2012
DOI: 10.1016/j.jpsychires.2012.05.002
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Sex determines which section of the SLC6A4 gene is linked to obsessive–compulsive symptoms in normal Chinese college students

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Cited by 16 publications
(9 citation statements)
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“…In addition, carrying one or two doses of the L A allele for the 5-HTTLPR + rs25531 polymorphism in SLC6A4 was associated with a 47% decrease in the odds of belonging to the Higher Fatigue class. While rs2020942 was linked with obsessive-compulsive symptoms 123 and risk for nonsyndromic cleft lip with or without cleft palate, 124 no studies have reported on associations between SLC6A4 rs2020942 and energy level.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, carrying one or two doses of the L A allele for the 5-HTTLPR + rs25531 polymorphism in SLC6A4 was associated with a 47% decrease in the odds of belonging to the Higher Fatigue class. While rs2020942 was linked with obsessive-compulsive symptoms 123 and risk for nonsyndromic cleft lip with or without cleft palate, 124 no studies have reported on associations between SLC6A4 rs2020942 and energy level.…”
Section: Discussionmentioning
confidence: 99%
“…Another reason could be a gender difference in genetic modulation of depression by 5-HTTLPR. A gender-specific genetic effect has been reported for 5-HTTLPR in many psychiatric phenotypes, particularly in terms of the interaction with an environmental effect 28,29. It is possible that the genetic effect is moderated in a gender-specific way.…”
Section: Discussionmentioning
confidence: 99%
“…In genetic association studies, gender wise analysis has been recommended in several earlier reports [8][9][10]. In view of only two male patients in the cohort they were excluded to maintain uniformity of analysis.…”
Section: Subjectsmentioning
confidence: 99%
“…MBL2 gene is located at chromosome 10 (10q11. [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20][21] and comprises of four exons. Three functional SNPs in exon 1 at codons 52 (rs5030737; C > T; Arg > Cys), 54 (rs1800450; G > A; Gly > Asp), and 57 (rs1800451; G > A; Gly > Glu), are known as D, B, and C variants, respectively, whereas A is the common non-mutated allele.…”
Section: Introductionmentioning
confidence: 99%