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Meta-analysis of association between obsessive-compulsive disorder and the 3′ region of neuronal glutamate transporter gene SLC1A1

✍ Scribed by Stewart, S.E.; Mayerfeld, C.; Arnold, P.D.; Crane, J.R.; O'Dushlaine, C.; Fagerness, J.A.; Yu, D.; Scharf, J.M.; Chan, E.; Kassam, F.; Moya, P.R.; Wendland, J.R.; Delorme, R.; Richter, M.A.; Kennedy, J.L.; Veenstra-VanderWeele, J.; Samuels, J.; Greenberg, B.D.; McCracken, J.T.; Knowles, J.A.; Fyer, A.J.; Rauch, S.L.; Riddle, M.A.; Grados, M.A.; Bienvenu, O.J.; Cullen, B.; Wang, Y.; Shugart, Y.Y.; Piacentini, J.; Rasmussen, S.; Nestadt, G.; Murphy, D.L.; Jenike, M.A.; Cook, E.H.; Pauls, D.L.; Hanna, G.L.; Mathews, C.A.


Book ID
120228625
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
290 KB
Volume
162
Category
Article
ISSN
1552-4841

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## Abstract SLC1A1 encodes a neuronal glutamate transporter and is a promising candidate gene for obsessive‐compulsive disorder (OCD). Several independent research groups have reported significant associations between OCD and single nucleotide polymorphisms (SNPs) in this gene. Previously, we evalu