Literature DB >> 17660461

A genome-wide scan for genes involved in primary vesicoureteric reflux.

H Kelly1, C M Molony, J M Darlow, M E Pirker, A Yoneda, A J Green, P Puri, D E Barton.   

Abstract

BACKGROUND: Vesicoureteric reflux (VUR) is the retrograde flow of urine from the bladder into the ureters. It is the most common urological anomaly in children, and a major cause of end-stage renal failure and hypertension in both children and adults. VUR is seen in approximately 1-2% of Caucasian newborns and is frequently familial. OBJECTIVE AND METHODS: In order to search for genetic loci involved in VUR, we performed a genome-wide linkage scan using 4710 single-nucleotide polymorphisms (SNPs) in 609 individuals from 129 Irish families with >1 affected member.
RESULTS: Nonparametric linkage (NPL) analysis of the dataset yielded moderately suggestive linkage at chromosome 2q37 (NPL(max) = 2.67, p<0.001). Analysis of a subset without any additional features, such as duplex kidneys, yielded a maximum NPL score of 4.1 (p = 0.001), reaching levels of genome-wide statistical significance. Suggestive linkage was also seen at 10q26 and 6q27, and there were several smaller peaks.
CONCLUSION: Our results confirm the previous conclusion that VUR is genetically heterogeneous, and support the identification of several disease-associated regions indicated by smaller studies, as well as indicating new regions of interest for investigation.

Entities:  

Mesh:

Year:  2007        PMID: 17660461      PMCID: PMC2752186          DOI: 10.1136/jmg.2007.051086

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  66 in total

1.  Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation.

Authors:  Paul J Batstone; Sheila Simpson; David T Bonthron; Wee T Keng; Doreen Hamilton; Linda Forsyth; Mark Sales; Norman Pratt; David Goudie
Journal:  Am J Med Genet A       Date:  2003-04-30       Impact factor: 2.802

Review 2.  Unrelated patients with a rearrangement of chromosome 2 causing duplication of 2p23 and deletion of 2q37.

Authors:  Linlea Armstrong; Judith E Allanson; David D Weaver; Carole J Bevan; Holly H Hobart
Journal:  Am J Med Genet A       Date:  2005-04-30       Impact factor: 2.802

Review 3.  Vesicoureteral reflux.

Authors:  Larry A Greenbaum; Hrair-George O Mesrobian
Journal:  Pediatr Clin North Am       Date:  2006-06       Impact factor: 3.278

4.  [Renal damage in vesicoureteral reflux associated to duplex pyeloureteral system].

Authors:  P Orellana; M E Pizarro; F García; P Baquedano
Journal:  Rev Esp Med Nucl       Date:  2005 Nov-Dec

Review 5.  Vesicoureteric reflux and renal malformations: a developmental problem.

Authors:  I J Murawski; I R Gupta
Journal:  Clin Genet       Date:  2006-02       Impact factor: 4.438

6.  [Vesicoureteral reflux in children with prenatal suspicion of urinary tract abnormalities].

Authors:  Grazyna Krzemień; Maria Roszkowska-Blaim; Izabella Kostro; Agnieszka Szmigielska; Jarosław Madzik
Journal:  Przegl Lek       Date:  2006

7.  Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.

Authors:  C A Bacino; C D Kashork; N A Davino; L G Shaffer
Journal:  Am J Med Genet       Date:  2000-06-05

8.  Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy-like phenotype.

Authors:  N Chassaing; P De Mas; M Tauber; M C Vincent; S Julia; G Bourrouillou; P Calvas; E Bieth
Journal:  Am J Med Genet A       Date:  2004-08-01       Impact factor: 2.802

9.  Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

Authors:  P Sanyanusin; L A Schimmenti; L A McNoe; T A Ward; M E Pierpont; M J Sullivan; W B Dobyns; M R Eccles
Journal:  Nat Genet       Date:  1995-04       Impact factor: 38.330

10.  Linkage analysis of complex diseases using microsatellites and single-nucleotide polymorphisms: application to alcoholism.

Authors:  Jérémie Nsengimana; Hélène Renard; David Goldgar
Journal:  BMC Genet       Date:  2005-12-30       Impact factor: 2.797

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  22 in total

1.  A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

Authors:  Patricia L Weng; Simone Sanna-Cherchi; Terry Hensle; Ellen Shapiro; Alan Werzberger; Gianluca Caridi; Claudia Izzi; Anita Konka; Adam C Reese; Rong Cheng; Samuel Werzberger; Richard N Schlussel; Robert D Burk; Joseph H Lee; Roberto Ravazzolo; Francesco Scolari; Gian Marco Ghiggeri; Kenneth Glassberg; Ali G Gharavi
Journal:  J Am Soc Nephrol       Date:  2009-05-14       Impact factor: 10.121

2.  Vesicoureteral reflux: genetic associations besides the Hinman syndrome.

Authors:  Shailendra Kapoor
Journal:  Clin Exp Nephrol       Date:  2008-07-09       Impact factor: 2.801

Review 3.  Genetics of vesicoureteral reflux.

Authors:  Prem Puri; Jan-Hendrik Gosemann; John Darlow; David E Barton
Journal:  Nat Rev Urol       Date:  2011-08-23       Impact factor: 14.432

4.  Mutation screening of ACKR3 and COPS8 in kidney cancer cases from the CONFIRM study.

Authors:  Maryam Mahmoodi; Tu Nguyen-Dumont; Fleur Hammet; Bernard J Pope; Daniel J Park; Melissa C Southey; John M Darlow; Fiona Bruinsma; Ingrid Winship
Journal:  Fam Cancer       Date:  2017-07       Impact factor: 2.375

5.  Primary, nonsyndromic vesicoureteric reflux and nephropathy in sibling pairs: a United Kingdom cohort for a DNA bank.

Authors:  Heather J Lambert; Aisling Stewart; Ambrose M Gullett; Heather J Cordell; Sue Malcolm; Sally A Feather; Judith A Goodship; Timothy H J Goodship; Adrian S Woolf
Journal:  Clin J Am Soc Nephrol       Date:  2011-03-24       Impact factor: 8.237

6.  TNXB mutations can cause vesicoureteral reflux.

Authors:  Rasheed A Gbadegesin; Patrick D Brophy; Adebowale Adeyemo; Gentzon Hall; Indra R Gupta; David Hains; Bartlomeij Bartkowiak; C Egla Rabinovich; Settara Chandrasekharappa; Alison Homstad; Katherine Westreich; Guanghong Wu; Yutao Liu; Danniele Holanda; Jason Clarke; Peter Lavin; Angelica Selim; Sara Miller; John S Wiener; Sherry S Ross; John Foreman; Charles Rotimi; Michelle P Winn
Journal:  J Am Soc Nephrol       Date:  2013-04-25       Impact factor: 10.121

7.  A single-center cohort of Canadian children with VUR reveals renal phenotypes important for genetic studies.

Authors:  Jasmine El Andalousi; Inga J Murawski; John-Paul Capolicchio; Mohamed El-Sherbiny; Roman Jednak; Indra R Gupta
Journal:  Pediatr Nephrol       Date:  2013-03-26       Impact factor: 3.714

8.  Mutations in the ROBO2 and SLIT2 genes are rare causes of familial vesico-ureteral reflux.

Authors:  Shulu Zu; Zsuzsa Bartik; Shengtian Zhao; Ulla Sillen; Agneta Nordenskjöld
Journal:  Pediatr Nephrol       Date:  2009-04-07       Impact factor: 3.714

9.  A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5.

Authors:  Christine E Briggs; Chao-Yu Guo; Cynthia Schoettler; Ilina Rosoklija; Andres Silva; Stuart B Bauer; Alan B Retik; Louis Kunkel; Hiep T Nguyen
Journal:  Eur J Hum Genet       Date:  2009-08-19       Impact factor: 4.246

10.  Genetic contribution and associated pathophysiology in end-stage renal disease.

Authors:  Suraksha Agrawal; Ss Agarwal; Sita Naik
Journal:  Appl Clin Genet       Date:  2010-08-05
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