Significant Association Between Rare IPO11-HTR1A Variants and Attention Deficit Hyperactivity Disorder in Caucasians

Creator(s)

Lingjun Zuo, Yale School of Medicine
Laura Saba, University of Colorado School of Medicine
Xiandong Lin, Fujian Provincial Cancer Hospital
Yunlong Tan, Beijing Huilongguan Hospital
Kesheng Wang, East Tennessee State University
John H. Krystal, Yale School of Medicine
Boris Tabakoff, University of Colorado School of Medicine
Xingguang Luo, Yale School of Medicine

Document Type

Article

Publication Date

10-1-2015

Description

We comprehensively examined the rare variants in the IPO11-HTR1A region to explore their roles in neuropsychiatric disorders. Five hundred seventy-three to 1,181 rare SNPs in subjects of European descent and 1,234-2,529 SNPs in subjects of African descent (0

Citation Information

Zuo, Lingjun; Saba, Laura; Lin, Xiandong; Tan, Yunlong; Wang, Kesheng; Krystal, John H.; Tabakoff, Boris; and Luo, Xingguang. 2015. Significant Association Between Rare IPO11-HTR1A Variants and Attention Deficit Hyperactivity Disorder in Caucasians. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. Vol.168(7). 544-556. https://doi.org/10.1002/ajmg.b.32329 PMID: 26079129 ISSN: 1552-4841