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GWAS Study

Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunction.

Imtiaz MA, Melas K, Tin A et al.

40963118 PubMed ID
GWAS Study Type
22730 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

IM
Imtiaz MA
MK
Melas K
TA
Tin A
TV
Talevi V
CH
Chen H
FM
Fornage M
SS
Shrestha S
GM
Gögele M
ED
Emmert D
PC
Pattaro C
PP
Pramstaller P
FF
Förster F
HK
Horn K
MT
Mosley TH
FC
Fuchsberger C
SM
Scholz M
BM
Breteler MMB
AN
Aziz NA
Chapter II

Abstract

Summary of the research findings

Olfactory dysfunction is among the earliest signs of many age-related neurodegenerative diseases and has been associated with increased mortality in older adults; however, its genetic basis remains largely unknown. Therefore, here we aimed to elucidate its genetic architecture through a genome-wide association study meta-analysis (GWMA).

22,730 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

22730
Total Participants
GWAS
Study Type
No
Replicated
European, African unspecified
Ancestry
U.S., Italy, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.