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Article

Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Oct 2015

Zuo Lingjun, Saba Laura, Lin Xiandong, Tan Yunlong, Wang Kesheng, Krystal John H, Tabakoff Boris, Luo Xingguang

Abstract excerpt

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 < minor allele frequency (MAF) < 0.05) were analyzed in a total of 49,268 subjects in 21 independent cohorts with 11 different neuropsychiatric disorders....

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Identifiers

PMID: 26079129
DOI: 10.1002/ajmg.b.32329
PMCID: PMC4851708

Genes

IPO11
MAF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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