Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data

Kim, W., Hecker, J., Barr, R. G., Boerwinkle, E., Cade, B., Correa, A., Dupuis, J., Gharib, S. A., Lange, L., London, S. J., Morrison, A. C., O’Connor, G. T., Oelsner, E. C., Psaty, B. M., Vasan, R. S., Redline, S., Rich, S. S., Rotter, J. I., … Yu, B. (2022). Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data. Human Molecular Genetics, 31(22), 3873–3885. https://doi.org/10.1093/hmg/ddac117
Authors:
Wonji Kim
Julian Hecker
R Graham Barr
Eric Boerwinkle
Brian Cade
Adolfo Correa
Josée Dupuis
Sina A Gharib
Leslie Lange
Stephanie J London
Alanna C Morrison
George T O'Connor
Elizabeth C Oelsner
Bruce M Psaty
Ramachandran S Vasan
Susan Redline
Stephen S Rich
Jerome I Rotter
Bing Yu
Christoph Lange
Ani Manichaikul
Jin J Zhou
Tamar Sofer
Edwin K Silverman
Dandi Qiao
Michael H Cho
Affiliated Authors:
R Graham Barr
Elizabeth C Oelsner
Publication Type:
Article
Unique ID:
10.1093/hmg/ddac117
PMID:
Publication Date:
Data Source:
PubMed

Record Created: