Search Results - "Villafuerte, Sandra M"
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Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population
Published in PloS one (13-09-2012)“…Several independent studies have supported the association of DYX1C1 with dyslexia, but its role in general reading development remains unclear. Here, we…”
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2
Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population
Published in PloS one (21-04-2016)“…The doublecortin domain-containing 2 (DCDC2) gene, which is located on chromosome 6p22.1, has been widely suggested to be a candidate gene for dyslexia, but…”
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3
Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression
Published in American journal of medical genetics (08-03-2002)“…An increasing amount of data suggests that affective disorders are related to dysregulation of the hypothalamic‐pituitary‐adrenal (HPA) axis, the…”
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4
SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A
Published in Psychiatric genetics (01-12-2009)“…Desensitization of serotonin 1A (HTR1A) and 1B (HTR1B) autoreceptors has been proposed to be involved in the delayed onset of response to selective serotonin…”
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5
Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder
Published in European journal of human genetics : EJHG (01-05-1999)“…Recent genetic studies have implicated chromosome 18 in bipolar disorder (BP) with putative loci in the pericentromeric region and on 18q. We reported linkage…”
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