human | Q5 |
P106 | occupation | researcher | Q1650915 |
Q33848895 | 2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy |
Q40943174 | A Comprehensive Multistate Model Analyzing Associations of Various Risk Factors With the Course of Breast Cancer in a Population-Based Cohort of Breast Cancer Cases |
Q37192589 | A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication |
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 |
Q35870483 | A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients |
Q30779634 | Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases |
Q35218520 | Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy |
Q43488772 | Association of pre-diagnosis physical activity with recurrence and mortality among women with breast cancer |
Q47296512 | Associations between adjuvant radiotherapy and different causes of death in a German breast cancer cohort |
Q46115524 | Body mass index and breast cancer survival: a Mendelian randomization analysis |
Q43519004 | Circulating 25-hydroxyvitamin D and postmenopausal breast cancer survival: Influence of tumor characteristics and lifestyle factors? |
Q35558033 | Coffee consumption modifies risk of estrogen-receptor negative breast cancer |
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 |
Q34594697 | Confirmation of the reduction of hormone replacement therapy-related breast cancer risk for carriers of the HSD17B1_937_G variant |
Q44846019 | Determinants of long-term fatigue in breast cancer survivors: results of a prospective patient cohort study |
Q44197715 | Determinants of newly diagnosed comorbidities among breast cancer survivors |
Q57416701 | Enterolactone concentrations and prognosis after postmenopausal breast cancer: Assessment of effect modification and meta-analysis |
Q35064451 | Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation |
Q35524465 | Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. |
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. |
Q35151684 | Genetic predisposition to in situ and invasive lobular carcinoma of the breast |
Q100426886 | Genetic variants in the regulatory T cell related pathway and colorectal cancer prognosis |
Q53163641 | Germline variants of base excision repair genes and breast cancer: A polymorphism in DNA polymerase gamma modifies gene expression and breast cancer risk. |
Q36276540 | Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization |
Q35102646 | Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk |
Q34038964 | Identification of new genetic susceptibility loci for breast cancer through consideration of gene-environment interactions |
Q36014067 | Identification of novel genetic markers of breast cancer survival |
Q35104068 | Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer |
Q34898735 | Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors |
Q34497352 | MicroRNA related polymorphisms and breast cancer risk |
Q28533813 | Mortality and recurrence risk in relation to the use of lipid-lowering drugs in a prospective breast cancer patient cohort |
Q28584533 | PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS |
Q56089175 | Pathway analysis of genetic variants in folate-mediated one-carbon metabolism-related genes and survival in a prospectively followed cohort of colorectal cancer patients |
Q57306202 | Polymorphisms in oxidative stress-related genes and mortality in breast cancer patients – Potential differential effects by radiotherapy? |
Q36583004 | Prediction of breast cancer risk based on profiling with common genetic variants |
Q55508030 | Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation. |
Q35155449 | Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia |
Q41065061 | Relationship between menopausal hormone therapy and mortality after breast cancer The MARIEplus study, a prospective case cohort |
Q40936032 | SNPs in transporter and metabolizing genes as predictive markers for oxaliplatin treatment in colorectal cancer patients |
Q35781316 | The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients |
Q36917100 | The UGT1A6_19_GG genotype is a breast cancer risk factor |
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