Author:
Raffield Laura M.,Iyengar Apoorva K.,Wang Biqi,Gaynor Sheila M.,Spracklen Cassandra N.,Zhong Xue,Kowalski Madeline H.,Salimi Shabnam,Polfus Linda M.,Benjamin Emelia J.,Bis Joshua C.,Bowler Russell,Cade Brian E.,Choi Won Jung,Comellas Alejandro P.,Correa Adolfo,Cruz Pedro,Doddapaneni Harsha,Durda Peter,Gogarten Stephanie M.,Jain Deepti,Kim Ryan W.,Kral Brian G.,Lange Leslie A.,Larson Martin G.,Laurie Cecelia,Lee Jiwon,Lee Seonwook,Lewis Joshua P.,Metcalf Ginger A.,Mitchell Braxton D.,Momin Zeineen,Muzny Donna M.,Pankratz Nathan,Park Cheol Joo,Rich Stephen S.,Rotter Jerome I.,Ryan Kathleen,Seo Daekwan,Tracy Russell P.,Viaud-Martinez Karine A.,Yanek Lisa R.,Zhao Lue Ping,Lin Xihong,Li Bingshan,Li Yun,Dupuis Josée,Reiner Alexander P.,Mohlke Karen L.,Auer Paul L.
Funder
National Institute of Diabetes and Digestive and Kidney Diseases
American Heart Association
Subject
Genetics(clinical),Genetics
Reference39 articles.
1. Whole-genome sequencing of rare disease patients in a national healthcare system;The NIHR BioResource on behalf of the 100000 Genomes Project;bioRxiv,2019
2. Whole genome sequencing in psychiatric disorders: the WGSPD consortium;Sanders;Nat. Neurosci.,2017
3. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program;Taliun;bioRxiv,2019
4. Genomic Analysis in the Age of Human Genome Sequencing;Lappalainen;Cell,2019
5. Genomics is failing on diversity;Popejoy;Nature,2016