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Yannis Trakadis

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Clinical Associate ProfessorDepartment of Human GeneticsMcGill University

Yannis Trakadis

Clinical Associate Professor

Department of Human Genetics

Faculty of Medicine and Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Clinical faculty often co-supervise; many graduate programs need a core faculty member as the main supervisor.
13 publications in the last five years, latest in 2026.
Senior (last) author on 4 recent papers, a sign of leading a research group.

These signals come from public records, including federal and provincial funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

Publications

285

Citations

Collaborators

Grants

Publications by year

Counts cover the publications linked to this profile. Citations and the h-index appear when the source records them.

Profiles and links

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Signals and details

Research

Read how they describe their research on their McGill University profile.

Latest papers

Selecting Candidates for Genetic Therapy: A Patient-Centered Framework.
Current gene therapy · 2026 · senior author
Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.
JIMD reports · 2025
Disease-Specific Prediction of Missense Variant Pathogenicity with DNA Language Models and Graph Neural Networks.
Bioengineering (Basel, Switzerland) · 2025 · senior author

All 25 publications

Latest funding

An innovative registry-based trials platform to improve clinical care, outcomes, and health policy for children with treatable rare diseases
CIHR · 2019 · Co-investigator
$2,754,009
Designing interventions to improve delivery of health care for children with inherited metabolic diseases: family and provider perspectives
CIHR · 2016 · Co-investigator
$738,224

All 2 grants and awards

25 publications.

Selecting Candidates for Genetic Therapy: A Patient-Centered Framework.

Henein M, Trakadis Y

Current gene therapy2026Senior author

DOI: 10.2174/0115665232471894260326103649 PMID: 42138146

Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.

Yuskiv N, Saad A, Potter BK, Stockler-Ipsiroglu S, Mitchell JJ, Hawken S, Tingley K, Pugliese M, Lamoureux M, Chow AJ, Kronick JB, Wilson K, Feigenbaum A, Goobie S, Inbar-Feigenberg M, Little J, Mercimek-Andrews S, Pender A, Prasad C, Schulze A, Trakadis Y, Ho G, Vallance H, Austin V, Vandersteen A, Yu AC, Rockman-Greenberg C, Mhanni AA, Chakraborty P

JIMD reports2025Open Access

DOI: 10.1002/jmd2.70042 PMID: 40901071

Disease-Specific Prediction of Missense Variant Pathogenicity with DNA Language Models and Graph Neural Networks.

Ghadie M, Sardaar S, Trakadis Y

Bioengineering (Basel, Switzerland)2025Senior author

DOI: 10.3390/bioengineering12101098 PMID: 41155097

Current landscape of clinical genetics knowledge and attitudes among Non-Geneticist Physicians - the McGill genetics education survey (McGES).

Abdullah-Maklan S, Trakadis Y

Journal of community genetics2025Senior author

DOI: 10.1007/s12687-025-00831-1 PMID: 41032227

Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency

Iverson R, Taljaard M, Geraghty MT, Pugliese M, Tingley K, Coyle D, Kronick JB, Wilson K, Austin V, Brunel-Guitton C

BMC Pediatrics20244 citationsOpen Access

DOI: 10.1186/s12887-023-04393-4 PMID: W4390840255

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production.

Ebstein F, Küry S, Most V, Rosenfelt C, Scott-Boyer MP, van Woerden GM, Besnard T, Papendorf JJ, Studencka-Turski M, Wang T, Hsieh TC, Golnik R, Baldridge D, Forster C, de Konink C, Teurlings SMW, Vignard V, van Jaarsveld RH, Ades L, Cogné B, Mignot C, Deb W, Jongmans MCJ, Cole FS, van den Boogaard MH, Wambach JA, Wegner DJ, Yang S, Hannig V, Brault JA, Zadeh N, Bennetts B, Keren B, Gélineau AC, Powis Z, Towne M, Bachman K, Seeley A, Beck AE, Morrison J, Westman R, Averill K, Brunet T, Haasters J, Carter MT, Osmond M, Wheeler PG, Forzano F, Mohammed S, Trakadis Y, Accogli A, Harrison R, Guo Y, Hakonarson H, Rondeau S, Baujat G, Barcia G, Feichtinger RG, Mayr JA, Preisel M, Laumonnier F, Kallinich T, Knaus A, Isidor B, Krawitz P, Völker U, Hammer E, Droit A, Eichler EE, Elgersma Y, Hildebrand PW, Bolduc F, Krüger E, Bézieau S

Science translational medicine202337 citationsOpen Access

DOI: 10.1126/scitranslmed.abo3189 PMID: 37256937

Paper II: thematic framework analysis of registry-based randomized controlled trials provided insights for designing trial ready registries.

Krause KR, Tay J, Douglas WA, Sammy A, Baba A, Goren K, Thombs BD, Howie AH, Oskoui M, Frøbert O, Trakadis Y, Little J, Potter BK, Butcher NJ, Offringa M

Journal of clinical epidemiology20238 citationsOpen Access

DOI: 10.1016/j.jclinepi.2023.04.015 PMID: 37146660

Ethical and practical considerations related to data sharing when collecting patient-reported outcomes in care-based child health research

Vanderhout S, Potter BK, Smith M, Butcher NJ, Vaters J, Chakraborty P, Adams J, Inbar-Feigenberg M, Offringa M, Speechley K

Quality of Life Research20234 citationsOpen Access

DOI: 10.1007/s11136-023-03393-2 PMID: W4362457870

Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity.

Gayden T, Crevier-Sorbo G, Jawhar W, Saint-Martin C, Eveleigh R, Gilardino MS, Anastasio N, Trakadis Y, Bassenden AV, Berghuis AM, Jabado N, Dudley RWR

Journal of neurosurgery. Pediatrics20233 citations

DOI: 10.3171/2023.1.peds22287 PMID: 36905673

An in-frame deletion affecting the critical acid loop of PPP2R5D is associated with a neonatal lethal form of PPP2R5D-related neurodevelopmental disorder.

Alhajaj G, Lacroix C, Trakadis Y, Garfinkle J, Srour M

American journal of medical genetics. Part A2023Open Access

DOI: 10.1002/ajmg.a.63307 PMID: 37248744

Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.

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Yannis Trakadis

Research

Latest papers

Latest funding

Selecting Candidates for Genetic Therapy: A Patient-Centered Framework.

Metabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.

Disease-Specific Prediction of Missense Variant Pathogenicity with DNA Language Models and Graph Neural Networks.

Current landscape of clinical genetics knowledge and attitudes among Non-Geneticist Physicians - the McGill genetics education survey (McGES).

Assessing the quality and value of metabolic chart data for capturing core outcomes for pediatric medium-chain acyl-CoA dehydrogenase (MCAD) deficiency

PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production.

Paper II: thematic framework analysis of registry-based randomized controlled trials provided insights for designing trial ready registries.

Ethical and practical considerations related to data sharing when collecting patient-reported outcomes in care-based child health research

Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity.

An in-frame deletion affecting the critical acid loop of PPP2R5D is associated with a neonatal lethal form of PPP2R5D-related neurodevelopmental disorder.

An innovative registry-based trials platform to improve clinical care, outcomes, and health policy for children with treatable rare diseases

Designing interventions to improve delivery of health care for children with inherited metabolic diseases: family and provider perspectives

Frequent collaborators

Beth Potter

Pranesh Chakraborty

John Mitchell

Julian Little

Kumanan Wilson

Komudi Siriwardena

Jagdeep Walia

Brenda Wilson

Doug Coyle

Douglas Coyle

Cheryl Rockman-Greenberg

Andreas Schulze

Kathy Speechley

Sylvia Stockler

Murray Alexander Potter

Jennifer MacKenzie

Michael Geraghty

Nancy Butcher

Martin Offringa

Michal Inbar-Feigenberg

Bruno Maranda

Robin Hayeems

Monica Taljaard

Anne-Marie Laberge

Neal Sondheimer

Alicia Chan