Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts.
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| Title: | Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts. |
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| Authors: | Shaffer JR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., LeClair J; Department of Computational and Systems Biology, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, School of Public Health, Boston University, Boston, Massachusetts., Carlson JC; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Feingold E; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Buxó CJ; Dental and Craniofacial Genomics Core, School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico., Christensen K; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark., Deleyiannis FWB; Department of Surgery, Plastic and Reconstructive Surgery, University of Colorado School of Medicine, Denver, Colorado., Field LL; Department of Medical Genetics, University of British Columbia, Vancouver, Canada., Hecht JT; Department of Pediatrics, McGovern Medical School and School of Dentistry UT Health at Houston, Houston, Texas., Moreno L; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa., Orioli IM; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil., Padilla C; Department of Pediatrics, College of Medicine; and Institute of Human Genetics, National Institutes of Health, University of the Philippines Manila, Manila, The Philippines.; Philippine Genome Center, University of the Philippines System, Manila, The Philippines., Vieira AR; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania., Wehby GL; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa., Murray JC; Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa., Weinberg SM; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Anthropology, Dietrich School of Arts and Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania., Marazita ML; Center for Craniofacial and Dental Genetics, Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Clinical and Translational Science, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Leslie EJ; Department of Human Genetics, Emory University School of Medicine, Emory University, Atlanta, Georgia. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2019 Mar; Vol. 179 (3), pp. 467-474. Date of Electronic Publication: 2018 Dec 24. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. |
| 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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| ISSN: | 1552-4833 |
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| DOI: | 10.1002/ajmg.a.61002 |
