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Author Details
Full Name
Arthur Jeremy Willsey
Affiliation
University of California san francisco
ORCID
Career Start Year
2012
Papers
42
H Index
33
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37366052
Pleiotropy of autism-associated chromatin regulators.
Development
2023
37366052
Pleiotropy of autism-associated chromatin regulators.
Development
2023
35440779
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.
Nat Rev Neurosci
2022
35440779
Genomics, convergent neuroscience and progress in understanding autism spectrum disorder.
Nat Rev Neurosci
2022
34411509
A convergent molecular network underlying autism and congenital heart disease.
Cell Syst
2021
33887193
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
33497602
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
34411509
A convergent molecular network underlying autism and congenital heart disease.
Cell Syst
2021
33887193
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
33497602
Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Neuron
2021
32294447
Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.
Cell Rep
2020
32294447
Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.
Cell Rep
2020
31771860
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Biol Psychiatry
2020
32467234
The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
33288503
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
31771860
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.
Biol Psychiatry
2020
33288503
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
32467234
The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryos.
Development
2020
30818990
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
Am J Psychiatry
2019
30818990
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.
Am J Psychiatry
2019
29549319
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Nat Neurosci
2018
30257206
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Cell Rep
2018
30545852
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
Science
2018
30053424
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
Cell
2018
30318412
Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.
Neuron
2018
29700473
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
Nat Genet
2018
29549319
Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Nat Neurosci
2018
30053424
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders.
Cell
2018
30257206
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis.
Cell Rep
2018
30318412
Neonatal Tbr1 Dosage Controls Cortical Layer 6 Connectivity.
Neuron
2018
30545852
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
Science
2018
29700473
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.
Nat Genet
2018
29184211
Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Nat Neurosci
2017
28472652
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
Neuron
2017
29184211
Whole genome sequencing in psychiatric disorders: the WGSPD consortium.
Nat Neurosci
2017
28253736
Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.
Am J Psychiatry
2017
28253736
Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.
Am J Psychiatry
2017
28472652
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.
Neuron
2017
26974344
Localized JNK signaling regulates organ size during development.
Elife
2016
26974344
Localized JNK signaling regulates organ size during development.
Elife
2016
27536211
The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.
Front Neurosci
2016
27536211
The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.
Front Neurosci
2016
25534755
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Biol Psychiatry
2015
25464374
Autism spectrum disorders: from genes to neurobiology.
Curr Opin Neurobiol
2015
25752243
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
Nat Commun
2015
25621974
No evidence for association of autism with rare heterozygous point mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contactins.
PLoS Genet
2015
25534755
A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Biol Psychiatry
2015
25973162
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus.
Mol Autism
2015
26402605
Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Neuron
2015
26605881
The PsychENCODE project.
Nat Neurosci
2015
1 - 50 of 84
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row(s) 1 - 30 of 30
Collaborators
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UCSF Weill Institute for Neurosciences, University of California san francisco
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Co-authored papers
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Co-authored papers
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Jeanselle Dea
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Co-authored papers
10
Benjamin M Neale
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Co-authored papers
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University of California san francisco
Co-authored papers
9
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Yale School of Medicine
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Mark J Daly
Massachusetts General Hospital
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Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
Co-authored papers
7
James S Sutcliffe
Vanderbilt Genetics Institute, Vanderbilt University
Co-authored papers
7
Christa Lese Martin
Autism and Developmental Medicine Institute
Co-authored papers
7
David H Ledbetter
University of Florida, College of Medicine-Jacksonville
Co-authored papers
7
Timothy W Yu
Harvard Medical School
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7
Christopher A Walsh
Broad Institute of MIT and Harvard
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7
Edwin H Cook
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7
Donna M Werling
Co-authored papers
7
Yuxiao Xu
University of California san francisco
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Eric Fombonne
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