Abstract is: Maria Teresa Landi is an Italian epidemiologist and oncologist who researches genetic and environmental determinants of lung cancer and melanoma. At the National Cancer Institute, she is a senior investigator in the integrative tumor epidemiology branch and a senior advisor for genomic epidemiology. Landi is an associate professor of epidemiology at the Johns Hopkins Bloomberg School of Public Health.
| human | Q5 |
| P973 | described at URL | https://blog.cirm.ca.gov/tag/dr-maria-teresa-landi/ |
| https://dceg.cancer.gov/about/staff-directory/landi-maria | ||
| P2671 | Google Knowledge Graph ID | /g/11c6f3zk2m |
| P496 | ORCID iD | 0000-0002-9727-7772 |
| P6023 | ResearchGate contributions ID | 39501369 |
| P1153 | Scopus author ID | 7005278728 |
| P4012 | Semantic Scholar author ID | 2605573 |
| P27 | country of citizenship | Italy | Q38 |
| P69 | educated at | University of Milan | Q46210 |
| ??? | http://www.wikidata.org/.well-known/genid/c4420bec0ee5c0e3de32fc1ba5915392 | ||
| P108 | employer | Johns Hopkins University | Q193727 |
| George Washington University | Q432637 | ||
| National Cancer Institute | Q664846 | ||
| Division of Cancer Epidemiology and Genetics, National Cancer Institute | Q45134916 | ||
| P734 | family name | Landi | Q21502104 |
| Landi | Q21502104 | ||
| Landi | Q21502104 | ||
| P735 | given name | Maria Teresa | Q9435438 |
| Maria Teresa | Q9435438 | ||
| P106 | occupation | epidemiologist | Q13416803 |
| physician-scientist | Q25141651 | ||
| oncologist | Q16062369 | ||
| P21 | sex or gender | female | Q6581072 |
| Q42754133 | A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma |
| Q98881133 | A Likelihood Ratio Test for Gene-Environment Interaction Based on the Trend Effect of Genotype Under an Additive Risk Model Using the Gene-Environment Independence Assumption |
| Q37319013 | A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer |
| Q39738163 | A Novel Pathway-Based Approach Improves Lung Cancer Risk Prediction Using Germline Genetic Variations |
| Q36808635 | A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL). |
| Q34145755 | A flexible Bayesian model for studying gene-environment interaction |
| Q34609753 | A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindreds |
| Q35281526 | A gene expression signature from peripheral whole blood for stage I lung adenocarcinoma |
| Q28943348 | A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3 |
| Q24657797 | A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma |
| Q28943367 | A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci |
| Q103052744 | A multifactorial score including autophagy for prognosis and care of COVID-19 patients |
| Q28391788 | A regression model for risk difference estimation in population-based case-control studies clarifies gender differences in lung cancer risk of smokers and never smokers |
| Q29417157 | A variant in FTO shows association with melanoma risk not due to BMI |
| Q57663920 | Abstract 1875: Lung cancer risk among hairdressers in SYNERGY – pooled analysis from case-control studies in Europe and Canada with detailed smoking data |
| Q57663922 | Abstract 1877: Lung cancer risk in painters: Results from the SYNERGY pooled analysis |
| Q59196342 | Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue |
| Q58074718 | Abstract 4593: Genome-wide association study identifies novel loci associated with osteosarcoma |
| Q57319428 | Abstract 4597: A novel variant in DNA repair gene GTF2H4 is associated with lung cancer risk: A reanalysis of GWAS datasets from the TRICL consortium |
| Q59196397 | Abstract 4710: A candidate gene expression signature of early stage lung adenocarcinoma from peripheral whole blood |
| Q59196371 | Abstract 630: Tobacco smoking women are not at higher risk than men for lung cancer |
| Q57307156 | Abstract 817: Mendelian randomization and mediation analysis of 5p15.33, telomere length and lung cancer risk |
| Q57319566 | Abstract 889: An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for theXRCC4SNPs |
| Q57319487 | Abstract 942: Imputation from The 1000 Genomes Project identifies rare large effect variants of BRCA2-K3326X and CHEK2-I157T as risk factors for lung cancer; a study from the TRICL consortium |
| Q29248338 | Alcohol and Lung Cancer Risk Among Never Smokers: A Pooled Analysis from the International Lung Cancer Consortium and the SYNERGY Study |
| Q33566820 | Alcohol consumption and lung cancer risk in the Environment and Genetics in Lung Cancer Etiology (EAGLE) study |
| Q93175408 | Alcohol consumption and lung cancer risk: A pooled analysis from the International Lung Cancer Consortium and the SYNERGY study |
| Q35040633 | An Efficient Stochastic Search for Bayesian Variable Selection with High-Dimensional Correlated Predictors |
| Q34709103 | An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs |
| Q36073255 | An exposure-weighted score test for genetic associations integrating environmental risk factors |
| Q24170413 | Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types |
| Q115209619 | Application of two job indices for general occupational demands in a pooled analysis of case-control studies on lung cancer |
| Q36854071 | Are women who smoke at higher risk for lung cancer than men who smoke? |
| Q44848841 | Aryl-hydrocarbon receptor-dependent pathway and toxic effects of TCDD in humans: a population-based study in Seveso, Italy |
| Q56893420 | Assessing the Incremental Contribution of Common Genomic Variants to Melanoma Risk Prediction in Two Population-Based Studies |
| Q34677186 | Assessment of human papillomavirus in lung tumor tissue |
| Q97070156 | Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers |
| Q36540914 | Associated Links Among Smoking, Chronic Obstructive Pulmonary Disease, and Small Cell Lung Cancer: A Pooled Analysis in the International Lung Cancer Consortium |
| Q91816031 | Association analysis of driver-gene related genetic variants identified novel lung cancer susceptibility loci with 20,871 lung cancer cases and 15,971 controls |
| Q40406762 | Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations |
| Q81235911 | Association of MC1R variants and risk of melanoma in melanoma-prone families with CDKN2A mutations |
| Q39137734 | Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project |
| Q28387253 | Association of a novel functional promoter variant (rs2075533 C>T) in the apoptosis gene TNFSF8 with risk of lung cancer--a finding from Texas lung cancer genome-wide association study |
| Q37415242 | Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families |
| Q37708402 | Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs |
| Q37511418 | Authors' response to: comment upon the article: impact of occupational carcinogens on lung cancer risk in a general population |
| Q36766090 | Authors' response to: qualitative job-exposure matrix--a tool for the quantification of population-attributable fractions for occupational lung carcinogens? |
| Q55073149 | Blood DNA methylation, nevi number, and the risk of melanoma. |
| Q45185406 | CYP1A1 and CYP1B1 genotypes, haplotypes, and TCDD-induced gene expression in subjects from Seveso, Italy |
| Q99353311 | Causal Relationships between Body Mass Index, Smoking, and Lung Cancer: Univariable and Multivariable Mendelian Randomization |
| Q24169697 | Characterization of large structural genetic mosaicism in human autosome |
| Q36266148 | Characterization of melanoma susceptibility genes in high-risk patients from Central Italy. |
| Q57664758 | Characterization of nonacral melanoma patients without typical risk factors |
| Q28595730 | Characterizing human lung tissue microbiota and its relationship to epidemiological and clinical features |
| Q37696685 | Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue |
| Q33509281 | Chronic obstructive pulmonary disease and altered risk of lung cancer in a population-based case-control study |
| Q35812982 | Cigarette smoking and lung cancer--relative risk estimates for the major histological types from a pooled analysis of case-control studies |
| Q38925681 | Cigarette smoking behaviour and blood metabolomics |
| Q112708329 | Clinical Implications of Inter- and Intratumor Heterogeneity of Immune Cell Markers in Lung Cancer |
| Q64458461 | Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma |
| Q47114132 | Common TDP1 Polymorphisms in Relation to Survival among Small Cell Lung Cancer Patients: A Multicenter Study from the International Lung Cancer Consortium |
| Q36944260 | Common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer |
| Q50706320 | Comprehensive evaluation of allele frequency differences of MC1R variants across populations. |
| Q98958099 | Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma |
| Q91296227 | Contribution of Common Genetic Variants to Familial Aggregation of Disease and Implications for Sequencing Studies |
| Q58317858 | Correspondence re: K. Toide et al., Aryl hydrocarbon hydroxylase represents CYP1B1, and not CYP1A1, in human freshly isolated white cells: trimodal distribution of Japanese population according to induction of CYP1B1 mRNA by environmental dioxins. 12 |
| Q28396029 | Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer |
| Q28388475 | Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations |
| Q57272122 | DNA Repair and Cell Cycle Control Genes and the Risk of Young-Onset Lung Cancer |
| Q43417561 | DNA repair, dysplastic nevi, and sunlight sensitivity in the development of cutaneous malignant melanoma |
| Q28389918 | Deciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controls |
| Q50224889 | Dermoscopic features of cutaneous melanoma are associated with clinical characteristics of patients and tumours and with MC1R genotype. |
| Q23916196 | Detectable clonal mosaicism and its relationship to aging and cancer |
| Q28385149 | Detectable clonal mosaicism from birth to old age and its relationship to cancer |
| Q93208038 | Diesel Engine Exhaust Exposure, Smoking, and Lung Cancer Subtype Risks: A Pooled Exposure-response Analysis of 14 Case-control Studies |
| Q33759681 | Dietary quercetin, quercetin-gene interaction, metabolic gene expression in lung tissue and lung cancer risk |
| Q35784652 | Duplication of CXC chemokine genes on chromosome 4q13 in a melanoma-prone family |
| Q34580731 | Education and lung cancer among never smokers |
| Q28394483 | Effect modification of the association of cumulative exposure and cancer risk by intensity of exposure and time since exposure cessation: a flexible method applied to cigarette smoking and lung cancer in the SYNERGY Study |
| Q62583131 | Elevated platelet count appears to be causally associated with increased risk of lung cancer: A Mendelian randomization analysis |
| Q33341194 | Environment And Genetics in Lung cancer Etiology (EAGLE) study: an integrative population-based case-control study of lung cancer |
| Q38602034 | Epigenome-wide analysis of DNA methylation in lung tissue shows concordance with blood studies and identifies tobacco smoke-inducible enhancers |
| Q57208344 | Erratum to “Increased lung cancer risk among bricklayers in an italian population-based case-control study” |
| Q57208345 | Erratum to “Increased lung cancer risk among bricklayers in an italian population-based case-control study” |
| Q57271291 | Erratum: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer |
| Q91399778 | Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT |
| Q101216820 | Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits |
| Q46812479 | Exposure to diesel motor exhaust and lung cancer risk in a pooled analysis from case-control studies in Europe and Canada |
| Q30837145 | Exposure-Response Analyses of Asbestos and Lung Cancer Subtypes in a Pooled Analysis of Case-Control Studies |
| Q33834679 | Family history of cancer and nonmalignant lung diseases as risk factors for lung cancer |
| Q37004819 | Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents |
| Q27908479 | Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome |
| Q58351991 | Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity |
| Q28384269 | Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci |
| Q35083710 | Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions |
| Q90455618 | Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma |
| Q33629880 | Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 |
| Q38850374 | Functional variants in DCAF4 associated with lung cancer risk in European populations |
| Q43012778 | GPC5 rs2352028 variant and risk of lung cancer in never smokers |
| Q36037230 | GSTM1 and GSTT1 copy numbers and mRNA expression in lung cancer |
| Q33320978 | Gene expression signature of cigarette smoking and its role in lung adenocarcinoma development and survival |
| Q36300831 | Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus |
| Q95327114 | Genetic and epigenetic intratumor heterogeneity impacts prognosis of lung adenocarcinoma |
| Q35729543 | Genetic determinants for promoter hypermethylation in the lungs of smokers: a candidate gene-based study |
| Q35999323 | Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study |
| Q59544908 | Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners |
| Q28383262 | Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers |
| Q40706710 | Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium |
| Q37419151 | Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia |
| Q36521749 | Genetic variants associated with longer telomere length are associated with increased lung cancer risk among never-smoking women in Asia: a report from the female lung cancer consortium in Asia |
| Q33678110 | Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium |
| Q31010279 | Genetic variation and willingness to participate in epidemiologic research: data from three studies |
| Q36360694 | Genetic variation in innate immunity and inflammation pathways associated with lung cancer risk |
| Q34973837 | Genome partitioning of genetic variation for complex traits using common SNPs |
| Q91792933 | Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes |
| Q21092142 | Genome-wide and candidate gene association study of cigarette smoking behaviors |
| Q28943345 | Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia |
| Q93270780 | Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility |
| Q28744574 | Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis |
| Q45069141 | Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence |
| Q28943520 | Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3 |
| Q28659283 | Genome-wide association study identifies multiple loci associated with bladder cancer risk |
| Q34314018 | Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer |
| Q37341178 | Genome-wide association study identifies three loci associated with melanoma risk |
| Q29416994 | Genome-wide association study identifies three new melanoma susceptibility loci |
| Q28659642 | Genome-wide association study identifies two susceptibility loci for osteosarcoma |
| Q90438214 | Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk |
| Q64124096 | Genome-wide association study of familial lung cancer |
| Q28943359 | Genome-wide interaction study of smoking and bladder cancer risk |
| Q36019187 | Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma |
| Q21144958 | Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption |
| Q37058633 | Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence |
| Q112716940 | Genomic and evolutionary classification of lung cancer in never smokers |
| Q52716844 | Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma. |
| Q38613449 | Germline variation at CDKN2A and associations with nevus phenotypes among members of melanoma families. |
| Q58317861 | Glucocorticoid use and melanoma risk |
| Q33705253 | HPV-associated lung cancers: an international pooled analysis. |
| Q30993368 | Handling of dioxin measurement data in the presence of non-detectable values: overview of available methods and their application in the Seveso chloracne study |
| Q34125199 | Heme-related gene expression signatures of meat intakes in lung cancer tissues |
| Q56437244 | High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL |
| Q114062122 | Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting |
| Q38598304 | Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history. |
| Q91864711 | Histologic features of melanoma associated with germline mutations of CDKN2A, CDK4, and POT1 in melanoma-prone families from the United States, Italy, and Spain |
| Q40033503 | Identification of 14-3-3 theta as an antigen that induces a humoral response in lung cancer |
| Q36754771 | Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry |
| Q36255653 | Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia |
| Q36331604 | Identification of shared and unique susceptibility pathways among cancers of the lung, breast, and prostate from genome-wide association studies and tissue-specific protein interactions |
| Q58351997 | Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk |
| Q36246568 | Identifying Host Genetic Variants Associated with Microbiome Composition by Testing Multiple Beta Diversity Matrices |
| Q92480678 | Immune-mediated genetic pathways resulting in pulmonary function impairment increase lung cancer susceptibility |
| Q24529869 | Immunologic effects of dioxin: new results from Seveso and comparison with other studies |
| Q28386338 | Impact of occupational carcinogens on lung cancer risk in a general population |
| Q46945115 | Impact of occupational carcinogens on lung cancer risk in a general population. |
| Q44803827 | Increased lung cancer risk among bricklayers in an Italian population-based case-control study |
| Q29417049 | Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls |
| Q34303807 | Influence of quercetin-rich food intake on microRNA expression in lung cancer tissues |
| Q36384402 | Informed conditioning on clinical covariates increases power in case-control association studies |
| Q35967379 | Inherited variation at chromosome 12p13.33, including RAD52, influences the risk of squamous cell lung carcinoma |
| Q38683029 | Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia |
| Q74615608 | Instrumental measurements of skin color and skin ultraviolet light sensitivity and risk of cutaneous malignant melanoma: a case-control study in an Italian population |
| Q37289032 | Intakes of red meat, processed meat, and meat mutagens increase lung cancer risk |
| Q45943258 | Integrating Clinical and Multiple Omics Data for Prognostic Assessment across Human Cancers. |
| Q99409494 | Integration of multiomic annotation data to prioritize and characterize inflammation and immune-related risk variants in squamous cell lung cancer |
| Q41193948 | Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA). |
| Q28394515 | International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants |
| Q30850865 | International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways |
| Q34425781 | Is previous respiratory disease a risk factor for lung cancer? |
| Q38730359 | Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes |
| Q34125066 | Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background |
| Q33723442 | Lower risk of lung cancer after multiple pneumonia diagnoses |
| Q40486328 | Lung Cancer Among Firefighters: Smoking-Adjusted Risk Estimates in a Pooled Analysis of Case-Control Studies |
| Q90157503 | Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15.33 TERT-CLPTM1Ll Region |
| Q40759340 | Lung cancer among coal miners, ore miners and quarrymen: smoking-adjusted risk estimates from the synergy pooled analysis of case-control studies |
| Q28393149 | Lung cancer and occupation in a population-based case-control study |
| Q52692653 | Lung cancer and socioeconomic status in a pooled analysis of case-control studies. |
| Q36817059 | Lung cancer prognosis before and after recurrence in a population-based setting |
| Q44000257 | Lung cancer risk among bakers, pastry cooks and confectionary makers: the SYNERGY study |
| Q28397018 | Lung cancer risk among bricklayers in a pooled analysis of case-control studies |
| Q41475032 | Lung cancer risk among cooks when accounting for tobacco smoking: a pooled analysis of case-control studies from Europe, Canada, New Zealand, and China |
| Q37268621 | Lung cancer risk among hairdressers: a pooled analysis of case-control studies conducted between 1985 and 2010. |
| Q101050476 | Lung cancer risk in painters: results from the SYNERGY pooled case-control study consortium |
| Q79815917 | MC1R germline variants confer risk for BRAF-mutant melanoma |
| Q99212231 | MC1R variants and cutaneous melanoma risk according to histological type, body site, and Breslow thickness: a pooled analysis from the M-SKIP project |
| Q54938332 | MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: a pooled analysis from the M-SKIP project. |
| Q92368080 | MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort |
| Q33715143 | MC1R variants increase risk of melanomas harboring BRAF mutations. |
| Q35230315 | MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project |
| Q81926997 | MC1R, ASIP, and DNA repair in sporadic and familial melanoma in a Mediterranean population |
| Q36707069 | MEGSA: A Powerful and Flexible Framework for Analyzing Mutual Exclusivity of Tumor Mutations |
| Q90883886 | MelaNostrum: a consensus questionnaire of standardized epidemiologic and clinical variables for melanoma risk assessment by the melanostrum consortium |
| Q34365732 | Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies |
| Q40228976 | Menstrual and reproductive factors and lung cancer risk: A pooled analysis from the international lung cancer consortium |
| Q28385292 | Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women |
| Q35184912 | MicroRNA expression differentiates histology and predicts survival of lung cancer |
| Q46461168 | Microarray analysis of gene expression in peripheral blood mononuclear cells from dioxin-exposed human subjects |
| Q34374866 | Mood disorders and risk of lung cancer in the EAGLE case-control study and in the U.S. Veterans Affairs inpatient cohort |
| Q113185709 | Multi-Trait Genetic Analysis Identifies Autoimmune Loci Associated with Cutaneous Melanoma |
| Q28290169 | Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. |
| Q39568294 | Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations |
| Q36367063 | Multistage analysis of variants in the inflammation pathway and lung cancer risk in smokers |
| Q31155880 | Mutations in the tyrosine kinase domain of the epidermal growth factor receptor in non-small cell lung cancer |
| Q28385029 | Neonatal thyroid function in Seveso 25 years after maternal exposure to dioxin |
| Q61917486 | No Evidence for Linkage with Melanoma in Italian Melanoma-Prone Families |
| Q31130933 | Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS data |
| Q28390824 | Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk |
| Q47233603 | Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer |
| Q33327597 | Nucleotide diversity and population differentiation of the melanocortin 1 receptor gene, MC1R. |
| Q34548993 | Nut Consumption and Lung Cancer Risk: Results from Two Large Observational Studies |
| Q33778268 | Obesity, metabolic factors and risk of different histological types of lung cancer: A Mendelian randomization study |
| Q44998973 | Occupational exposure to organic dust increases lung cancer risk in the general population |
| Q36070302 | Occupational prestige, social mobility and the association with lung cancer in men |
| Q44226927 | On combining family and case-control studies |
| Q34540748 | On the interplay of telomeres, nevi and the risk of melanoma |
| Q57210627 | Outdoor particulate matter (PM10) exposure and lung cancer risk in the EAGLE study |
| Q39346675 | P1.04: Defining the Genetic Architecture of Lung Cancer Etiology: Track: Prevention, Early Detection, Epidemiology and Tobacco Control |
| Q93206509 | POT1 germline mutations but not TERT promoter mutations are implicated in melanoma susceptibility in a large cohort of Spanish melanoma families |
| Q38984784 | Pathway-analysis of published genome-wide association studies of lung cancer: A potential role for the CYP4F3 locus |
| Q91721813 | Peritoneal mesothelioma and asbestos exposure: a population-based case-control study in Lombardy, Italy |
| Q33455775 | Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression |
| Q37619240 | Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families |
| Q48403202 | Plasma levels of dioxins, furans, non-ortho-PCBs, and TEQs in the Seveso population 17 years after the accident. |
| Q39449490 | Pleiotropic Analysis of Lung Cancer and Blood Triglycerides |
| Q28383788 | Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia |
| Q36719039 | Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls |
| Q60934832 | Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls |
| Q94562441 | Protein-altering germline mutations implicate novel genes related to lung cancer development |
| Q90242034 | Publisher Correction: Shared heritability and functional enrichment across six solid cancers |
| Q88214332 | Publisher correction: Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 |
| Q30498925 | Quality control and quality assurance in genotypic data for genome-wide association studies |
| Q33751971 | Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma |
| Q28943461 | Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer |
| Q36721847 | Reproductive and hormonal factors and the risk of lung cancer: the EAGLE study |
| Q93208034 | Respirable Crystalline Silica Exposure, Smoking, and Lung Cancer Subtype Risks: A Pooled Analysis of Case-control Studies |
| Q41022944 | Risk factors for keratinocyte skin cancer in patients diagnosed with melanoma, a large retrospective study |
| Q61118451 | Shared heritability and functional enrichment across six solid cancers |
| Q64004349 | Shared heritability and functional enrichment across six solid cancers |
| Q36214274 | Somatic Genomics and Clinical Features of Lung Adenocarcinoma: A Retrospective Study. |
| Q104691963 | Sub-multiplicative interaction between polygenic risk score and household coal use in relation to lung adenocarcinoma among never-smoking women in Asia |
| Q29248340 | Susceptibility loci of CNOT6 in the general mRNA degradation pathway and lung cancer risk - a re-analysis of eight GWASs |
| Q28645948 | TCDD-mediated alterations in the AhR-dependent pathway in Seveso, Italy, 20 years after the accident |
| Q39998496 | TERT promoter mutations in melanoma survival |
| Q28265076 | Telomerase reverse transcriptase locus polymorphisms and cancer risk: a field synopsis and meta-analysis |
| Q34372389 | The 19q12 bladder cancer GWAS signal: association with cyclin E function and aggressive disease |
| Q28397565 | The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia |
| Q34333988 | The effect on melanoma risk of genes previously associated with telomere length |
| Q96576422 | The genomic and epigenomic evolutionary history of papillary renal cell carcinomas |
| Q36255637 | The role of haplotype in 15q25.1 locus in lung cancer risk: results of scanning chromosome 15. |
| Q29248193 | Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21 |
| Q33813187 | Time to smoke first morning cigarette and lung cancer in a case-control study |
| Q91158802 | Transcriptome-wide association study reveals candidate causal genes for lung cancer |
| Q47409401 | Using imputed genotype data in the joint score tests for genetic association and gene-environment interactions in case-control studies |
| Q37642319 | VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions |
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| Maria Teresa Landi | wikipedia | |
| ml | മരിയ തെരേസ ലാൻഡി | wikipedia |
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