KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design-Reference-Cited by-同舟云学术

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KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design

Published:2022-10 Issue:10 Volume:109 Page:1761-1776
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Yang Yi,Wang Chen,Liu Linxi,Buxbaum Joseph,He Zihuai,Ionita-Laza Iuliana

Funder

NIA

National Institutes of Health

National Institute of Mental Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference67 articles.

1. Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from saudi families;Al-Mubarak;Sci. Rep.,2017

2. Evidence supporting wnt2 as an autism susceptibility gene;Wassink;Am. J. Med. Genet.,2001

3. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations;O’Roak;Nat. Genet.,2011

4. The role of family-based designs in genome-wide association studies;Laird;Stat. Sci.,2009

5. Family-based designs in the age of large-scale gene-association studies;Laird;Nat. Rev. Genet.,2006

Cited by 1 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. KnockoffHybrid: A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies;The American Journal of Human Genetics;2024-07

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