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GWAS Study

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.

Verbitsky M, Krithivasan P, Batourina E et al.

33597122 PubMed ID
GWAS Study Type
6761 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

VM
Verbitsky M
KP
Krithivasan P
BE
Batourina E
KA
Khan A
GS
Graham SE
MM
Marasà M
KH
Kim H
LT
Lim TY
WP
Weng PL
SE
Sánchez-Rodríguez E
MA
Mitrotti A
AD
Ahram DF
ZF
Zanoni F
FD
Fasel DA
WR
Westland R
SM
Sampson MG
ZJ
Zhang JY
BM
Bodria M
KB
Kil BH
SS
Shril S
GL
Gesualdo L
TF
Torri F
SF
Scolari F
IC
Izzi C
VW
van Wijk JAE
SM
Saraga M
SD
Santoro D
CG
Conti G
BD
Barton DE
DM
Dobson MG
PP
Puri P
FS
Furth SL
WB
Warady BA
PI
Pisani I
FE
Fiaccadori E
AL
Allegri L
DM
Degl'Innocenti ML
PG
Piaggio G
AS
Alam S
GM
Gigante M
ZG
Zaza G
EP
Esposito P
LF
Lin F
SA
Simões-E-Silva AC
BA
Brodkiewicz A
DD
Drozdz D
ZK
Zachwieja K
MM
Miklaszewska M
SM
Szczepanska M
AP
Adamczyk P
TM
Tkaczyk M
TD
Tomczyk D
SP
Sikora P
MM
Mizerska-Wasiak M
KG
Krzemien G
SA
Szmigielska A
ZM
Zaniew M
LV
Lozanovski VJ
GZ
Gucev Z
II
Ionita-Laza I
SI
Stanaway IB
CD
Crosslin DR
WC
Wong CS
HF
Hildebrandt F
BJ
Barasch J
KE
Kenny EE
LR
Loos RJF
LB
Levy B
GG
Ghiggeri GM
HH
Hakonarson H
LA
Latos-Bieleńska A
MA
Materna-Kiryluk A
DJ
Darlow JM
TV
Tasic V
WC
Willer C
KK
Kiryluk K
SS
Sanna-Cherchi S
MC
Mendelsohn CL
GA
Gharavi AG
Chapter II

Abstract

Summary of the research findings

Vesicoureteral reflux (VUR) is a common, familial genitourinary disorder, and a major cause of pediatric urinary tract infection (UTI) and kidney failure. The genetic basis of VUR is not well understood.

1,395 European ancestry cases, 5,366 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6761
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.