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Our Work

At the Vivante Lab, we are committed to advancing the understanding of the genetic and molecular basis of chronic kidney disease (CKD) to enable earlier diagnosis, improve risk prediction, and ultimately develop targeted gene-based therapies for patients.

 

Our research spans the full spectrum of translational nephrogenetics—from gene discovery to therapy. We combine comprehensive genomic analysis with functional studies of novel disease-causing genes, and actively pursue the development of precision treatments based on molecular insights.

 

A cornerstone of our work is the Israeli Kidney Failure Genetic Cohort, a nationwide miltuethnic initiative established by our team. This unique resource includes over 3,000 individuals recruited from more than 50 dialysis units across Israel, representing a wide range of ethnic backgrounds and clinical phenotypes.

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We also collaborate closely with the National Nephrogenetic Clinic at Sheba Medical Center, led by Prof. Asaf Vivante. The clinic serves as Israel’s central referral center for genetic kidney diseases diagnosis, monitoring and treatment.

 

By integrating next-generation sequencing, cellular and animal models, and innovative therapeutic platforms, the Vivante Lab is positioned at the forefront of translational kidney genetics research. Our goal is to bridge the gap between rare disease discovery and clinical implementation, while fostering collaboration and training the next generation of physician-scientists and geneticists.

01

Unravel Known and Novel CKD Causing Genes

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This project aims to identify both known and previously unrecognized genetic causes of chronic kidney disease (CKD). Leveraging our national Israeli Kidney Failure Genetic Cohort and a diverse range of clinical phenotypes, we apply advanced genomic technologies, including whole exome and genome sequencing, to uncover monogenic contributors to CKD. By integrating detailed clinical data with high-resolution genetic analysis, we seek to expand the catalog of disease-causing genes and refine molecular diagnoses across populations.

02

Study Novel Mechanisms For Genetic Kidney Diseases

In this project, we investigate the biological pathways and cellular mechanisms underlying newly identified genetic kidney diseases. Using in vitro models, patient-derived cells, and in vivo systems, we explore how specific gene variants disrupt kidney development and function. Our goal is to move beyond gene discovery and uncover the molecular basis of disease, paving the way for mechanistic insights and potential therapeutic targets.

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03

Develop Gene-Based Therapies

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This project focuses on translating genetic discoveries into targeted therapeutic strategies for patients with inherited kidney diseases. We develop and test gene-based approaches, including RNA therapies and antisense oligonucleotides (ASOs), aimed at correcting or modulating the effects of pathogenic variants. By combining insights from our genetic and functional studies with innovative delivery platforms, we strive to advance precision medicine for rare kidney disorders.

Our Funding

Our group has been awarded multiple prestigious and competitive research grants, made possible through the generous support of leading funding organizations. These contributions have been instrumental in advancing our research and driving innovation in the field of genetic kidney disease.

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We gratefully acknowledge the support of our primary funding partners:

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