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Inferring Relevant Cell Types for Complex Traits by Using Single-Cell Gene Expression.
Calderon, Diego; Bhaskar, Anand; Knowles, David A; Golan, David; Raj, Towfique; Fu, Audrey Q; Pritchard, Jonathan K.
Afiliación
  • Calderon D; Program in Biomedical Informatics, Stanford University, Stanford, CA 94305, USA. Electronic address: dcal@stanford.edu.
  • Bhaskar A; Department of Genetics, Stanford University, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA.
  • Knowles DA; Department of Genetics, Stanford University, Stanford, CA 94305, USA; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Golan D; Faculty of Industrial Engineering & Management, Technion, Haifa 3200003, Israel.
  • Raj T; Department of Neuroscience, Mount Sinai School of Medicine, New York, NY 10029, USA; Department of Genetics and Genomic Sciences, Mount Sinai School of Medicine, New York, NY 10029, USA.
  • Fu AQ; Department of Statistical Science, University of Idaho, Moscow, ID 83844, USA.
  • Pritchard JK; Department of Genetics, Stanford University, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford University, Stanford, CA 94305, USA; Department of Biology, Stanford University, Stanford, CA 94305, USA.
Am J Hum Genet ; 101(5): 686-699, 2017 Nov 02.
Article en En | MEDLINE | ID: mdl-29106824
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Programas Informáticos / Oligodendroglía / Microglía / Análisis de la Célula Individual / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Esquizofrenia / Programas Informáticos / Oligodendroglía / Microglía / Análisis de la Célula Individual / Enfermedad de Alzheimer Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos