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Search Results to Christian Marshall

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Marshall, Christian

Item TypeName
Concept Autism Spectrum Disorder
Academic Article Contribution of SHANK3 mutations to autism spectrum disorder.
Academic Article Structural variation of chromosomes in autism spectrum disorder.
Academic Article Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder.
Academic Article Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
Academic Article Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.
Academic Article Functional impact of global rare copy number variation in autism spectrum disorders.
Academic Article Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
Academic Article Gene and miRNA expression profiles in autism spectrum disorders.
Academic Article Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder.
Academic Article Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.
Academic Article A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Academic Article Rare deletions at the neurexin 3 locus in autism spectrum disorder.
Academic Article Detection and characterization of copy number variation in autism spectrum disorder.
Academic Article SHANK1 Deletions in Males with Autism Spectrum Disorder.
Academic Article Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation.
Academic Article Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing.
Academic Article Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Academic Article Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families.
Academic Article Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.
Academic Article Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Academic Article Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder.
Academic Article Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
Academic Article Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Academic Article Whole-genome sequencing of quartet families with autism spectrum disorder.
Academic Article Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
Academic Article Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Academic Article Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Academic Article Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10.
Academic Article Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Academic Article Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.
Academic Article A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Academic Article A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.
Academic Article Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders.
Academic Article A framework for an evidence-based gene list relevant to autism spectrum disorder.

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  • Autism Spectrum Disorder