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
Machine learning in prediction and classification of type 1 diabetes.
Nature genetics · 2026 · senior author
What Proportion of Antibody-Negative Type 1 Diabetes Cases Have a Nonautoimmune Etiology? A Genetics-Based Estimate.
Diabetes · 2026 · senior author
Development and validation of a trans-ancestry polygenic risk score for type 1 diabetes.
Diabetologia · 2026
Latest funding
- $5,999,552
Canadian Population Screening for Risk of Type 1 Diabetes Research Consortium
CIHR · 2023 · Co-investigator
- $1,132,200
Driver somatic mutations in autoimmunity
CIHR · 2019 · Nominated PI
- $1,086,301
Precision diagnostics in childhood diabetes; therapeutic implications
CIHR · 2018 · Nominated PI
84 publications.
Machine learning in prediction and classification of type 1 diabetes.
Li Y, Polychronakos C
What Proportion of Antibody-Negative Type 1 Diabetes Cases Have a Nonautoimmune Etiology? A Genetics-Based Estimate.
Nicodemo JL, Makri A, Polychronakos C
Development and validation of a trans-ancestry polygenic risk score for type 1 diabetes.
Jumentier B, Qu HQ, Lu T, Liu K, Kleinbrink EL, Klein K, Belbellaj W, Gamache I, Ferrat L, Butler-Laporte G, Li Y, Hakonarson H, Wu W, Polychronakos C, Greenwood CMT, Manousaki D
Metabolome-wide Mendelian randomisation reveals causal links between circulating metabolites and type 1 diabetes.
Jumentier B, Gamache I, Michalek DA, Chen WM, Onengut-Gumuscu S, Rich SS, Polychronakos C, Manousaki D
Investigating TSHR gene variants in consanguineous families: novel insights into variable expression in familial congenital hypothyroidism.
Nadeali Z, Mohammadi-Zaniani Z, Biglari S, Molavi N, Zardoui K, Mirfendereski S, Hashemipour M, Tabatabaiefar MA, Polychronakos C
Non-syndromic WFS1 mutations are not a rare cause of diabetes in Pakistan.
Rafique I, Mir A, Popovic N, Vanpoperinghe A, Nadeem Saqib MA, Fawwad A, Basit A, Naeem M, Polychronakos C, Makri A
Population-based prevalence of self-reported pediatric diabetes and screening for undiagnosed type 2 diabetes in Chinese children in years 2017-2019, a cross-sectional study.
Wu W, Zhang JW, Li Y, Huang K, Chen RM, Maimaiti M, Luo JS, Chen SK, Wu D, Zhu M, Wang CL, Su Z, Liang Y, Yao H, Wei HY, Zheng RX, Du HW, Luo FH, Li P, Wang E, Polychronakos C, Fu JF
Parsing the spectrum of allelic architectures in diabetes.
Li Y, Polychronakos C
Clinical application of immune repertoire sequencing in solid organ transplant.
Wong P, Cina DP, Sherwood KR, Fenninger F, Sapir-Pichhadze R, Polychronakos C, Lan J, Keown PA
Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator.
Cardinale CJ, Chang X, Wei Z, Qu HQ, Bradfield JP, Polychronakos C, Hakonarson H
Canadian Population Screening for Risk of Type 1 Diabetes Research Consortium
Principal investigators: Wherrett, Diane K; Delorme, Sasha; Chakraborty, Pranesh K; Hayeems, Robin Z; Kastner, Monika; L'Espérance, Audrey; Manousaki, Despoina; Marwaha, Ashish K; McGavock, Jonathan M; Pow, Conrad; Senior, Peter A; Tsui, Albert K; Verchere, Bruce C; Witteman, Holly M
Keywords: Autoantibodies; Consortium; Diabetic Ketoacidosis; Genetic Risk Score; Metabolic Monitoring; Population; Screening; Type 1 Diabetes
Driver somatic mutations in autoimmunity
Principal investigators: Polychronakos, Constantin
Keywords: Autoimmunity; Celiac Disease; Clonal Expansion; Post-Zygotic Mutations; T-Lymphocytes; Type 1 Diabetes
Precision diagnostics in childhood diabetes; therapeutic implications
Principal investigators: Polychronakos, Constantin
Keywords: Diabetes; Dominant; Exome; Mendelian; Mody; Monogenic; Neonatal; Recessive
Antigen-specific functional properties and molecular profiling of autoreactive T-cells in individuals at risk for type 1 diabetes.
Principal investigators: Piccirillo, Ciriaco A
Keywords: Antigen-Specific; Autoreactive Tcr Sequences; Biomarkers; Epigenetics; Immune Regulation; Regulatory T Cells; T Cells; Type 1 Diabetes (Recent-Onset)
A genome-wide search for exonic variants affecting translational efficiency
Principal investigators: Polychronakos, Constantin
Keywords: Complex Trait; Diabetes; Genetic Variation; Genome-Wide Associatin; Mass Spectrometry; Polysomes; Protein Quantification; Proteomics; Ribosomes; Translation
Molecular alterations in type 1 diabetes
Principal investigators: Polychronakos, Constantin
Keywords: Blood Cells; Clonal Expansion; Comparative Genomic Hybridisation; Diabetes; Lymph Nodes; Lymphocytes; Microarrays; Molecular Alterations; Personalised Medicine; Proliferation
The Role of Rare and Somatic Variants in Ageing-Related Disease
Principal investigators: Richards, Brent
Keywords: Ageing; Epigenetic Modification; Genetic Epidemiology; Genomics; Osteoporosis; Rare Base Pair Variation; Somatic Mutation
From population-based gene identification studies to molecular biology: a genetic epidemiology training program
Principal investigators: Infante-Rivard, Claire; Labbe, Aurelie; Polychronakos, Constantin; Richards, Brent; Sladek, Robert G
Keywords: Bioinformatics; Gene Characterization; Gene Identification; Genetic Epidemiology; Methods In Genetic Epidemiology; Molecular Biology
CIHR Training Program in Integrative Approaches to Human Health
Principal investigators: Hallett, Michael T
Keywords: Bioinformatics; Cancer; Complex Diseases; Computational Biology; Genomics; Imaging; Mathematical Modelling; Orphan Diseases; Proteomics; Quantitative Biology; Systems Biology
Genetic Epidemiology of Osteoporotic Fractures; From Susceptibility Genes to Susceptible Populations
Principal investigators: Richards, Brent
Keywords: Aging; Fracture; Genetic Epidemiology; Human Genetics; Osteoporosis
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
- Pediatrics
- Human Genetics
- Oncology
- Medicine
- Pédiatrie
- Physics
- Neurology and Neurosurgery
- 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.
Despoina Manousaki
Pédiatrie
5 shared papers, latest 2026
Tomi Pastinen
Human Genetics
3 shared papers, latest 2013
Ruth Sapir-Pichhadze
Medicine
2 shared papers, latest 2023
Michael Pollak
Oncology
2 shared papers, latest 2022
Jacek Majewski
Human Genetics
2 shared papers, latest 2010
Robert Sladek
Physics
2 shared papers, latest 2009
Nada Jabado
Pediatrics
2 shared papers, latest 2010
Cynthia Goodyer
Pharmacology and Therapeutics
1 shared papers, latest 2011
Laurent Legault
Faculty
1 shared papers, latest 2017
Meranda Nakhla
Nutrition
1 shared papers, latest 2005
Jo Knight
Psychiatry
1 shared papers, latest 2016
Laurent Legault
Faculty
1 shared papers, latest 2017
Meranda Nakhla
Faculty
1 shared papers, latest 2005
Martin Olivier
Pathologie et microbiologie vétérinaire
1 shared papers, latest 2019
Steven Paraskevas
Chemical Engineering
1 shared papers, latest 2011
Roberta La Piana
Neurology and Neurosurgery
1 shared papers, latest 2021
James Lan
Nephrology
1 shared papers, latest 2023
Nadine Taleb
Faculty
1 shared papers, latest 2011
Eriskay Liston
Faculty
1 shared papers, latest 2021
Daniela Pohl
Pediatrics
1 shared papers, latest 2021
Bernard Brais
Neurology and Neurosurgery
1 shared papers, latest 2021
Jerry Pelletier
Biochemistry
1 shared papers, latest 2013
Elsa Rossignol
Neurosciences
1 shared papers, latest 2021
Alan Peterson
Oncology
1 shared papers, latest 2017
Martin Olivier
Medicine
1 shared papers, latest 2019
Elin Grundberg
Faculty
1 shared papers, latest 2010
Ciriaco Piccirillo
Microbiology and Immunology
1 shared papers, latest 2020
Marc Prentki
Nutrition
1 shared papers, latest 2007
A short, specific email works best. This draft uses one of their recent papers; replace the parts in brackets with your own details before sending.