Phenome-wide Burden of Copy-Number Variation in the UK Biobank-Reference-Cited by-同舟云学术

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Phenome-wide Burden of Copy-Number Variation in the UK Biobank

Published:2019-08 Issue:2 Volume:105 Page:373-383
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Aguirre Matthew^ORCID,Rivas Manuel A.,Priest James

Funder

Stanford University

National Institute of Health center for Multi- and Trans-ethnic Mapping of Mendelian and Complex Diseases

National Human Genome Research Institute (NHGRI) of the National Institutes of Health

Stanford University Department of Pediatrics

National Heart Lung and Blood Institute

Chan-Zuckerberg Biohub

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference68 articles.

1. Global diversity, population stratification, and selection of human copy-number variation;Sudmant;Science,2015

2. Mapping copy number variation by population-scale genome sequencing;Mills;Nature,2011

3. Copy number variations and human genetic disease;Mikhail;Curr. Opin. Pediatr.,2014

4. Microdeletion syndromes;Carvill;Curr. Opin. Genet. Dev.,2013

5. Recent segmental duplications in the human genome;Bailey;Science,2002

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