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  3. SCSB Colloquium Series – One brain, many genomes: somatic mutation and genomic diversity in human brain
20151106_Walsh at bench cropped.jpg
Simons Center for the Social Brain
SCSB Colloquium Series

SCSB Colloquium Series – One brain, many genomes: somatic mutation and genomic diversity in human brain

Speaker(s)
SCSB Colloquium Series – Christopher A. Walsh, M.D., Ph.D.
Register
Add to CalendarAmerica/New_YorkSCSB Colloquium Series – One brain, many genomes: somatic mutation and genomic diversity in human brain11/18/2020 9:00 pm11/18/2020 10:00 pmWebinar
November 18, 2020
9:00 pm - 10:00 pm
Location
Webinar
Contact
Alexandra Sokhina
    Description

    Date: Wednesday, November 18, 2020
    Location: Zoom Webinar – Registration Required
    Register in advance for this webinar: click here  
    * After registering, you will receive a confirmation email containing information on how to join the webinar.

    Speaker: Christopher A. Walsh, M.D., Ph.D.
    Affiliation:
    Chief of Genetics and Genomics, Boston Children’s Hospital, Investigator, Howard Hughes Medical Institute, Professor of Pediatrics and Neurology, Harvard Medical School
    Host: Dr. Mriganka Sur

    Talk title: One brain, many genomes: somatic mutation and genomic diversity in human brain

    Abstract: Although it had long been assumed that the genomes of all neurons are identical, recent work has shown that every cell division causes mutations even during normal development, and that postmitotic neurons continue to accumulate mutations throughout life. Clonal somatic mutations create a mosaic brain that in some cases is associated with epileptic brain malformations and autism spectrum disorders, and may contribute to other neuropsychiatric diseases. The mutations that arise during development also represent a permanent forensic cell lineage map of the body.  This lecture will discuss mutations that distinguish the genome of one neuron from the neuron next to it in human brain, and the implications for normal brain development, and neurological diseases.

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