List of works - Asaf Vivante

A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux

scientific article

A human integrin-α3 mutation confers major renal developmental defects

scientific article

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

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

Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center

scientific article

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

scientific article published on 01 April 2019

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

scientific article published on November 26, 2012

Cardiovascular and metabolic risk factors in inherited autoinflammation

scientific article published on 25 July 2014

Congenital diaphragmatic hernia: 22 years experience in a single tertiary medical center

scientific article

Etiology and long-term outcome of extrahepatic portal vein obstruction in children ⬇️

scientific article published on October 21, 2010

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

Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases

scientific article published on 05 August 2017

Exploring the genetic basis of early-onset chronic kidney disease

scientific article

Familial autosomal recessive renal tubular acidosis: importance of early diagnosis.

scientific article

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

scientific article

Hematuria and risk for end-stage kidney disease ⬇️

scientific article published on May 1, 2013

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

scientific article published in February 2018

Intracardiac thrombus and pulmonary aneurysms in an adolescent with Behçet disease

scientific article published on 11 October 2008

Keeping the heart in mind when managing hemolytic: uremic syndrome

scientific article published on July 1, 2011

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract

scientific article

Mortality risk factors associated with familial Mediterranean fever among a cohort of 1.25 million adolescents

scientific article published on 16 March 2013

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

scientific article

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

scientific article

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

scientific article

Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on 27 October 2017

Overweight in adolescence is related to increased risk of future urothelial cancer

scientific article published on 18 April 2012

Persistent asymptomatic isolated microscopic hematuria in Israeli adolescents and young adults and risk for end-stage renal disease

scientific article published in August 2011

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

scientific article published on 6 February 2017

Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature

Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling

scientific article published on 21 March 2013

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

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

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 29 January 2016

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

scientific article published on 21 December 2018

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

scientific article published on 26 February 2018

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

scientific article

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

scientific article published on 8 September 2017

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

scientific article

List of works by Asaf Vivante

A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux

A human integrin-α3 mutation confers major renal developmental defects

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).

Adolescent Obesity and Paternal Country of Origin Predict Renal Cell Carcinoma: A Cohort Study of 1.1 Million 16 to 19-Year-Old Males ⬇️

Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center

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

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

Cardiovascular and metabolic risk factors in inherited autoinflammation

Congenital diaphragmatic hernia: 22 years experience in a single tertiary medical center

Etiology and long-term outcome of extrahepatic portal vein obstruction in children ⬇️

Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract

Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases

Exploring the genetic basis of early-onset chronic kidney disease

Familial autosomal recessive renal tubular acidosis: importance of early diagnosis.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Hematuria and risk for end-stage kidney disease ⬇️

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

Intracardiac thrombus and pulmonary aneurysms in an adolescent with Behçet disease

Keeping the heart in mind when managing hemolytic: uremic syndrome

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract

Mortality risk factors associated with familial Mediterranean fever among a cohort of 1.25 million adolescents

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

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

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

Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract

Overweight in adolescence is related to increased risk of future urothelial cancer

Persistent asymptomatic isolated microscopic hematuria in Israeli adolescents and young adults and risk for end-stage renal disease

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

Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature

Renal hypodysplasia associates with a WNT4 variant that causes aberrant canonical WNT signaling

SAT-244 The Association between Obesity and Secular Trend of Stature: A Nationwide Study of 2.8 Million Adolescents over Five Decades.

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

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

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

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

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome

Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

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