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Thomas Kitzler

Has grant

Scientist

Research Institute of the McGill University Health Centre

Canada

Research Interests

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Professors in Canada Professors in Cell Biology Cell Biology professors in Canada

Recent Grants

Grant: Open

Autosomal recessive variants in TNS1 constitute a novel cause of proteinuric renal disease due to mesangial cell dysfunction.

Open Date: 2026-04-01

Close Date: 2032-03-01

Grant: Open

Toward Equitable Genetic Services for Hereditary Kidney Disease: A Canadian Needs Assessment and Implementation Toolkit

Open Date: 2026-01-01

Close Date: 2027-12-31

Grant: Open

The Zebrafish Variant Resolution Program: Mapping the Genetic Landscape of Primary Ciliary Dyskinesia to Enable Targeted Therapies

Open Date: 2025-09-01

Close Date: 2027-08-01

Grant: Open

A comprehensive approach to study novel monogenic causes of CAKUT in humans

Open Date: 2024-07-01

Close Date: 2027-06-01

Grant: Close

Uncovering novel genotype-phenotype relationships in chronic kidney disease

Open Date: 2024-06-01

Close Date: 2024-08-31

Articles (16)

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2026

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2025

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2024

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2023

Collaborators (9)

Abdulrahman Aldeeri

Harvard University

UNITED STATES

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Justin Chun

Assistant Professor

University of Calgary

CANADA

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Miguel Barroso-Gil

Laboratory teacher (profesor colaborador doctor de prácticas de laboratorio)

Universidad CEU San Pablo

SPAIN

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Timothy Yu

Associate Member

Broad Institute

UNITED STATES

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Konstantin Deutsch

Senior Scientist, Discovery Research

UNITED STATES

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Elena Torban

CANADA

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Paul Goodyer

Professor

McGill University

CANADA

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Zachary Thomas Sentell

McGill University

CANADA

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Kirollos Yousef

Assistant Professor

Children's Hospital of Richmond at Virginia Commonwealth University Children's Pavilion

UNITED STATES

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Thomas Kitzler

Research Interests

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Recent Grants

Articles (16)

Expanding the Phenotypic Spectrum of TXNDC15‐Related Ciliopathies to Include Joubert Syndrome

Swimming Upstream to Understand Congenital Anomalies of the Kidney and Urinary Tract: Zebrafish Models for Developmental Biology, Disease Mechanisms, and Functional Interpretation of Genetic Variation

Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure—Implications for Mitochondrial Genetic Testing in Nephrology

Use of patient-derived cell models for characterization of compound heterozygous hypomorphic C2CD3 variants in a patient with isolated nephronophthisis

Contiguous Gene Deletion Involving COL4A1 and COL4A2 in a Patient with Thin Basement Membrane Nephropathy: A Case Report

Genetic Assessment of Living Kidney Transplant Donors: A Survey of Canadian Practices

Proximity-based proteomics (BioID) uncovers the Rho GTPase interactome in kidney podocytes

Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions

Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome

Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis

Epigenomic and phenotypic characterization of DEGCAGS syndrome

Primary cilia and actin regulatory pathways in renal ciliopathies.

Characterization of Rho-Family of Small GTPases Interactome in Podocytes

Collaborative effort: managing Bardet-Biedl syndrome in pediatric patients. Case series and a literature review

Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature

Understanding the Current Landscape of Kidney Disease in Canada to Advance Precision Medicine Guided Personalized Care

Collaborators (9)

Abdulrahman Aldeeri

Justin Chun

Miguel Barroso-Gil

Timothy Yu

Konstantin Deutsch

Elena Torban

Paul Goodyer

Zachary Thomas Sentell

Kirollos Yousef

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