A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases-Reference-Cited by-同舟云学术

A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases

Published:2012-01-11 Issue:7 Volume:40 Page:e53-e53
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Li Miao-Xin¹¹¹¹,Gui Hong-Sheng¹,Kwan Johnny S. H.¹¹,Bao Su-Ying¹,Sham Pak C.¹¹¹¹

Affiliation:

1. Department of Psychiatry, 2State Key Laboratory for Cognitive and Brain Sciences, 3Centre for Reproduction, Development and Growth, 4Genome Research Centre, 5Department of Medicine and 6Department of Biochemistry, University of Hong Kong, Pokfulam, Hong Kong, China

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/40/7/e53/25334663/gkr1257.pdf

Reference30 articles.

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4. Learning from molecular genetics: novel insights arising from the definition of genes for monogenic and type 2 diabetes;McCarthy;Diabetes,2008

5. Exploring the unknown: assumptions about allelic architecture and strategies for susceptibility variant discovery;McCarthy;Genome Med.,2009

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