Exome‐wide assessment of isolated biliary atresia: A report from the <scp>National Birth Defects Prevention Study</scp> using child–parent trios and a case–control design to identify novel rare variants

Pagna Sok(Baylor College of Medicine), Philip J. Lupo(Emory Healthcare), Elizabeth Blue(University of Washington), Marcia L. Feldkamp(University of Utah), Yunping Lei(Baylor College of Medicine), Qingchang Meng(Baylor College of Medicine), Gary M. Shaw(Stanford University), Andrew F. Olshan(University of North Carolina at Chapel Hill), Donna M. Muzny(Baylor College of Medicine), Faith Pangilinan(National Human Genome Research Institute), Austin L. Brown(Baylor College of Medicine), Paul A. Romitti(Faculty of Public Health), Jennita Reefhuis(Centers for Disease Control and Prevention), A. J. Agopian(The University of Texas Health Science Center at Houston), Lynn M. Almli(Centers for Disease Control and Prevention), Richard A. Gibbs(Baylor College of Medicine), Marilyn L. Browne(New York State Department of Health), Michael J. Bamshad(University of Washington), Jessica X. Chong(Brotman Baty Institute), Mary M. Jenkins(Centers for Disease Control and Prevention), Mark A. Canfield(Texas Department of State Health Services), Wendy N. Nembhard(Arkansas Children's Hospital), James C. Mullikin(Human Genome Sciences (United States)), Sanjiv Harpavat(Emory University), Richard H. Finnell(Baylor College of Medicine), Denise M. Kay(New York State Department of Health), Jeremy M. Schraw(Baylor College of Medicine), Aniko Sabo(Baylor College of Medicine), Shannon Dugan‐Perez(Baylor College of Medicine), Martha M. Werler(Boston University), Suzan L. Carmichael(Stanford Medicine), Lawrence C. Brody(National Institutes of Health), Cynthia A. Moore(Chesapeake Public Schools)
American Journal of Medical Genetics Part A
March 21, 2023
Cited by 7


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