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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants

Bioinformatics, 2015-11, Vol.31 (21), p.3555-3557

2015

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Harnessing cancer genomes for precision oncology

Nature genetics, 2024-09, Vol.56 (9), p.1768-1769

Chanock, Stephen J.

2024

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How the germline informs the somatic landscape

Nature genetics, 2021-11, Vol.53 (11), p.1523-1525

Chanock, Stephen J.

2021

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LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation

Bioinformatics, 2018-03, Vol.34 (5), p.887-889

2018

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The paradox of mutations and cancer

Science (American Association for the Advancement of Science), 2018-11, Vol.362 (6417), p.893-894

Chanock, Stephen J

2018

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LDlinkR : An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations

Frontiers in genetics, 2020-02, Vol.11, p.157-157

2020

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Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies

Nature genetics, 2013-04, Vol.45 (4), p.400-405

2013

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Thousands of short cuts to genetic testing

Nature (London), 2018-10, Vol.562 (7726), p.1-2

Chanock, Stephen J

2018

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A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits

American journal of human genetics, 2012-05, Vol.90 (5), p.821-835

2012

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Gene editing reveals the effect of thousands of variants in a key cancer gene

Nature (London), 2018-10, Vol.562 (7726), p.201-202

Chanock, Stephen J.

2018

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

Nature genetics, 2010-07, Vol.42 (7), p.570-575

2010

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Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (13), p.3767-3772

2016

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Interpretable, non-mechanistic forecasting using empirical dynamic modeling and interactive visualization

PloS one, 2023-04, Vol.18 (4), p.e0277149

2023

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Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

American journal of human genetics, 2010-06, Vol.86 (6), p.929-942

2010

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Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes

PLoS genetics, 2020-10, Vol.16 (10), p.e1009078-e1009078

2020

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Integration Analysis of Three Omics Data Using Penalized Regression Methods: An Application to Bladder Cancer

PLoS genetics, 2015-12, Vol.11 (12), p.e1005689

2015

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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Nature genetics, 2014-05, Vol.46 (5), p.482-486

2014

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Current status of genome-wide association studies in cancer

Human genetics, 2011-07, Vol.130 (1), p.59-78

2011

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Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery

Genes chromosomes & cancer, 2018-03, Vol.57 (3), p.140-149

2018

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High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

BMC genomics, 2009-11, Vol.10 (1), p.561-561, Article 561

2009

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Mosaic Y Loss Is Moderately Associated with Solid Tumor Risk

Cancer research (Chicago, Ill.), 2019-02, Vol.79 (3), p.461-466

2019

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Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank

Scientific reports, 2018-08, Vol.8 (1), p.12316-10, Article 12316

2018

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Genetic Susceptibility Loci for Breast Cancer by Estrogen Receptor Status

Clinical cancer research, 2008-12, Vol.14 (24), p.8000-8009

2008

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A spectrum of severe familial liver disorders associate with telomerase mutations

PloS one, 2009-11, Vol.4 (11), p.e7926-e7926

2009

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Detectable clonal mosaicism from birth to old age and its relationship to cancer

Nature genetics, 2012-06, Vol.44 (6), p.642-650

2012

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LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants

Harnessing cancer genomes for precision oncology

How the germline informs the somatic landscape

LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation

The paradox of mutations and cancer

LDlinkR : An R Package for Rapidly Calculating Linkage Disequilibrium Statistics in Diverse Populations

Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies

Thousands of short cuts to genetic testing

A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits

Gene editing reveals the effect of thousands of variants in a key cancer gene

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

Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses

Interpretable, non-mechanistic forecasting using empirical dynamic modeling and interactive visualization

Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes

Integration Analysis of Three Omics Data Using Penalized Regression Methods: An Application to Bladder Cancer

Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Current status of genome-wide association studies in cancer

Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays

Mosaic Y Loss Is Moderately Associated with Solid Tumor Risk

Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank

Genetic Susceptibility Loci for Breast Cancer by Estrogen Receptor Status

A spectrum of severe familial liver disorders associate with telomerase mutations

Detectable clonal mosaicism from birth to old age and its relationship to cancer

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