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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Justice, Cristina M; Cuellar, Araceli; Bala, Krithi; Sabourin, Jeremy A; Cunningham, Michael L; Crawford, Karen; Phipps, Julie M; Zhou, Yan; Cilliers, Deirdre; Byren, Jo C; Johnson, David; Wall, Steven A; Morton, Jenny E V; Noons, Peter; Sweeney, Elizabeth; Weber, Astrid; Rees, Katie E M; Wilson, Louise C; Simeonov, Emil; Kaneva, Radka; Yaneva, Nadezhda; Georgiev, Kiril; Bussarsky, Assen; Senders, Craig; Zwienenberg, Marike; Boggan, James; Roscioli, Tony; Tamburrini, Gianpiero; Barba, Marta; Conway, Kristin; Sheffield, Val C; Brody, Lawrence; Mills, James L; Kay, Denise; Sicko, Robert J; Langlois, Peter H; Tittle, Rachel K; Botto, Lorenzo D; Jenkins, Mary M; LaSalle, Janine M; Lattanzi, Wanda; Wilkie, Andrew O M; Wilson, Alexander F; Romitti, Paul A; Boyadjiev, Simeon A.
Afiliación
  • Justice CM; Genometrics Section, Computational and Statistical Genomics Branch, Division of Intramural Research, NHGRI, NIH, Baltimore, MD, USA.
  • Cuellar A; Department of Pediatrics, University of California Davis, 4625 2nd Avenue, Research Building II, Sacramento, CA, 95817, USA.
  • Bala K; Department of Pediatrics, University of California Davis, 4625 2nd Avenue, Research Building II, Sacramento, CA, 95817, USA.
  • Sabourin JA; Genometrics Section, Computational and Statistical Genomics Branch, Division of Intramural Research, NHGRI, NIH, Baltimore, MD, USA.
  • Cunningham ML; Department of Pediatrics, Division of Craniofacial Medicine, Seattle Children's Craniofacial Center, Seattle Children's Research Institute, University of Washington, Seattle, WA, USA.
  • Crawford K; MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Phipps JM; MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Zhou Y; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Cilliers D; MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • Byren JC; Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Johnson D; Craniofacial Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Wall SA; Craniofacial Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Morton JEV; Craniofacial Unit, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Noons P; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
  • Sweeney E; Birmingham Craniofacial Unit, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
  • Weber A; Birmingham Craniofacial Unit, Birmingham Women's and Children's Hospitals NHS Foundation Trust, Birmingham, UK.
  • Rees KEM; Department of Clinical Genetics, Liverpool Women's NHS Foundation Trust, Liverpool, England, UK.
  • Wilson LC; Department of Clinical Genetics, Liverpool Women's NHS Foundation Trust, Liverpool, England, UK.
  • Simeonov E; Clinical Genetics Service, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Kaneva R; Clinical Genetics Service, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
  • Yaneva N; National Institute of Pediatrics, Sofia Medical University, Sofia, Bulgaria.
  • Georgiev K; Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University of Sofia, Sofia, Bulgaria.
  • Bussarsky A; National Genetic Laboratory, University Hospital of Obstetrics and Gynecology "Maichin Dom", Medical University of Sofia, Sofia, Bulgaria.
  • Senders C; Department of Neurosurgery, University Hospital 'St. Ivan Rilski', Medical University of Sofia, Sofia, Bulgaria.
  • Zwienenberg M; Department of Neurosurgery, University Hospital 'St. Ivan Rilski', Medical University of Sofia, Sofia, Bulgaria.
  • Boggan J; Department of Otolaryngology, Head and Neck Surgery, University of California Davis, Sacramento, CA, USA.
  • Roscioli T; Department of Neurosurgery, University of California Davis, Sacramento, CA, USA.
  • Tamburrini G; Department of Neurosurgery, University of California Davis, Sacramento, CA, USA.
  • Barba M; Neuroscience Research Australia, University of New South Wales, Sydney, Australia.
  • Conway K; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Sheffield VC; Section of Neurosurgery, Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Brody L; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
  • Mills JL; Section of Experimental Biology, Department of Life Science and Public Health, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Kay D; Department of Epidemiology, College of Public Health, The University of Iowa, 145 N Riverside Dr, S416 CPHB, Iowa City, IA, 52242, USA.
  • Sicko RJ; Department of Pediatrics, Division of Medical Genetics, Carver College of Medicine, The University of Iowa, Iowa City, IA, USA.
  • Langlois PH; Gene and Environment Interaction Section, NHGRI, Bethesda, NIHMD, USA.
  • Tittle RK; Epidemiology Branch, Eunice Kennedy Shriver NICHD, NIH, Bethesda, MD, USA.
  • Botto LD; Division of Genetics, NYS Department of Health, Wadsworth CenterAlbany, NY, USA.
  • Jenkins MM; Division of Genetics, NYS Department of Health, Wadsworth CenterAlbany, NY, USA.
  • LaSalle JM; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA.
  • Lattanzi W; Department of Nutritional Sciences, University of Texas at Austin, Austin, TX, USA.
  • Wilkie AOM; Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT, USA.
  • Wilson AF; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Romitti PA; Department of Medical Microbiology and Immunology, Genome Center, and MIND Institute, University of California Davis, Davis, CA, USA.
  • Boyadjiev SA; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Hum Genet ; 139(8): 1077-1090, 2020 Aug.
Article en En | MEDLINE | ID: mdl-32266521

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Craneosinostosis / Polimorfismo de Nucleótido Simple / Proteína Morfogenética Ósea 7 Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Craneosinostosis / Polimorfismo de Nucleótido Simple / Proteína Morfogenética Ósea 7 Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos