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Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data

Karen Y. He; Xiaoyin Li; Tanika N. Kelly; Jingjing Liang; Brian E. Cade; Themistocles L. Assimes; Lewis C. Becker; Amber L. Beitelshees; Adam P. Bress; Yen-Pei Christy Chang; Yii-Der Ida Chen; Paul S. de Vries; Ervin R. Fox; Nora Franceschini; Anna Furniss; Yan Gao; Xiuqing Guo; Jeffrey Haessler; Shih-Jen Hwang; Marguerite Ryan Irvin; Rita R. Kalyani; Ching-Ti Liu; Chunyu Liu; Lisa Warsinger Martin; May E. Montasser; Paul M. Muntner; Stanford Mwasongwe; Walter Palmas; Alex P. Reiner; Daichi Shimbo; Jennifer A. Smith; Beverly M. Snively; Lisa R. Yanek; Eric Boerwinkle; Adolfo Correa; L. Adrienne Cupples; Jiang He; Sharon L. R. Kardia; Charles Kooperberg; Rasika A. Mathias; Braxton D. Mitchell; Bruce M. Psaty; Ramachandran S. Vasan; D. C. Rao; Stephen S. Rich; Jerome I. Rotter; James G. Wilson; Aravinda Chakravarti; Alanna C. Morrison; Daniel Levy; Donna K. Arnett; Susan Redline; Xiaofeng Zhu
Human Genetics · Vol. 138, Issue 2 · pp. 199-210 · 2019

Abstract

Abstract is unavailable.

Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2019-02-01
Publication Year2019
Volume138
Issue2
Pages199-210
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-019-01975-0

Access Information

NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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