This profile is built from public research funding records (CIHR, NSERC and SSHRC) and PubMed. We have not imported them from a University of Toronto directory, so their courses and email address may be missing. Find their university profile.
Research
Latest papers
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for Hematuria.
Kidney international reports · 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome.
Kidney international reports · 2026
Genotype-Based Molecular Mechanisms in Alport Syndrome.
Journal of the American Society of Nephrology : JASN · 2025 · senior author
Latest funding
- $432,226
Identifying causal pathways for hematuria using comprehensive omics strategies: genomics, transcriptomics, metabolomics and proteomics
CIHR · 2023 · Co-investigator
- $6,000
Pax2 Mediates Glomerular Repair
CIHR · 2023 · Supervisor
- $105,000
The role of transcription factor PAX2 in mediating glomerular repair in a mouse model of focal segmental glomerulosclerosis
CIHR · 2022 · Supervisor
32 publications.
Autosomal Type IV Collagen Genes Display Sex Differences in Genetic Risk for Hematuria.
Lona-Durazo F, Dinsmore IR, McNulty MT, Sampson MG, Forest L, Mirshahi T, Chang AR, Paterson AD, Barua M, Gagliano Taliun SA
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome.
Oates TM, Barua M, Gear S, Turner AN, Lennon R, Kai H, Gale DP, Aksenova M, Savige J, Gross O, Massella L, Miner JH, Deltas C
Genotype-Based Molecular Mechanisms in Alport Syndrome.
Caparali EB, De Gregorio V, Barua M
Podocytes in health and glomerular disease.
Cunanan J, Zhang D, Peired AJ, Barua M
Collagen formation, function and role in kidney disease.
De Gregorio V, Barua M, Lennon R
Association of Genetically Predicted Skipping of COL4A4 Exon 27 with Hematuria and Albuminuria.
Lona-Durazo F, Omachi K, Fermin D, Eichinger F, Troost JP, Lin MH, Dinsmore IR, Mirshahi T, Chang AR, Miner JH, Paterson AD, Barua M, Gagliano Taliun SA
Genetic Causes of Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis.
Caparali EB, De Gregorio V, Barua M
Mice with a Pax2 missense variant display impaired glomerular repair.
Cunanan J, Rajyam SS, Sharif B, Udwan K, Rana A, De Gregorio V, Ricardo S, Elia A, Brooks B, Weins A, Pollak M, John R, Barua M
Author Correction: GWAS for the composite traits of hematuria and albuminuria.
Gagliano Taliun SA, Dinsmore IR, Mirshahi T, Chang AR, Paterson AD, Barua M
Correction: The 2019 and 2021 International workshops on Alport syndrome.
Daga S, Ding J, Deltas C, Savige J, Lipska-Ziętkiewicz BS, Hoefele J, Flinter F, Gale DP, Aksenova M, Kai H, Perin L, Barua M, Torra R, Miner JH, Massella L, Ljubanović DG, Lennon R, Weinstock AB, Knebelmann B, Cerkauskaite A, Gear S, Gross O, Turner AN, Baldassarri M, Pinto AM, Renieri A
Identifying causal pathways for hematuria using comprehensive omics strategies: genomics, transcriptomics, metabolomics and proteomics
Principal investigators: Gagliano Taliun, Sarah A
Keywords: Chronic Kidney Disease; Fsgs; Genome-Wide Association Study; Mechanistic Subtypes
Pax2 Mediates Glomerular Repair
Principal investigators: Cunanan, Joanna
Keywords: Focal Segmental Glomerulosclerosis (Fsgs); Parietal Epithelial Cells (Pecs); Pax2; Podocytes
The role of transcription factor PAX2 in mediating glomerular repair in a mouse model of focal segmental glomerulosclerosis
Principal investigators: Cunanan, Joanna
Keywords: Cell Lineage Fate Mapping; Chronic Kidney Disease; Focal Segmental Glomerulosclerosis; Pax2; Proteomics; Repair And Regeneration; Single-Cell Rna Sequencing; Super Resolution Microscopy
Pax2 Mediates Glomerular Repair
Principal investigators: Barua, Moumita
Keywords: Glomerulus; Kidney; Pax2; Regeneration
Genetic Determinants of Focal and Segmental Glomerulosclerosis (FSGS)
Principal investigators: Barua, Moumita; Paterson, Andrew D
Keywords: Chronic Kidney Disease; Fsgs; Genome-Wide Association Study; Mechanistic Subtypes
Genetic Determinants of Focal and Segmental Glomerulosclerosis (FSGS)
Principal investigators: Barua, Moumita; Paterson, Andrew D
Keywords: Chronic Kidney Disease; Fsgs; Genetics; Genome-Wide Association Study; Polygenic Risk Score; Proteinuria; Transcription-Wide Association Study
Molecular Diagnosis in Adult-onset Familial and Sporadic Focal and Segmental Glomerulosclerosis
Principal investigators: Barua, Moumita
Keywords: Fsgs; Gene Mapping; Molecular Genetics; Next-Generation Sequencing; Podocyte
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
- Sanjeev Sockalingam and Timothy Jackson: 20 shared papers
- Sanjeev Sockalingam and Satya Dash: 12 shared papers
- York Pei and Moumita Barua: 6 shared papers
- Michelle Hladunewich and Heather Reich: 6 shared papers
- Satya Dash and Timothy Jackson: 6 shared papers
- York Pei and Daniel Cattran: 5 shared papers
- Joshua Tepper and Danielle Martin: 5 shared papers
- York Pei and Heather Reich: 4 shared papers
- York Pei and Ana Konvalinka: 4 shared papers
- Michelle Hladunewich and Daniel Cattran: 4 shared papers
- Michelle Hladunewich and Moumita Barua: 3 shared papers
- Daniel Cattran and Heather Reich: 3 shared papers
- April Khademi and Julien Meyer: 3 shared papers
- Daniel Cattran and Moumita Barua: 2 shared papers
- Moumita Barua and April Khademi: 2 shared papers
- Amber Molnar and Kara Schick-Makaroff: 1 shared paper
- Amber Molnar and Moumita Barua: 1 shared paper
- Amber Molnar and Ana Konvalinka: 1 shared paper
- Tomoko Takano and Moumita Barua: 1 shared paper
- Tomoko Takano and Todd Fairhead: 1 shared paper
- Michelle Hladunewich and Todd Fairhead: 1 shared paper
- Heather Reich and Moumita Barua: 1 shared paper
- Heather Reich and Ana Konvalinka: 1 shared paper
- Heather Reich and Todd Fairhead: 1 shared paper
- Sanjeev Sockalingam and Moumita Barua: 1 shared paper
- Joshua Tepper and Moumita Barua: 1 shared paper
- Kara Schick-Makaroff and Moumita Barua: 1 shared paper
- Kara Schick-Makaroff and Ana Konvalinka: 1 shared paper
- Moumita Barua and Ana Konvalinka: 1 shared paper
- Moumita Barua and Satya Dash: 1 shared paper
- Moumita Barua and Timothy Jackson: 1 shared paper
- Moumita Barua and Danielle Martin: 1 shared paper
- Moumita Barua and Todd Fairhead: 1 shared paper
- Moumita Barua and Julien Meyer: 1 shared paper
- Medicine/Nephrology
- Department of Medicine
- Centre for Urban Health Solutions
- Pediatrics
- No Department/Division
- Other
Co-authors at University of Toronto, colored by department. Thicker lines mean more shared papers; select anyone to open their profile and their own map.
York Pei
Department of Medicine
6 shared papers, latest 2021
Michelle Hladunewich
Medicine/Nephrology
3 shared papers, latest 2023
April Khademi
Faculty
2 shared papers, latest 2022
Daniel Cattran
Medicine/Nephrology
2 shared papers, latest 2021
Timothy Jackson
Faculty
1 shared papers, latest 2019
Satya Dash
Faculty
1 shared papers, latest 2019
Danielle Martin
Centre for Urban Health Solutions
1 shared papers, latest 2018
Julien Meyer
Faculty
1 shared papers, latest 2022
Ana Konvalinka
Medicine/Nephrology
1 shared papers, latest 2017
Todd Fairhead
Department of Medicine
1 shared papers, latest 2022
Sanjeev Sockalingam
Faculty
1 shared papers, latest 2019
Joshua Tepper
Faculty
1 shared papers, latest 2018
Amber Molnar
Department of Medicine
1 shared papers, latest 2017
Kara Schick-Makaroff
Pediatrics
1 shared papers, latest 2017
Tomoko Takano
No Department/Division
1 shared papers, latest 2022
Heather Reich
Medicine/Nephrology
1 shared papers, latest 2021
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