The landscape of copy number variations in Finnish families with autism spectrum disorders.
Kanduri, Chakravarthi; Kantojärvi, Katri; Salo, Paula M; Vanhala, Raija; Buck, Gemma; Blancher, Christine; Lähdesmäki, Harri; Järvelä, Irma.
; 9(1): 9-16, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26052927
Increased female autosomal burden of rare copy number variants in human populations and in autism families.
Synergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism.
Structure and function of neonatal social communication in a genetic mouse model of autism.
The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Heritable aspects of biological motion perception and its covariation with autistic traits.
Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder.
Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.