Menu
GWAS Study

Different Pigmentation Risk Loci for High-Risk Monosomy 3 and Low-Risk Disomy 3 Uveal Melanomas.

Mobuchon L, Derrien AC, Houy A et al.

34424336 PubMed ID
GWAS Study Type
2024 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ML
Mobuchon L
DA
Derrien AC
HA
Houy A
VT
Verrier T
PG
Pierron G
CN
Cassoux N
MM
Milder M
DJ
Deleuze JF
BA
Boland A
SG
Scelo G
CG
Cancel-Tassin G
CO
Cussenot O
RM
Rodrigues M
NJ
Noirel J
MM
Machiela MJ
SM
Stern MH
Chapter II

Abstract

Summary of the research findings

Uveal melanoma (UM), a rare malignant tumor of the eye, is predominantly observed in populations of European ancestry. UMs carrying a monosomy 3 (M3) frequently relapse mainly in the liver, whereas UMs with disomy 3 (D3) are associated with more favorable outcome. Here, we explored the UM genetic predisposition factors in a large genome-wide association study (GWAS) of 1142 European UM patients and 882 healthy controls .

1,142 European ancestry cases, 882 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

2024
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
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.