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Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism.
Rigor in science and science reporting: updated guidelines for submissions to Molecular Autism.
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations.
Did Hans Asperger actively assist the Nazi euthanasia program?
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Prospective investigation of FOXP1 syndrome.
Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome.
Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID.
Ultrastructural analyses in the hippocampus CA1 field in Shank3-deficient mice.
Understanding autism in the light of sex/gender.
Transcriptomic changes in the frontal cortex associated with paternal age.
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.
Neuropathology of the posteroinferior occipitotemporal gyrus in children with autism.
A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome.
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.
Capping four years of growth of Molecular Autism: impact factor coming in 2014.
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.
DSM-5: the debate continues.
Insulin-like growth factor-1 rescues synaptic and motor deficits in a mouse model of autism and developmental delay.
Optimizing the phenotyping of rodent ASD models: enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features.
Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication.
Genetics in psychiatry: common variant association studies.
A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.
Molecular Autism: accelerating and integrating research into neurodevelopmental conditions.