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GWAS Study

Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.

Clancy RM, Marion MC, Kaufman KM et al.

20662065 PubMed ID
GWAS Study Type
3467 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CR
Clancy RM
MM
Marion MC
KK
Kaufman KM
RP
Ramos PS
AA
Adler A
HJ
Harley JB
LC
Langefeld CD
BJ
Buyon JP
Chapter II

Abstract

Summary of the research findings

Objective: Cardiac manifestations of neonatal lupus, comprising atrioventricular conduction defects and cardiomyopathy, occur in fetuses exposed to anti-Ro/SSA antibodies, and carry substantial mortality. There is strong evidence of a genetic contribution to the risk. This study was undertaken to evaluate single-nucleotide polymorphisms (SNPs) for associations with cardiac neonatal lupus.

116 European ancestry cases, 3,351 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3467
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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