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Research
Latest papers
Contiguous Gene Deletion Involving COL4A1 and COL4A2 in a Patient with Thin Basement Membrane Nephropathy: A Case Report.
Nephron · 2026
Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology.
Clinical genetics · 2026
Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.
Nephron · 2024
Latest funding
- $95,608
Toward Equitable Genetic Services for Hereditary Kidney Disease: A Canadian Needs Assessment and Implementation Toolkit
CIHR · 2025 · Nominated PI
3 publications.
Contiguous Gene Deletion Involving COL4A1 and COL4A2 in a Patient with Thin Basement Membrane Nephropathy: A Case Report.
Henein M, Russo F, Bernard C, Cybulsky AV, Kitzler TM
Biallelic TMEM126B Variants as a Novel Cause of Kidney Failure-Implications for Mitochondrial Genetic Testing in Nephrology.
Sentell ZT, Cheung ACT, Russo F, Bernard C, Suri R, Cybulsky AV, Buhas D, Kitzler TM
Phenotypic Discordance among Siblings with Autosomal Recessive Polycystic Kidney Disease: Case Report and Review of the Literature.
Henein M, Russo F, Sentell ZT, Goupil R, Kitzler TM
Toward Equitable Genetic Services for Hereditary Kidney Disease: A Canadian Needs Assessment and Implementation Toolkit
Principal investigators: Russo, Felicia; Kitzler, Thomas M
Keywords: Educational Toolkit; Genetic Counselling; Genetic Service Delivery; Inherited Kidney Disease; Renal Genetics Clinic
From CIHR, NSERC and SSHRC funding decisions: CIHR since 2008, NSERC since 1991 and SSHRC since 1998, including their latest published competition results.
Frequent collaborators
- Medicine
- Medicine/Nephrology
- Other
Co-authors at McGill University, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
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