Menu
GWAS Study

Genome-wide association study reveals novel loci for adult type 1 diabetes in a 5-year nested case-control study.

Gao Y, Chen S, Gu WY et al.

35047121 PubMed ID
GWAS Study Type
1589 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GY
Gao Y
CS
Chen S
GW
Gu WY
FC
Fang C
HY
Huang YT
GY
Gao Y
LY
Lu Y
SJ
Su J
WM
Wu M
ZJ
Zhang J
XM
Xu M
ZZ
Zhang ZL
Chapter II

Abstract

Summary of the research findings

Type 1 diabetes (T1D) is a severe and prevalent metabolic disease. Due to its high heredity, an increasing number of genome-wide association studies have been performed, most of which were from hospital-based case-control studies with a relatively small sample size. The association of single nucleotide polymorphisms (SNPs) and T1D has been less studied and is less understood in natural cohorts.

381 Chinese ancestry cases, 377 Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1589
Total Participants
GWAS
Study Type
Yes
Replicated
404 Chinese ancestry cases, 427 Chinese ancestry controls
Replication Participants
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

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.