estimating risks for variants of unknown significance according to their predicted pathogenicity classes with application to BRCA1. |
| Q34767345 | Estimating single nucleotide polymorphism associations using pedigree data: applications to breast cancer |
| Q59292166 | Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants |
| Q57306021 | Estrogen Receptor Polymorphism at Codon 325 and Risk of Breast Cancer in Women Before Age Forty |
| Q57100396 | Ethnicity and Risk for Colorectal Cancers Showing Somatic BRAF V600E Mutation or CpG Island Methylator Phenotype |
| Q37481884 | Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA). |
| Q33894527 | Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium |
| Q35653910 | Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk |
| Q36070164 | Evidence for BRAF mutation and variable levels of microsatellite instability in a syndrome of familial colorectal cancer |
| Q73286319 | Evidence for genetic associations between asthma, atopy, and bronchial hyperresponsiveness: a study of 8- to 18-yr-old twins |
| Q36720821 | Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors |
| Q35064451 | Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation |
| Q37342144 | Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation |
| Q45918948 | Explaining variance in the cumulus mammographic measures that predict breast cancer risk: a twins and sisters study. |
| Q50871791 | Expression of MUC2, MUC5AC, MUC5B, and MUC6 mucins in colorectal cancers and their association with the CpG island methylator phenotype. |
| Q34209800 | FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer |
| Q37594336 | FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium |
| Q33949054 | FMR1 intron 1 methylation predicts FMRP expression in blood of female carriers of expanded FMR1 alleles |
| Q36886224 | Factors in childhood as predictors of asthma in adult life |
| Q45201853 | Factors influencing asthma remission: a longitudinal study from childhood to middle age. |
| Q57265888 | Familial Patterns of Covariation for Cardiovascular Risk Factors in Adults: The Victorian Family Heart Study |
| Q57306010 | Familial Risks, Early-Onset Breast Cancer, and BRCA1 and BRCA2 Germline Mutations |
| Q44325842 | Familial aggregation of a disease consequent upon correlation between relatives in a risk factor measured on a continuous scale |
| Q52553115 | Familial and genomic analyses of postural changes in systolic and diastolic blood pressure. |
| Q43256458 | Familial correlations in postmenopausal serum concentrations of sex steroid hormones and other mitogens: a twins and sisters study |
| Q71444475 | Familial temporal lobe epilepsy: a common disorder identified in twins |
| Q37308563 | Family history of breast cancer and all-cause mortality after breast cancer diagnosis in the Breast Cancer Family Registry |
| Q33625221 | Family history of colorectal cancer in BRAF p.V600E-mutated colorectal cancer cases |
| Q57265514 | Family history-based colorectal cancer screening in Australia: A modelling study of the costs, benefits, and harms of different participation scenarios |
| Q45137915 | Family-based association study of IGF1 microsatellites and height, weight, and body mass index |
| Q51811339 | Family-based genetic association study of insulin-like growth factor I microsatellite markers and premenopausal breast cancer risk. |
| Q36397847 | Female Hormonal Factors and the Risk of Endometrial Cancer in Lynch Syndrome |
| Q37236216 | Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs). |
| Q36068167 | Fine-Mapping of Common Genetic Variants Associated with Colorectal Tumor Risk Identified Potential Functional Variants |
| Q36111237 | Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus |
| Q35524465 | Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. |
| Q61230414 | Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes |
| Q92480972 | Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes |
| Q35056061 | Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes |
| Q35063160 | Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk |
| Q39844032 | Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer |
| Q36248936 | Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk |
| Q34903062 | Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1. |
| Q37367871 | Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1. |
| Q37002930 | Five endometrial cancer risk loci identified through genome-wide association analysis |
| Q34979715 | Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium |
| Q44768684 | Foods, nutrients and prostate cancer |
| Q44326161 | Fracture risk and height: an association partly accounted for by cortical porosity of relatively thinner cortices |
| Q39260899 | Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study |
| Q34756357 | Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases |
| Q44770755 | Frequency of ejaculation and risk of prostate cancer |
| Q46060108 | From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes |
| Q36124728 | Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus |
| Q36742577 | Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers |
| Q47822741 | Gene-based analysis of regulatory variants identifies 4 putative novel asthma risk genes related to nucleotide synthesis and signaling |
| Q34406143 | Gene-environment interaction involving recently identified colorectal cancer susceptibility Loci |
| Q40137431 | Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium |
| Q47812751 | Gene-wide association study between the aromatase gene (CYP19A1) and female pattern hair loss |
| Q74426396 | Genes and family environment explain correlations between blood pressure and body mass index |
| Q33994469 | Genes involved with folate uptake and distribution and their association with colorectal cancer risk |
| Q37389405 | Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer |
| Q41598426 | Genetic analysis of systolic blood pressure in Melbourne families |
| Q40363977 | Genetic and Environmental Causes of Variation in the Difference Between Biological Age Based on DNA Methylation and Chronological Age for Middle-Aged Women |
| Q38376969 | Genetic and Environmental Factors in Invasive Cervical Cancer: Design and Methods of a Classical Twin Study |
| Q57306006 | Genetic and Histopathologic Evaluation ofBRCA1andBRCA2DNA Sequence Variants of Unknown Clinical Significance |
| Q100943997 | Genetic and environmental causes of variation in epigenetic aging across the lifespan |
| Q54202681 | Genetic and environmental factors affecting birth size variation: a pooled individual-based analysis of secular trends and global geographical differences using 26 twin cohorts. |
| Q37503420 | Genetic and environmental influences on adult human height across birth cohorts from 1886 to 1994. |
| Q94687003 | Genetic and environmental influences on human height from infancy through adulthood at different levels of parental education |
| Q51802906 | Genetic and environmental influences on variation in balance performance among female twin pairs aged 21-82 years. |
| Q46653715 | Genetic and environmental variances of bone microarchitecture and bone remodeling markers: a twin study |
| Q60310914 | Genetic and environmental variation in Eysenck Personality Questionnaire scales measured on Australian adolescent twins |
| Q98164511 | Genetic and environmental variation in educational attainment: an individual-based analysis of 28 twin cohorts |
| Q35578513 | Genetic determinants of bone mass in adults. A twin study |
| Q35999323 | Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study |
| Q49111373 | Genetic factors associated with altered sodium transport in human hypertension: a twin study. |
| Q51611349 | Genetic factors in bone turnover. |
| Q37739048 | Genetic modifiers of CHEK2*1100delC-associated breast cancer risk |
| Q54940815 | Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. |
| Q90436522 | Genetic predictors of circulating 25-hydroxyvitamin D and prognosis after colorectal cancer |
| Q37281843 | Genetic predictors of circulating 25-hydroxyvitamin d and risk of colorectal cancer |
| Q35925620 | Genetic predisposition to ductal carcinoma in situ of the breast |
| Q35151684 | Genetic predisposition to in situ and invasive lobular carcinoma of the breast |
| Q52561250 | Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. |
| Q33586578 | Genetic variability in the MTHFR gene and colorectal cancer risk using the colorectal cancer family registry |
| Q100426886 | Genetic variants in the regulatory T cell related pathway and colorectal cancer prognosis |
| Q46432976 | Genetic variants in the vitamin D receptor gene and prostate cancer risk |
| Q26775022 | Genetic variants within the hTERT gene and the risk of colorectal cancer in Lynch syndrome |
| Q35022825 | Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers |
| Q35179897 | Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study |
| Q35078297 | Genetic variation in UGT genes modify the associations of NSAIDs with risk of colorectal cancer: colon cancer family registry |
| Q34378972 | Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade |
| Q36422109 | Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium |
| Q37332589 | Genetic variation in the inflammation and innate immunity pathways and colorectal cancer risk |
| Q33643330 | Genetic variation in the vitamin D receptor (VDR) and the vitamin D-binding protein (GC) and risk for colorectal cancer: results from the Colon Cancer Family Registry |
| Q34656420 | Genetic variations in SMAD7 are associated with colorectal cancer risk in the colon cancer family registry |
| Q74081659 | Genetic, common environment, and individual specific components of variance for bone mineral density in 10- to 26-year-old females: a twin study |
| Q43167965 | Genetic, functional, and histopathological evaluation of two C-terminal BRCA1 missense variants |
| Q30000080 | Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent |
| Q33609333 | Genetics for population and public health |
| Q40755776 | Genetics of asthma and hay fever in Australian twins. |
| Q34198753 | Genetics of epilepsy: The testimony of twins in the molecular era |
| Q38092403 | Genetics of febrile seizure subtypes and syndromes: a twin study |
| Q73485962 | Genetics of haemostasis |
| Q45024538 | Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21. |
| Q36159275 | Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer |
| Q39002788 | Genome-Wide Measures of Peripheral Blood Dna Methylation and Prostate Cancer Risk in a Prospective Nested Case-Control Study |
| Q28388497 | Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types |
| Q30313778 | Genome-wide analysis identifies 12 loci influencing human reproductive behavior |
| Q28305142 | Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype |
| Q36842233 | Genome-wide association analysis identifies three new breast cancer susceptibility loci |
| Q35996692 | Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer |
| Q63681757 | Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer |
| Q24622610 | Genome-wide association studies identify four ER negative-specific breast cancer risk loci |
| Q45068755 | Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci |
| Q95329367 | Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses |
| Q28943520 | Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 |
| Q35061252 | Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk |
| Q28924380 | Genome-wide association study identifies new prostate cancer susceptibility loci |
| Q24645441 | Genome-wide association study identifies novel breast cancer susceptibility loci |
| Q29417131 | Genome-wide association study identifies novel loci predisposing to cutaneous melanoma |
| Q37341178 | Genome-wide association study identifies three loci associated with melanoma risk |
| Q29416994 | Genome-wide association study identifies three new melanoma susceptibility loci |
| Q37140021 | Genome-wide association study of colorectal cancer identifies six new susceptibility loci |
| Q64040390 | Genome-wide association study of germline variants and breast cancer-specific mortality |
| Q91265679 | Genome-wide association study of peripheral blood DNA methylation and conventional mammographic density measures |
| Q51764859 | Genome-wide average DNA methylation is determined in utero. |
| Q29417001 | Genome-wide diet-gene interaction analyses for risk of colorectal cancer |
| Q36190531 | Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses |
| Q40636379 | Genome-wide measures of DNA methylation in peripheral blood and the risk of urothelial cell carcinoma: a prospective nested case-control study |
| Q34321689 | Genome-wide search for gene-gene interactions in colorectal cancer |
| Q63977685 | Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients With Lynch Syndrome |
| Q59566871 | Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility |
| Q38823212 | Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk |
| Q34949154 | Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study |
| Q33901605 | Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development |
| Q57265601 | Germline HOXB13 p.Gly84Glu mutation and risk of colorectal cancer |
| Q37337396 | Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study |
| Q35735103 | Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry |
| Q59756250 | Germline Variation and Breast Cancer Incidence: A Gene-Based Association Study and Whole-Genome Prediction of Early-Onset Breast Cancer |
| Q45733546 | Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women |
| Q40200164 | Global measures of peripheral blood-derived DNA methylation as a risk factor in the development of mature B-cell neoplasms |
| Q48178998 | Growing pains: twin family study evidence for genetic susceptibility and a genetic relationship with restless legs syndrome |
| Q57100233 | HFE C282Y Homozygosity Is Associated with an Increased Risk of Total Hip Replacement for Osteoarthritis |
| Q37274209 | HFE C282Y homozygotes are at increased risk of breast and colorectal cancer |
| Q37149526 | HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity |
| Q34101222 | HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 microg/L are at low risk of hemochromatosis |
| Q39247003 | HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women |
| Q36503369 | HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG). |
| Q57306020 | HRAS1 Rare Minisatellite Alleles and Breast Cancer in Australian Women Under Age Forty Years |
| Q42626992 | Hallux Valgus, By Nature or Nurture? A Twin Study |
| Q35382206 | Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers |
| Q57748112 | Heavy domestic, but not recreational, physical activity is associated with low back pain: Australian Twin low BACK pain (AUTBACK) study |
| Q57471595 | Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study |
| Q36276540 | Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization |
| Q46872589 | Heritability of macular thickness determined by optical coherence tomography |
| Q48611340 | Heritability of mammographic density, a risk factor for breast cancer. |
| Q52371352 | Heritable DNA methylation marks associated with susceptibility to breast cancer. |
| Q33330850 | Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics |
| Q35037312 | Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2 |
| Q34765405 | Hi-Plex targeted sequencing is effective using DNA derived from archival dried blood spots |
| Q39597471 | High and low mammographic density human breast tissues maintain histological differential in murine tissue engineering chambers |
| Q35247458 | High performance computing enabling exhaustive analysis of higher order single nucleotide polymorphism interaction in Genome Wide Association Studies |
| Q40502668 | Histological markers that predict clinical recurrence in ductal carcinoma in situ of the breast: an Australian population-based study |
| Q28596814 | Hormonal contraception increases risk of asthma among obese but decreases it among nonobese subjects: a prospective, population-based cohort study |
| Q57265814 | Hormone Replacement Therapy, Percent Mammographic Density, and Sensitivity of Mammography |
| Q57265782 | Hormone therapy and breast cancer: what factors modify the association? |
| Q71382176 | Hot flushes, menstrual status, and hormone levels in a population-based sample of midlife women |
| Q45288967 | House dust mite sensitization in toddlers predicts current wheeze at age 12 years |
| Q45965999 | How do individuals decide whether to accept or decline an offer of genetic testing for colorectal cancer? |
| Q37639436 | How do researchers manage genetic results in practice? The experience of the multinational Colon Cancer Family Registry |
| Q35225559 | How do women at increased, but unexplained, familial risk of breast cancer perceive and manage their risk? A qualitative interview study |
| Q39409779 | Hyperinsulinaemia and obesity in aborigines of south-eastern Australia, with comparisons from rural and urban Europid populations |
| Q35102646 | Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk |
| Q29417155 | Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array |
| Q29416993 | Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis |
| Q29417065 | Identification of IL6R and chromosome 11q13.5 as risk loci for asthma |
| Q37416078 | Identification of Lynch syndrome among patients with colorectal cancer |
| Q37004125 | Identification of STOML2 as a putative novel asthma risk gene associated with IL6R. |
| Q37008880 | Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk |
| Q36069872 | Identification of a common variant with potential pleiotropic effect on risk of inflammatory bowel disease and colorectal cancer |
| Q29417013 | Identification of a melanoma susceptibility locus and somatic mutation in TET2. |
| Q36062033 | Identification of a novel percent mammographic density locus at 12q24. |
| Q34975918 | Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript |
| Q39321320 | Identification of fifteen novel germline variants in the BRCA1 3'UTR reveals a variant in a breast cancer case that introduces a functional miR-103 target site |
| Q36859142 | Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer |
| Q36086247 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus |
| Q37074763 | Identification of new genetic risk factors for prostate cancer |
| Q34038964 | Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions |
| Q57170142 | Identification of nine new susceptibility loci for endometrial cancer |
| Q36014067 | Identification of novel genetic markers of breast cancer survival |
| Q29417022 | Identification of seven new prostate cancer susceptibility loci through a genome-wide association study |
| Q34048230 | Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis |
| Q46103372 | Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer |
| Q57305995 | Image-guided sampling reveals increased stroma and lower glandular complexity in mammographically dense breast tissue |
| Q36335636 | Immunohistochemical testing of conventional adenomas for loss of expression of mismatch repair proteins in Lynch syndrome mutation carriers: a case series from the Australasian site of the colon cancer family registry |
| Q39314150 | Impaired glucose tolerance, hyperinsulinemia, and hypertriglyceridemia in Australian aborigines from the desert |
| Q38912872 | Improved quality of risk-reducing salpingo-oophorectomy in Australasian women at high risk of pelvic serous cancer |
| Q57265784 | In Reply: |
| Q34185064 | Incorporation of twins in the regressive logistic model for pedigree disease data |
| Q40686588 | Increase in the self-reported prevalence of asthma and hay fever in adults over the last generation: a matched parent-offspring study. |
| Q53400538 | Increased COX-2 expression in epithelial and stromal cells of high mammographic density tissues and in a xenograft model of mammographic density. |
| Q34250215 | Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations |
| Q37708268 | Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry |
| Q57305946 | Inference about causation between body mass index and DNA methylation in blood from a twin family study |
| Q34249252 | Inference about causation from examination of familial confounding: application to longitudinal twin data on mammographic density measures that predict breast cancer risk |
| Q43199954 | Influence of high-dose estrogen exposure during adolescence on mammographic density for age in adulthood |
| Q50352967 | InforMD: a new initiative to raise public awareness about breast density. |
| Q35104068 | Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer |
| Q44509051 | Innovations in the statistical analysis of twin studies. |
| Q48503138 | Interaction between polymorphisms in aspirin metabolic pathways, regular aspirin use and colorectal cancer risk: A case-control study in unselected white European populations. |
| Q57265634 | Interleukin-6 promoter variants, prostate cancer risk, and survival |
| Q51579135 | International Consortium on Mammographic Density: Methodology and population diversity captured across 22 countries. |
| Q35458070 | International network of twin registries (INTR): building a platform for international collaboration |
| Q90690238 | Interval breast cancer risk associations with breast density, family history and breast tissue aging |
| Q34898735 | Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors |
| Q28264901 | Iron-overload-related disease in HFE hereditary hemochromatosis |
| Q57265722 | Is BRCA2 c.9079 G > A a predisposing variant for early onset breast cancer? |
| Q53227682 | Is MSH2 a breast cancer susceptibility gene? |
| Q50109358 | Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations? |
| Q57265815 | Is There Overlap Between the Genetic Determinants of Mammographic Density and Bone Mineral Density? |
| Q58417105 | Is benign rolandic epilepsy genetically determined? |
| Q39581403 | Is breast cancer risk associated with alcohol intake before first full-term pregnancy? |
| Q36225575 | Is childhood immunisation associated with atopic disease from age 7 to 32 years? |
| Q34480659 | Is there a positive association between mammographic density and bone mineral density? |
| Q38955532 | Is this back pain killing me? All-cause and cardiovascular-specific mortality in older Danish twins with spinal pain |
| Q64279327 | Joint association of mammographic density adjusted for age and body mass index and polygenic risk score with breast cancer risk |
| Q47190168 | Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium |
| Q36254149 | Key concepts in genetic epidemiology |
| Q97595643 | Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival |
| Q57191573 | Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair |
| Q28267893 | Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair |
| Q29416989 | Large-scale genotyping identifies 41 new loci associated with breast cancer risk |
| Q46590053 | Lifetime alcohol consumption and upper aero-digestive tract cancer risk in the Melbourne Collaborative Cohort Study |
| Q47646485 | Lifetime alcohol intake and risk of non-Hodgkin lymphoma: Findings from the Melbourne Collaborative Cohort Study |
| Q39102623 | Lifetime alcohol intake is associated with an increased risk of KRAS+ and BRAF-/KRAS- but not BRAF+ colorectal cancer |
| Q52220393 | Likelihood-based approach to estimating twin concordance for dichotomous traits. |
| Q43843244 | Limited influence of germline genetic variation on all-cause mortality in women with early onset breast cancer: evidence from gene-based tests, single-marker regression, and whole-genome prediction |
| Q35000837 | Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome). |
| Q24802704 | Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA) |
| Q39035043 | Longitudinal Study of Mammographic Density Measures That Predict Breast Cancer Risk |
| Q52456412 | Longitudinal analysis of lung function growth in healthy children and adolescents. |
| Q35119701 | Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium |
| Q53345216 | Low somatic K-ras mutation frequency in colorectal cancer diagnosed under the age of 45 years. |
| Q24618839 | Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X |
| Q34375540 | Lynch syndrome-associated breast cancers do not overexpress chromosome 11-encoded mucins |
| Q33767027 | Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry |
| Q35019782 | MC1R genotype as a predictor of early-onset melanoma, compared with self-reported and physician-measured traditional risk factors: an Australian case-control-family study |
| Q35088518 | MC1R genotypes and risk of melanoma before age 40 years: a population-based case-control-family study |
| Q57265792 | Macrophage Inhibitory Cytokine-1 H6D Polymorphism, Prostate Cancer Risk, and Survival |
| Q44439883 | Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer |
| Q48729158 | Magnetic resonance imaging and late-onset epilepsy. |
| Q36043843 | Mammographic breast density and breast cancer: evidence of a shared genetic basis |
| Q36274404 | Mammographic breast density as an intermediate phenotype for breast cancer |
| Q48596722 | Mammographic densities during the menopausal transition: a longitudinal study of Australian-born women |
| Q33859833 | Mammographic density and ageing: A collaborative pooled analysis of cross-sectional data from 22 countries worldwide |
| Q44758736 | Mammographic density and candidate gene variants: a twins and sisters study |
| Q37018080 | Mammographic density and risk of breast cancer by mode of detection and tumor size: a case-control study |
| Q47116028 | Mammographic density and risk of breast cancer by tumor characteristics: a case-control study |
| Q40232863 | Mammographic density and risk of breast cancer in Korean women |
| Q37517477 | Mammographic density assessed on paired raw and processed digital images and on paired screen-film and digital images across three mammography systems |
| Q41010078 | Mammographic density defined by higher than conventional brightness thresholds better predicts breast cancer risk |
| Q36057738 | Mammographic density phenotypes and risk of breast cancer: a meta-analysis |
| Q38194952 | Mammographic density-a review on the current understanding of its association with breast cancer |
| Q37358052 | Mammographic density: a heritable risk factor for breast cancer |
| Q36337267 | Meanings of abortion in context: accounts of abortion in the lives of women diagnosed with breast cancer |
| Q36373793 | Measures of familial aggregation depend on definition of family history: meta-analysis for colorectal cancer |
| Q37123422 | Measuring, and identifying predictors of women's perceptions of three types of breast cancer risk: population risk, absolute risk and comparative risk |
| Q74459833 | Mechanisms of bone loss following allogeneic and autologous hemopoietic stem cell transplantation |
| Q38463411 | Medical radiation exposure and breast cancer risk: findings from the Breast Cancer Family Registry |
| Q56435948 | Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK |
| Q35815677 | Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk |
| Q89685277 | Mendelian Randomization of Circulating Polyunsaturated Fatty Acids and Colorectal Cancer Risk |
| Q37100729 | Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer |
| Q30252873 | Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer |
| Q56089167 | Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer |
| Q114182490 | Mendelian randomisation study of smoking exposure in relation to breast cancer risk |
| Q93370418 | Mendelian randomization analysis of C-reactive protein on colorectal cancer risk |
| Q35784595 | Mendelian randomization study of height and risk of colorectal cancer |
| Q70512162 | Menopausal symptoms in Australian women |
| Q50016433 | Menopause-Related Appendicular Bone Loss is Mainly Cortical and Results in Increased Cortical Porosity. |
| Q34091855 | Meta-analysis of 8q24 for seven cancers reveals a locus between NOV and ENPP2 associated with cancer development |
| Q36333368 | Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. |
| Q35670184 | Meta-analysis of new genome-wide association studies of colorectal cancer risk |
| Q30558412 | Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery |
| Q36208014 | Methylation of Breast Cancer Predisposition Genes in Early-Onset Breast Cancer: Australian Breast Cancer Family Registry |
| Q34497352 | MicroRNA related polymorphisms and breast cancer risk |
| Q57265760 | Microsatellite Instability Markers for Identifying Early-Onset Colorectal Cancers Caused by Germ-Line Mutations in DNA Mismatch Repair Genes |
| Q47973656 | Misperceptions of ovarian cancer risk in women at increased risk for hereditary ovarian cancer |
| Q34123806 | Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls |
| Q42698804 | Modeling the probability that Ashkenazi Jewish women carry a founder mutation in BRCA1 or BRCA2. |
| Q57305979 | Molecular Characterization and Cancer Risk Associated with BRCA1 and BRCA2 Splice Site Variants Identified in Multiple-Case Breast Cancer Families |
| Q57306007 | Molecular characterization and cancer risk associated withBRCA1 andBRCA2 splice site variants identified in multiple-case breast cancer families |
| Q37066133 | Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening |
| Q39926554 | Mother's smoking and complex lung function of offspring in middle age: A cohort study from childhood |
| Q24658557 | Multigene testing of moderate-risk genes: be mindful of the missense |
| Q21144952 | Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer |
| Q36897003 | Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer |
| Q50582715 | Multiple loci on 8q24 associated with prostate cancer susceptibility. |
| Q33988405 | Multiple loci with different cancer specificities within the 8q24 gene desert |
| Q28268180 | Multiple newly identified loci associated with prostate cancer susceptibility |
| Q30491647 | Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium |
| Q40808150 | Multivitamin, calcium and folic acid supplements and the risk of colorectal cancer in Lynch syndrome |
| Q36087551 | Mutation deep within an intron of MSH2 causes Lynch syndrome |
| Q35972599 | Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry |
| Q36853854 | Nandrolone decanoate and intranasal calcitonin as therapy in established osteoporosis |
| Q36663501 | Natural history of HFE simple heterozygosity for C282Y and H63D: a prospective 12-year study |
| Q38075521 | Nature or nurture in low back pain? Results of a systematic review of studies based on twin samples |
| Q37356243 | Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. |
| Q57265727 | No Association between Common Chemokine and Chemokine Receptor Gene Variants and Prostate Cancer Risk |
| Q30374367 | No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. |
| Q24800108 | No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer |
| Q48064622 | No evidence of MMTV-like env sequences in specimens from the Australian Breast Cancer Family Study |
| Q34642008 | No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk |
| Q37308596 | No evidence that GATA3 rs570613 SNP modifies breast cancer risk |
| Q37079859 | No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing |
| Q44122211 | No increased risk of breast cancer associated with alcohol consumption among carriers of BRCA1 and BRCA2 mutations ages <50 years |
| Q45834583 | No strong association between second to fourth digit ratio (2D:4D) and adult anthropometric measures with emphasis on adiposity |
| Q35752042 | Novel Associations between Common Breast Cancer Susceptibility Variants and Risk-Predicting Mammographic Density Measures |
| Q56359054 | Novel Common Genetic Susceptibility Loci for Colorectal Cancer |
| Q47248476 | Novel associations between blood DNA methylation and body mass index in middle-aged and older adults |
| Q44766689 | Obesity and outcomes in premenopausal and postmenopausal breast cancer |
| Q51599913 | Obesity, diabetes, and hyperlipidemia in a central Australian aboriginal community with a long history of acculturation. |
| Q58416998 | Obstetric Events as a Risk Factor for Febrile Seizures: A Community-Based Twin Study |
| Q91557009 | Occupational exposure to solvents and lung function decline: A population based study |
| Q53559785 | Occupational exposures to solvents and metals are associated with fixed airflow obstruction. |
| Q36591738 | Odds per adjusted standard deviation: comparing strengths of associations for risk factors measured on different scales and across diseases and populations |
| Q36696565 | Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations |
| Q34398269 | Oral contraceptive use and risk of early-onset breast cancer in carriers and noncarriers of BRCA1 and BRCA2 mutations |
| Q45898816 | P-236Screening practices of Australians at population and familial risk following the partial roll-out of the National Bowel Cancer Screening Program, 2009-2012. |
| Q28584533 | PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS |
| Q47143943 | PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1. |
| Q34778710 | PIK3CA activating mutation in colorectal carcinoma: associations with molecular features and survival |
| Q33879359 | Parent of origin effects on age at colorectal cancer diagnosis |
| Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
| Q64126036 | Parental Education and Genetics of BMI from Infancy to Old Age: A Pooled Analysis of 29 Twin Cohorts |
| Q51807648 | Parity and decreased use of oral contraceptives as predictors of asthma in young women. |
| Q34061135 | Past recreational physical activity, body size, and all-cause mortality following breast cancer diagnosis: results from the Breast Cancer Family Registry |
| Q34102606 | Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study |
| Q43707600 | Pedigree analysis of blood pressure in subjects from rural Greece and relatives who migrated to Melbourne, Australia |
| Q27851443 | Penetrance analysis of the PALB2 c.1592delT founder mutation |
| Q37337361 | Perceived versus predicted risks of colorectal cancer and self-reported colonoscopies by members of mismatch repair gene mutation-carrying families who have declined genetic testing |
| Q36094483 | Performance of PREMM(1,2,6), MMRpredict, and MMRpro in detecting Lynch syndrome among endometrial cancer cases |
| Q35965705 | Phenotype and polyp landscape in serrated polyposis syndrome: a series of 100 patients from genetics clinics |
| Q33820828 | Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study |
| Q89454638 | Physical activity and risks of breast and colorectal cancer: a Mendelian randomisation analysis |
| Q44277666 | Physical activity, body size and composition, and risk of ovarian cancer |
| Q34059662 | Plasma concentration of Propionibacterium acnes antibodies and prostate cancer risk: results from an Australian population-based case-control study |
| Q45350463 | Plasma phospholipid fatty acids, dietary fatty acids and prostate cancer risk |
| Q37570238 | Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia |
| Q62583133 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes |
| Q41495374 | Polymorphisms affecting vitamin D-binding protein modify the relationship between serum vitamin D (25[OH]D3) and food allergy |
| Q36066735 | Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression |
| Q47590869 | Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics |
| Q34606248 | Population-based estimate of prostate cancer risk for carriers of the HOXB13 missense mutation G84E. |
| Q73022855 | Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein-truncating mutations in BRCA1 and BRCA2. Australian Breast Cancer Family Study |
| Q35587015 | Population-based estimate of the contribution of TP53 mutations to subgroups of early-onset breast cancer: Australian Breast Cancer Family Study |
| Q45062920 | Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry |
| Q36287185 | Population-based family studies in genetic epidemiology |
| Q33566677 | Population-based, case-control-family design to investigate genetic and environmental influences on melanoma risk: Australian Melanoma Family Study |
| Q30674792 | Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin data |
| Q36009831 | Practical problems with clinical guidelines for breast cancer prevention based on remaining lifetime risk |
| Q37353677 | Prediagnosis reproductive factors and all-cause mortality for women with breast cancer in the breast cancer family registry |
| Q34102617 | Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models |
| Q60044938 | Predicting interval and screen-detected breast cancers from mammographic density defined by different brightness thresholds |
| Q92055460 | Prediction and clinical utility of a contralateral breast cancer risk model |
| Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
| Q40986564 | Prediction of functional outcome and tissue loss in acute cortical infarction |
| Q37179473 | Predictors of mammographic density: insights gained from a novel regression analysis of a twin study |
| Q40414575 | Predictors of participation in clinical and psychosocial follow-up of the kConFab breast cancer family cohort |
| Q46561468 | Predictors of the use of complementary and alternative medicine (CAM) by women at high risk for breast cancer |
| Q36176973 | Preterm birth and low birth weight continue to increase the risk of asthma from age 7 to 43. |
| Q30275554 | Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer |
| Q35180844 | Prevalence and predictors of germline CDKN2A mutations for melanoma cases from Australia, Spain and the United Kingdom |
| Q36903452 | Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families |
| Q57265876 | Prevalence of self-reported arm morbidity following treatment for breast cancer in the Australian Breast Cancer Family Study |
| Q38614073 | Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis |
| Q57306049 | Progesterone receptor polymorphisms and risk of breast cancer: results from two Australian breast cancer studies |
| Q57265847 | Prognosis of Premenopausal Breast Cancer and Childbirth Prior to Diagnosis |
| Q37185723 | Prospective validation of the breast cancer risk prediction model BOADICEA and a batch-mode version BOADICEACentre |
| Q49072154 | Prospectively measured levels of serum follicle-stimulating hormone, estradiol, and the dimeric inhibins during the menopausal transition in a population-based cohort of women. |
| Q57265692 | Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studies |
| Q37331108 | Prostate screening uptake in Australian BRCA1 and BRCA2 carriers |
| Q38820804 | Protective and Harmful Effects of Physical Activity for Low Back Pain: A Protocol for the AUstralian Twin BACK Pain (AUTBACK) Feasibility Study |
| Q37121690 | Psychosocial factors and survival of young women with breast cancer: a population-based prospective cohort study |
| Q35046454 | Public health aspects of genetic screening for hereditary haemochromatosis in Australia |
| Q52978550 | Publication policy or publication bias? |
| Q55508030 | Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation. |
| Q90242034 | Publisher Correction: Shared heritability and functional enrichment across six solid cancers |
| Q36178929 | Pulmonary function after bone marrow transplantation for chronic myeloid leukaemia. |
| Q34801092 | Quality assessment and correlation of microsatellite instability and immunohistochemical markers among population- and clinic-based colorectal tumors results from the Colon Cancer Family Registry |
| Q35648055 | Quantifying the cumulative effect of low-penetrance genetic variants on breast cancer risk |
| Q34540638 | RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study |
| Q36009422 | RAD51B in Familial Breast Cancer |
| Q61132086 | RESPONSE LETTER TO DR. GAU ET AL |
| Q73740231 | RESPONSE: re: HRAS1 rare minisatellite alleles and breast cancer in australian women under age forty years |
| Q28652308 | Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study |
| Q28652056 | Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers |
| Q28730692 | Rare mutations in XRCC2 increase the risk of breast cancer |
| Q35608690 | Rare variants in the ATM gene and risk of breast cancer |
| Q37373918 | Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer |
| Q28743906 | Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study |
| Q36790169 | Rationale for, and approach to, studying modifiers of risk in persons with a genetic predisposition to colorectal cancer |
| Q57265799 | Rationale for, and approach to, studying modifiers of risk in persons with a genetic predisposition to colorectal cancer |
| Q52041110 | Re: "Presenting statistical uncertainty in trends and dose-response relations". |
| Q54331515 | Re: Microsatellite instability and BRAF mutation testing in colorectal cancer prognostication. |
| Q45151860 | Re: On the use of familial aggregation in population-based case probands for calculating penetrance |
| Q73600014 | Re: Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers |
| Q56611123 | Re: Prospective Studies of Dairy Product and Calcium Intakes and Prostate Cancer Risk: A Meta-Analysis |
| Q57265637 | Reasons for ongoing participation in a longitudinal cohort study |
| Q90439909 | Recreational Physical Activity Is Associated with Reduced Breast Cancer Risk in Adult Women at High Risk for Breast Cancer: A Cohort Study of Women Selected for Familial and Genetic Risk |
| Q34964012 | Red meat intake, NAT2, and risk of colorectal cancer: a pooled analysis of 11 studies |
| Q50787795 | Red meat, chicken, and fish consumption and risk of colorectal cancer. |
| Q72113471 | Reduced femoral neck bone density in the daughters of women with hip fractures: the role of low peak bone density in the pathogenesis of osteoporosis |
| Q56436732 | Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer |
| Q48018693 | Regressive logistic and proportional hazards disease models for within-family analyses of measured genotypes, with application to a CYP17 polymorphism and breast cancer |
| Q42658024 | Regressive logistic modeling of familial aggregation for asthma in 7,394 population-based nuclear families |
| Q64101959 | Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study |
| Q50908249 | Relationship of endogenous sex hormones to lipids and blood pressure in mid-aged women. |
| Q37125404 | Reliability of DNA methylation measures from dried blood spots and mononuclear cells using the HumanMethylation450k BeadArray |
| Q51421695 | Remodeling markers are associated with larger intracortical surface area but smaller trabecular surface area: a twin study. |
| Q57305959 | Reply |
| Q43232465 | Reply to comment on: 'Second to fourth digit ratio (2D:4D), breast cancer risk factors, and breast cancer risk: a prospective cohort study'. |
| Q47160276 | Reproductive factors as risk modifiers of breast cancer in BRCA mutation carriers and high-risk non-carriers |
| Q45951126 | Reproductive profiles and risk of breast cancer subtypes: a multi-center case-only study. |
| Q37632099 | Reproductive risk factors and oestrogen/progesterone receptor-negative breast cancer in the Breast Cancer Family Registry |
| Q54309392 | Results of a genome-wide linkage analysis in prostate cancer families ascertained through the ACTANE consortium. |
| Q40925733 | Retired elite female ballet dancers and nonathletic controls have similar bone mineral density at weightbearing sites |
| Q57789353 | Revised Australian national guidelines for colorectal cancer screening: family history |
| Q35815958 | Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci |
| Q47638801 | Risk factors and preventive strategies for breast cancer. |
| Q48555890 | Risk factors for breast cancer associated with mammographic features in Singaporean chinese women. |
| Q36671526 | Risk factors for breast cancer in young women by oestrogen receptor and progesterone receptor status |
| Q33641289 | Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics |
| Q39162382 | Risk factors for low back pain: insights from a novel case-control twin study |
| Q40789385 | Risk factors for metachronous colorectal cancer following a primary colorectal cancer: A prospective cohort study. |
| Q35750765 | Risk factors for uncommon histologic subtypes of breast cancer using centralized pathology review in the Breast Cancer Family Registry |
| Q37710973 | Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer |
| Q43793012 | Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study |
| Q37300024 | Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042. |
| Q33699887 | Risk of metachronous colon cancer following surgery for rectal cancer in mismatch repair gene mutation carriers |
| Q37085786 | Risk of pancreatic cancer in breast cancer families from the breast cancer family registry |
| Q57265859 | Risk of prostate cancer associated with a family history in an era of rapid increase in prostate cancer diagnosis (Australia) |
| Q38627833 | Risk of uterine cancer for BRCA1 and BRCA2 mutation carriers |
| Q37968395 | Risk prediction models for colorectal cancer: a review |
| Q50787592 | Risk-reducing surgery, screening and chemoprevention practices of BRCA1 and BRCA2 mutation carriers: a prospective cohort study. |
| Q38717239 | Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers |
| Q30492977 | Risks of Lynch syndrome cancers for MSH6 mutation carriers |
| Q46763659 | Risks of cancers for carriers of monoallelic MUTYH mutation with a family history of colorectal cancer |
| Q36621452 | Risks of colorectal and other cancers after endometrial cancer for women with Lynch syndrome |
| Q36486798 | Risks of primary extracolonic cancers following colorectal cancer in lynch syndrome |
| Q34266707 | Role of tumour molecular and pathology features to estimate colorectal cancer risk for first-degree relatives |
| Q36545934 | SNP-SNP interaction analysis of NF-κB signaling pathway on breast cancer survival |
| Q36322904 | SNPs and breast cancer risk prediction for African American and Hispanic women |
| Q38108742 | Screening participation for people at increased risk of colorectal cancer due to family history: a systematic review and meta-analysis |
| Q38099956 | Screening participation predictors for people at familial risk of colorectal cancer: a systematic review |
| Q36429192 | Screening practices of Australian men and women categorized as "at or slightly above average risk" of colorectal cancer |
| Q35739938 | Screening practices of unaffected people at familial risk of colorectal cancer |
| Q34628788 | Second to fourth digit ratio (2D:4D) and concentrations of circulating sex hormones in adulthood |
| Q35212668 | Second to fourth digit ratio (2D:4D) and prostate cancer risk in the Melbourne Collaborative Cohort Study |
| Q36385301 | Second to fourth digit ratio (2D:4D), breast cancer risk factors, and breast cancer risk: a prospective cohort study |
| Q34020691 | Segregation analyses of 1,476 population-based Australian families affected by prostate cancer |
| Q40603558 | Sensitization to milk, egg and peanut from birth to 18 years: A longitudinal study of a cohort at risk of allergic disease |
| Q59654873 | Serum Vitamin D and Falls in Older Women in Residential Care in Australia |
| Q29417074 | Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study |
| Q21999082 | Sexual factors and prostate cancer |
| Q50964155 | Sexuality, hormones and the menopausal transition. |
| Q61118451 | Shared heritability and functional enrichment across six solid cancers |
| Q64004349 | Shared heritability and functional enrichment across six solid cancers |
| Q46793899 | Should older people in residential care receive vitamin D to prevent falls? Results of a randomized trial |
| Q51118570 | Should the grading of colorectal adenocarcinoma include microsatellite instability status? |
| Q33658220 | Smoking and colorectal cancer in Lynch syndrome: results from the Colon Cancer Family Registry and the University of Texas M.D. Anderson Cancer Center |
| Q56995007 | Smoking and prostate cancer: Findings from an Australian case-control study |
| Q36567692 | Socio-economic status and survival from breast cancer for young, Australian, urban women |
| Q50137108 | Socioeconomic status and cancer mortality and incidence in Melbourne. |
| Q36405971 | Somatic mutations of the coding microsatellites within the beta-2-microglobulin gene in mismatch repair-deficient colorectal cancers and adenomas |
| Q57306051 | Stability of BAT26 in Lynch syndrome colorectal tumours |
| Q98394077 | Stochastic epigenetic mutations are associated with risk of breast cancer, lung cancer and mature B-cell neoplasms |
| Q71477306 | Streptokinase increases luxury perfusion after stroke |
| Q36960378 | Stroke topography and outcome in relation to hyperglycaemia and diabetes |
| Q43076184 | Suggestive evidence for a site specific prostate cancer gene on chromosome 1p36. The CRC/BPG UK Familial Prostate Cancer Study Coordinators and Collaborators. The EU Biomed Collaborators |
| Q34128569 | Sunbed use during adolescence and early adulthood is associated with increased risk of early-onset melanoma |
| Q90355497 | Sunscreen Use and Melanoma Risk Among Young Australian Adults |
| Q34568530 | Supercomputing enabling exhaustive statistical analysis of genome wide association study data: Preliminary results |
| Q33566957 | TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer |
| Q37122297 | Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers |
| Q38842051 | Testing for Gene-Environment Interactions Using a Prospective Family Cohort Design: Body Mass Index in Early and Later Adulthood and Risk of Breast Cancer. |
| Q33534461 | The 4q27 locus and prostate cancer risk |
| Q24810265 | The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women |
| Q69576158 | The Australian NHMRC Twin Registry. A resource for the Australian scientific community |
| Q30882439 | The Australian Twin Registry |
| Q46594966 | The BARD1 Cys557Ser polymorphism and breast cancer risk: an Australian case-control and family analysis |
| Q36615665 | The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions |
| Q43754304 | The BRCA2 372 HH genotype is associated with risk of breast cancer in Australian women under age 60 years. |
| Q49817640 | The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity. |
| Q24806109 | The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer |
| Q36417802 | The CODATwins Project: The Cohort Description of Collaborative Project of Development of Anthropometrical Measures in Twins to Study Macro-Environmental Variation in Genetic and Environmental Effects on Anthropometric Traits |
| Q57265871 | The CYP3A4*1B polymorphism has no functional significance and is not associated with risk of breast or ovarian cancer |
| Q40700905 | The Charles Perkins Centre's Twins Research Node |
| Q91178389 | The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer |
| Q64116004 | The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With or Mutations |
| Q47348286 | The Mental Adjustment to Cancer (MAC) scale: replication and refinement in 632 breast cancer patients |
| Q57265735 | The RAD51D E233G variant and breast cancer risk: population-based and clinic-based family studies of Australian women |
| Q35781316 | The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients |
| Q51129428 | The age of puberty determines sexual dimorphism in bone structure: a male/female co-twin control study. |
| Q24797305 | The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers |
| Q37391248 | The association of tumor microsatellite instability phenotype with family history of colorectal cancer |
| Q40723364 | The associations between childhood asthma and atopy, and parental asthma, hay fever and smoking |
| Q51182041 | The biology of panic-genetic evidence. |
| Q72714387 | The bone density of female twins discordant for tobacco use |
| Q24655454 | The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations |
| Q53335555 | The common variant rs1447295 on chromosome 8q24 and prostate cancer risk: results from an Australian population-based case-control study. |
| Q67558093 | The effect of aging on intact PTH and bone density in women |
| Q72607251 | The effect of pregnancy on the epilepsies: a study of 37 pregnancies |
| Q51620165 | The effects of diet differing in fat, carbohydrate, and fiber on carbohydrate and lipid metabolism in type II diabetes. |
| Q33178370 | The effects of gonadectomy on bone size, mass, and volumetric density in growing rats are gender-, site-, and growth hormone-specific |
| Q51048048 | The endocrinology of the menopausal transition: a cross-sectional study of a population-based sample. |
| Q43480606 | The heritability of mammographically dense and nondense breast tissue |
| Q46112463 | The heritability of prostate cancer—letter |
| Q61974616 | The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations |
| Q58198339 | The iPrevent Online Breast Cancer Risk Assessment and Risk Management Tool: Usability and Acceptability Testing |
| Q37681773 | The interaction between farming/rural environment and TLR2, TLR4, TLR6 and CD14 genetic polymorphisms in relation to early- and late-onset asthma |
| Q46096589 | The interplay between the effects of lifetime asthma, smoking, and atopy on fixed airflow obstruction in middle age. |
| Q24806016 | The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia |
| Q51439350 | The natural history of serum iron indices for HFE C282Y homozygosity associated with hereditary hemochromatosis. |
| Q35476902 | The potential value of sibling controls compared with population controls for association studies of lifestyle-related risk factors: an example from the Breast Cancer Family Registry |
| Q40091643 | The prevalence and risk factors of epiretinal membranes: the Melbourne Collaborative Cohort Study |
| Q68110886 | The prevalence of glucose intolerance in aborigines and Europids of south-eastern Australia |
| Q43993679 | The progesterone receptor exon 4 Val660Leu G/T polymorphism and risk of breast cancer in Australian women. |
| Q35587027 | The role of SMAD4 in early-onset colorectal cancer |
| Q52282627 | The role of genes in tobacco smoking during adolescence and young adulthood: a multivariate behaviour genetic investigation. |
| Q36142060 | The role of genetic breast cancer susceptibility variants as prognostic factors |
| Q38025481 | The roles of genetic and environmental factors on risk of cervical cancer: a review of classical twin studies |
| Q46912143 | The rs743572 common variant in the promoter of CYP17A1 is not associated with prostate cancer risk or circulating hormonal levels |
| Q43829398 | The steroid 5alpha-reductase type II TA repeat polymorphism is not associated with risk of breast or ovarian cancer in Australian women. |
| Q39393845 | The treatment-seeking woman at menopause |
| Q34622507 | The use of DNA from archival dried blood spots with the Infinium HumanMethylation450 array |
| Q51004176 | The value of the Hospital Anxiety and Depression Scale (HADS) for comparing women with early onset breast cancer with population-based reference women. |
| Q35799767 | Tools for translational epigenetic studies involving formalin-fixed paraffin-embedded human tissue: applying the Infinium HumanMethyation450 Beadchip assay to large population-based studies |
| Q40239027 | Total and beverage-specific alcohol intake and the risk of aggressive prostate cancer: a case-control study |
| Q51887153 | Towards more effective and equitable genetic testing for BRCA1 and BRCA2 mutation carriers. |
| Q38407261 | Tracing 8,600 participants 36 years after recruitment at age seven for the Tasmanian Asthma Study |
| Q34270911 | Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. |
| Q89961489 | Transcriptome-wide association study of breast cancer risk by estrogen-receptor status |
| Q41368391 | Transitioning to routine breast cancer risk assessment and management in primary care: what can we learn from cardiovascular disease? |
| Q51828985 | Tumor characteristics and family history in relation to mammographic density and breast cancer: The French E3N cohort. |
| Q40713486 | Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts |
| Q36924465 | Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry |
| Q37003285 | Tumour morphology predicts PALB2 germline mutation status |
| Q40080751 | Twin birth changes DNA methylation of subsequent siblings |
| Q36622764 | Twin concordance for a binary trait. I. Statistical models illustrated with data on drinking status |
| Q35200130 | Twin concordance for a binary trait. II. Nested analysis of ever-smoking and ex-smoking traits and unnested analysis of a "committed-smoking" trait |
| Q40767111 | Twin concordance for a binary trait: III. A bivariate analysis of hay fever and asthma |
| Q48513343 | Twin studies for the prognosis, prevention and treatment of musculoskeletal conditions. |
| Q57242585 | Twin study of genetic and environmental influences on adult body size, shape and composition |
| Q43703848 | Twin study of genetic and environmental influences on glucose tolerance and indices of insulin sensitivity and secretion |
| Q37401258 | Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project |
| Q51974477 | Two ATM variants and breast cancer risk. |
| Q92994868 | Two truncating variants in FANCC and breast cancer risk |
| Q57265834 | Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer |
| Q37583398 | Use of a Novel Nonparametric Version of DEPTH to Identify Genomic Regions Associated with Prostate Cancer Risk |
| Q36469169 | Use of folic acid-containing supplements after a diagnosis of colorectal cancer in the Colon Cancer Family Registry |
| Q57265740 | Using Mammographic Density to Improve Breast Cancer Screening Outcomes |
| Q33763777 | Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model |
| Q31061546 | Using bivariate models to understand between- and within-cluster regression coefficients, with application to twin data |
| Q28394774 | Using functional data analysis models to estimate future time trends in age-specific breast cancer mortality for the United States and England-Wales |
| Q30681302 | Using longitudinal data to define the perimenopause by menstrual cycle characteristics |
| Q34613556 | Using mammographic density to predict breast cancer risk: dense area or percentage dense area |
| Q57265924 | Validation of Questionnaire and Bronchial Hyperresponsiveness against Respiratory Physician Assessment in the Diagnosis of Asthma |
| Q36503573 | Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG) |
| Q47128258 | Validation study of risk prediction models for female relatives of Australian women with breast cancer |
| Q56994850 | Variants in the Prostate-Specific Antigen (PSA) Gene and Prostate Cancer Risk, Survival, and Circulating PSA |
| Q46647254 | Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry |
| Q37367984 | Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease |
| Q48629163 | Volumetric analysis of cerebral hypoperfusion on SPECT: validation and reliability. |
| Q47334605 | Weight change and prostate cancer incidence and mortality |
| Q40462333 | Who remembers whether they had asthma as children? |
| Q34586198 | Whole exome sequencing suggests much of non-BRCA1/BRCA2 familial breast cancer is due to moderate and low penetrance susceptibility alleles |
| Q47662548 | Why Accurate Knowledge of Zygosity is Important to Twins |
| Q74202884 | Why are the majority of hereditary cases of early-onset breast cancer sporadic? A simulation study |
| Q63352871 | Within-family studies for Mendelian randomization: avoiding dynastic, assortative mating, and population stratification biases |
| Q73050997 | Yield from colonoscopic screening in people with a strong family history of common colorectal cancer |
| Q36161705 | Zygosity Differences in Height and Body Mass Index of Twins From Infancy to Old Age: A Study of the CODATwins Project |
| Q36678510 | iPrevent®: a tailored, web-based, decision support tool for breast cancer risk assessment and management |
| Q44458999 | kConFab: a research resource of Australasian breast cancer families. Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer |
| Q37414133 | rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk |
| Q59270783 | ‘Next-generation’ genome wide association studies |
| John Hopper (scientist) | wikipedia |
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