Search Results - "Villafuerte, Sandra M."

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  1. 1

    Association of the DYX1C1 dyslexia susceptibility gene with orthography in the Chinese population by Zhang, Yuping, Li, Jun, Tardif, Twila, Burmeister, Margit, Villafuerte, Sandra M, McBride-Chang, Catherine, Li, Hong, Shi, Bingjie, Liang, Weilan, Zhang, Zhixiang, Shu, Hua

    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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    Journal Article
  2. 2

    Association of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese Population by Zhang, Yuping, Li, Jun, Song, Shuang, Tardif, Twila, Burmeister, Margit, Villafuerte, Sandra M, Su, Mengmeng, McBride, Catherine, Shu, Hua

    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. 3

    Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression by Villafuerte, Sandra M., Del-Favero, Jurgen, Adolfsson, Rolf, Souery, Daniel, Massat, Isabelle, Mendlewicz, Julien, Van Broeckhoven, Christine, Claes, Stephan

    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. 4

    SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A by Villafuerte, Sandra M, Vallabhaneni, Kamala, Sliwerska, Elzbieta, McMahon, Francis J, Young, Elizabeth A, Burmeister, Margit

    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. 5

    Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder by Verheyen, G R, Villafuerte, S M, Del-Favero, J, Souery, D, Mendlewicz, J, Van Broeckhoven, C, Raeymaekers, P

    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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