Raphael Bernier

Children referred for possible sexual abuse: medical findings in 2384 children.

Autism-related language, personality, and cognition in people with absolute pitch: results of a preliminary study.

Early regression in social communication in autism spectrum disorders: a CPEA Study.

Individuals with autism spectrum disorder show normal responses to a fear potential startle paradigm.

Familial autoimmune thyroid disease as a risk factor for regression in children with Autism Spectrum Disorder: a CPEA Study.

Is there a 'regressive phenotype' of Autism Spectrum Disorder associated with the measles-mumps-rubella vaccine? A CPEA Study.

Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale.

ERP evidence of atypical face processing in young children with autism.

Becoming a face expert: a computerized face-training program for high-functioning individuals with autism spectrum disorders.

Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.

Neurobiological correlates of social functioning in autism.

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Psychopathology, families, and culture: autism.

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.

Evidence for broader autism phenotype characteristics in parents from multiple-incidence autism families.

A multisite study of the clinical diagnosis of different autism spectrum disorders.

Evidence for involvement of GNB1L in autism.

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

Developmental changes in mu suppression to observed and executed actions in autism spectrum disorders.

Tympanostomy tube placement in children with autism.

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

The broader autism phenotype and its implications on the etiology and treatment of autism spectrum disorders.

Social attention: a possible early indicator of efficacy in autism clinical trials.

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

The broader autism phenotype in simplex and multiplex families.

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.

The role of imitation in the observed heterogeneity in EEG mu rhythm in autism and typical development.

Guidelines and Best Practices for Electrophysiological Data Collection, Analysis and Reporting in Autism.

Brief report: social skills, internalizing and externalizing symptoms, and respiratory sinus arrhythmia in autism.

A quarter century of progress on the early detection and treatment of autism spectrum disorder.

Update on diagnostic classification in autism.

Nonverbal and verbal cognitive discrepancy profiles in autism spectrum disorders: influence of age and gender.

A genotype-first approach to defining the subtypes of a complex disease.