Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations. - Test2 - elhamkhani - TriplyDB

Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.

Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.

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Pharmacologic Therapy of Diabetes and Overall Cancer Risk and Mortality: A Meta-Analysis of 265 Studies Zinc transporter genes and urological cancers: integrated analysis suggests a role for ZIP11 in bladder cancer.Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article Systematic evaluation of underlying defects in DNA repair as an approach to case-only assessment of familial prostate cancer Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing.The Rise and Rise of Exome Sequencing.Association score testing for rare variants and binary traits in family data with shared controls.Evidence from a familial case suggests maternal inheritance of primary biliary cholangitis.Genetic and experimental evidence for the involvement of the CD6 lymphocyte receptor in psoriasis.

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Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.

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Case-only exome sequencing and ...... : study design considerations.

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Journal of Medical Genetics

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Case-only exome sequencing and ...... : study design considerations.

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Daniel J Schaid

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Eric D Wieben

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Gloria M Petersen

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Hu Li

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Hugues Sicotte

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Lang Wu

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Initial sequencing and analysis of the human genome

Chapter 11: Genome-wide association studies

Integrative annotation of variants from 1092 humans: application to cancer genomics

Predicting deleterious amino acid substitutions

An integrated map of genetic variation from 1,092 human genomes

Finding the missing heritability of complex diseases

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

Five years of GWAS discovery

International network of cancer genome projects.

Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas

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