This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a McGill University directory, so their courses may be missing. Find their university profile.
Research
Latest papers
Identification of intradialytic hemodynamic phenotypes using latent profile analysis.
Clinical kidney journal · 2026
Proteome-wide Mendelian randomization identifies APOM and TNXB as actionable mediators of steroid-sensitive nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) · 2026
USP40 protects podocytes by deubiquitylating integrin β1.
Biochemical and biophysical research communications · 2026
Latest funding
- $95,608
Toward Equitable Genetic Services for Hereditary Kidney Disease: A Canadian Needs Assessment and Implementation Toolkit
CIHR · 2025 · Co-investigator
- $1,101,600
Autosomal recessive variants in TNS1 constitute a novel cause of proteinuric renal disease due to mesangial cell dysfunction.
CIHR · 2025 · Co-investigator
- $47,000
Mechanistic landscape of Rho GTPase regulation in the kidney
NSERC · 2024 · Principal investigator
76 publications.
Identification of intradialytic hemodynamic phenotypes using latent profile analysis.
Baroz F, Suri RS, Sharma A, Tom A, Takano T, Brophy JM, Beaubien-Souligny W, Mavrakanas TA
Proteome-wide Mendelian randomization identifies APOM and TNXB as actionable mediators of steroid-sensitive nephrotic syndrome.
Heydari D, Langlois S, Norouzi M, Myette RL, Samuel S, Zhou S, Takano T, Butler-Laporte G, Downie ML
USP40 protects podocytes by deubiquitylating integrin β1.
Mikami N, Fukushima T, Takematsu H, Kiuchi Z, Fukuhara D, Tanaka E, Kimura T, Suehiro J, Fukutomi T, Kobayashi K, Pastan I, Nagata M, Takano T, Matsusaka T, Akimoto Y, Kawanishi K, Yan K
Clusterin marks maladaptive regenerative responses throughout the kidney following ischemia-reperfusion injury.
Masztalerz A, Joumier L, Zhen S, Takano T, Lemay S, Malleshaiah M, Gregorieff A
Recurrent Neuro-Renal Syndrome With Acute Kidney Injury From Anti-Pan-Neurofascin Antibody Resurgence: A Case Report.
De Saint Gilles D, Rafat C, Devaux JJ, Marois C, Leclerc S, Takano T, Brochériou I, Elatram N, Husser F, Mesnard L, Buob D, Mousseaux C
Proximity-based proteomics (BioID) uncovers the Rho GTPase interactome in kidney podocytes.
Ibrahim S, Matsuda J, Nurcombe ZW, Boulais J, Aoudjit L, Foxman E, Kazan C, Suzuki S, Leclerc S, Shimada N, Kitzler T, Coté JF, Takano T
Mouse nephron formation is impaired by moderate dose arsenical exposure.
Alonso CAI, Haverfield J, Regalado G, Sellami S, Gagnon N, Rajaram A, Fiset PO, Takano T, Ryan AK, Mann KK, Gupta IR
Rac1 Suppression by the Focal Adhesion Protein GIT ArfGAP2 and Podocyte Protection.
Shimada N, Matsuda J, Asano-Matsuda K, Tokuchi M, Aoudjit L, Masztalerz A, Lemay S, Takano T, Isaka Y
Enhanced Gαq Signaling in TSC2-Deficient Cells Is Required for Their Neoplastic Behavior.
Tréfier A, Tousson-Abouelazm N, Yamani L, Ibrahim S, Joung KB, Pietrobon A, Yockell-Lelievre J, Hébert TE, Ladak RJ, Takano T, Nellist M, Namkung Y, Chatenet D, Stanford WL, Laporte SA, Kristof AS
The autoimmune architecture of childhood idiopathic nephrotic syndrome.
Al-Aubodah TA, Piccirillo CA, Trachtman H, Takano T
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
Autosomal recessive variants in TNS1 constitute a novel cause of proteinuric renal disease due to mesangial cell dysfunction.
Principal investigators: Kitzler, Thomas M; Downie, Mallory L
Keywords: Chronic Renal Failure; Exome And Genome Sequencing; Proteinuric Renal Disease; Zebrafish
Mechanistic landscape of Rho GTPase regulation in the kidney
Principal investigators: Takano, Tomoko
Keywords: rho gtpase; protein-protein interaction; rna profiling; cell signaling; podocytes; endothelial cells; glomerular filtration
Multi-omics for precision medicine in paediatric steroid sensitive nephrotic syndrome
Principal investigators: Downie, Mallory L
Keywords: Genomics; Gwas; Mendelian Randomization; Nephrotic Syndrome; Pediatric; Proteomics; Ssns; Structural Variant
Identification, description, and prognostic significance of latent classes based on hemodynamic indicators for patients on maintenance hemodialysis.
Principal investigators: Mavrakanas, Thomas; Beaubien-Souligny, William
Keywords: Hemodynamic Phenotypes; Intradialytic Hypertension; Intradialytic Hypotension; Latent Class Analysis; Maintenance Hemodialysis; Phenotype Prognostic Association; Unsupervised Machine Learning
Pathogenesis of idiopathic nephrotic syndrome: defining the role of B cells and autoantibodies reactive to podocyte proteins
Principal investigators: Takano, Tomoko; Piccirillo, Ciriaco A
Keywords: Nephrotic Syndrome
The Molecules and Mechanisms Mediating Kidney Health and Disease (M3K) Meeting and Investigator Summit
Principal investigators: Torban, Elena
Keywords: Biomarkers; Canadian; Disease Models; Diversity; Genetics; Kidney; Kidney Injury; Knowledge Translation; Mechanisms Of Disease; Molecular Biology
Elucidating the factors dictating regulatory T cell function in immune-mediated glomerular diseases.
Principal investigators: Al-Aubodah, Tho-Alfakar
Keywords: Alarmins; Autoimmunity; Cytokines; Effector T Cells; Flow Cytometry; Glomerular Diseases; Immune Cell Culture; Nephrotoxic Nephritis; Plasticity; Regulatory T Cells
Defining the immune dysfunction in childhood nephrotic syndrome: Toward therapeutic reversal without glucocorticoids
Principal investigators: Takano, Tomoko; Piccirillo, Ciriaco A; Samuel, Susan M
Keywords: Lymphocytes; Minimal Change Disease; Nephrotic Syndrome; Rituximab
Role of beta-PIX and CdGAP in the pathogenesis of proteinuria
Principal investigators: Takano, Tomoko
Keywords: Podocytes; Proteinuria; Rho Gtpases
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/Nephrology
- Medicine
- Nephrology
- Molecular and Cellular Biology
- Medicine/Cardiology
- Human Genetics
- Psychiatry
- 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.
Nina Jones
Molecular and Cellular Biology
5 shared papers, latest 2022
Elena Torban
Medicine/Nephrology
3 shared papers, latest 2022
Sunny Hartwig
Biomedical Sciences
2 shared papers, latest 2022
Nathalie Lamarche-Vane
Anatomy and Cell Biology
2 shared papers, latest 2022
Lakshman Gunaratnam
Medicine/Nephrology
2 shared papers, latest 2022
Marie Hudson
Psychiatry
2 shared papers, latest 2020
Nathalie Lamarche-Vane
Faculty
2 shared papers, latest 2022
Jacek Majewski
Human Genetics
2 shared papers, latest 2019
Abhinav Sharma
Medicine/Cardiology
2 shared papers, latest 2026
Alex Gregorieff
Faculty
2 shared papers, latest 2026
Steven Arora
Pediatrics
2 shared papers, latest 2019
Allison Dart
Pediatrics and Child Health
1 shared papers, latest 2019
Adeera Levin
Nephrology
1 shared papers, latest 2022
Stanley Nattel
Medicine
1 shared papers, latest 2013
Ruth Sapir-Pichhadze
Medicine
1 shared papers, latest 2017
Moumita Barua
Faculty
1 shared papers, latest 2022
Louise Larose
Medicine
1 shared papers, latest 2006
Kevin Burns
Department of Medicine
1 shared papers, latest 2022
Ji Zhang
Faculty
1 shared papers, latest 2020
Casimiro Gerarduzzi
Medicine
1 shared papers, latest 2022
Sonia Del Rincon
Oncology
1 shared papers, latest 2020
Rahul Chanchlani
Population Health Research Institute (PHRI) (Joint Institute)
1 shared papers, latest 2019
Nader Khalidi
Medicine
1 shared papers, latest 2020
Darren Bridgewater
Pathology & Molecular Medicine
1 shared papers, latest 2022
Margaret Larche
Medicine
1 shared papers, latest 2020
James Scholey
Medicine/Nephrology
1 shared papers, latest 2022
Catherine Clase
Medicine
1 shared papers, latest 2022
Shannon Scott
Pediatrics
1 shared papers, latest 2017
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