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Search Results to Jacob Vorstman

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 Vorstman, Jacob

Item TypeName
Concept Genotype
Academic Article Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia.
Academic Article Proline affects brain function in 22q11DS children with the low activity COMT 158 allele.
Academic Article Systematic genotype-phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism.
Academic Article A double hit implicates DIAPH3 as an autism risk gene.
Academic Article Dissecting the clinical heterogeneity of autism spectrum disorders through defined genotypes.
Academic Article A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.
Academic Article Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.
Academic Article Association study of copy number variants with brain volume in schizophrenia patients and healthy controls.
Academic Article Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.
Academic Article Individual common variants exert weak effects on the risk for autism spectrum disorders.
Academic Article Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.
Academic Article Genome-wide burden of deleterious coding variants increased in schizophrenia.
Academic Article The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
Academic Article Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.

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