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Author Details

Edwin H Cook
1986
318
93
PMIDPaper TitleJournal TitlePublished Year
34905409Maternal Duplication 15q11-13 Syndrome with Autism Spectrum Disorder: Mood Stabilization by Carbamazepine.Journal of Child and Adolescent Psychopharmacology2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
34183358Recurrent <i>de novo</i> missense variants in <i>GNB2</i> can cause syndromic intellectual disability.J Med Genet2022
33909211Case Report: Association of Comorbid Psychiatric Disorders and Sigmoid Prolapse with de novo POGZ Mutation.Journal of Autism and Developmental Disorders2022
33229037Elevated Polygenic Burden for Autism Spectrum Disorder Is Associated With the Broad Autism Phenotype in Mothers of Individuals With Autism Spectrum Disorder.Biol Psychiatry2021
34285202Contextualizing genetic risk score for disease screening and rare variant discovery.Nat Commun2021
32791992Properties of beta oscillations in Dup15q syndrome.Journal of Neurodevelopmental Disorders2020
32317787A framework for an evidence-based gene list relevant to autism spectrum disorder.Nat Rev Genet2020
31729143Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study.American Journal of Medical Genetics, Part A2020
31654560Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials.American Journal of Medical Genetics, Part A2020
30988527A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data.Nat Neurosci2019
31857874Familiality of behavioral flexibility and response inhibition deficits in autism spectrum disorder (ASD).Molecular Autism2019
31619160Vocabulary comprehension in adults with fragile X syndrome (FXS).J Neurodev Disord2019
30542208Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1-2 (BP1-BP2) in a large cohort of samples referred for genetic diagnosis.J Hum Genet2019
30927179Whole Blood Serotonin Levels and Platelet 5-HT Binding in Autism Spectrum Disorder.Journal of Autism and Developmental Disorders2019
30901256Lovastatin Treatment of a Patient with a Protein Truncating Variant.Journal of Child and Adolescent Psychopharmacology2019
30392628Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.J Am Acad Child Adolesc Psychiatry2018
29052841Cognitive mechanisms of inhibitory control deficits in autism spectrum disorder.Journal of Child Psychology and Psychiatry and Allied Disciplines2018
29930110Analysis of shared heritability in common disorders of the brain.Science2018
28244813Pharmacogenomics of autism spectrum disorder.Pharmacogenomics2017
28344757Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.Mol Autism2017
28407363De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.Am J Med Genet A2017
28401654Is there sexual dimorphism of hyperserotonemia in autism spectrum disorder?Autism Res2017
28263302Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.Nat Neurosci2017
27748740Arbaclofen in Children and Adolescents with Autism Spectrum Disorder: A Randomized, Controlled, Phase 2 Trial.Neuropsychopharmacology2017
28163169Does MAOA increase susceptibility to prenatal stress in young children?Neurotoxicol Teratol2017
277171695HT receptor blockade in dorsomedial striatum reduces repetitive behaviors in BTBR mice.Genes, Brain and Behavior2017
27542772STAMS: STRING-assisted module search for genome wide association studies and application to autism.Bioinformatics2016
25744963CYP2A6 Longitudinal Effects in Young Smokers.Nicotine and Tobacco Research2016
27346079Constance E. Lieber, Theodore R. Stanley, and the Enduring Impact of Philanthropy on Psychiatry Research.Biol Psychiatry2016
27242401Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes.Frontiers in Neuroscience2016
26744772Confirmation of the Factor Structure and Measurement Invariance of the Children's Scale of Hostility and Aggression: Reactive/Proactive in Clinic-Referred Children With and Without Autism Spectrum Disorder.Journal of Child and Adolescent Psychopharmacology2016
27328765The impact of genotype calling errors on family-based studies.Sci Rep2016
27218684Mortality in isodicentric chromosome 15 syndrome: The role of SUDEP.Epilepsy Behav2016
27030804Commentary on "Platelet Studies in Autism Spectrum Disorder Patients and First-Degree Relatives".Molecular Autism2016
27158270Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome.J Neurodev Disord2016
26581695Separating Family-Level and Direct Exposure Effects of Smoking During Pregnancy on Offspring Externalizing Symptoms: Bridging the Behavior Genetic and Behavior Teratologic Divide.Behavior Genetics2016
27920663ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-, and .Frontiers in Neuroscience2016
27977700A Quantitative Electrophysiological Biomarker of Duplication 15q11.2-q13.1 Syndrome.PLoS ONE2016
27727243Alterations in the functional neural circuitry supporting flexible choice behavior in autism spectrum disorders.Translational Psychiatry2016
25158072Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.Am J Psychiatry2015
25450139Preliminary evidence for the interaction of the oxytocin receptor gene (oxtr) and face processing in differentiating prenatal smoking patterns.Neuroscience Letters2015
25277794UGT1A and UGT2B genetic variation alters nicotine and nitrosamine glucuronidation in european and african american smokers.Cancer Epidemiol Biomarkers Prev2015
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
25653359Feedforward and feedback motor control abnormalities implicate cerebellar dysfunctions in autism spectrum disorder.Journal of Neuroscience2015
25568282A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.Bioinformatics2015
25684064Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice.Neuropsychopharmacology2015
25807484Loss of δ-catenin function in severe autism.Nature2015
25421404The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.Mol Psychiatry2015
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Vanderbilt University Medical Center
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University of California los angeles
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Icahn School of Medicine at Mount Sinai
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The Hospital for Sick Children
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Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
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Hospital for Sick Children, University of Toronto
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Rush University Medical College
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UCSF Weill Institute for Neurosciences, University of California san francisco
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University of California
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Oregon Health & Science University (OHSU)
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INSERM U
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Icahn School of Medicine at Mount Sinai
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University of Florida, College of Medicine-Jacksonville
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Office of the Clinical Director, National Institute on Alcohol Abuse and Alcoholism.
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Massachusetts General Hospital
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