Raphael Bernier

Affiliated with

Research Area

Biography

Raphael Bernier has not added Biography.
If you are Raphael Bernier and would like to personalize this page please email our Author Liaison for assistance.

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