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Bondy, B., Kuznik, J., Baghai, T., Schule, C., Zwanzger, P., Minov, C., de Jonge, S., Rupprecht, R., Meyer, H., Engel, R. R., Eisenmenger, W. and Ackenheil, M. (2000) Lack of Association of Serotonin-2A Receptor Gene Polymorphism (T102C) with Suicidal Ideation and Suicide. American Journal of Medical Genetics (Neuropsychiatric Genetics), 96, 831-835.
https://doi.org/10.1002/1096-8628(20001204)96:6<831::AID-AJMG27>3.0.CO;2-K

has been cited by the following article:

• TITLE: 5-HTR2A Polymorphisms rs6311 and rs6313 and Major Depressive Disorder: A Meta-Analysis

  AUTHORS: Krystal Castle White, Angie K. McDonald, David M. Compton

  KEYWORDS: Genetic Predisposition to Disease, Receptors, Serotonin, Polymorphism, Single Nucleotide, Genetics, Behavioral

  JOURNAL NAME: Journal of Behavioral and Brain Science, Vol.12 No.10, October 18, 2022

  ABSTRACT: rs6311 and rs6313 are two Single Nucleotide Polymorphisms (SNPs) on the Serotonin Receptor 2A gene (5-HTR2A) in complete linkage disequilibrium. Numerous gene association studies have examined the relationships between one or both of these two polymorphisms and Major Depressive Disorder (MDD), with conflicting results. The present meta-analysis examined 19 case-control gene association studies, 9 of which included rs6311 (n = 3382), and 15 of which included rs6313 (n = 5590). The strength of relationship with MDD was assessed by pooled odds ratios and 95% confidence intervals for both SNPs according to four genetic models. Heterogeneity was measured by Q and I2. Subgrouping was performed by minor allele and by ethnicity. Results were nonsignificant for all models and subgroups, suggesting that genotype alone does not play a major role in genetic susceptibility to depression. The potential for epistatic, epigenetic, and regulatory RNA interactions with these SNPs is discussed, and future areas of research are recommended.