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GWAS Study

Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia.

Kornilov SA, Tan M, Aljughaiman A et al.

31620175 PubMed ID
GWAS Study Type
354 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KS
Kornilov SA
TM
Tan M
AA
Aljughaiman A
NO
Naumova OY
GE
Grigorenko EL
Chapter II

Abstract

Summary of the research findings

Recent studies of the genetic foundations of cognitive ability rely on large samples (in extreme, hundreds of thousands) of individuals from relatively outbred populations of mostly European ancestry. Hypothesizing that the genetic foundation of cognitive ability depends on the broader population-specific genetic context, we performed a genome-wide association study and homozygosity mapping of cognitive ability estimates obtained through latent variable modeling in a sample of 354 children from a consanguineous population of Saudi Arabia. Approximately half of the sample demonstrated significantly elevated homozygosity levels indicative of inbreeding, and among those with elevated levels, homozygosity was negatively associated with cognitive ability. Further homozygosity mapping identified a specific run, inclusive of the GRIA4 gene, that survived corrections for multiple testing for association with cognitive ability. The results suggest that in a consanguineous population, a notable proportion of the variance in cognitive ability in the normal range in children might be regulated by population-specific mechanisms such as patterns of elevated homozygosity. This observation has implications for the field's understanding of the etiological bases of intelligence and its variability around the world.

354 Saudi Arabian ancestry children

Chapter III

Study Statistics

Key metrics and study information

354
Total Participants
GWAS
Study Type
No
Replicated
Greater Middle Eastern (Middle Eastern, North African or Persian)
Ancestry
Saudi Arabia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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