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Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
Kim, Sonia Nan; Viswanadham, Vinayak V; Doan, Ryan N; Dou, Yanmei; Bizzotto, Sara; Khoshkhoo, Sattar; Huang, August Yue; Yeh, Rebecca; Chhouk, Brian; Truong, Alex; Chappell, Kathleen M; Beaudin, Marc; Barton, Alison; Akula, Shyam K; Rento, Lariza; Lodato, Michael; Ganz, Javier; Szeto, Ryan A; Li, Pengpeng; Tsai, Jessica W; Hill, Robert Sean; Park, Peter J; Walsh, Christopher A.
Afiliação
  • Kim SN; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Viswanadham VV; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Doan RN; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Dou Y; Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, 02115, MA, USA.
  • Bizzotto S; Department of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.
  • Khoshkhoo S; Bioinformatics and Integrative Genomics Program, Harvard Medical School, Boston, 02115, MA, USA.
  • Huang AY; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Yeh R; Department of Biomedical Informatics, Harvard Medical School, Boston, 02115, MA, USA.
  • Chhouk B; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Truong A; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Chappell KM; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Beaudin M; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Barton A; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Akula SK; Department of Neurology, Brigham and Women's Hospital, Boston, 02115, MA, USA.
  • Rento L; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Lodato M; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
  • Ganz J; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Szeto RA; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Li P; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Tsai JW; Research Computing, Harvard Medical School, Boston, 02115, MA, USA.
  • Hill RS; Research Computing, Harvard Medical School, Boston, 02115, MA, USA.
  • Park PJ; Division of Genetics and Genomics, Manton Center for Orphan Disease Research, Department of Pediatrics, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, 02115, MA, USA.
  • Walsh CA; Departments of Pediatrics and Neurology, Harvard Medical School, Boston, 02115, MA, USA.
bioRxiv ; 2023 Nov 06.
Article em En | MEDLINE | ID: mdl-37986891
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article