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List of works by Asaf Vivante

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Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract

scientific article
Body Mass Index in 1.2 Million Adolescents and Risk for End-Stage Renal Disease

scientific article published on November 26, 2012
Exploring the genetic basis of early-onset chronic kidney disease

scientific article published on January 11, 2016
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

scientific article published on January 8, 2014
Persistent Asymptomatic Isolated Microscopic Hematuria in Israeli Adolescents and Young Adults and Risk for End-Stage Renal Disease

scientific article published on August 17, 2011
Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on April 3, 2014
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

scientific article
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

scientific article
Renal Hypodysplasia Associates with a Wnt4 Variant that Causes Aberrant Canonical Wnt Signaling

scientific article published on March 21, 2013
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

scientific article published on 8 September 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

scientific article
History of Childhood Kidney Disease and Risk of Adult End-Stage Renal Disease

scientific article published in February 2018
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

scientific article published on 5 May 2016
Adolescent Obesity and Paternal Country of Origin Predict Renal Cell Carcinoma: A Cohort Study of 1.1 Million 16 to 19-Year-Old Males

scientific article published on November 16, 2012
A new MALDI-TOF-based assay for monitoring JAK2 V617F mutation level in patients undergoing allogeneic stem cell transplantation (allo SCT) for classic myeloproliferative disorders (MPD).

scientific article published on 14 August 2007
Mortality risk factors associated with familial Mediterranean fever among a cohort of 1.25 million adolescents

scientific article published on 16 March 2013
Etiology and long-term outcome of extrahepatic portal vein obstruction in children

scientific article published on October 21, 2010
Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on October 27, 2017
A human integrin-α3 mutation confers major renal developmental defects

scientific article
The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 21 December 2018
Intracardiac thrombus and pulmonary aneurysms in an adolescent with Behçet disease

scientific article published on 11 October 2008
Hematuria and risk for end-stage kidney disease

scientific article published on May 1, 2013
Overweight in adolescence is related to increased risk of future urothelial cancer

scientific article published on 18 April 2012
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center

scientific article
Prehypertension among 2.19 million adolescents and future risk for end-stage renal disease

scientific article published on 6 February 2017
Cardiovascular and metabolic risk factors in inherited autoinflammation

scientific article published on 25 July 2014
Familial autosomal recessive renal tubular acidosis: importance of early diagnosis

scientific article
Mutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome

scientific article
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract

scientific article published on January 29, 2016
Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases

scientific article published on 05 August 2017
Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 01 April 2019
Congenital diaphragmatic hernia: 22 years experience in a single tertiary medical center

scientific article
Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report

scientific article
Keeping the heart in mind when managing hemolytic: uremic syndrome

scientific article published on July 1, 2011
SAT-244 The Association between Obesity and Secular Trend of Stature: A Nationwide Study of 2.8 Million Adolescents over Five Decades

scientific article published on 30 April 2019
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux

scientific article
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome

scientific article published on 26 February 2018

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