Risultati della ricerca - Thibodeau, My Linh

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

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Whole genome and whole transcriptome genomic profiling of a metastatic eccrine porocarcinoma di Thibodeau, My Linh, Bonakdar, Melika, Zhao, Eric, Mungall, Karen L., Reisle, Caralyn, Zhang, Wei, Bye, Morgan H., Thiessen, Nina, Bleile, Dustin, Mungall, Andrew J., Ma, Yussanne P., Jones, Martin R., Renouf, Daniel J., Lim, Howard J., Yip, Stephen, Ng, Tony, Ho, Cheryl, Laskin, Janessa, Marra, Marco A., Schrader, Kasmintan A., Jones, Steven J. M.

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Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline CHEK2:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcin... di Thibodeau, My Linh, Reisle, Caralyn, Zhao, Eric, Martin, Lee Ann, Alwelaie, Yazeed, Mungall, Karen L., Ch'ng, Carolyn, Thomas, Ruth, Ng, Tony, Yip, Stephen, J. Lim, Howard, Sun, Sophie, Young, Sean S., Karsan, Aly, Zhao, Yongjun, Mungall, Andrew J., Moore, Richard A., J. Renouf, Daniel, Gelmon, Karen, Ma, Yussanne P., Hayes, Malcolm, Laskin, Janessa, Marra, Marco A., Schrader, Kasmintan A., Jones, Steven J. M.

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Corrigendum: Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline CHEK2:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal... di Thibodeau, My Linh, Reisle, Caralyn, Zhao, Eric, Martin, Lee Ann, Alwelaie, Yazeed, Mungall, Karen L., Ch'ng, Carolyn, Thomas, Ruth, Ng, Tony, Yip, Stephen, Lim, Howard, Sun, Sophie, Young, Sean S., Karsan, Aly, Zhao, Yongjun, Mungall, Andrew J., Moore, Richard A., Renouf, Daniel, Gelmon, Karen, Ma, Yussanne P., Hayes, Malcolm, Laskin, Janessa, Marra, Marco A., Schrader, Kasmintan A., Jones, Steven J.M.

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Establishing a Framework for the Clinical Translation of Germline Findings in Precision Oncology di Dixon, Katherine, Young, Sean, Shen, Yaoqing, Thibodeau, My Linh, Fok, Alexandra, Pleasance, Erin, Zhao, Eric, Jones, Martin, Aubert, Geraldine, Armstrong, Linlea, Virani, Alice, Regier, Dean, Gelmon, Karen, Renouf, Dan, Chia, Stephen, Bosdet, Ian, Rassekh, S Rod, Deyell, Rebecca J, Yip, Stephen, Fisic, Ana, Titmuss, Emma, Abadi, Shirin, Jones, Steven J M, Sun, Sophie, Karsan, Aly, Marra, Marco, Laskin, Janessa, Lim, Howard, Schrader, Kasmintan A

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Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing di Thibodeau, My Linh, O’Neill, Kieran, Dixon, Katherine, Reisle, Caralyn, Mungall, Karen L., Krzywinski, Martin, Shen, Yaoqing, Lim, Howard J., Cheng, Dean, Tse, Kane, Wong, Tina, Chuah, Eric, Fok, Alexandra, Sun, Sophie, Renouf, Daniel, Schaeffer, David F., Cremin, Carol, Chia, Stephen, Young, Sean, Pandoh, Pawan, Pleasance, Stephen, Pleasance, Erin, Mungall, Andrew J., Moore, Richard, Yip, Stephen, Karsan, Aly, Laskin, Janessa, Marra, Marco A., Schrader, Kasmintan A., Jones, Steven J. M.

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Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis di Thibodeau, My Linh, Zhao, Eric Y., Reisle, Caralyn, Ch'ng, Carolyn, Wong, Hui-Li, Shen, Yaoqing, Jones, Martin R., Lim, Howard J., Young, Sean, Cremin, Carol, Pleasance, Erin, Zhang, Wei, Holt, Robert, Eirew, Peter, Karasinska, Joanna, Kalloger, Steve E., Taylor, Greg, Majounie, Elisa, Bonakdar, Melika, Zong, Zusheng, Bleile, Dustin, Chiu, Readman, Birol, Inanc, Gelmon, Karen, Lohrisch, Caroline, Mungall, Karen L., Mungall, Andrew J., Moore, Richard, Ma, Yussanne P., Fok, Alexandra, Yip, Stephen, Karsan, Aly, Huntsman, David, Schaeffer, David F., Laskin, Janessa, Marra, Marco A., Renouf, Daniel J., Jones, Steven J.M., Schrader, Kasmintan A.

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Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes di Goudie, Catherine, Witkowski, Leora, Cullinan, Noelle, Reichman, Lara, Schiller, Ian, Tachdjian, Melissa, Armstrong, Linlea, Blood, Katherine A., Brossard, Josée, Brunga, Ledia, Cacciotti, Chantel, Caswell, Kimberly, Cellot, Sonia, Clark, Mary Egan, Clinton, Catherine, Coltin, Hallie, Felton, Kathleen, Fernandez, Conrad V., Fleming, Adam J., Fuentes-Bolanos, Noemi, Gibson, Paul, Grant, Ronald, Hammad, Rawan, Harrison, Lynn W., Irwin, Meredith S., Johnston, Donna L., Kane, Sarah, Lafay-Cousin, Lucie, Lara-Corrales, Irene, Larouche, Valerie, Mathews, Natalie, Meyn, M. Stephen, Michaeli, Orli, Perrier, Renée, Pike, Meghan, Punnett, Angela, Ramaswamy, Vijay, Say, Jemma, Somers, Gino, Tabori, Uri, Thibodeau, My Linh, Toupin, Annie-Kim, Tucker, Katherine M., van Engelen, Kalene, Vairy, Stephanie, Waespe, Nicolas, Warby, Meera, Wasserman, Jonathan D., Whitlock, James A., Sinnett, Daniel, Jabado, Nada, Nathan, Paul C., Shlien, Adam, Kamihara, Junne, Deyell, Rebecca J., Ziegler, David S., Nichols, Kim E., Dendukuri, Nandini, Malkin, David, Villani, Anita, Foulkes, William D.

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