Menu
Currency
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
43 Views
Scroll to explore
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

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.