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.
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| Title: | 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. |
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| Authors: | Sok P; Pediatrics, Baylor College of Medicine, Houston, Texas, USA., Sabo A; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Almli LM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Jenkins MM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Nembhard WN; Fay W. Boozman College of Public Health, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Agopian AJ; Department of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas School of Public Health, Houston, Texas, USA., Bamshad MJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA.; Brotman Baty Institute for Precision Medicine, Seattle, Washington, USA., Blue EE; Brotman Baty Institute for Precision Medicine, Seattle, Washington, USA.; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, USA., Brody LC; Genetics and Environment Interaction Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Brown AL; Pediatrics, Baylor College of Medicine, Houston, Texas, USA., Browne ML; Birth Defects Registry, New York State Department of Health, Albany, New York, USA.; Department of Epidemiology and Biostatistics, School of Public Health, University at Albany, Rensselaer, New York, USA., Canfield MA; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA., Carmichael SL; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA., Chong JX; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA.; Brotman Baty Institute for Precision Medicine, Seattle, Washington, USA., Dugan-Perez S; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Feldkamp ML; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA., Finnell RH; Department of Medicine, Center for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA., Gibbs RA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Kay DM; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA., Lei Y; Department of Medicine, Center for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA., Meng Q; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Moore CA; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Mullikin JC; Genetics and Environment Interaction Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Muzny D; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA., Olshan AF; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, North Carolina, USA., Pangilinan F; Genetics and Environment Interaction Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Reefhuis J; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Romitti PA; Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa, USA., Schraw JM; Pediatrics, Baylor College of Medicine, Houston, Texas, USA., Shaw GM; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA., Werler MM; Department of Epidemiology, Boston University, Boston, Massachusetts, USA., Harpavat S; Pediatrics, Baylor College of Medicine, Houston, Texas, USA.; Gastroenterology, Hepatology and Nutrition, Texas Children's Hospital, Houston, Texas, USA., Lupo PJ; Pediatrics, Baylor College of Medicine, Houston, Texas, USA. |
| Corporate Authors: | University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program, the National Birth Defects Prevention Study |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2023 Jun; Vol. 191 (6), pp. 1546-1556. Date of Electronic Publication: 2023 Mar 21. |
| Publication Type: | Journal Article; Research Support, U.S. Gov't, P.H.S.; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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