DNA copy number variations in children with vesicoureteral reflux and urinary tract infections

Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT)

(2018) Yasmine Neirijnck et al.   KIDNEY INTERNATIONAL

Genetic- and Lifestyle-dependent Dental Caries Defined by the Acidic Proline-rich Protein Genes PRH1 and PRH2

(2017) Nicklas Strömberg et al.   EBioMedicine

Identification of a specific agonist of human TAS2R14 from Radix Bupleuri through virtual screening, functional evaluation and binding studies

(2017) Yuxin Zhang et al.   Scientific Reports

SMASH, a fragmentation and sequencing method for genomic copy number analysis

(2016) Zihua Wang et al.   GENOME RESEARCH

Genetics of Vesicoureteral Reflux

(2015) F. Nino et al.   CURRENT GENOMICS

Genomic imbalances in pediatric patients with chronic kidney disease

(2015) Miguel Verbitsky et al.   JOURNAL OF CLINICAL INVESTIGATION

Large multiallelic copy number variations in humans

(2015) Robert E Handsaker et al.   NATURE GENETICS

Fibroblast growth factor receptor signaling in kidney and lower urinary tract development

(2015) Kenneth A. Walker et al.   PEDIATRIC NEPHROLOGY

Human gene copy number variation and infectious disease

(2014) Edward J. Hollox et al.   HUMAN GENETICS

Antimicrobial Prophylaxis for Children with Vesicoureteral Reflux

(2014)   NEW ENGLAND JOURNAL OF MEDICINE

Urinary tract infection and vesicoureteral reflux in children with mild antenatal hydronephrosis

(2014) A. Sencan et al.   Journal of Pediatric Urology

Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes

(2013) Patrick D. Brophy et al.   HUMAN GENETICS

TNXB Mutations Can Cause Vesicoureteral Reflux

(2013) R. A. Gbadegesin et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Mutations in DSTYK and Dominant Urinary Tract Malformations

(2013) S. Sanna-Cherchi et al.   NEW ENGLAND JOURNAL OF MEDICINE

The RIVUR Trial: Profile and Baseline Clinical Associations of Children With Vesicoureteral Reflux

(2013) M. A. Carpenter et al.   PEDIATRICS

A new genome scan for primary nonsyndromic vesicoureteric reflux emphasizes high genetic heterogeneity and shows linkage and association with various genes already implicated in urinary tract development

(2013) J. M. Darlow et al.   Molecular Genetics & Genomic Medicine

Chromosomal variation in lymphoblastoid cell lines

(2012) Matthew D. Shirley et al.   HUMAN MUTATION

Renal anomalies in Alagille syndrome: A disease-defining feature

(2011) Binita M. Kamath et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genetics of vesicoureteral reflux

(2011) Prem Puri et al.   Nature Reviews Urology

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

(2011) Dan Levy et al.   NEURON

The genetics of primary, nonsyndromic vesicoureteral reflux

(2010) Fernando Carvas et al.   CURRENT OPINION IN UROLOGY

High Incidence of Vesicoureteral Reflux in Mice With Fgfr2 Deletion in Kidney Mesenchyma

(2010) David S. Hains et al.   JOURNAL OF UROLOGY

Microarray-Based Genomic DNA Profiling Technologies in Clinical Molecular Diagnostics

(2009) Y. Shen et al.   CLINICAL CHEMISTRY

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

(2009) Christine E Briggs et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux

(2009) H. J. Cordell et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

A Recessive Gene for Primary Vesicoureteral Reflux Maps to Chromosome 12p11-q13

(2009) P. L. Weng et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Vesicoureteral Reflux

(2008) G. Williams et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity

(2008) Maria Luisa Conte et al.   PEDIATRIC NEPHROLOGY