Search Results - "Reichert, Jennifer G"
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Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT
Published in BMC medical genomics (16-10-2008)“…It has previously been shown that specific microdeletions and microduplications, many of which also associated with cognitive impairment (CI), can present with…”
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Family-based association study of TPH1 and TPH2 polymorphisms in autism
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05-12-2006)“…The TPH1 and TPH2 genes encode the rate‐limiting enzymes that control serotonin biosynthesis, and serotonin is clearly altered in autism. In the current study,…”
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Linkage and Association of the Mitochondrial Aspartate Glutamate Carrier SLC25A12 Gene With Autism
Published in The American journal of psychiatry (01-04-2004)“…OBJECTIVE: Autism autistic disorder (MIM number 209850) is a complex, largely genetic psychiatric disorder. The authors recently mapped a susceptibility locus…”
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An analysis of candidate autism loci on chromosome 2q24-q33: Evidence for association to the STK39 gene
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05-10-2008)“…A susceptibility locus for autism was identified to the chromosome 2q24–q33 region in independent cohorts of families, especially in subsets clinically defined…”
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Lack of Evidence for Association of the Serotonin Transporter Gene SLC6A4 with Autism
Published in Biological psychiatry (1969) (15-07-2006)“…The serotonin transporter (5-HTT) has long been considered likely to play a role in autism. Hyperserotonemia has been consistently found in a proportion of…”
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Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors
Published in Psychiatric genetics (01-12-2006)“…An autism susceptibility locus (AUTS1, MIM#608636) has been identified in chromosome 7q31. NrCAM is a candidate gene for AUTS1 because it is expressed in the…”
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Autism and ultraconserved non-coding sequence on chromosome 7q
Published in Psychiatric genetics (01-02-2006)“…Autism has been linked to a broad region on chromosome 7q that contains a large number of genes involved in transcription and development. This region is also…”
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Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05-06-2007)“…Mutations in the PTEN gene are associated with a broad spectrum of disorders, including Cowden syndrome (CS), Bannayan–Riley–Ruvalcaba syndrome, Proteus…”
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