Raphael A Bernier


Ontology type: schema:Person     


Person Info

NAME

Raphael A

SURNAME

Bernier

Publications in SciGraph latest 50 shown

  • 2021-12-02 Sex Differences in Autism: Examining Intrinsic and Extrinsic Factors in Children and Adolescents Enrolled in a National ASD Cohort in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2021-09-13 Resting state EEG in youth with ASD: age, sex, and relation to phenotype in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2021-07-26 Recent ultra-rare inherited variants implicate new autism candidate risk genes in NATURE GENETICS
  • 2021-07-26 The Early Start Denver Model Intervention and Mu Rhythm Attenuation in Autism Spectrum Disorders in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2021-07-13 Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism in HUMAN GENOMICS
  • 2021-07-01 Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome in NATURE GENETICS
  • 2021-06-21 Reflections on the genetics-first approach to advancements in molecular genetic and neurobiological research on neurodevelopmental disorders in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2021-04-19 Clinical delineation of SETBP1 haploinsufficiency disorder in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2021-04-19 Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders in GENOME MEDICINE
  • 2021-03-14 Bruxism in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Visual-Motor Function in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Neurophysiology in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Rote Memory in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 California Verbal Learning Test, Children’s Version (CVLT-C) in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Mismatch Negativity in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Stanford-Binet Intelligence Scales and Revised Versions in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-14 Face Perception in ENCYCLOPEDIA OF AUTISM SPECTRUM DISORDERS
  • 2021-03-08 Language and Aggressive Behaviors in Male and Female Youth with Autism Spectrum Disorder in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2020-11-11 Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2020-10-21 Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders in NATURE COMMUNICATIONS
  • 2020-10-01 Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders in NATURE COMMUNICATIONS
  • 2020-06-02 Neural responsivity to social rewards in autistic female youth in TRANSLATIONAL PSYCHIATRY
  • 2020-05-29 Weaker neural suppression in autism in NATURE COMMUNICATIONS
  • 2020-05-24 Brief Report: Can a Composite Heart Rate Variability Biomarker Shed New Insights About Autism Spectrum Disorder in School-Aged Children? in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2020-04-21 A framework for an evidence-based gene list relevant to autism spectrum disorder in NATURE REVIEWS GENETICS
  • 2020-03-03 Imaging-genetics of sex differences in ASD: distinct effects of OXTR variants on brain connectivity in TRANSLATIONAL PSYCHIATRY
  • 2019-10-15 Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders in NATURE COMMUNICATIONS
  • 2019-07-12 AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders in NATURE COMMUNICATIONS
  • 2019-04-10 Trauma and Autism Spectrum Disorder: Review, Proposed Treatment Adaptations and Future Directions in JOURNAL OF CHILD & ADOLESCENT TRAUMA
  • 2019-03-05 Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication in TRANSLATIONAL PSYCHIATRY
  • 2019-01-16 Psychiatric disorders in children with 16p11.2 deletion and duplication in TRANSLATIONAL PSYCHIATRY
  • 2019-01-15 Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene in TRANSLATIONAL PSYCHIATRY
  • 2018-12-17 Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity in NATURE GENETICS
  • 2018-12-13 Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model in MOLECULAR AUTISM
  • 2018-12-03 Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes in GENETICS IN MEDICINE
  • 2018-10-01 Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder in HUMAN GENETICS
  • 2017-12-05 A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-10-24 Prospective investigation of FOXP1 syndrome in MOLECULAR AUTISM
  • 2017-10-05 Clinical phenotype of ASD-associated DYRK1A haploinsufficiency in MOLECULAR AUTISM
  • 2017-09-08 Erratum to: Interactive Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2017-08-30 Gene Disrupting Mutations Associated with Regression in Autism Spectrum Disorder in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2017-08-02 Interactive Effects of Prenatal Antidepressant Exposure and Likely Gene Disrupting Mutations on the Severity of Autism Spectrum Disorder in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2017-06-19 Hotspots of missense mutation identify novel neurodevelopmental disorder genes and functional domains in NATURE NEUROSCIENCE
  • 2017-05-26 Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
  • 2017-02-13 Targeted sequencing identifies 91 neurodevelopmental disorder risk genes with autism and developmental disability biases in NATURE GENETICS
  • 2016-12-13 Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism in MOLECULAR PSYCHIATRY
  • 2016-11-15 Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism in HUMAN GENETICS
  • 2016-05-21 Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication in JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
  • 2016-01-13 De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-07-24 Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications in JOURNAL OF NEURODEVELOPMENTAL DISORDERS
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