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Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer's and Parkinson's diseases.
Corces, M Ryan; Shcherbina, Anna; Kundu, Soumya; Gloudemans, Michael J; Frésard, Laure; Granja, Jeffrey M; Louie, Bryan H; Eulalio, Tiffany; Shams, Shadi; Bagdatli, S Tansu; Mumbach, Maxwell R; Liu, Boxiang; Montine, Kathleen S; Greenleaf, William J; Kundaje, Anshul; Montgomery, Stephen B; Chang, Howard Y; Montine, Thomas J.
Afiliación
  • Corces MR; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Shcherbina A; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA, USA.
  • Kundu S; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
  • Gloudemans MJ; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Frésard L; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Granja JM; Department of Computer Science, Stanford University, Stanford, CA, USA.
  • Louie BH; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Eulalio T; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
  • Shams S; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Bagdatli ST; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA, USA.
  • Mumbach MR; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
  • Liu B; Program in Biophysics, Stanford University, Stanford, CA, USA.
  • Montine KS; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Greenleaf WJ; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA, USA.
  • Kundaje A; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Montgomery SB; Department of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.
  • Chang HY; Center for Personal Dynamic Regulomes, Stanford University, Stanford, CA, USA.
  • Montine TJ; Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA.
Nat Genet ; 52(11): 1158-1168, 2020 11.
Article en En | MEDLINE | ID: mdl-33106633
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Encéfalo / Enfermedad de Alzheimer / Neuronas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Encéfalo / Enfermedad de Alzheimer / Neuronas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos