Raymond H. Kim

University Health Network

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Research Interests

Biostatistics

Internal Medicine

Medical Science

Cancer Biology

Cancer Genetics

Genomic Instability

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Recent Grants

Grant: Close

Cell-free DNA as a biomarker in Neurofibromatosis 1

Open Date: 2019-02-01

Close Date: 2021-02-01

Articles25

Collaborators11

Vera Bril

University of Toronto

Tracy Stockley

Department Head

University Health Network

Robyn Whitney

McMaster University

Jennifer Brooks

Associate Professor

University of Toronto

Gareth Evans

The University of Manchester

UNITED KINGDOM

Andrea Eisen

McMaster University

Christopher Maxwell

The University of British Columbia

Kelly Metcalfe

Professor and Associate Dean, Research & External Relations

University of Toronto

Ozgur Mete

Clinician Teacher, Professor of Pathology

University of Toronto

Philippe Després

Institut universitaire de cardiologie et de pneumologie de Québec

Saadet Mercimek‐Andrews

How do I reach out?

Meet Kite AI

Raymond H. Kim

How do I reach out?

Contact this professor

Research Interests

Ask ApplyKite AI

Recent Grants

Articles25

Parity, breastfeeding, and the risk of early-onset breast cancer in women with a BRCA1 pathogenic variant

Ovarian cancer after breast cancer in women with a BRCA1 or BRCA2 pathogenic variant

At-home Breast Oncology care Delivered with EHealth solutions (ABODE) study protocol: a randomised controlled trial

An Innovative Strategy for Collecting Family Health History: An Effectiveness-Implementation Trial in Primary Care Clinics

Rare germline ETV6 variant associated with thrombocytopenia and acute leukemia

TRIAGE-GS: protocol for a randomised controlled trial of a genomics-first approach to rare disease diagnosis for patients awaiting assessment by a clinical geneticist

Prostate-Related Germline Variant Frequencies Detected in a Cohort of Men With Metastatic Prostate Cancer in Northern India.

Framework for Standardized Genetic Testing Recommendations for Chronic Kidney Disease in Ontario.

Myelodysplastic syndrome diagnosed by genetic testing for hereditary cancer: a case report

Psychological and emotional impacts of communicating breast cancer risk using multifactorial assessment with polygenic risk score: findings from PERSPECTIVE I&amp;I

Implementing Multifactorial Risk Assessment with Polygenic Risk Scores for Personalized Breast Cancer Screening in the Population Setting: Challenges and Opportunities

Epilepsy in neurofibromatosis type 1: Prevalence, phenotype, and genotype in adults

Next generation of free? Points to consider when navigating sponsored genetic testing

FLCN-Driven Functional Adrenal Cortical Carcinoma with High Mitotic Tumor Grade: Extending the Endocrine Manifestations of Birt-Hogg-Dubé Syndrome

Oncologist-led germline genetic testing for uveal melanoma

Congenital Myopathy Due to Pathogenic Missense Variant in the MYBPC1 Gene

Retrospective analysis of Canadian adults with tuberous sclerosis complex

Using Whole Genome Sequence Findings to Assess gene-disease Causality in Cardiomyopathy and Arrhythmia Patients

VHL mosaicism: the added value of multi-tissue analysis.

Clinical implementation of genetic testing in adults for hereditary hematologic malignancy syndromes

Association between time to therapeutic INR and length of stay following mechanical heart valve surgery

Challenges and practical solutions for managing secondary genomic findings in primary care

Stay at home: implementation and impact of virtualising cancer genetic services during COVID-19

Incidental findings from cancer next generation sequencing panels.

The evolving role of germline genetic testing and management in prostate cancer: Report from the Princess Margaret Cancer Centre International Retreat.

Collaborators11

Vera Bril

Tracy Stockley

Robyn Whitney

Jennifer Brooks

Gareth Evans

Andrea Eisen

Christopher Maxwell

Kelly Metcalfe

Ozgur Mete

Philippe Després

Saadet Mercimek‐Andrews

How do I reach out?

Psychological and emotional impacts of communicating breast cancer risk using multifactorial assessment with polygenic risk score: findings from PERSPECTIVE I&I