Raymond H Kim
University of Toronto
H-index: 32
North America-Canada
Top articles of Raymond H Kim
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
P548: Universal germline genetic testing for breast cancer at the Princess Margaret Cancer Centre | Genetics in Medicine Open | Larissa Peck Maria Carolina Sanabria-Salas Sarah Ridd Helia Purnaghshband Wes Morrison | 2024/1/1 |
P843: Development of a logic model to inform a measurement strategy for a provincial genetics program: Approach and lessons learned | Genetics in Medicine Open | Husayn Marani Tharsiya Martin Wilson Yu Kathleen Bell Rachel Healey | 2024/1/1 |
P860: A health systems framework to advance equity in medical genetics policy and practice | Genetics in Medicine Open | Muna Aden Kathleen Bell Andrea Guerin Raymond Kim | 2024/1/1 |
Expanding the phenotypic spectrum of NOTCH1 variants: Clinical manifestations in families with congenital heart disease | Rebekah Jobling Kaitlin Stanley Kelsey Kalbfleisch Olivia Moran Rajiv Chaturvedi | 2024/1/17 | |
Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis | Kelly Metcalfe Tomasz Huzarski Jacek Gronwald Joanne Kotsopoulos Raymond Kim | 2024/2/10 | |
PATHFINDER 2: A prospective study to evaluate safety and performance of a multi-cancer early detection test in a population setting | Age | Karthik V Giridhar Michael J Demeure Raymond H Kim Justin A Chen Shirish Gadgeel | 2024/4/5 |
P169: Characterizing the phenotypic spectrum and estimated penetrance of families with pathogenic loss of function variants in the FLT4 gene | Genetics in Medicine Open | Olivia Moran Cherith Somerville Miriam Reuter Kelsey Kalbfleisch Marci Schwartz | 2024/1/1 |
O16: The new normal: Six years of mainstreaming germline genetic testing across cancer sites | Genetics in Medicine Open | Larissa Peck Sarah Ridd Jeanna McCuaig Emily Thain Brittany Gillies | 2024/1/1 |
P108: Myelodysplastic syndrome (MDS) detected by germline genetic testing for hereditary cancer | Genetics in Medicine Open | Larissa Peck Sarah Ridd Janet Malcolmson Raymond Kim | 2024/1/1 |
Feasibility of BRCA1 and BRCA2 testing among Nigerian women with breast cancer | European Journal of Surgical Oncology | Funmilola Wuraola Jenine Ramruthan Emma Reel Andrea Covelli Anna Dare | 2024/2/1 |
Early Cancer Detection in Li–Fraumeni Syndrome with Cell-Free DNA | Cancer Discovery | Derek Wong Ping Luo Leslie E Oldfield Haifan Gong Ledia Brunga | 2024/1/12 |
Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib | NPJ Genomic Medicine | KM Ingley M Zatzman AM Fontebasso W Lo V Subasri | 2024/3/27 |
P474: Precision child health: Integrating a consultative pharmacogenetics (PGx) program into clinical care at the Hospital for Sick Children | Genetics in Medicine Open | Iris Cohn Olivia Moran Kaitlin Stanley Sierra Scodellaro April Kennedy | 2024/1/1 |
P078: Identification of novel germline mutations and copy-number variations in patients with small cell lung cancer | Genetics in Medicine Open | Sami Ul Haq Gregory Downs Luna Jia Zhan Danielle Sacdalan Janice Li | 2024/1/1 |
O07: Haploinsufficiency of EIF3A and EIF3B cause a clinically variable phenotype characterized by neurodevelopmental abnormalities and congenital heart defects | Genetics in Medicine Open | Cherith Somerville Ersa Erkut Marci Schwartz Xin Chen Roozbeh Manshaei | 2024/1/1 |
P103: Operationalizing structured curated scientific literature (CIViC and Hypothesis) in developing gene-specific recommendations of the ClinGen VHL Variant Curation Expert Panel | Genetics in Medicine Open | Deborah Ritter Chansonette Badduke Michael Anderson Arpad Danos Kurston Doonanco | 2024/1/1 |
“I just wanted more”: Hereditary cancer syndromes patients’ perspectives on the utility of circulating tumour DNA testing for cancer screening | European Journal of Human Genetics | Ella Adi-Wauran Marc Clausen Salma Shickh Anna R Gagliardi Avram Denburg | 2024/2 |
Epilepsy in Neurofibromatosis Type 1: Prevalence, Phenotype, and Genotype in Adults | Epilepsy Research | Julien Hébert Robert J De Santis Lubna Daniyal Shabber Mannan Eduardo Ng | 2024/3/2 |
P541: Development of a provincial genetics program in Ontario | Genetics in Medicine Open | Kathleen Bell Raymond Kim Aaron Pollett Wilson Yu Syed Ahmed | 2024/1/1 |
P538: Curious but cautious: Patients’ preferences for all types of clinically actionable genomic incidental results | Genetics in Medicine Open | Salma Shickh Rita Kodida Chloe Mighton Marc Clausen Emma Reble | 2024/1/1 |
