Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.

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Bibliographic Details
Title: Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Authors: Carlson JC; 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., Nidey NL; Department of Epidemiology, College of Public Health, University of Iowa, Iowa City, Iowa., Butali A; Department of Oral Pathology, Radiology and Medicine, Dows Institute for Dental Research, College of Dentistry, University of Iowa, Iowa City, Iowa., Buxo 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 FW; Department of Surgery, Plastic and Reconstructive Surgery Division, University of Colorado School of Medicine, Denver, Colorado., Hecht JT; Department of Pediatrics, McGovern Medical School and School of Dentistry, UT Health at Houston, Houston, Texas., Field LL; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada., Moreno-Uribe LM; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa., Orioli IM; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil., Poletta FA; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.; CEMIC-CONICET: Center for Medical Education and Clinical Research 'Norberto Quirno', Buenos Aires, Argentina., Padilla C; Department of Pediatrics, College of Medicine, University of the Philippines, Manila, Philippines.; The Philippine Genome Center, University of the Philippines System, Manilla, Philippines., Vieira AR; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Weinberg SM; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Wehby GL; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa., 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., Murray JC; Department of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, Iowa., Marazita ML; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania., Leslie EJ; Department of Human Genetics, Emory University School of Medicine, Emory University, Atlanta, Georgia.
Source: Genetic epidemiology [Genet Epidemiol] 2018 Oct; Vol. 42 (7), pp. 664-672. Date of Electronic Publication: 2018 Sep 11.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8411723 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-2272 (Electronic) Linking ISSN: 07410395 NLM ISO Abbreviation: Genet Epidemiol Subsets: MEDLINE
Database: MEDLINE Ultimate
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