Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study.
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| Title: | Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study. |
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| Authors: | Blue EE; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, USA.; Brotman-Baty Institute for Precision Medicine, Seattle, Washington, USA., Moore KJ; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., North KE; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Desrosiers TA; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Carmichael SL; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA., White JJ; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA., Chong JX; Brotman-Baty Institute for Precision Medicine, Seattle, Washington, USA.; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA., Bamshad MJ; Brotman-Baty Institute for Precision Medicine, Seattle, Washington, USA.; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USA.; Division of Genetic Medicine, Seattle Children's Hospital, Seattle, Washington, USA.; Department of Genome Sciences, University of Washington School of Medicine, Seattle, Washington, USA., Jenkins MM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Almli LM; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia, USA., Brody LC; Division of Genomics and Society, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Freedman SF; Department of Ophthalmology, Duke University Medical Center, Durham, North Carolina, 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, College of Public Health, The University of Iowa, Iowa City, Iowa, USA., Shaw GM; Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA., Werler M; Department of Epidemiology, School of Public Health, Boston University, Boston, Massachusetts, USA.; Slone Epidemiology Center at Boston University, Boston, Massachusetts, USA., Kay DM; Division of Genetics, Wadsworth Center, New York State Department of Health, Albany, New York, USA., Browne ML; New York State Department of Health, Birth Defects Registry, Albany, New York, USA.; Department of Epidemiology and Biostatistics, University at Albany School of Public Health, Rensselaer, New York, USA., Feldkamp ML; Division of Medical Genetics, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah, USA., Finnell RH; Center for Precision Environmental Health, Departments of Molecular and Cellular Biology and Medicine, Baylor College of Medicine, Houston, Texas, USA., Nembhard WN; Department of Epidemiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA., Pangilinan F; Division of Genomics and Society, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA., Olshan AF; Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA. |
| Corporate Authors: | National Institutes of Health Intramural Sequencing Center, University of Washington Center for Mendelian Genomics, National Birth Defects Prevention Study |
| Source: | Birth defects research [Birth Defects Res] 2024 Jul; Vol. 116 (7), pp. e2384. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: John Wiley & Sons, Inc Country of Publication: United States NLM ID: 101701004 Publication Model: Print Cited Medium: Internet ISSN: 2472-1727 (Electronic) NLM ISO Abbreviation: Birth Defects Res Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2472-1727 |
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| DOI: | 10.1002/bdr2.2384 |
