(Q37890286)

24 August 2017

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title

Current status of genome-wide association studies in cancer (English)

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genome-wide association study

24 August 2017

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2

Stephen J Chanock

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24 August 2017

Charles C Chung

1

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24 August 2017

16 June 2011

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24 August 2017

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24 August 2017

130

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24 August 2017

59-78

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24 August 2017

1

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https://scigraph.springernature.com/pub.10.1007/s00439-011-1030-9

24 August 2017

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cites work

A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Variation in KLK genes, prostate-specific antigen and risk of prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Multiple loci on 8q24 associated with prostate cancer susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A common variant associated with prostate cancer in European and African populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Telomerase mutations in families with idiopathic pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Evaluating coverage of genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common variants at 19p13 are associated with susceptibility to ovarian cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A spectrum of severe familial liver disorders associate with telomerase mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Replicating genotype-phenotype associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association studies in cancer--current and future directions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A systematic approach to understand the functional consequences of non-protein coding risk regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common regulatory variation impacts gene expression in a cell type-dependent manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Progress and challenges in genome-wide association studies in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A map of human genome variation from population-scale sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study identifies novel breast cancer susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Risk of gastric cancer and peptic ulcers in relation to ABO blood type: a cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Multiple newly identified loci associated with prostate cancer susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Overview of model-free methods for linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

SNPs in cancer research and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Value of adding single-nucleotide polymorphism genotypes to a breast cancer risk model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Multiple regions within 8q24 independently affect risk for prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Linkage of early-onset familial breast cancer to chromosome 17q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Multiple ADH genes are associated with upper aerodigestive cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

The balance between heritable and environmental aetiology of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association studies for common diseases and complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Germline p16 mutations in familial melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Estimating missing heritability for disease from genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A new multipoint method for genome-wide association studies by imputation of genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A decade's perspective on DNA sequencing technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

GSTM1 null and NAT2 slow acetylation genotypes, smoking intensity and bladder cancer risk: results from the New England bladder cancer study and NAT2 meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Population structure and eigenanalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Molecular portraits of human breast tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Principal components analysis corrects for stratification in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association study of testicular germ cell tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Searching for genetic determinants in the new millennium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Systematic variation in gene expression patterns in human cancer cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study identifies five susceptibility loci for glioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

New common variants affecting susceptibility to basal cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Population genomics of human gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Two newly identified genetic determinants of pigmentation in Europeans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Evidence for two independent prostate cancer risk-associated loci in the HNF1B gene at 17q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Inherited genetic markers discovered to date are able to identify a significant number of men at considerably elevated risk for prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Multiple loci identified in a genome-wide association study of prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Germline genomic variants associated with childhood acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Adult-onset pulmonary fibrosis caused by mutations in telomerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study identifies five new breast cancer susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association studies in common cancers--what have we learnt?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Performance of common genetic variants in breast-cancer risk models

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Common 5p15.33 and 6p21.33 variants influence lung cancer risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Established prostate cancer susceptibility variants are not associated with disease outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Admixture mapping comes of age

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

ABO blood group and the risk of pancreatic cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Identification of the breast cancer susceptibility gene BRCA2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Adjusting for covariates in logistic regression models

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Inherited genetic variant predisposes to aggressive but not indolent prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Identification of a new prostate cancer susceptibility locus on chromosome 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Two independent prostate cancer risk-associated Loci at 11q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

MYEOV: A candidate gene for DNA amplification events occurring centromeric toCCND1in breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Beyond odds ratios — communicating disease risk based on genetic profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

21 January 2018

When the smoke clears ..

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1030-9

Telomerase expression in B-cell chronic lymphocytic leukemia predicts survival and delineates subgroups of patients with the same igVH mutation status and different outcome

21 January 2018

1 reference

12 December 2020

Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.

1 reference

12 December 2020

Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32).

1 reference

12 December 2020

Fine mapping the KLK3 locus on chromosome 19q13.33 associated with prostate cancer susceptibility and PSA levels

1 reference

12 December 2020

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

1 reference

12 December 2020

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

1 reference

12 December 2020

Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.

1 reference

12 December 2020

Population substructure and control selection in genome-wide association studies

1 reference

12 December 2020

Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP

1 reference

12 December 2020

What's the best statistic for a simple test of genetic association in a case-control study?

1 reference

12 December 2020

A second generation human haplotype map of over 3.1 million SNPs

1 reference

12 December 2020

International network of cancer genome projects

1 reference

12 December 2020

The genetic interpretation of area under the ROC curve in genomic profiling

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia

1 reference

12 December 2020

A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group

1 reference

12 December 2020

Polygenes, risk prediction, and targeted prevention of breast cancer

1 reference

12 December 2020

Hundreds of variants clustered in genomic loci and biological pathways affect human height

1 reference

12 December 2020

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

1 reference

12 December 2020

A comprehensive resequence analysis of the KLK15-KLK3-KLK2 locus on chromosome 19q13.33.

1 reference

12 December 2020

Copy number variation at 1q21.1 associated with neuroblastoma

1 reference

12 December 2020

Synthetic associations created by rare variants do not explain most GWAS results

1 reference

12 December 2020

Lung cancer susceptibility locus at 5p15.33

1 reference

12 December 2020

An Icelandic example of the impact of population structure on association studies

1 reference

12 December 2020

Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

1 reference

12 December 2020

Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer

1 reference

12 December 2020

Comprehensive genomic characterization defines human glioblastoma genes and core pathways

1 reference

12 December 2020

Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer

1 reference

12 December 2020

Identification of seven new prostate cancer susceptibility loci through a genome-wide association study

1 reference

12 December 2020

The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia

1 reference

12 December 2020

A twist on admixture mapping

1 reference

12 December 2020

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

12 December 2020

Cumulative association of five genetic variants with prostate cancer

1 reference

12 December 2020

GWAS identifies a common breast cancer risk allele among BRCA1 carriers

1 reference

12 December 2020

Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer

1 reference

12 December 2020

The Sequence of the Human Genome

1 reference

12 December 2020

A single nucleotide polymorphism tags variation in the arylamine N-acetyltransferase 2 phenotype in populations of European background

1 reference

12 December 2020

Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility

1 reference

12 December 2020

Rare variants create synthetic genome-wide associations

1 reference

12 December 2020

Blood type and family cancer history in relation to precancerous gastric lesions

1 reference

12 December 2020

Lymphoid malignancies in U.S. Asians: incidence rate differences by birthplace and acculturation

1 reference

12 December 2020

Analysis of the 10q11 cancer risk locus implicates MSMB and NCOA4 in human prostate tumorigenesis

1 reference

12 December 2020

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

1 reference

12 December 2020

The International HapMap Project

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

Identification of a novel prostate cancer susceptibility variant in the KLK3 gene transcript

1 reference

12 December 2020

10.1007/S00439-011-1030-9

Identifiers

DOI

1 reference

24 August 2017

1 reference

PubMed ID

21678065