Approaches to studying the impact of 22q11.2 copy number variants-Reference-Cited by-同舟云学术

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Approaches to studying the impact of 22q11.2 copy number variants

Published:2023-07 Issue:7 Volume:110 Page:1216-1218
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bassett Anne S.,McDonald-McGinn Donna M.,Boot Erik,Óskarsdóttir Sólveig,Yuen Ryan K.C.

Funder

W. Garfield Weston Foundation

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference14 articles.

1. The impact of 22q11.2 copy-number variants on human traits in the general population;Zamariolli;Am. J. Hum. Genet.,2023

2. Large-scale copy number polymorphism in the human genome;Sebat;Science,2004

3. Global variation in copy number in the human genome;Redon;Nature,2006

4. Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank;Crawford;J. Med. Genet.,2019

5. Effects of pathogenic CNVs on physical traits in participants of the UK Biobank;Owen;BMC Genom.,2018

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Young adults with a 22q11.2 microdeletion and the cost of aging with complexity in a population-based context;Genetics in Medicine;2024-05

2. Polygenic risk for triglyceride levels in the presence of a high impact rare variant;BMC Medical Genomics;2023-11-08

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