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GWAS Study

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.

Kanai M, Akiyama M, Takahashi A et al.

29403010 PubMed ID
GWAS Study Type
128305 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KM
Kanai M
AM
Akiyama M
TA
Takahashi A
MN
Matoba N
MY
Momozawa Y
IM
Ikeda M
IN
Iwata N
IS
Ikegawa S
HM
Hirata M
MK
Matsuda K
KM
Kubo M
OY
Okada Y
KY
Kamatani Y
Chapter II

Abstract

Summary of the research findings

Clinical measurements can be viewed as useful intermediate phenotypes to promote understanding of complex human diseases. To acquire comprehensive insights into the underlying genetics, here we conducted a genome-wide association study (GWAS) of 58 quantitative traits in 162,255 Japanese individuals. Overall, we identified 1,407 trait-associated loci (P < 5.0 × 10-8), 679 of which were novel. By incorporating 32 additional GWAS results for complex diseases and traits in Japanese individuals, we further highlighted pleiotropy, genetic correlations, and cell-type specificity across quantitative traits and diseases, which substantially expands the current understanding of the associated genetics and biology. This study identified both shared polygenic effects and cell-type specificity, represented by the genetic links among clinical measurements, complex diseases, and relevant cell types. Our findings demonstrate that even without prior biological knowledge of cross-phenotype relationships, genetics corresponding to clinical measurements successfully recapture those measurements' relevance to diseases, and thus can contribute to the elucidation of unknown etiology and pathogenesis.

128,305 Japanese ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

128305
Total Participants
GWAS
Study Type
No
Replicated
East Asian
Ancestry
Japan
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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