Raphael Bernier

Department of Psychiatry, University of Washington

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2014

Other Publications

Article	Year
Children referred for possible sexual abuse: medical findings in 2384 children. Child abuse & neglect\| PubMed ID: 12201160	2002
Autism-related language, personality, and cognition in people with absolute pitch: results of a preliminary study. Journal of autism and developmental disorders\| PubMed ID: 12757355	2003
Early regression in social communication in autism spectrum disorders: a CPEA Study. Developmental neuropsychology\| PubMed ID: 15843100	2005
Individuals with autism spectrum disorder show normal responses to a fear potential startle paradigm. Journal of autism and developmental disorders\| PubMed ID: 16167091	2005
Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study. Journal of autism and developmental disorders\| PubMed ID: 16598435	2006
Is there a 'regressive phenotype' of Autism Spectrum Disorder associated with the measles-mumps-rubella vaccine? A CPEA Study. Journal of autism and developmental disorders\| PubMed ID: 16729252	2006
Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale. Journal of autism and developmental disorders\| PubMed ID: 16868845	2007
ERP evidence of atypical face processing in young children with autism. Journal of autism and developmental disorders\| PubMed ID: 16897400	2006
Becoming a face expert: a computerized face-training program for high-functioning individuals with autism spectrum disorders. Developmental neuropsychology\| PubMed ID: 18443967	2008
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature\| PubMed ID: 19404256	2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature\| PubMed ID: 19404257	2009
Neurobiological correlates of social functioning in autism. Clinical psychology review\| PubMed ID: 20570622	2010
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16. Human genetics\| PubMed ID: 20963441	2011
Psychopathology, families, and culture: autism. Child and adolescent psychiatric clinics of North America\| PubMed ID: 21056350	2010
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. Nature genetics\| PubMed ID: 21572417	2011
Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families. Autism research : official journal of the International Society for Autism Research\| PubMed ID: 21905246	2012
A multisite study of the clinical diagnosis of different autism spectrum disorders. Archives of general psychiatry\| PubMed ID: 22065253	2012
Evidence for involvement of GNB1L in autism. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics\| PubMed ID: 22095694	2012
Relative burden of large CNVs on a range of neurodevelopmental phenotypes. PLoS genetics\| PubMed ID: 22102821	2011
Developmental changes in mu suppression to observed and executed actions in autism spectrum disorders. Social cognitive and affective neuroscience\| PubMed ID: 22302843	2012
Tympanostomy tube placement in children with autism. Journal of developmental and behavioral pediatrics : JDBP\| PubMed ID: 22343482	2012
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature\| PubMed ID: 22495309	2012
The broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders. Autism research and treatment\| PubMed ID: 22937250	2011
Social attention: a possible early indicator of efficacy in autism clinical trials. Journal of neurodevelopmental disorders\| PubMed ID: 22958480	2012
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders. Journal of medical genetics\| PubMed ID: 23054248	2012
The broader autism phenotype in simplex and multiplex families. Journal of autism and developmental disorders\| PubMed ID: 23117424	2013
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. Science (New York, N.Y.)\| PubMed ID: 23160955	2012
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder. American journal of human genetics\| PubMed ID: 23375656	2013
The role of imitation in the observed heterogeneity in EEG mu rhythm in autism and typical development. Brain and cognition\| PubMed ID: 23511847	2013
Guidelines and Best Practices for Electrophysiological Data Collection, Analysis and Reporting in Autism. Journal of autism and developmental disorders\| PubMed ID: 23975145	2013
Brief report: social skills, internalizing and externalizing symptoms, and respiratory sinus arrhythmia in autism. Journal of autism and developmental disorders\| PubMed ID: 23982488	2014
A quarter century of progress on the early detection and treatment of autism spectrum disorder. Development and psychopathology\| PubMed ID: 24342850	2013
Update on diagnostic classification in autism. Current opinion in psychiatry\| PubMed ID: 24441420	2014
Nonverbal and verbal cognitive discrepancy profiles in autism spectrum disorders: influence of age and gender. American journal on intellectual and developmental disabilities\| PubMed ID: 24450323	2014
A genotype-first approach to defining the subtypes of a complex disease. Cell\| PubMed ID: 24581488	2014