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GWAS Study

Ultra-rare genetic variation in relapsing polychondritis: a whole-exome sequencing study.

Luo Y, Ferrada MA, Sikora KA et al.

37918895 PubMed ID
GWAS Study Type
2989 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LY
Luo Y
FM
Ferrada MA
SK
Sikora KA
RC
Rankin C
AH
Alessi HD
KD
Kastner DL
DZ
Deng Z
ZM
Zhang M
MP
Merkel PA
KV
Kraus VB
AA
Allen AS
GP
Grayson PC
Chapter II

Abstract

Summary of the research findings

Objective: Relapsing polychondritis (RP) is a systemic inflammatory disease of unknown aetiology. The objective of this study was to examine the contribution of rare genetic variations to RP.

66 non-Hispanic European American ancestry cases, 2,923 non-Hispanic European American ancestry controls

Chapter III

Study Statistics

Key metrics and study information

2989
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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Analysis In Progress

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