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Author Details

James S Sutcliffe
Vanderbilt Genetics Institute, Vanderbilt University
1988
130
67
PMIDPaper TitleJournal TitlePublished Year
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
35841203A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.Am J Med Genet B Neuropsychiatr Genet2022
35751013Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data.J Neurodev Disord2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
35841203A phenome-wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data.Am J Med Genet B Neuropsychiatr Genet2022
35751013Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data.J Neurodev Disord2022
33261099An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder.Int J Mol Sci2020
33261099An Automated Functional Annotation Pipeline That Rapidly Prioritizes Clinically Relevant Genes for Autism Spectrum Disorder.Int J Mol Sci2020
30755521Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in <i>SLC6A3</i>.Proc Natl Acad Sci U S A2019
30755521Structural, functional, and behavioral insights of dopamine dysfunction revealed by a deletion in <i>SLC6A3</i>.Proc Natl Acad Sci U S A2019
31316544The Drosophila Gene <i>Sulfateless</i> Modulates Autism-Like Behaviors.Front Genet2019
30988527A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.Nat Neurosci2019
31316544The Drosophila Gene <i>Sulfateless</i> Modulates Autism-Like Behaviors.Front Genet2019
30988527A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.Nat Neurosci2019
30392628Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.J Am Acad Child Adolesc Psychiatry2018
30392628Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.J Am Acad Child Adolesc Psychiatry2018
29038237The Gain-of-Function Integrin β3 Pro33 Variant Alters the Serotonin System in the Mouse Brain.J Neurosci2017
28344757Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.Mol Autism2017
28401654Is there sexual dimorphism of hyperserotonemia in autism spectrum disorder?Autism Res2017
29038237The Gain-of-Function Integrin β3 Pro33 Variant Alters the Serotonin System in the Mouse Brain.J Neurosci2017
28301091Shorter sleep duration is associated with social impairment and comorbidities in ASD.Autism Res2017
28130356A Novel Human <i>CAMK2A</i> Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors.J Neurosci2017
28301091Shorter sleep duration is associated with social impairment and comorbidities in ASD.Autism Res2017
28130356A Novel Human <i>CAMK2A</i> Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors.J Neurosci2017
28401654Is there sexual dimorphism of hyperserotonemia in autism spectrum disorder?Autism Res2017
28344757Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.Mol Autism2017
27328765The impact of genotype calling errors on family-based studies.Sci Rep2016
27328765The impact of genotype calling errors on family-based studies.Sci Rep2016
25270638Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.Bioinformatics2015
25741436Zn(2+) reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder.Mol Autism2015
25534755A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Biol Psychiatry2015
25270638Consensus Genotyper for Exome Sequencing (CGES): improving the quality of exome variant genotypes.Bioinformatics2015
25655306Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.Am J Med Genet A2015
25774383Rare autism-associated variants implicate syntaxin 1 (STX1 R26Q) phosphorylation and the dopamine transporter (hDAT R51W) in dopamine neurotransmission and behaviors.EBioMedicine2015
25568282A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.Bioinformatics2015
25432440Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.Hum Genet2015
25684064Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice.Neuropsychopharmacology2015
26402605Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Neuron2015
26402605Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Neuron2015
25684064Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice.Neuropsychopharmacology2015
25655306Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.Am J Med Genet A2015
25774383Rare autism-associated variants implicate syntaxin 1 (STX1 R26Q) phosphorylation and the dopamine transporter (hDAT R51W) in dopamine neurotransmission and behaviors.EBioMedicine2015
25741436Zn(2+) reverses functional deficits in a de novo dopamine transporter variant associated with autism spectrum disorder.Mol Autism2015
25432440Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.Hum Genet2015
25568282A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.Bioinformatics2015
25534755A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Biol Psychiatry2015
24695082Pro32Pro33 mutations in the integrin β3 PSI domain result in αIIbβ3 priming and enhanced adhesion: reversal of the hypercoagulability phenotype by the Src inhibitor SKI-606.Mol Pharmacol2014
25363760Synaptic, transcriptional and chromatin genes disrupted in autism.Nature2014
25313507SLC6A3 coding variant Ala559Val found in two autism probands alters dopamine transporter function and trafficking.Transl Psychiatry2014
25392729The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.Mol Autism2014
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Collaborators

Edwin H Cook
Co-authored papers 41
Jonathan L Haines
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 23
Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
Co-authored papers 21
Bernie Devlin
Co-authored papers 20
Arthur L Beaudet
Baylor College of Medicine
Co-authored papers 19
Daniel H Geschwind
University of California los angeles
Co-authored papers 18
David H Ledbetter
University of Florida, College of Medicine-Jacksonville
Co-authored papers 18
Gerard D Schellenberg
Co-authored papers 16
Kathryn Roeder
Co-authored papers 15
Stephan J Sanders
Co-authored papers 14
Lambertus Klei
Co-authored papers 14
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers 14
Catherine Lord
University of California los angeles
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Hilary Coon
Co-authored papers 13
Peter Szatmari
Hospital for Sick Children, University of Toronto
Co-authored papers 13
Margaret A Pericak-Vance
Co-authored papers 13
Eric Fombonne
Oregon Health & Science University (OHSU)
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Louise Gallagher
Co-authored papers 12
Matthew W State
UCSF Weill Institute for Neurosciences, University of California san francisco
Co-authored papers 12
Nicholas G Campbell
Co-authored papers 12
Emily L Crawford
Co-authored papers 11
Michael Gill
Co-authored papers 11
Veronica J Vieland
The Ohio State University
Co-authored papers 10
Geraldine Dawson
Co-authored papers 10
John I Nurnberger
Stark Neurosciences Research Institute, Indiana University School of Medicine
Co-authored papers 10
Stephen J Guter
Co-authored papers 10
Mark J Daly
Massachusetts General Hospital
Co-authored papers 10
Catalina Betancur
Co-authored papers 9
Joseph Piven
Oregon Health & Science University
Co-authored papers 9
Susan L Christian
Seattle Children's Research Institute
Co-authored papers 9
Release 1.2