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Author Details

Matthew W State
UCSF Weill Institute for Neurosciences, University of California san francisco
1997
144
69
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36797480New and emerging approaches to treat psychiatric disorders.Nat Med2023
36475375In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review.Am J Psychiatry2023
36797480New and emerging approaches to treat psychiatric disorders.Nat Med2023
37366052Pleiotropy of autism-associated chromatin regulators.Development2023
37366052Pleiotropy of autism-associated chromatin regulators.Development2023
36475375In Search of Biomarkers to Guide Interventions in Autism Spectrum Disorder: A Systematic Review.Am J Psychiatry2023
35440779Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.Nat Rev Neurosci2022
35440779Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.Nat Rev Neurosci2022
32668441Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.Neuropsychopharmacology2021
33887193Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.Neuron2021
33497602Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.Neuron2021
32668441Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.Neuropsychopharmacology2021
33384012Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.Am J Psychiatry2021
33887193Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.Neuron2021
33497602Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.Neuron2021
33384012Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.Am J Psychiatry2021
32294447Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.Cell Rep2020
32268104Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.Cell Rep2020
31949163Autism spectrum disorder.Nat Rev Dis Primers2020
32294447Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.Cell Rep2020
32467234The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.Development2020
33288503Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.Development2020
31949163Autism spectrum disorder.Nat Rev Dis Primers2020
33288503Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.Development2020
32467234The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.Development2020
32268104Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.Cell Rep2020
29325623Tourette disorder and other tic disorders.Handb Clin Neurol2018
30359605Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder.Neuron2018
30545854Integrative functional genomic analysis of human brain development and neuropsychiatric risks.Science2018
30257206De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.Cell Rep2018
30545852Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.Science2018
30053424The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.Cell2018
30318412Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.Neuron2018
29700473An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.Nat Genet2018
29549319Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2018
29325623Tourette disorder and other tic disorders.Handb Clin Neurol2018
30053424The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.Cell2018
30257206De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.Cell Rep2018
30318412Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.Neuron2018
30545854Integrative functional genomic analysis of human brain development and neuropsychiatric risks.Science2018
30545852Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.Science2018
30359605Lost in Translation: Traversing the Complex Path from Genomics to Therapeutics in Autism Spectrum Disorder.Neuron2018
29700473An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.Nat Genet2018
29549319Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2018
27431290Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.Mol Psychiatry2017
28472652De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Neuron2017
29100089De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.Am J Hum Genet2017
29184211Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2017
29170230Molecular and cellular reorganization of neural circuits in the human lineage.Science2017
27431290Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.Mol Psychiatry2017
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Collaborators

Stephan J Sanders
Co-authored papers 44
Arthur Jeremy Willsey
University of California san francisco
Co-authored papers 35
Richard P Lifton
The Rockefeller University
Co-authored papers 28
Shrikant Mane
Yale School of Medicine
Co-authored papers 24
Bernie Devlin
Co-authored papers 22
Murat Gunel
Yale School of Medicine
Co-authored papers 21
Nenad Sestan
Yale School of Medicine
Co-authored papers 21
Daniel H Geschwind
University of California los angeles
Co-authored papers 20
Kaya Bilguvar
Acibadem Mehmet Ali Aydinlar University
Co-authored papers 17
Kathryn Roeder
Co-authored papers 16
Lambertus Klei
Co-authored papers 16
Edwin H Cook
Co-authored papers 14
Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
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James S Sutcliffe
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Massachusetts General Hospital
Co-authored papers 12
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Massachusetts General Hospital
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Christopher E Mason
Feil Family Brain and Mind Research Institute.
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Christopher A Walsh
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Christa Lese Martin
Autism and Developmental Medicine Institute
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University of California san francisco
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Timothy W Yu
Harvard Medical School
Co-authored papers 9
Donna M Werling
Co-authored papers 8
David H Ledbetter
University of Florida, College of Medicine-Jacksonville
Co-authored papers 8
Thomas M Morgan
Co-authored papers 8
Catherine Lord
University of California los angeles
Co-authored papers 8
Jay A Tischfield
Co-authored papers 8
Helen Rankin Willsey
University of California san francisco
Co-authored papers 7
Mingfeng Li
Co-authored papers 7
Eric Fombonne
Oregon Health & Science University (OHSU)
Co-authored papers 7
Li Liu
Co-authored papers 7
Release 1.2