Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants
Shannon Dugan‐Perez(Baylor College of Medicine), Pagna Sok(Baylor College of Medicine), 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), Faith Pangilinan(National Human Genome Research Institute), 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), Marilyn L. Browne(New York State Department of Health), Philip J. Lupo(Emory Healthcare), 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), D. Muzny(Baylor College of Medicine), Martha M. Werler(Boston University), Ann L. Brown(University of Cincinnati), Lawrence C. Brody(National Institutes of Health), M. Bamshad(University of Utah), Richard A. Gibbs(Baylor College of Medicine), S. Carmichael, University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program, the National Birth Defects Prevention Study, Cynthia A. Moore(Chesapeake Public Schools)
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