The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia |
|
Abstract 287: Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue |
|
Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types |
|
Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families |
|
Authors' response to: qualitative job-exposure matrix--a tool for the quantification of population-attributable fractions for occupational lung carcinogens? |
|
CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF. |
|
Characterization of large structural genetic mosaicism in human autosomes |
|
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma |
|
Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer |
|
Cutaneous phenotype andMC1R variants as modifying factors for the development of melanoma inCDKN2A G101W mutation carriers from 4 countries |
|
Detectable clonal mosaicism and its relationship to aging and cancer |
|
Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome |
|
Fine mapping of 14q24.1 breast cancer susceptibility locus |
|
Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers |
|
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 |
|
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility |
|
Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population |
|
A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma |
|
Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture |
|
Geographical variation in the penetrance of CDKN2A mutations for melanoma |
|
Heterogeneity of risk for melanoma and pancreatic and digestive malignancies |
|
High-risk Melanoma Susceptibility Genes and Pancreatic Cancer, Neural System Tumors, and Uveal Melanoma across GenoMEL |
|
Impact of occupational carcinogens on lung cancer risk in a general population |
|
Improved imputation of common and uncommon SNPs with a new reference set. |
|
Individuals at high risk of melanoma, 1988: |
|
Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations |
|
The landscape of recombination in African Americans |
|
Large-scale fine mapping of the HNF1B locus and prostate cancer risk |
|
Leukocyte DNA methylation and colorectal cancer among male smokers |
|
Lung cancer and occupation in a population-based case-control study |
|
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry |
|
Mosaic loss of chromosome Y is associated with common variation near TCL1A |
|
Multiple loci identified in a genome-wide association study of prostate cancer |
|
Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals |
|
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cells |
|
A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies |
|
Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression |
|
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families |
|
Potential excess mortality in BRCA1/2 mutation carriers beyond breast, ovarian, prostate, and pancreatic cancers, and melanoma |
|
A Pragmatic Testing-Eligibility Framework for Population Mutation Screening: The Example of BRCA1/2 |
|
Rare germline variants in known melanoma susceptibility genes in familial melanoma. |
|
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma |
|
Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2. |
|
Reply to 'Mosaic loss of chromosome Y in leukocytes matters' |
|
Reproductive and hormonal factors and the risk of lung cancer: the EAGLE study |
|
Risk for malignancies of infectious etiology among adult survivors of specific non-Hodgkin lymphoma subtypes |
|
Risk of Soft Tissue Sarcomas by Individual Subtype in Survivors of Hereditary Retinoblastoma |
|
Risk of subsequent malignant neoplasms in long-term hereditary retinoblastoma survivors after chemotherapy and radiotherapy |
|
Sebaceous carcinoma epidemiology and genetics: Emerging concepts and clinical implications for screening, prevention, and treatment |
|
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma |
|
Successful use of whole genome amplified DNA from multiple source types for high-density Illumina SNP microarrays. |
|
Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations |
|
Thyroid Cancer after Childhood Exposure to External Radiation: An Updated Pooled Analysis of 12 Studies |
|
Two susceptibility loci identified for prostate cancer aggressiveness |
|
Variation of second cancer risk by family history of retinoblastoma among long-term survivors |
|
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene |
|
Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility |
|