Gary A Heiman

10PUBLICATIONS
83CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesGenetically modified animalsDevelopmental genetics (incl. sex determination)Aboriginal and Torres Strait Islander child health and wellbeing
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Publications (10)

|Nov 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders.

Belinda Wang, Matthew N Tran, Sheng Wang

|Nov 13, 2025
A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron Excitability.

Cara Nasello, G Duygu Yilmaz, Lauren A Poppi

|Apr 29, 2024
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice.

Cara Nasello, Lauren A Poppi, Junbing Wu

|Dec 06, 2023
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD.

Sheng Wang, Belinda Wang, Vanessa Drury

|Dec 08, 2022
Polygenic and environmental determinants of tics in the Avon Longitudinal Study of Parents and Children.

Mohamed Abdulkadir, Jay A Tischfield, Gary A Heiman

|Feb 23, 2022
Genetic counseling certificate program: A program evaluation of undergraduate exposure to genetic counseling.

Erin McGraw, Jessica Rispoli, Michele B Horner

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Frequent Collaborators

4 joint publications

Thomas V Fernandez

3 joint publications

Jay A Tischfield

3 joint publications

Jinchuan Xing

3 joint publications

Joshua K Thackray