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Author Details

Arthur Jeremy Willsey
University of California san francisco
2012
42
33
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37366052Pleiotropy of autism-associated chromatin regulators.Development2023
37366052Pleiotropy of autism-associated chromatin regulators.Development2023
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
34411509A convergent molecular network underlying autism and congenital heart disease.Cell Syst2021
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
34411509A convergent molecular network underlying autism and congenital heart disease.Cell Syst2021
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
32294447Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.Cell Rep2020
32294447Enhancing WNT Signaling Restores Cortical Neuronal Spine Maturation and Synaptogenesis in Tbr1 Mutants.Cell Rep2020
31771860De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.Biol Psychiatry2020
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
31771860De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism.Biol Psychiatry2020
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
30818990Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.Am J Psychiatry2019
30818990Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies.Am J Psychiatry2019
29549319Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2018
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
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
30545852Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.Science2018
29700473An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.Nat Genet2018
29184211Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2017
28472652De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Neuron2017
29184211Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Nat Neurosci2017
28253736Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.Am J Psychiatry2017
28253736Identification of Developmental and Behavioral Markers Associated With Genetic Abnormalities in Autism Spectrum Disorder.Am J Psychiatry2017
28472652De Novo Coding Variants Are Strongly Associated with Tourette Disorder.Neuron2017
26974344Localized JNK signaling regulates organ size during development.Elife2016
26974344Localized JNK signaling regulates organ size during development.Elife2016
27536211The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.Front Neurosci2016
27536211The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.Front Neurosci2016
25534755A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Biol Psychiatry2015
25464374Autism spectrum disorders: from genes to neurobiology.Curr Opin Neurobiol2015
25752243The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.Nat Commun2015
25621974No 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 Genet2015
25534755A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Biol Psychiatry2015
25973162The female protective effect in autism spectrum disorder is not mediated by a single genetic locus.Mol Autism2015
26402605Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Neuron2015
26605881The PsychENCODE project.Nat Neurosci2015
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Collaborators

UCSF Weill Institute for Neurosciences, University of California san francisco
Co-authored papers 35
Co-authored papers 23
Co-authored papers 14
Co-authored papers 12
University of California los angeles
Co-authored papers 11
Co-authored papers 11
Yale School of Medicine
Co-authored papers 10
University of California san francisco
Co-authored papers 10
Massachusetts General Hospital
Co-authored papers 10
University of California san francisco
Co-authored papers 9
Yale School of Medicine
Co-authored papers 9
Massachusetts General Hospital
Co-authored papers 8
Icahn School of Medicine at Mount Sinai
Co-authored papers 7
Vanderbilt Genetics Institute, Vanderbilt University
Co-authored papers 7
Autism and Developmental Medicine Institute
Co-authored papers 7
University of Florida, College of Medicine-Jacksonville
Co-authored papers 7
Harvard Medical School
Co-authored papers 7
Broad Institute of MIT and Harvard
Co-authored papers 7
Co-authored papers 7
Co-authored papers 7
University of California san francisco
Co-authored papers 6
Oregon Health & Science University (OHSU)
Co-authored papers 6
University of California los angeles
Co-authored papers 6
University of Michigan ann arbor
Co-authored papers 5
University of California san francisco
Co-authored papers 5
Co-authored papers 5
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
University of California san francisco
Co-authored papers 4