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Author Details

Stephen J Guter
1998
35
20
PMIDPaper TitleJournal TitlePublished Year
33909211Case Report: Association of Comorbid Psychiatric Disorders and Sigmoid Prolapse with de novo POGZ Mutation.Journal of Autism and Developmental Disorders2022
34183358Recurrent <i>de novo</i> missense variants in <i>GNB2</i> can cause syndromic intellectual disability.J Med Genet2022
31729143Clinical and neurocognitive issues associated with Bosch-Boonstra-Schaaf optic atrophy syndrome: A case study.American Journal of Medical Genetics, Part A2020
30901256Lovastatin Treatment of a Patient with a Protein Truncating Variant.Journal of Child and Adolescent Psychopharmacology2019
31619160Vocabulary comprehension in adults with fragile X syndrome (FXS).J Neurodev Disord2019
30927179Whole Blood Serotonin Levels and Platelet 5-HT Binding in Autism Spectrum Disorder.Journal of Autism and Developmental Disorders2019
30392628Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.J Am Acad Child Adolesc Psychiatry2018
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
28407363De novo unbalanced translocation (4p duplication/8p deletion) in a patient with autism, OCD, and overgrowth syndrome.Am J Med Genet A2017
27920663ASD and Genetic Associations with Receptors for Oxytocin and Vasopressin-, and .Frontiers in Neuroscience2016
27242401Variants in Adjacent Oxytocin/Vasopressin Gene Region and Associations with ASD Diagnosis and Other Autism Related Endophenotypes.Frontiers in Neuroscience2016
26151311An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview-Revised data.J Biomed Inform2015
26313485Escitalopram pharmacogenetics: CYP2C19 relationships with dosing and clinical outcomes in autism spectrum disorder.Pharmacogenetics and Genomics2015
26262902Pharmacogenetic Study of Serotonin Transporter and 5HT2A Genotypes in Autism.Journal of Child and Adolescent Psychopharmacology2015
24768552Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.Am J Hum Genet2014
25363760Synaptic, transcriptional and chromatin genes disrupted in autism.Nature2014
23443968Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.Am J Med Genet A2013
23956104Parental broader autism subphenotypes in ASD affected families: relationship to gender, child's symptoms, SSRI treatment, and platelet serotonin.Autism Research2013
21996756A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Hum Genet2012
22843504Individual common variants exert weak effects on the risk for autism spectrum disorders.Hum Mol Genet2012
22065253A multisite study of the clinical diagnosis of different autism spectrum disorders.Arch Gen Psychiatry2012
21609426A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders.Mol Autism2011
21881965Repetitive behavior profiles: Consistency across autism spectrum disorder cohorts and divergence from Prader-Willi syndrome.Journal of Neurodevelopmental Disorders2011
20663923A genome-wide scan for common alleles affecting risk for autism.Hum Mol Genet2010
20844286Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.Sci Transl Med2010
20679591Neurobehavioral abnormalities in first-degree relatives of individuals with autism.Arch Gen Psychiatry2010
20531469Functional impact of global rare copy number variation in autism spectrum disorders.Nature2010
20020537A pharmacogenetic study of escitalopram in autism spectrum disorders.Autism Research2010
19154646Impaired inhibitory control is associated with higher-order repetitive behaviors in autism spectrum disorders.Psychological Medicine2009
17069541A prospective, open-label trial of memantine in the treatment of cognitive, behavioral, and memory dysfunction in pervasive developmental disorders.Journal of Child and Adolescent Psychopharmacology2006
17069542Effect of CX516, an AMPA-modulating compound, on cognition and behavior in fragile X syndrome: a controlled trial.J Child Adolesc Psychopharmacol2006
15782081An open-label trial of escitalopram in pervasive developmental disorders.Journal of the American Academy of Child and Adolescent Psychiatry2005
11920155Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder.Mol Psychiatry2002
9545402Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.Am J Hum Genet1998
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