Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants
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Published:2023-01
Issue:1
Volume:4
Page:100163
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ISSN:2666-2477
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Container-title:Human Genetics and Genomics Advances
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language:en
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Short-container-title:Human Genetics and Genomics Advances
Author:
Young Kristin L.ORCID, Fisher Virginia, Deng Xuan, Brody Jennifer A., Graff Misa, Lim Elise, Lin Bridget M., Xu Hanfei, Amin Najaf, An Ping, Aslibekyan Stella, Fohner Alison E., Hidalgo Bertha, Lenzini Petra, Kraaij Robert, Medina-Gomez Carolina, Prokić Ivana, Rivadeneira Fernando, Sitlani Colleen, Tao Ran, van Rooij Jeroen, Zhang Di, Broome Jai G., Buth Erin J., Heavner Benjamin D., Jain Deepti, Smith Albert V., Barnes Kathleen, Boorgula Meher Preethi, Chavan Sameer, Darbar Dawood, De Andrade Mariza, Guo Xiuqing, Haessler Jeffrey, Irvin Marguerite R., Kalyani Rita R., Kardia Sharon L.R., Kooperberg Charles, Kim Wonji, Mathias Rasika A., McDonald Merry-Lynn, Mitchell Braxton D., Peyser Patricia A., Regan Elizabeth A., Redline Susan, Reiner Alexander P., Rich Stephen S., Rotter Jerome I., Smith Jennifer A., Weiss Scott, Wiggins Kerri L., Yanek Lisa R., Arnett Donna, Heard-Costa Nancy L., Leal Suzanne, Lin Danyu, McKnight Barbara, Province Michael, van Duijn Cornelia M., North Kari E., Cupples L. Adrienne, Liu Ching-Ti
Funder
National Institute on Aging National Heart Lung and Blood Institute NHGRI NIDDK National Center for Advancing Translational Sciences European Commission Sixth Framework Programme NC TraCS European Commission Seventh Framework Programme for Research and Technological Development ZonMw Russian Foundation for Basic Research Netherlands Organisation for Scientific Research
Subject
Genetics (clinical),Molecular Medicine
Cited by
2 articles.
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