| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/SJ.MP.4001970 |
| P698 | PubMed publication ID | 17453059 |
| P50 | author | Jack Samuels | Q37615968 |
| Virginia L Willour | Q58371410 | ||
| P2093 | author name string | Wang Y | |
| Riddle MA | |||
| Valle D | |||
| Shugart YY | |||
| Hoehn-Saric R | |||
| Murphy DL | |||
| Detera-Wadleigh S | |||
| Liang KY | |||
| Cullen B | |||
| Nestadt G | |||
| Bienvenu OJ | |||
| Grados MA | |||
| Wendland JR | |||
| P2860 | cites work | Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder | Q24646169 |
| Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype | Q34273765 | ||
| Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder | Q34658088 | ||
| Does measurement instrument moderate the association between the serotonin transporter gene and anxiety-related personality traits? A meta-analysis | Q35984302 | ||
| Exploratory factor analysis of obsessive-compulsive patients and association with 5-HTTLPR polymorphism | Q43938287 | ||
| Lack of evidence for association between serotonin transporter gene (5-HTTLPR) and obsessive-compulsive disorder by case control and family association study in humans | Q44917299 | ||
| Evidence for linkage disequilibrium between serotonin transporter protein gene (SLC6A4) and obsessive compulsive disorder | Q47806910 | ||
| Association of the serotonin transporter promoter regulatory region polymorphism and obsessive-compulsive disorder. | Q51980891 | ||
| A family study of obsessive-compulsive disorder. | Q52079769 | ||
| Single-nucleotide polymorphism analysis by pyrosequencing | Q73775865 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | obsessive-compulsive disorder | Q178190 |
| P304 | page(s) | 422-423 | |
| P577 | publication date | 2007-05-01 | |
| P1433 | published in | Molecular Psychiatry | Q6895973 |
| P1476 | title | Rare plus common SERT variants in obsessive-compulsive disorder | |
| P478 | volume | 12 |
| Q34975117 | A large-scale screen for coding variants in SERT/SLC6A4 in autism spectrum disorders |
| Q58408137 | Pilot study on HTR2A promoter polymorphism, −1438G/A (rs6311) and a nearby copy number variation showed association with onset and severity in early onset obsessive–compulsive disorder |
| Q38959036 | Rodent models of obsessive compulsive disorder: Evaluating validity to interpret emerging neurobiology |
| Q60501981 | The Behavioral Genetics of Serotonin: Relevance to Anxiety and Depression |
| Q61632407 | The Serotonergic System in Obsessive-Compulsive Disorder |
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