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Matthew W State

13PUBLICATIONS

141CO-AUTHORS

Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Genome structure and regulation

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Publications (13)

Sort by Publication Date:

|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

|Mar 06, 2025

Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility.

Kate E McCluskey, Katherine M Stovell, Karen Law

|Dec 16, 2024

Convergence of autism proteins at the cilium.

Elina Kostyanovskaya, Micaela C Lasser, Belinda Wang

|Jun 10, 2024

Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility.

Kate E McCluskey, Katherine M Stovell, Karen Law

|Dec 11, 2023

A foundational atlas of autism protein interactions reveals molecular convergence.

Belinda Wang, Rasika Vartak, Yefim Zaltsman

|Dec 06, 2023

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

Sheng Wang, Belinda Wang, Vanessa Drury

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Frequent Collaborators

7 joint publications

A Jeremy Willsey

6 joint publications

Jeanselle Dea

5 joint publications

Helen Rankin Willsey

5 joint publications

Belinda Wang

4 joint publications

Sheng Wang

3 joint publications

Elina Kostyanovskaya

3 joint publications

Kate E McCluskey

3 joint publications

Nenad Sestan

3 joint publications

Nawei Sun

3 joint publications

Karen Law

Frequent Collaborators

7 joint publications

A Jeremy Willsey

6 joint publications

Jeanselle Dea

5 joint publications

Helen Rankin Willsey

5 joint publications

Belinda Wang

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