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Matthew State
Matthew State
Verified email at ucsf.edu - Homepage
Title
Cited by
Year
Genome-wide association study points to novel locus for gilles de la tourette syndrome
F Tsetsos, A Topaloudi, P Jain, Z Yang, D Yu, P Kolovos, Z Tumer, ...
Biological psychiatry 96 (2), 114-124, 2024
92024
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility
KE McCluskey, KM Stovell, K Law, E Kostyanovskaya, J Schmidt, ...
bioRxiv, 2024.05. 28.593642, 2024
2024
Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD
S Wang, B Wang, V Drury, S Drake, N Sun, H Alkhairo, J Arbelaez, ...
Nature communications 14 (1), 8077, 2023
42023
A foundational atlas of autism protein interactions reveals molecular convergence
B Wang, R Vartak, Y Zaltsman, ZZC Naing, K Hennick, B Polacco, ...
62023
Pleiotropy of autism-associated chromatin regulators
M Lasser, N Sun, Y Xu, S Wang, S Drake, K Law, S Gonzalez, B Wang, ...
Development 150 (14), 2023
102023
New and emerging approaches to treat psychiatric disorders
KW Scangos, MW State, AH Miller, JT Baker, LM Williams
Nature medicine 29 (2), 317-333, 2023
452023
In search of biomarkers to guide interventions in autism spectrum disorder: a systematic review
M Parellada, Á Andreu-Bernabeu, M Burdeus, A San José Cáceres, ...
American Journal of Psychiatry 180 (1), 23-40, 2023
332023
Autism-associated transcriptional regulators target shared loci proximal to brain-expressed genes
SF Darbandi, JY An, K Lim, NF Page, L Liang, AR Ypsilanti, ...
bioRxiv, 2022.10. 17.512583, 2022
12022
6.7 Translating Gene Discovery into Treatments in ASD
M State
Journal of the American Academy of Child & Adolescent Psychiatry 61 (10), S136, 2022
2022
Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder
S Wang, B Wang, V Drury, S Drake, N Sun, H Alkhairo, J Arbelaez, ...
medRxiv, 2022.09. 22.22280248, 2022
12022
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder
HR Willsey, AJ Willsey, B Wang, MW State
Nature Reviews Neuroscience 23 (6), 323-341, 2022
1112022
Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
E Markenscoff-Papadimitriou, F Binyameen, S Whalen, J Price, K Lim, ...
Cell reports 37 (10), 2021
422021
FROM BENCH TO BEDSIDE: INVESTIGATING BIOLOGICAL MECHANISMS OF SEX DIFFERENCES IN AUTISM SPECTRUM DISORDER
EJ Hoffman, D Manoli, M State
Journal of the American Academy of Child & Adolescent Psychiatry 60 (10), S293, 2021
2021
A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders
CM Diaz-Caneja, MW State, RJ Hagerman, S Jacquemont, O Marin, ...
European Neuropsychopharmacology 48, 49-88, 2021
342021
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience
HR Willsey, CRT Exner, Y Xu, A Everitt, N Sun, B Wang, J Dea, ...
Neuron 109 (5), 788-804. e8, 2021
952021
Autism spectrum disorder genetics and the search for pathological mechanisms
DS Manoli, MW State
American Journal of Psychiatry 178 (1), 30-38, 2021
1022021
Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders
VB Searles Quick, B Wang, MW State
Neuropsychopharmacology 46 (1), 55-69, 2021
352021
The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos
HR Willsey, Y Xu, A Everitt, J Dea, CRT Exner, AJ Willsey, MW State, ...
Development 147 (21), dev189290, 2020
412020
BRIDGING THE GAP FROM BENCH TO BEDSIDE IN CHILDHOOD NEUROPSYCHIATRIC DISORDERS
EJ Hoffman, D Manoli, M State
Journal of the American Academy of Child & Adolescent Psychiatry 59 (10), S313, 2020
2020
A chromatin accessibility atlas of the developing human telencephalon
E Markenscoff-Papadimitriou, S Whalen, P Przytycki, R Thomas, ...
Cell 182 (3), 754-769. e18, 2020
752020
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