Association study of the serotonin transporter gene polymorphism in obsessive-compulsive disorder

International Journal of Neuropsychopharmacology

Volumn 4, Issue 3, 2001, Pages 269-272

  Camarena, Beatriz ^a   Rinetti, Gina ^a   Cruz, Carlos ^a   Hernández, Sandra ^a   Ramón De La Fuente, Juan ^b   Nicolini, Humberto ^a  

^a INSTITUTO NACIONAL DE PSIQUIATRÍA RAMÓN DE LA FUENTE MUÑIZ   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

Author keywords

Association study; Family based method; OCD; Serotonin transporter gene

Indexed keywords

NUCLEIC ACID BASE; SEROTONIN TRANSPORTER; SEROTONIN UPTAKE INHIBITOR;

ADULT; ALLELE; ARTICLE; BASE PAIRING; CONTROLLED STUDY; FAMILY; FEMALE; GENE DELETION; GENE INSERTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC RISK; HAPLOTYPE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MEXICO; OBSESSION; PRIORITY JOURNAL; PROMOTER REGION; SAMPLE SIZE;

ADULT; ALLELES; CARRIER PROTEINS; FEMALE; GENOTYPE; HUMANS; MALE; MEMBRANE GLYCOPROTEINS; MEMBRANE TRANSPORT PROTEINS; MEXICO; NERVE TISSUE PROTEINS; OBSESSIVE-COMPULSIVE DISORDER; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS); SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;

EID: 0035703869     PISSN: 14611457     EISSN: None     Source Type: Journal    
DOI: 10.1017/S1461145701002516     Document Type: Article

References (24)

1. Intact coding region of the serotonin transporter gene in obsessive-compulsive disorder
2. The serotonin hypothesis of obsessive-compulsive disorder
3. Association of the serotonin transporter promoter regulatory region polymorphism and obsessive-compulsive disorder
4. Obsessive-compulsive disorder, response to serotonin reuptake inhibitors and the serotonin transporter gene
5. Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder
6. Concurrent validity of the DIS experience with psychiatric patients in Mexico City
7. Increased prevalence of the seven-repeat variant of the dopamine D4 receptor gene in patients with obsessive-compulsive disorder with tics
8. Genomic control for association studies
9. Neuroticism is not associated with the serotonin transporter (5-HTTLPR) polymorphism
10. Serotonin transporter protein (SLC6A4) allele and haplotype frequencies and linkage disequilibria in African- and European-American and Japanese populations and in alcohol-dependent subjects
11. Linkage mapping of serotonin transporter protein gene SLC6A4 on chromosome 17
12. Variability in the serotonin transporter gene and increased risk for major depression with melancholia
13. Allelic variation of human serotonin transporter gene expression
14. Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder
15. Obsessive-compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): A negative association study in the Afrikaner population
16. A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies
17. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
18. Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive-compulsive disorder
19. Understanding the genetic basis of obsessive-compulsive disorder
20. Traducción al español y confiabilidad de la escala de Yale-Brown para el trastorno obsesivo-compulsivo
21. Role of serotonin transporter promoter repeat length polymorphism (5-HTTLPR) in seasonality and seasonal affective disorder
22. Serotonin transporter gene (5-HTTLPR) is not associated with depressive symptomatology in mood disorders
23. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
24. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations