Rare APC promoter 1B variants in gastric cancer kindreds unselected for fundic gland polyposis

por Dixon, Katherine, Senz, Janine, Kaurah, Pardeep, Huntsman, David G, Schrader, Kasmintan A
Publicado 2021

CDKN2A founder mutation in pancreatic ductal adenocarcinoma patients without cutaneous features of Familial Atypical Multiple Mole Melanoma (FAMMM) syndrome

por Cremin, Carol, Howard, Sarah, Le, Lyly, Karsan, Aly, Schaeffer, David F., Renouf, Daniel, Schrader, Kasmintan A.
Publicado 2018

Genetic testing for hereditary cancer syndromes: patient recommendations for improved risk communication

por Pollard, Samantha, Kalloger, Steve, Weymann, Deirdre, Sun, Sophie, Nuk, Jennifer, Schrader, Kasmintan A., Regier, Dean A.
Publicado 2020

Germline Testing and Somatic Tumor Testing for BRCA1/2 Pathogenic Variants in Ovarian Cancer: What Is the Optimal Sequence of Testing?

por Kwon, Janice S., Tinker, Anna V., Santos, Jennifer, Compton, Katie, Sun, Sophie, Schrader, Kasmintan A., Karsan, Aly
Publicado 2022

Severe Late Toxicity After Adjuvant Breast Radiotherapy in a Patient with a Germline Ataxia Telangiectasia Mutated Gene: Future Treatment Decisions

por Dosani, Maryam, Schrader, Kasmintan A, Nichol, Alan, Sun, Sophie, Shenkier, Tamara, Lohn, Zoe, Aubertin, Gudrun, Tyldesley, Scott
Publicado 2017

Development and early‐stage evaluation of a patient portal to enhance familial communication about hereditary cancer susceptibility testing: A patient‐driven approach

por Pollard, Samantha, Weymann, Deirdre, Loewen, Rosalie, Nuk, Jennifer, Sun, Sophie, Schrader, Kasmintan A., Hessels, Chiquita, Regier, Dean A.
Publicado 2023

A population-based analysis of germline BRCA1 and BRCA2 testing among ovarian cancer patients in an era of histotype-specific approaches to ovarian cancer prevention

por Hanley, Gillian E., McAlpine, Jessica N., Miller, Dianne, Huntsman, David, Schrader, Kasmintan A., Blake Gilks, C., Mitchell, Gillian
Publicado 2018

Parent-of-origin detection and chromosome-scale haplotyping using long-read DNA methylation sequencing and Strand-seq

por Akbari, Vahid, Hanlon, Vincent C.T., O’Neill, Kieran, Lefebvre, Louis, Schrader, Kasmintan A., Lansdorp, Peter M., Jones, Steven J.M.
Publicado 2022

Hereditary diffuse gastric cancer: association with lobular breast cancer

por Schrader, Kasmintan A., Masciari, Serena, Boyd, Niki, Wiyrick, Sara, Kaurah, Pardeep, Senz, Janine, Burke, Wylie, Lynch, Henry T., Garber, Judy E., Huntsman, David G.
Publicado 2007

Matching methods in precision oncology: An introduction and illustrative example

por Weymann, Deirdre, Laskin, Janessa, Jones, Steven J.M., Lim, Howard, Renouf, Daniel J., Roscoe, Robyn, Schrader, Kasmintan A., Sun, Sophie, Yip, Stephen, Marra, Marco A., Regier, Dean A.
Publicado 2020

The cost and cost trajectory of whole‐genome analysis guiding treatment of patients with advanced cancers

por Weymann, Deirdre, Laskin, Janessa, Roscoe, Robyn, Schrader, Kasmintan A., Chia, Stephen, Yip, Stephen, Cheung, Winson Y., Gelmon, Karen A., Karsan, Aly, Renouf, Daniel J., Marra, Marco, Regier, Dean A.
Publicado 2017

Early-stage economic analysis of research-based comprehensive genomic sequencing for advanced cancer care

por Weymann, Deirdre, Laskin, Janessa, Jones, Steven J. M., Roscoe, Robyn, Lim, Howard J., Renouf, Daniel J., Schrader, Kasmintan A., Sun, Sophie, Yip, Stephen, Marra, Marco A., Regier, Dean A.
Publicado 2021

The Specificity of the FOXL2 c.402C>G Somatic Mutation: A Survey of Solid Tumors

por Schrader, Kasmintan A., Gorbatcheva, Bella, Senz, Janine, Heravi-Moussavi, Alireza, Melnyk, Nataliya, Salamanca, Clara, Maines-Bandiera, Sarah, Cooke, Susanna L., Leung, Peter, Brenton, James D., Gilks, C. Blake, Monahan, John, Huntsman, David G.
Publicado 2009

Oncology Clinic-Based Hereditary Cancer Genetic Testing in a Population-Based Health Care System

por Richardson, Matthew, Min, Hae Jung, Hong, Quan, Compton, Katie, Mung, Sze Wing, Lohn, Zoe, Nuk, Jennifer, McCullum, Mary, Portigal-Todd, Cheryl, Karsan, Aly, Regier, Dean, Brotto, Lori A., Sun, Sophie, Schrader, Kasmintan A.
Publicado 2020

Assessment of SLX4 Mutations in Hereditary Breast Cancers

por Shah, Sohela, Kim, Yonghwan, Ostrovnaya, Irina, Murali, Rajmohan, Schrader, Kasmintan A., Lach, Francis P., Sarrel, Kara, Rau-Murthy, Rohini, Hansen, Nichole, Zhang, Liyng, Kirchhoff, Tomas, Stadler, Zsofia, Robson, Mark, Vijai, Joseph, Offit, Kenneth, Smogorzewska, Agata
Publicado 2013

Whole-genome and transcriptome profiling of a metastatic thyroid-like follicular renal cell carcinoma

por Ko, Jenny J., Grewal, Jasleen K., Ng, Tony, Lavoie, Jean-Michel, Thibodeau, My Linh, Shen, Yaoqing, Mungall, Andrew J., Taylor, Greg, Schrader, Kasmintan A., Jones, Steven J.M., Kollmannsberger, Christian, Laskin, Janessa, Marra, Marco A.
Publicado 2018

Evaluating the impact of universal Lynch syndrome screening in a publicly funded healthcare system

por Lee, Petra W. C., Bedard, Angela C., Samimi, Setareh, Beard, Vivienne K., Hong, Quan, Bedard, James E. J., Gilks, Blake, Schaeffer, David F., Wolber, Robert, Kwon, Janice S., Lim, Howard J., Sun, Sophie, Schrader, Kasmintan A.
Publicado 2020

Quality of life drives patients’ preferences for secondary findings from genomic sequencing

por Mighton, Chloe, Carlsson, Lindsay, Clausen, Marc, Casalino, Selina, Shickh, Salma, McCuaig, Laura, Joshi, Esha, Panchal, Seema, Semotiuk, Kara, Ott, Karen, Elser, Christine, Eisen, Andrea, Kim, Raymond H., Lerner-Ellis, Jordan, Carroll, June C., Glogowski, Emily, Schrader, Kasmintan, Bombard, Yvonne
Publicado 2020

Defining the heterogeneity of unbalanced structural variation underlying breast cancer susceptibility by nanopore genome sequencing

por Dixon, Katherine, Shen, Yaoqing, O’Neill, Kieran, Mungall, Karen L., Chan, Simon, Bilobram, Steve, Zhang, Wei, Bezeau, Marjorie, Sharma, Alshanee, Fok, Alexandra, Mungall, Andrew J., Moore, Richard, Bosdet, Ian, Thibodeau, My Linh, Sun, Sophie, Yip, Stephen, Schrader, Kasmintan A., Jones, Steven J. M.
Publicado 2023

Gynecologic Cancer Risk and Genetics: Informing an Ideal Model of Gynecologic Cancer Prevention

por Tindale, Lauren C., Zhantuyakova, Almira, Lam, Stephanie, Woo, Michelle, Kwon, Janice S., Hanley, Gillian E., Knoppers, Bartha, Schrader, Kasmintan A., Peacock, Stuart J., Talhouk, Aline, Dummer, Trevor, Metcalfe, Kelly, Pashayan, Nora, Foulkes, William D., Manchanda, Ranjit, Huntsman, David, Stuart, Gavin, Simard, Jacques, Dawson, Lesa
Publicado 2022