Author:
Mukherjee Souhrid,Cassini Thomas A.,Hu Ningning,Yang Tao,Li Bian,Shen Wangzhen,Moth Christopher W.,Rinker David C.,Sheehan Jonathan H.,Cogan Joy D.,Newman John H.,Hamid Rizwan,Macdonald Robert L.,Roden Dan M.,Meiler Jens,Kuenze Georg,Phillips John A.,Capra John A.
Funder
National Institutes of Health
American Heart Association
Office of Strategic Coordination
Vanderbilt University
Subject
Genetics (clinical),Molecular Medicine
Reference80 articles.
1. Targeted capture and massively parallel sequencing of 12 human exomes;Ng;Nature,2009
2. ARTICLE finding disease variants in mendelian disorders by using sequence data: methods and applications;Ionita-Laza;Am. J. Hum. Genet.,2011
3. Exome sequencing identifies the cause of a mendelian disorder;Ng;Nat. Genet.,2010
4. COMMENTARY International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases;Boycott,2017
5. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities;Chong,2015
Cited by
4 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