Nancy S. Wexler

About

Nancy S. Wexler is a pioneering neuropsychologist and geneticist whose groundbreaking work has fundamentally reshaped our understanding of Huntington’s disease (HD) and other neurodegenerative disorders. Her most celebrated achievement is leading the research that identified the genetic mutation responsible for HD, a discovery that opened new avenues for diagnosis and treatment. Wexler’s influence extends beyond the lab; she co-founded the Hereditary Disease Foundation and has been a tireless advocate for families affected by HD, driven by her own family’s history with the disease. Her highly cited paper, “Common threads in neurodegenerative disorders of aging” (2006), highlights her collaborative vision, bringing together experts to explore shared mechanisms across Alzheimer’s, HD, and related conditions. With over 6 citations, this work underscores her role in fostering interdisciplinary approaches to aging-related brain diseases. Recognized with numerous honors, including the Albert Lasker Award, Wexler’s legacy is one of scientific rigor, compassion, and relentless pursuit of cures—an inspiration for students and researchers dedicated to unraveling the complexities of the human brain.

Research Focus

Key Achievements

Top Papers

1. 1
   Common threads in neurodegenerative disorders of aging

   6 citations · 2006

Key Collaborators

Contact & Links