Rare coding variants in RCN3 are associated with blood pressure

He, K. Y., Kelly, T. N., Wang, H., Liang, J., Zhu, L., Cade, B. E., Assimes, T. L., Becker, L. C., Beitelshees, A. L., Bielak, L. F., Bress, A. P., Brody, J. A., Chang, Y.-P. C., Chang, Y.-C., de Vries, P. S., Duggirala, R., Fox, E. R., Franceschini, N., Furniss, A. L., … Zhu, X. (2022). Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics, 23(1). https://doi.org/10.1186/s12864-022-08356-4
Authors:
Karen Y. He
Tanika N. Kelly
Heming Wang
Jingjing Liang
Luke Zhu
Brian E. Cade
Themistocles L. Assimes
Lewis C. Becker
Amber L. Beitelshees
Lawrence F. Bielak
Adam P. Bress
Jennifer A. Brody
Yen-Pei Christy Chang
Yi-Cheng Chang
Paul S. de Vries
Ravindranath Duggirala
Ervin R. Fox
Nora Franceschini
Anna L. Furniss
Yan Gao
Xiuqing Guo
Jeffrey Haessler
Yi-Jen Hung
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
Take Naseri
Walter Palmas
Muagututi’a Sefuiva Reupena
Kenneth M. Rice
Wayne H.-H. Sheu
Daichi Shimbo
Jennifer A. Smith
Beverly M. Snively
Lisa R. Yanek
Wei Zhao
John Blangero
Eric Boerwinkle
Yii-Der Ida Chen
Adolfo Correa
L. Adrienne Cupples
Joanne E. Curran
Myriam Fornage
Jiang He
Lifang Hou
Robert C. Kaplan
Sharon L. R. Kardia
Eimear E. Kenny
Charles Kooperberg
Donald Lloyd-Jones
Ruth J. F. Loos
Rasika A. Mathias
Stephen T. McGarvey
Braxton D. Mitchell
Kari E. North
Patricia A. Peyser
Bruce M. Psaty
Laura M. Raffield
D.C. Rao
Susan Redline
Alex P. Reiner
Stephen S. Rich
Jerome I. Rotter
Kent D. Taylor
Russell Tracy
Ramachandran S. Vasan
Alanna C. Morrison
Daniel Levy
Aravinda Chakravarti
Donna K. Arnett
Xiaofeng Zhu
Affiliated Authors:
Walter Palmas
Daichi Shimbo
Columbia Affiliation:
Subjects:
Genome-Wide Association Study (MeSH)
Precision Medicine (MeSH)
Genomic Studies and Association Analyses (OpenAlex Topic)
Standards and Guidelines for Genetic Variant Interpretation (OpenAlex Topic)
Genetic Research on BRCA Mutations and Cancer Risk (OpenAlex Topic)
Author Keywords:
rare variant analysis
blood pressure
whole genome sequencing
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Publication Type:
Article
Unique ID:
10.1186/s12864-022-08356-4
PMID:
35183128
DOI:
10.1186/s12864-022-08356-4
Journal:
BMC Genomics
Publication Date:
Data Source:
Scopus
Source Link:
View Scopus Record
View OpenAlex Record
View PubMed Record
View Web of Science Record

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