Raymond H Kim (R H Kim, Raymond Kim)

Loop profile Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 47

Top Venues

Cancer discovery

NPJ genomic medicine

Journal of medical genetics

Cancers

University of Toronto

University of Toronto (BSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Toronto

Canada

Assistant Professor :: Medicine

University Health Network

Canada

Medical Geneticist :: Medical Oncology and Hematology

Hospital for Sick Children

Canada

Medical Geneticist :: Clinical and Metabolic Genetics

Education History

University of Toronto

Canada

BSC :: Immunology

Publications

Meghan J Walker, Kristina M Blackmore, Amy Chang, Laurence Lambert-Côté, Annie Turgeon, Antonis C Antoniou, Kathleen A Bell, Mireille J M Broeders, Jennifer D Brooks, Tim Carver, Jocelyne Chiquette, Philippe Després, Douglas F Easton, Andrea Eisen, Laurence Eloy, Dafydd Gareth Evans, Samantha Fienberg, Yann Joly, Raymond H Kim, Shana J Kim, Bartha Maria Knoppers, Aisha K Lofters, Hermann Nabi, Jean-Sébastien Paquette, Nora Pashayan, Amanda J Sheppard, Tracy L Stockley, Michel Dorval, Jacques Simard, Anna M Chiarelli
Implementing Multifactorial Risk Assessment with Polygenic Risk Scores for Personalized Breast Cancer Screening in the Population Setting: Challenges and Opportunities. Cancers 16 (11) (2024)
Katrina M Ingley, Matthew Zatzman, A M Fontebasso, W Lo, Vallijah Subasri, A Goldenberg, Y Li, S Davidson, N Kanwar, L Waldman, L Brunga, Y Babichev, E G Demicco, A Gupta, M Szybowska, S Thipphavong, D Malkin, A Villani, Adam Shlien, R A Gladdy, Raymond H Kim
Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib. NPJ genomic medicine 9 (1) (2024)
Katrina M Ingley, Matthew Zatzman, A M Fontebasso, W Lo, Vallijah Subasri, A Goldenberg, Y Li, S Davidson, N Kanwar, L Waldman, L Brunga, Y Babichev, E G Demicco, A Gupta, M Szybowska, S Thipphavong, D Malkin, A Villani, Adam Shlien, R A Gladdy, Raymond H Kim
Genomic and clinical characterization of a familial GIST kindred intolerant to imatinib. NPJ genomic medicine 9 (1) (2024)
Derek Wong, Maha Tageldein, Ping Luo, Erik Ensminger, Jeffrey Bruce, Leslie Oldfield, Haifan Gong, Nicholas William Fischer, Brianne Laverty, Vallijah Subasri, Scott Davidson, Reem Khan, Anita Villani, Adam Shlien, Raymond H Kim, David Malkin, Trevor J Pugh
Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patterns. Nature communications 15 (1) (2024)
Derek Wong, Maha Tageldein, Ping Luo, Erik Ensminger, Jeffrey Bruce, Leslie Oldfield, Haifan Gong, Nicholas William Fischer, Brianne Laverty, Vallijah Subasri, Scott Davidson, Reem Khan, Anita Villani, Adam Shlien, Raymond H Kim, David Malkin, Trevor J Pugh
Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patterns. Nature communications 15 (1) (2024)
Meghan J Walker, Kristina M Blackmore, Amy Chang, Laurence Lambert-Côté, Annie Turgeon, Antonis C Antoniou, Kathleen A Bell, Mireille J M Broeders, Jennifer D Brooks, Tim Carver, Jocelyne Chiquette, Philippe Després, Douglas F Easton, Andrea Eisen, Laurence Eloy, Dafydd Gareth Evans, Samantha Fienberg, Yann Joly, Raymond H Kim, Shana J Kim, Bartha Maria Knoppers, Aisha K Lofters, Hermann Nabi, Jean-Sébastien Paquette, Nora Pashayan, Amanda J Sheppard, Tracy L Stockley, Michel Dorval, Jacques Simard, Anna M Chiarelli
Implementing Multifactorial Risk Assessment with Polygenic Risk Scores for Personalized Breast Cancer Screening in the Population Setting: Challenges and Opportunities. Cancers 16 (11) (2024)
Derek Wong, Maha Tageldein, Ping Luo, Erik Ensminger, Jeffrey Bruce, Leslie Oldfield, Haifan Gong, Nicholas William Fischer, Brianne Laverty, Vallijah Subasri, Scott Davidson, Reem Khan, Anita Villani, Adam Shlien, Raymond H Kim, David Malkin, Trevor J Pugh
Cell-free DNA from germline TP53 mutation carriers reflect cancer-like fragmentation patterns. Nature communications 15 (1) (2024)
Kirsten Bartels, Samantha Afonso, Lindsay Brown, Claudia Carriles, Raymond H Kim, Joanna Lazier, Saadet Mercimek-Mahmutoglu, Tanya N Nelson, Ian Stedman, Emily Thain, Rachel Vanneste, Lauren Chad
Next generation of free? Points to consider when navigating sponsored genetic testing. Journal of medical genetics (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Derek Wong, Ping Luo, Leslie E Oldfield, Haifan Gong, Ledia Brunga, Ron Rabinowicz, Vallijah Subasri, Clarissa Chan, Tiana Downs, Kirsten M Farncombe, Beatrice Luu, Maia Leigh Norman, Julia A Sobotka, Precious Uju, Jenna Eagles, Stephanie Pedersen, Johanna Wellum, Arnavaz Danesh, Stephenie D Prokopec, Eric Y Zhao, Nadia Znassi, Lawrence E Heisler, Richard Jovelin, Bernard Lam, Beatriz E Lujan-Toro, Kayla Marsh, Yogi Sundaravadanam, Dax Torti, Carina Man, Anna Goldenberg, Wei Xu, Patrick Veit-Haibach, Andrea Schwarz Doria, David Malkin, Raymond H Kim, Trevor J Pugh
Early Cancer Detection in Li-Fraumeni Syndrome with Cell-Free DNA. Cancer discovery (2023)
Rita Kodida, Emma Reble, Marc Clausen, Salma Shickh, Chloe Mighton, Jordan Sam, Nicole Forster, Seema Panchal, Melyssa Aronson, Kara Semotiuk, Tracy Graham, Yael Silberman, Susan Randall Armel, Jeanna M McCuaig, Iris Cohn, Chantal F Morel, Christine Elser, Andrea Eisen, June C Carroll, Emily Glogowski, Kasmintan A Schrader, Vanessa Di Gioacchino, Jordan Lerner- Ellis, Raymond H Kim, Yvonne Bombard, null null
A model for the return and referral of all clinically significant secondary findings of genomic sequencing. Journal of medical genetics (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller
Genomic patterns of malignant peripheral nerve sheath tumor (MPNST) evolution correlate with clinical outcome and are detectable in cell-free DNA. Cancer discovery (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Vinaya Bhandari, Raymond H Kim, Hanna Faghfoury, Josh Silver, Raymond H Chan, Qiliang Ding, Marci Lb Schwartz, Vera Bril
Congenital myopathy due to pathogenic missense variant in the MYBPC1 gene. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2023)
Yiming Wang, Qiliang Ding, Stephenie Prokopec, Kirsten M Farncombe, Jeffrey Bruce, Selina Casalino, Jeanna McCuaig, Marta Szybowska, Kalene van Engelen, Jordan Lerner-Ellis, Trevor J Pugh, Raymond H Kim
Germline whole genome sequencing in adults with multiple primary tumors. Familial cancer (2023)
Dominique Pal, Nicole Forster, Monika Madan, Robyn Whitney, Kirsten M Farncombe, Raymond H Kim
Retrospective analysis of Canadian adults with tuberous sclerosis complex. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2023)
Aishwarya Rajesh Krishnan, Marci L B Schwartz, Cherith Somerville, Qiliang Ding, Raymond H Kim
Using whole genome sequence findings to assess gene-disease causality in cardiomyopathy and arrhythmia patients. Future cardiology (2023)
Renee Hofstedter, María Carolina Sanabria-Salas, Maria Di Jiang, Shereen Ezzat, Ozgur Mete, Raymond H Kim
FLCN-Driven Functional Adrenal Cortical Carcinoma with High Mitotic Tumor Grade: Extending the Endocrine Manifestations of Birt-Hogg-Dubé Syndrome. Endocrine pathology (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Ella Adi-Wauran, Marc Clausen, Salma Shickh, Anna R Gagliardi, Avram Denburg, Leslie E Oldfield, Jordan Sam, Emma Reble, Suvetha Krishnapillai, Deirdre Weymann, Nancy N Baxter, Lesa Dawson, Lynette S Penney, William D Foulkes, Mark Basik, Sophie Sun, Kasmintan A Schrader, Aly Karsan, Aaron Pollett, Trevor J Pugh, null null, Raymond H Kim, Yvonne Bombard
"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 : EJHG (2023)
Brittany Gillies, Hatem Krema, Anning Chao, Leonardo Lando, Kirsten M Farncombe, Marcus Butler, Filiberto Altomare, Raymond H Kim
Oncologist-led germline genetic testing for uveal melanoma. Ophthalmic genetics (2023)
Dominique Pal, Nicole Forster, Monika Madan, Robyn Whitney, Kirsten M Farncombe, Raymond H Kim
Retrospective Analysis of Canadian Adults with Tuberous Sclerosis Complex. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques (2023)
Isidro Cortes-Ciriano, Christopher D Steele, Katherine Piculell, Alyaa Al-Ibraheemi, Vanessa Eulo, Marilyn M Bui, Aikaterini Chatzipli, Brendan C Dickson, Dana C Borcherding, Andrew Feber, Alon Galor, Jesse Hart, Kevin B Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Colin Miller, Yoshihiro Nishida, Paula Z Proszek, Jonathan Serrano, R Taylor Sundby, Jeffrey J Szymanski, Nicole J Ullrich, David H Viskochil, Xia Wang, Matija Snuderl, Peter J Park, Adrienne M Flanagan, Angela C Hirbe, Nischalan Pillay, David T Miller, null null
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. Cancer discovery 13 (3) (2023)
Andreea Chiorean, Kirsten M Farncombe, Sean Delong, Veronica Andric, Safa Ansar, Clarissa Chan, Kaitlin Clark, Arpad M Danos, Yizhuo Gao, Rachel H Giles, Anna Goldenberg, Payal Jani, Kilannin Krysiak, Lynzey Kujan, Samantha Macpherson, Eamonn R Maher, Liam G McCoy, Yasser Salama, Jason Saliba, Lana Sheta, Malachi Griffith, Malachi Griffith, Lauren Erdman, Arun Ramani, Raymond H Kim
Large scale genotype- and phenotype-driven machine learning in Von Hippel-Lindau disease. Human mutation 43 (9) (2022)
Salma Shickh, Daena Hirjikaka, Marc Clausen, Rita Kodida, Chloe Mighton, Emma Reble, Jordan Sam, Seema Panchal, Melyssa Aronson, Tracy Graham, Susan Randall Armel, Emily Glogowski, Christine Elser, Andrea Eisen, June C Carroll, Cheryl Shuman, Emily Seto, Nancy N Baxter, Adena Scheer, Serena Shastri-Estrada, Geoff Feldman, Kevin E Thorpe, Kasmintan A Schrader, Jordan Lerner- Ellis, Raymond H Kim, Hanna Faghfoury, Yvonne Bombard
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service delivery. BMJ open 12 (4) (2022)
Leslie E Oldfield, Jessica Grzybowski, Sylvie Grenier, Elizabeth Chao, Gregory S Downs, Kirsten M Farncombe, Tracy L Stockley, Ozgur Mete, Raymond H Kim
VHL mosaicism: the added value of multi-tissue analysis. NPJ genomic medicine 7 (1) (2022)
Agnes Sebastian, June C Carroll, Meredith Vanstone, Marc Clausen, Rita Kodida, Emma Reble, Chloe Mighton, Salma Shickh, Melyssa Aronson, Andrea Eisen, Christine Elser, Jordan Lerner-Ellis, Raymond H Kim, Yvonne Bombard
Widening the lens of actionability: A qualitative study of primary care providers' views and experiences of managing secondary genomic findings. European journal of human genetics : EJHG (2021)
Lucas Colombo Godoy, George Tomlinson, Asmaa M Abumuamar, Michael E Farkouh, Madeleine Rudolph, Filio Billia, Iris Cohn, Gil Marcus, Raymond H Kim, Vivek Rao, Patrick R Lawler
Association between time to therapeutic INR and length of stay following mechanical heart valve surgery. Journal of cardiac surgery 37 (1) (2021)
Jeanna M McCuaig, Emily Thain, Janet Malcolmson, Sareh Keshavarzi, Susan Randall Armel, Raymond H Kim
A Comparison of Patient-Reported Outcomes Following Consent for Genetic Testing Using an Oncologist- or Genetic Counselor-Mediated Model of Care. Current oncology (Toronto, Ont.) 28 (2) (2021)
Nika Maani, Karen Panabaker, Jeanna M McCuaig, Kathleen Buckley, Kara Semotiuk, Kirsten M Farncombe, Peter Ainsworth, Seema Panchal, Bekim Sadikovic, Susan Randall Armel, Hanxin Lin, Raymond H Kim
Incidental findings from cancer next generation sequencing panels. NPJ genomic medicine 6 (1) (2021)
Raymond H Kim, Xiangling Wang, Andrew J Evans, Steven C Campbell, Jane K Nguyen, Kirsten M Farncombe, Charis Eng
Early-onset renal cell carcinoma in PTEN harmatoma tumour syndrome. NPJ genomic medicine 5 (2020)
Marta Szybowska, Ozgur Mete, Evan Weber, Josh Silver, Raymond H Kim
Neuroendocrine Neoplasms Associated with Germline Pathogenic Variants in the Homologous Recombination Pathway. Endocrine pathology 30 (3) (2020)
Maia Leigh Norman, Janet Malcolmson, Susan Randall Armel, Brittany Gillies, Brian Ou, Emily Thain, Jeanna Marie McCuaig, Raymond H Kim
Stay at home: implementation and impact of virtualising cancer genetic services during COVID-19. Journal of medical genetics (2020)
Salma Shickh, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Conxi Lázaro, Jessica Gu, Jamie Goltz, Dakota Kleinman, Abdul Noor, Sam Khalouei, Chloe Mighton, Emma Reble, Rita Kodida, Yvonne Bombard, Stephanie DiTroia, Samantha Baxter, Nicholas Watkins, Melanie Care, Arnon Adler, Sheri Horsburgh, Oana Morar, Jillian Murphy, Dayna-Lynn Nevay, Marta Szybowska, Melyssa Aronson, Seema Panchal, Ruth Godoy, Spring Holter, Susan Randall Armel, Kara Semotiuk, Christine Elser, Raymond H Kim, David Chitayat, Joyce So, Hanna Faghfoury, Josh Silver, Chantal F Morel, Jordan Lerner- Ellis
Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study. Journal of medical genetics 58 (4) (2020)
Miriam S Reuter, Rajiv R Chaturvedi, Eriskay Liston, Roozbeh Manshaei, Ritu B Aul, Sarah Bowdin, Iris Cohn, Meredith Curtis, Priya Dhir, Robin Z Hayeems, S Mohsen Hosseini, Reem Khan, Linh G Ly, Christian R Marshall, Luc Mertens, John B A Okello, Sergio L Pereira, Akshaya Raajkumar, Mike Seed, Bhooma Thiruvahindrapuram, Stephen W Scherer, Raymond H Kim, Rebekah K Jobling
The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease. Genetics in medicine : official journal of the American College of Medical Genetics 22 (6) (2020)
Raymond H Kim, Xiangling Wang, Andrew J Evans, Steven C Campbell, Jane K Nguyen, Kirsten M Farncombe, Charis Eng
Early-onset renal cell carcinoma in PTEN harmatoma tumour syndrome. NPJ genomic medicine 5 (1) (2020)
David T Miller, Isidro Cortes-Ciriano, Nischalan Pillay, Angela C Hirbe, Matija Snuderl, Marilyn M Bui, Katherine Piculell, Alyaa Al-Ibraheemi, Brendan C Dickson, Jesse Hart, Kevin Jones, Justin T Jordan, Raymond H Kim, Daniel Lindsay, Yoshihiro Nishida, Nicole J Ullrich, Xia Wang, Peter J Park, Adrienne M Flanagan
Genomics of MPNST (GeM) Consortium: Rationale and Study Design for Multi-Omic Characterization of NF1-Associated and Sporadic MPNSTs. Genes 11 (4) (2020)
Yasser Salama, Saleh Albanyan, Marta Szybowska, Garrett Bullivant, Bailey Gallinger, Rachel H Giles, Sylvia Asa, Chansonette Badduke, Andreea Chiorean, Harriet Druker, Shereen Ezzat, Fady Hannah-Shmouni, Karen G Hernandez, Cara Inglese, Payal Jani, Yuvreet Kaur, Hatem Krema, Lior Krimus, Normand Laperriere, Zsuzanna Lichner, Ozgur Mete, Marisa Sit, Gelareh Zadeh, Michael A S Jewett, David Malkin, Tracy Stockley, Jonathan D Wasserman, Wei Xu, Nathan F Schachter, Raymond H Kim
Comprehensive characterization of a Canadian cohort of von Hippel-Lindau disease patients. Clinical genetics 96 (5) (2019)
Nika Maani, Shelley Westergard, Joanna Yang, Anabel M Scaranelo, Stephanie Telesca, Emily Thain, Nathan F Schachter, Jeanna M McCuaig, Raymond H Kim
NF1 Patients Receiving Breast Cancer Screening: Insights from The Ontario High Risk Breast Screening Program. Cancers 11 (5) (2019)
Carolyn Piccinin, Seema Panchal, Nicholas Watkins, Raymond H Kim
An update on genetic risk assessment and prevention: the role of genetic testing panels in breast cancer. Expert review of anticancer therapy 19 (9) (2019)
Neda Stjepanovic, Tracy L Stockley, Philippe L Bedard, Jeanna M McCuaig, Melyssa Aronson, Spring Holter, Kara Semotiuk, Natasha B Leighl, Raymond Jang, Monika K Krzyzanowska, Amit M Oza, Abha Gupta, Christine Elser, Lailah Ahmed, Lisa Wang, Suzanne Kamel-Reid, Lillian L Siu, Raymond H Kim
Additional germline findings from a tumor profiling program. BMC medical genomics 11 (1) (2018)
Jeanna M McCuaig, Tracy L Stockley, Patricia Shaw, Michael Fung-Kee-Fung, Alon D Altman, James Bentley, Marcus Q Bernardini, Beatrice Cormier, Hal Hirte, Katharina Kieser, Andree MacMillan, Wendy S Meschino, Karen Panabaker, Renee Perrier, Diane Provencher, Kasmintan A Schrader, Kimberly Serfas, Eva Tomiak, Nora Wong, Sean S Young, Walter Henri Gotlieb, Paul Hoskins, Raymond H Kim, null null
Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap. Journal of medical genetics 55 (9) (2018)
Jeanna M McCuaig, Susan Randall Armel, Melanie Care, Alexandra Volenik, Raymond H Kim, Kelly A Metcalfe
Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer. Cancers 10 (11) (2018)
Nardin Samuel, Resham Ejaz, Josh Silver, Shereen Ezzat, Robert J Cusimano, Raymond H Kim
Primary mediastinal paraganglioma associated with a familial variant in the succinate dehydrogenase B subunit gene. Journal of surgical oncology 117 (2) (2017)
Sarah Bowdin, Adel Gilbert, Emma C Bedoukian, Christopher Carew, Margaret P Adam, John Belmont, Barbara A Bernhardt, Barbara B Biesecker, Hans Tomas Bjornsson, Miriam Blitzer, Lisa C A D'Alessandro, Matthew A Deardorff, Laurie Demmer, Alison M Elliott, Gerald L Feldman, Ian A Glass, Gail Herman, Lucia Hindorff, Fuki Hisama, Louanne Hudgins, A Micheil Innes, Laird Jackson, David L Veenstra, Raymond H Kim, Bruce R Korf, David H Ledbetter, Mindy Li, Eriskay Liston, Christian Marshall, Livija Medne, M Stephen Meyn, Nasim Monfared, Cynthia C Morton, John J Mulvihill, Sharon E Plon, Heidi Rehm, Amy Roberts, Cheryl Shuman, Nancy B Spinner, D James Stavropoulos, Kathleen D Valverde, Darrel J Waggoner, Alisha Wilkens, Ronald D Cohn, Ian D Krantz
Recommendations for the integration of genomics into clinical practice. Genetics in medicine : official journal of the American College of Medical Genetics 18 (11) (2016)

Raymond H Kim.css-eqlu8i{font-size:small;padding-left:4px;} (R H Kim, Raymond Kim)

Publication Activity (10 Years)

Top Topics

Top Venues

Raymond H Kim (R H Kim, Raymond Kim)