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GWAS Study

Genome-wide association identifies diverse causes of common variable immunodeficiency.

Orange JS, Glessner JT, Resnick E et al.

21497890 PubMed ID
GWAS Study Type
3319 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OJ
Orange JS
GJ
Glessner JT
RE
Resnick E
SK
Sullivan KE
LM
Lucas M
FB
Ferry B
KC
Kim CE
HC
Hou C
WF
Wang F
CR
Chiavacci R
KS
Kugathasan S
SJ
Sleasman JW
BR
Baldassano R
PE
Perez EE
CH
Chapel H
CC
Cunningham-Rundles C
HH
Hakonarson H
Chapter II

Abstract

Summary of the research findings

Common variable immunodeficiency (CVID) is a heterogeneous immune defect characterized by hypogammaglobulinemia, failure of specific antibody production, susceptibility to infections, and an array of comorbidities.

179 European ancestry cases, 1,917 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3319
Total Participants
GWAS
Study Type
Yes
Replicated
109 European ancestry cases, 1,114 European ancestry controls
Replication Participants
European
Ancestry
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.