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Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts.
Carlson, Jenna C; Nidey, Nichole L; Butali, Azeez; Buxo, Carmen J; Christensen, Kaare; Deleyiannis, Frederic W-D; Hecht, Jacqueline T; Field, L Leigh; Moreno-Uribe, Lina M; Orioli, Ieda M; Poletta, Fernando A; Padilla, Carmencita; Vieira, Alexandre R; Weinberg, Seth M; Wehby, George L; Feingold, Eleanor; Murray, Jeffrey C; Marazita, Mary L; Leslie, Elizabeth J.
Afiliação
  • Carlson JC; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Nidey NL; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Butali A; Department of Epidemiology, College of Public Health, University of Iowa, Iowa City, Iowa.
  • Buxo CJ; Department of Oral Pathology, Radiology and Medicine, Dows Institute for Dental Research, College of Dentistry, University of Iowa, Iowa City, Iowa.
  • Christensen K; Dental and Craniofacial Genomics Core, School of Dental Medicine, University of Puerto Rico, San Juan, Puerto Rico.
  • Deleyiannis FW; Department of Epidemiology, Institute of Public Health, University of Southern Denmark, Odense, Denmark.
  • Hecht JT; Department of Surgery, Plastic and Reconstructive Surgery Division, University of Colorado School of Medicine, Denver, Colorado.
  • Field LL; Department of Pediatrics, McGovern Medical School and School of Dentistry, UT Health at Houston, Houston, Texas.
  • Moreno-Uribe LM; Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada.
  • Orioli IM; Department of Orthodontics, College of Dentistry, University of Iowa, Iowa City, Iowa.
  • Poletta FA; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.
  • Padilla C; Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
  • Vieira AR; ECLAMC (Latin American Collaborative Study of Congenital Malformations) at INAGEMP (National Institute of Population Medical Genetics), Rio de Janeiro, Brazil.
  • Weinberg SM; CEMIC-CONICET: Center for Medical Education and Clinical Research "Norberto Quirno", Buenos Aires, Argentina.
  • Wehby GL; Department of Pediatrics, College of Medicine, University of the Philippines, Manila, Philippines.
  • Feingold E; The Philippine Genome Center, University of the Philippines System, Manilla, Philippines.
  • Murray JC; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Marazita ML; Department of Oral Biology, Center for Craniofacial and Dental Genetics, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Leslie EJ; Department of Health Management and Policy, College of Public Health, University of Iowa, Iowa City, Iowa.
Genet Epidemiol ; 42(7): 664-672, 2018 10.
Article em En | MEDLINE | ID: mdl-30277614

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Fenda Labial / Fissura Palatina / Caracteres Sexuais / Predisposição Genética para Doença / Alelos / Estudo de Associação Genômica Ampla Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Fenda Labial / Fissura Palatina / Caracteres Sexuais / Predisposição Genética para Doença / Alelos / Estudo de Associação Genômica Ampla Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2018 Tipo de documento: Article