Faculty profile

Catherine Goudie

ResearcherMcGill University

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 and email address may be missing. Find their university profile.

Catherine Goudie

Researcher

Health Sciences

McGill University

Montreal, Quebec, Canada

Supervision signals

Has led research grants, which requires an independent research appointment. Ask their department whether they supervise graduate students.
24 publications in the last five years, latest in 2026.
Senior (last) author on 5 recent papers, a sign of leading a research group.
Principal investigator on 2 research grants (2 CIHR), most recently in 2023.

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

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Publications

Citations

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Collaborators

Grants

Publications by year

Counts cover the works listed on the university profile; citation counts come from Dimensions.

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Signals and details

Research

Cancer Predisposition Syndrome Ehealth Genetics Cancer Clinical Utility Ethics Global Health Liability

Latest papers

Rare solid tumours as indicators of hereditary cancer syndromes.
European journal of human genetics : EJHG · 2026
The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility.
Genetics in medicine : official journal of the American College of Medical Genetics · 2026
The Real-World use of McGill interactive pediatric OncoGenetic guidelines (MIPOGG): A Cross-Sectional survey.
Journal of the National Cancer Institute · 2026 · senior author

All 38 publications

Latest funding

Towards patient-centred precision oncology care for children and youth: Understanding psychosocial impacts and experiences through patient and professional perspectives
CIHR · 2024 · Co-investigator
$1,013,626
Leveraging precision medicine and eHealth to predict cancer predisposition syndromes in children: A Canadian initiative to redress global health disparities in cancer genetics
CIHR · 2023 · Nominated PI
$703,800
Rationalizing Genetic Referral Practices in Pediatric Oncology: An eHealth Decision-Support Tool for Identifying Cancer Predisposition Syndromes
CIHR · 2018 · Nominated PI
$325,124

All 3 grants and awards

38 publications.

Rare solid tumours as indicators of hereditary cancer syndromes.

Rivera B, Torrezan GT, Roca C, Goudie C, Foulkes WD

European journal of human genetics : EJHG2026

DOI: 10.1038/s41431-026-02091-0 PMID: 41917266

The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility.

Poole E, Xiao B, Luca S, Assamad D, Abbott LS, Armstrong L, Boycott KM, Carroll JC, Chad L, De Bie I, Denburg A, Deyell RJ, Elliott AM, Goudie C, Laberge AM, Mucha BE, Peltekova IT, Quinlan B, Sawyer SL, Smith M, Villani A, Ungar WJ, Hayeems RZ, P-GUIDE Study Team

Genetics in medicine : official journal of the American College of Medical Genetics2026

DOI: 10.1016/j.gim.2026.102670 PMID: 42554147

The Real-World use of McGill interactive pediatric OncoGenetic guidelines (MIPOGG): A Cross-Sectional survey.

Higuera-Ornelas J, Rueda Martinez M, Reichman L, Budd C, Hammond L, Mistry A, Carter M, Cruz Marino T, Palma L, Bombard Y, Saulnier C, Goudie C

Journal of the National Cancer Institute2026Senior author

DOI: 10.1093/jnci/djag272 PMID: 42549886

Tumor patterns and cancer risk in carriers of TP53 exonic germline variants that alter mRNA splicing.

Schönegger D, Montellier E, Blanchet S, Freycon C, Monti P, Goudie C, Bougeard G, Kratz CP, Hainaut P, Reymer A

European journal of human genetics : EJHG2026

DOI: 10.1038/s41431-026-02061-6 PMID: 41776348

Germline analysis of an international cohort of pediatric diffuse midline glioma patients.

Mateos MK, Ajuyah P, Fuentes-Bolanos N, El-Kamand S, Barahona P, Altekoester AK, Mayoh C, Holliday H, Liu J, Cui L, Pfaff E, Mackay A, Resnick AC, Pinese M, Lau LMS, Khuong-Quang DA, Dias K, Goudie C, Salkeld A, Rokita JL, Jones DTW, Juretic N, Hayden E, Pfister SM, Kramm CM, Blattner-Johnson M, Jabado N, Tsoli M, Vittorio O, Mueller S, Guo Y, Tucker K, Waszak SM, Perreault S, Jones C, Wong-Erasmus M, Cowley MJ, Ziegler DS

Neuro-oncology2025

DOI: 10.1093/neuonc/noaf061 PMID: 40072012

How does personal utility depend on clinical setting? Evidence from 3 cohorts.

Poole E, Luca S, Assamad D, Xiao B, Yan J, Xia YY, Abbott LS, Armstrong L, Birch P, Boycott KM, Carroll JC, Chad L, Chitayat D, Denburg A, Deyell RJ, Elliott AM, Goudie C, Laberge AM, Maio M, Peltekova IT, Quinlan B, Sawyer SL, Silver R, Smith M, Teitelbaum R, Villani A, Ungar WJ, Hayeems RZ, P-GUIDE Study Team

Genetics in medicine open2025

DOI: 10.1016/j.gimo.2025.103453 PMID: 41089267

BRCA1/2 germline sequencing in children and adolescents with cancer: it is the context that matters.

Goudie C

Journal of the National Cancer Institute2025First author

DOI: 10.1093/jnci/djae339 PMID: 39847476

Genomic sequencing in paediatric oncology: navigating conflicting roles and responsibilities.

Goudie C, Zawati MH, Knoppers BM, Laberge AM

Journal of medical genetics2025First author

DOI: 10.1136/jmg-2024-110410 PMID: 39653388

Clustering of TP53 variants into functional classes correlates with cancer risk and identifies different phenotypes of Li-Fraumeni syndrome.

Montellier E, Lemonnier N, Penkert J, Freycon C, Blanchet S, Amadou A, Chuffart F, Fischer NW, Achatz MI, Levine AJ, Goudie C, Malkin D, Bougeard G, Kratz CP, Hainaut P

iScience2024

DOI: 10.1016/j.isci.2024.111296 PMID: 39634561

Germline p.R181H variant in TP53 in a family exemplifying the genotype-phenotype correlations in Li-Fraumeni syndrome.

Freycon C, Palma L, Budd C, Coulombe F, Witkowski L, Hainaut P, Foulkes WD, Goudie C

Familial cancer2024Senior author

DOI: 10.1007/s10689-024-00419-7 PMID: 39261343

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Catherine Goudie

Research

Latest papers

Latest funding

Rare solid tumours as indicators of hereditary cancer syndromes.

The Patient-reported Genetic testing Utility InDEx: A novel measure of personal utility.

The Real-World use of McGill interactive pediatric OncoGenetic guidelines (MIPOGG): A Cross-Sectional survey.

Tumor patterns and cancer risk in carriers of TP53 exonic germline variants that alter mRNA splicing.

Germline analysis of an international cohort of pediatric diffuse midline glioma patients.

How does personal utility depend on clinical setting? Evidence from 3 cohorts.

BRCA1/2 germline sequencing in children and adolescents with cancer: it is the context that matters.

Genomic sequencing in paediatric oncology: navigating conflicting roles and responsibilities.

Clustering of TP53 variants into functional classes correlates with cancer risk and identifies different phenotypes of Li-Fraumeni syndrome.

Germline p.R181H variant in TP53 in a family exemplifying the genotype-phenotype correlations in Li-Fraumeni syndrome.

Towards patient-centred precision oncology care for children and youth: Understanding psychosocial impacts and experiences through patient and professional perspectives

Leveraging precision medicine and eHealth to predict cancer predisposition syndromes in children: A Canadian initiative to redress global health disparities in cancer genetics

Rationalizing Genetic Referral Practices in Pediatric Oncology: An eHealth Decision-Support Tool for Identifying Cancer Predisposition Syndromes

Frequent collaborators

David Malkin

Nada Jabado

Avram Denburg

Anne-Marie Laberge

Uri Tabori

Adam Fleming

Paul Gibson

Adam Shlien

Lauren Chad

Sonia Cellot

Marc Beltempo

Gabriel Altit

Gabriel Altit

Marc Beltempo

Cynthia Hawkins

Nandini Dendukuri

Valérie Larouche

Vijay Ramaswamy

Carol Swallow

Mohamed Abdelhaleem

Gino Somers

Eric Bouffet

Sebastien Perreault

Daniel Sinnett

Nathalie Auger

Maureen Smith

Nancy Low

Yvonne Bombard

Rosanna Weksberg

Annie Huang

Jacek Majewski

Johann Hitzler

Petros Pechlivanoglou

Michel Duval

David Chitayat