Melyssa Aronson

University Health Network — Canada

Medicine · Health Sciences

44h-index8.8kcitations243works1.92yr avg
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Research Topics

Genetic factors in colorectal cancer(136), Cancer Genomics and Diagnostics(63), BRCA gene mutations in cancer(48), Glioma Diagnosis and Treatment(41), Colorectal Cancer Screening and Detection(41)

Publications241 total

Patterns of hypermutation shape tumorigenesis and immunotherapy response in mismatch-repair-deficient glioma
Nature Genetics·2025
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdens
Genetics in Medicine·2025Open Access
Hereditary diffuse gastric cancer spectrum associated with germline <i>CTNNA1</i> loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls
Gut·2025· 3 citedOpen Access
Comprehensively Testing the Function of Missense Variation in the <i>STK11</i> Tumour Suppressor
2025Open Access
The development and usability of ‘The Genetics Navigator’: a digital solution for adult and paediatric clinical genetics services
European Journal of Human Genetics·2025· 2 citedOpen Access
Canadian consensus for the assessment and testing of Lynch syndrome
Journal of Medical Genetics·2025· 2 citedOpen Access
Psychological impact of risk-reducing surgery for gynecologic cancer among women with Lynch syndrome
Gynecologic Oncology Reports·2025Open Access
Psychological Impact of Risk-Reducing Surgery for Gynecologic Cancer Among Women with Lynch Syndrome
SSRN Electronic Journal·2025Open Access
P686: Opportunistic screening for broad range of clinically relevant secondary findings: Outcomes of exome analysis in the Incidental Genomics RCT
Genetics in Medicine Open·2025Open Access
P547: An imperfect system: Access to genetic testing and hereditary cancer syndrome care-A national survey
Genetics in Medicine Open·2025Open Access
P298: Decoding ambiguity: Evaluating the psychological harms and utility of returning cancer variants of uncertain significance
Genetics in Medicine Open·2025Open Access
The landscape of primary mismatch repair deficient gliomas in children, adolescents, and young adults: a multi-cohort study
The Lancet Oncology·2024· 14 cited
Clinical Utility of Genomic Sequencing for Hereditary Cancer Syndromes: An Observational Cohort Study
JCO Precision Oncology·2024· 1 cited
Gynecologic cancer screening among women with Lynch syndrome: Information and healthcare access needs
Patient Education and Counseling·2024Open Access
Opportunistic genomic screening has clinical utility: An interventional cohort study
Genetics in Medicine·2024· 5 citedOpen Access
Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation protocol
BMJ Open·2024· 1 citedOpen Access
“Should I Let Them Know I Have This?”: Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer Syndromes
Public Health Genomics·2024· 4 citedOpen Access
Genetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations
BMJ Open·2024· 2 citedOpen Access
Autistic traits in youth with familial adenomatous polyposis: A Dutch–Canadian case–control study
American Journal of Medical Genetics Part B Neuropsychiatric Genetics·2024· 3 citedOpen Access
OTHR-30. THE CLINICAL AND BIOLOGICAL LANDSCAPE OF CNS CANCERS IN CONSTITUTIONAL MISMATCH REPAIR DEFICIENCY: AN IRRDC COHORT STUDY
Neuro-Oncology·2024Open Access
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Frequent Co-authors

Steven Gallinger(17), Uri Tabori(15), Carol Durno(14), Éric Bouffet(12), Cynthia Hawkins(11), Aaron Pollett(11), David Malkin(10), Rina Dvir(9), Melissa Edwards(9), Brittany Campbell(8), Roula Farah(8), Adam Shlien(8), David Samuel(8), Steve Gallinger(8), John L. Hopper(8), Daniel D. Buchanan(8), Mark A. Jenkins(8), Kara Semotiuk(8), Mark Clendenning(8), Valérie Larouche(7)