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Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variants.
Bureau, Alexandre; Begum, Ferdouse; Taub, Margaret A; Hetmanski, Jacqueline B; Parker, Margaret M; Albacha-Hejazi, Hasan; Scott, Alan F; Murray, Jeffrey C; Marazita, Mary L; Bailey-Wilson, Joan E; Beaty, Terri H; Ruczinski, Ingo.
Afiliación
  • Bureau A; Département de Médecine Sociale et Préventive, Université Laval, Québec City, Québec, Canada.
  • Begum F; Centre de recherche CERVO, Québec City, Québec, Canada.
  • Taub MA; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Hetmanski JB; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Parker MM; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Albacha-Hejazi H; Channing Division of Network Medicine, Harvard Medical School, Boston, Massachusetts.
  • Scott AF; Prime Health Clinic  Jeddah, Riyadh, Saudi Arabia.
  • Murray JC; Institute of Genetic Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland.
  • Marazita ML; Department of Pediatrics, School of Medicine, University of Iowa, Iowa City, Iowa.
  • Bailey-Wilson JE; Department of Oral Biology, School of Dental Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
  • Beaty TH; Inherited Disease Research Branch, National Human Genome Research Institute, Baltimore, Maryland.
  • Ruczinski I; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Genet Epidemiol ; 43(1): 37-49, 2019 02.
Article en En | MEDLINE | ID: mdl-30246882
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linaje / Variación Genética / Análisis de Secuencia de ADN / Predisposición Genética a la Enfermedad Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Linaje / Variación Genética / Análisis de Secuencia de ADN / Predisposición Genética a la Enfermedad Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá