A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3 - Top-Institutions - MDSpire

A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3

  • By

  • Michaela Yuen

  • Katharine Zhang

  • Rhett G. Marchant

  • Ryosuke Ishimura

  • Mark Graham

  • May Aung-Htut

  • Samantha Bryen

  • Rocio Rius

  • Lee Marshall

  • Nader Aryamanesh

  • Gregory Dziaduch

  • Himanshu Joshi

  • Ben Weisburd

  • Steve D. Wilton

  • Meredith Wilson

  • Russell Gear

  • Lucy Hennington

  • Stephanie Lau

  • Helen Doyle

  • Michael Krivanek

  • Richard J. Leventer

  • Susan M. White

  • Sarah A. Sandaradura

  • Masaaki Komatsu

  • Frances J. Evesson

  • Sandra T. Cooper

  • April 27, 2026

  • 0 min

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Top Institutions in Neurology

Brief introduction explaining scope and methodology.

  • #1

    Broad Institute of MIT and Harvard
    Broad Institute of MIT and Harvard

    Cambridge, MA

    Key Differentiators

    • Neurogenetics
    • Genomics
    • Rare Disease Research

  • #2

    Children’s Hospital of Philadelphia (CHOP) Center for Applied Genomics
    Children’s Hospital of Philadelphia (CHOP) Center for Applied Genomics

    Philadelphia, PA

    Key Differentiators

    • Pediatric Neurogenetics
    • Genomic Medicine
    • Rare Disease Diagnostics

  • #3

    University of California, San Francisco (UCSF) Weill Institute for Neurosciences
    University of California, San Francisco (UCSF) Weill Institute for Neurosciences

    San Francisco, CA

    Key Differentiators

    • Neurogenetics
    • Molecular Neuroscience
    • Neurodevelopmental Disorders

  • #4

    The Rockefeller University
    The Rockefeller University

    New York, NY

    Key Differentiators

    • Molecular Biology
    • Neurogenetics
    • Cellular Neuroscience

  • #5

    The Murdoch Children’s Research Institute
    The Murdoch Children’s Research Institute

    Melbourne, VIC

    Key Differentiators

    • Pediatric Genomics
    • Neurodevelopmental Disorders
    • Rare Disease Research

Original Source(s)

A significant neurodevelopmental disorder associated with a South Asian founder mutation in the UFMylation adaptor CDK5RAP3

  • by Michaela Yuen, Katharine Zhang, Rhett G. Marchant, Ryosuke Ishimura, Mark Graham, May Aung-Htut, Samantha Bryen, Rocio Rius, Lee Marshall, Nader Aryamanesh, Gregory Dziaduch, Himanshu Joshi, Ben Weisburd, Steve D. Wilton, Meredith Wilson, Russell Gear, Lucy Hennington, Stephanie Lau, Helen Doyle, Michael Krivanek, Richard J. Leventer, Susan M. White, Sarah A. Sandaradura, Masaaki Komatsu, Frances J. Evesson, Sandra T. Cooper

  • April 27, 2026

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