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Paper Details

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.
Am J Med Genet A
2
2023
Alagille syndrome, BA, Birth Defects, IFRD2, NOTCH2, PAVs, PKD1L1, biliary atresia, birth defects, child, children, disease gene, gastrointestinal conditions, genes, isolated biliary atresia, mother
Author NameAffiliation
Aniko SaboBaylor College of Medicine
Wendy N NembhardFay W. Boozman College of Public Health, University of Arkansas for Medical Sciences
Michael J BamshadUniversity of Washington
Michael J BamshadBrotman Baty Institute for Precision Medicine
Michael J BamshadUniversity of Washington
Michael J BamshadBrotman Baty Institute for Precision Medicine
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
Lawrence C BrodyNational Human Genome Research Institute, National Institutes of Health
Jessica X ChongUniversity of Washington
Jessica X ChongBrotman Baty Institute for Precision Medicine
Jessica X ChongUniversity of Washington
Jessica X ChongBrotman Baty Institute for Precision Medicine
Shannon DuganBaylor College of Medicine
Shannon DuganBaylor College of Medicine
Richard H FinnellCenter for Precision Environmental Health, Baylor College of Medicine
Richard A GibbsBaylor College of Medicine
Richard A GibbsBaylor College of Medicine
Yunping LeiCenter for Precision Environmental Health, Baylor College of Medicine
James C MullikinNational Human Genome Research Institute, National Institutes of Health
James C MullikinNational Human Genome Research Institute, National Institutes of Health
Donna M MuznyBaylor College of Medicine
Donna M MuznyBaylor College of Medicine
Andrew F OlshanUniversity of North Carolina
Sanjiv HarpavatBaylor College of Medicine
Sanjiv HarpavatTexas Children's Hospital
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Release 1.2