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GWAS Study

Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.

Wuttke M, Wong CS, Wühl E et al.

26420894 PubMed ID
GWAS Study Type
1141 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WM
Wuttke M
WC
Wong CS
WE
Wühl E
ED
Epting D
LL
Luo L
HA
Hoppmann A
DA
Doyon A
LY
Li Y
SB
Sözeri B
TD
Thurn D
HM
Helmstädter M
HT
Huber TB
BT
Blydt-Hansen TD
KA
Kramer-Zucker A
MO
Mehls O
MA
Melk A
QU
Querfeld U
FS
Furth SL
WB
Warady BA
SF
Schaefer F
KA
Köttgen A
Chapter II

Abstract

Summary of the research findings

Chronic kidney disease (CKD) in children is characterized by rapid progression and a high incidence of end-stage renal disease and therefore constitutes an important health problem. While unbiased genetic screens have identified common risk variants influencing renal function and CKD in adults, the presence and identity of such variants in pediatric CKD are unknown.

up to 744 European ancestry child cases, up to 397 Turkish ancestry child cases

Chapter III

Study Statistics

Key metrics and study information

1141
Total Participants
GWAS
Study Type
No
Replicated
European, Other
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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