Kasmintan A Schrader (Intan Schrader)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 26

Top Topics

Acute Lymphoblastic Leukemia

Top Venues

Health expectations : an international journal of public participation in health care and health policy

Journal of medical genetics

Nature communications

JCO precision oncology

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

Publications

Rebecca J Deyell, Yaoqing Shen, Emma Titmuss, Katherine Dixon, Laura M Williamson, Erin D Pleasance, Jessica M T Nelson, Sanna Abbasi, Martin Krzywinski, Linlea Armstrong, Melika Bonakdar, Carolyn Ch'ng, Eric Chuah, Chris Dunham, Alexandra Fok, Martin R Jones, Anna F Lee, Yussanne Ma, Richard A Moore, Andrew J Mungall, Karen L Mungall, Paul C Rogers, Kasmintan A Schrader, Alice Virani, Kathleen Wee, Sean S Young, Yongjun Zhao, Steven J M Jones, Janessa Laskin, Marco A Marra, Shahrad Rod Rassekh
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers. Nature communications 15 (1) (2024)
Rebecca J Deyell, Yaoqing Shen, Emma Titmuss, Katherine Dixon, Laura M Williamson, Erin D Pleasance, Jessica M T Nelson, Sanna Abbasi, Martin Krzywinski, Linlea Armstrong, Melika Bonakdar, Carolyn Ch'ng, Eric Chuah, Chris Dunham, Alexandra Fok, Martin R Jones, Anna F Lee, Yussanne Ma, Richard A Moore, Andrew J Mungall, Karen L Mungall, Paul C Rogers, Kasmintan A Schrader, Alice Virani, Kathleen Wee, Sean S Young, Yongjun Zhao, Steven J M Jones, Janessa Laskin, Marco A Marra, Shahrad Rod Rassekh
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers. Nature communications 15 (1) (2024)
Carol Cremin, Angela C Bedard, Quan Hong, Sze Wing Mung, Jennifer Nuk, Andrew Wong, Husain Akbar, Eugene Cheung, Daniel Renouf, David Schaeffer, Sophie Sun, Kasmintan A Schrader
Improving Access to Hereditary Testing in Pancreatic Ductal Carcinoma. JCO precision oncology 8 (2024)
Rebecca J Deyell, Yaoqing Shen, Emma Titmuss, Katherine Dixon, Laura M Williamson, Erin D Pleasance, Jessica M T Nelson, Sanna Abbasi, Martin Krzywinski, Linlea Armstrong, Melika Bonakdar, Carolyn Ch'ng, Eric Chuah, Chris Dunham, Alexandra Fok, Martin R Jones, Anna F Lee, Yussanne Ma, Richard A Moore, Andrew J Mungall, Karen L Mungall, Paul C Rogers, Kasmintan A Schrader, Alice Virani, Kathleen Wee, Sean S Young, Yongjun Zhao, Steven J M Jones, Janessa Laskin, Marco A Marra, Shahrad Rod Rassekh
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancers. Nature communications 15 (1) (2024)
Samantha Pollard, Deirdre Weymann, Rosalie Loewen, Jennifer Nuk, Sophie Sun, Kasmintan A Schrader, Chiquita Hessels, Deirdre Weymann
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach. Health expectations : an international journal of public participation in health care and health policy (2023)
Samantha Pollard, Deirdre Weymann, Rosalie Loewen, Jennifer Nuk, Sophie Sun, Kasmintan A Schrader, Chiquita Hessels, Deirdre Weymann
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach. Health expectations : an international journal of public participation in health care and health policy 26 (2) (2023)
Samantha Pollard, Deirdre Weymann, Rosalie Loewen, Jennifer Nuk, Sophie Sun, Kasmintan A Schrader, Chiquita Hessels, Deirdre Weymann
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach. Health expectations : an international journal of public participation in health care and health policy 26 (2) (2023)
Erica S Tsang, Veronika Csizmok, Laura M Williamson, Erin Pleasance, James T Topham, Joanna M Karasinska, Emma Titmuss, Kasmintan A Schrader, Stephen Yip, Basile Tessier-Cloutier, Karen Mungall, Tony Ng, Sophie Sun, Howard J Lim, Jonathan M Loree, Janessa Laskin, Marco A Marra, Steven J M Jones, David F Schaeffer, Daniel J Renouf
Homologous recombination deficiency signatures in gastrointestinal and thoracic cancers correlate with platinum therapy duration. NPJ precision oncology 7 (1) (2023)
Katherine Dixon, Yaoqing Shen, Kieran O'Neill, Karen L Mungall, Simon Chan, Steve Bilobram, Wei Zhang, Marjorie Bezeau, Alshanee Sharma, Alexandra Fok, Andrew J Mungall, Richard Moore, Ian Bosdet, My Linh Thibodeau, Sophie Sun, Stephen Yip, Kasmintan A Schrader, Steven J M Jones
Defining the heterogeneity of unbalanced structural variation underlying breast cancer susceptibility by nanopore genome sequencing. European journal of human genetics : EJHG (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)
Samantha Pollard, Deirdre Weymann, Rosalie Loewen, Jennifer Nuk, Sophie Sun, Kasmintan A Schrader, Chiquita Hessels, Deirdre Weymann
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach. Health expectations : an international journal of public participation in health care and health policy 26 (2) (2023)
Samantha Pollard, Deirdre Weymann, Rosalie Loewen, Jennifer Nuk, Sophie Sun, Kasmintan A Schrader, Chiquita Hessels, Deirdre Weymann
Development and early-stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient-driven approach. Health expectations : an international journal of public participation in health care and health policy 26 (2) (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)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Janice S Kwon, Sarah A Cook, Jennifer Santos, Katie Compton, Sophie Sun, Kasmintan A Schrader, Aly Karsan
Germline Testing and Somatic Tumor Testing for <i>BRCA1/2</i> Pathogenic Variants in Ovarian Cancer: What Is the Optimal Sequence of Testing? JCO precision oncology 6 (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Xi Luo, Jamie L Maciaszek, Bryony A Thompson, Huei San Leong, Katherine Dixon, Sónia Sousa, Michael Anderson, Maegan E Roberts, Kristy Lee, Amanda B Spurdle, Arjen R Mensenkamp, Terra Brannan, Carolina Pardo, Zarina Yelskaya, Tina Pesaran, Sainan Wei, Grace-Ann Fasaye, Chimene Kesserwan, Brian H Shirts, Jeremy L Davis, Carla Oliveira, Sharon E Plon, Kasmintan A Schrader, Rachid Karam, null null
Optimising clinical care through CDH1 -specific germline variant curation: improvement of clinical assertions and updated curation guidelines. Journal of medical genetics (2022)
Lauren C Tindale, Almira Zhantuyakova, Stephanie Lam, Michelle Woo, Janice S Kwon, Gillian E Hanley, Bartha Knoppers, Kasmintan A Schrader, Stuart J Peacock, Aline Talhouk, Trevor Dummer, Kelly Metcalfe, Nora Pashayan, William D Foulkes, Ranjit Manchanda, David Huntsman, Gavin Stuart, Jacques Simard, Lesa Dawson
Gynecologic Cancer Risk and Genetics: Informing an Ideal Model of Gynecologic Cancer Prevention. Current oncology (Toronto, Ont.) 29 (7) (2022)
Salma Shickh, Leslie E Oldfield, Marc Clausen, Chloe Mighton, Agnes Sebastian, Alessia Calvo, Nancy N Baxter, Lesa Dawson, Lynette S Penney, William Foulkes, Mark Basik, Sophie Sun, Kasmintan A Schrader, Dean A Regier, Aly Karsan, Aaron Pollett, Trevor J Pugh, Raymond H Kim, Yvonne Bombard, null null
"Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome Management. The oncologist 27 (5) (2022)
Eryn F Braley, Angela C Bedard, Jennifer Nuk, Quan Hong, James E J Bedard, Sophie Sun, Kasmintan A Schrader
Patient ethnicity and cascade genetic testing: a descriptive study of a publicly funded hereditary cancer program. Familial cancer (2021)
Petra W C Lee, Angela C Bedard, Setareh Samimi, Vivienne K Beard, Quan Hong, James E J Bedard, Blake Gilks, David F Schaeffer, Robert Wolber, Janice S Kwon, Howard J Lim, Sophie Sun, Kasmintan A Schrader
Evaluating the impact of universal Lynch syndrome screening in a publicly funded healthcare system. Cancer medicine 9 (18) (2020)
Katherine Dixon, Janine Senz, Pardeep Kaurah, David G Huntsman, Kasmintan A Schrader
Rare APC promoter 1B variants in gastric cancer kindreds unselected for fundic gland polyposis. Gut 70 (7) (2020)
My Linh Thibodeau, Kieran O'Neill, Katherine Dixon, Caralyn Reisle, Karen L Mungall, Martin Krzywinski, Yaoqing Shen, Howard J Lim, Dean Cheng, Kane Tse, Tina Wong, Eric Chuah, Alexandra Fok, Sophie Sun, Daniel Renouf, David F Schaeffer, Carol Cremin, Stephen Chia, Sean Young, Pawan Pandoh, Stephen Pleasance, Erin Pleasance, Andrew J Mungall, Richard Moore, Stephen Yip, Aly Karsan, Janessa Laskin, Marco A Marra, Kasmintan A Schrader, Steven J M Jones
Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 22 (11) (2020)
Katherine Dixon, Sean Young, Yaoqing Shen, My Linh Thibodeau, Alexandra Fok, Erin Pleasance, Eric Zhao, Martin Jones, Geraldine Aubert, Linlea Armstrong, Alice Virani, Deirdre Weymann, Karen A Gelmon, Dan Renouf, Stephen Chia, Ian Bosdet, S Rod Rassekh, Rebecca J Deyell, Stephen Yip, Ana Fisic, Emma Titmuss, Shirin Abadi, Steven J M Jones, Sophie Sun, Aly Karsan, Marco A Marra, Janessa Laskin, Howard Lim, Kasmintan A Schrader
Establishing a Framework for the Clinical Translation of Germline Findings in Precision Oncology. JNCI cancer spectrum 4 (5) (2020)
Samantha Pollard, Steve E Kalloger, Deirdre Weymann, Sophie Sun, Jennifer Nuk, Kasmintan A Schrader, Deirdre Weymann
Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication. Health expectations : an international journal of public participation in health care and health policy 23 (4) (2020)
Kristy Lee, Kate Krempely, Maegan E Roberts, Michael J Anderson, Fátima Carneiro, Elizabeth Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David Huntsman, Pardeep Kaurah, Chimene Kesserwan, Tyler Landrith, Shuwei Li, Arjen R Mensenkamp, Carla Oliveira, Carolina Pardo, Tina Pesaran, Matthew Richardson, Thomas P Slavin, Amanda B Spurdle, Mackenzie Trapp, Leora Witkowski, Charles S Yi, Liying Zhang, Sharon E Plon, Kasmintan A Schrader, Rachid Karam
Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants. Human mutation 39 (11) (2019)