Cause and Consequences of Genetic and Epigenetic Alterations in Human Cancer von Sadikovic, B, Al-Romaih, K, Squire, J A, Zielenska, M

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A genome-wide DNA methylation signature for SETD1B-related syndrome von Krzyzewska, I M, Maas, S M, Henneman, P, Lip, K V D, Venema, A, Baranano, K, Chassevent, A, Aref-Eshghi, E, van Essen, A J, Fukuda, T, Ikeda, H, Jacquemont, M, Kim, H-G, Labalme, A, Lewis, S M E, Lesca, G, Madrigal, I, Mahida, S, Matsumoto, N, Rabionet, R, Rajcan-Separovic, E, Qiao, Y, Sadikovic, B, Saitsu, H, Sweetser, D A, Alders, M, Mannens, M M A M

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Endothelin-1 Regulation Is Entangled in a Complex Web of Epigenetic Mechanisms in Diabetes von BISWAS, S., FENG, B., THOMAS, A., CHEN, S., AREF-ESHGHI, E., SADIKOVIC, B., CHAKRABARTI, S.

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Next Generation Sequencing in the Study of Hyperferritinemia von Sadikovic, B, Levstik, A, Adams, P

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DNA methylation epi-signature is associated with two molecularly and phenotypically distinct clinical subtypes of Phelan-McDermid syndrome von Schenkel, L C, Aref-Eshghi, E, Rooney, K, Kerkhof, J, Levy, M A, McConkey, H, Rogers, R C, Phelan, K, Sarasua, S M, Jain, L, Pauly, R, Boccuto, L, DuPont, B, Cappuccio, G, Brunetti-Pierri, N, Schwartz, C E, Sadikovic, B

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PROVIDING TIMELY PATIENT-CENTERED MOLECULAR DIAGNOSTIC TESTING FOR PATIENTS WITH ACUTE MYELOID LEUKEMIA: A QUALITY IMPROVEMENT STUDY von Qureshi, A., Ho, J., Schenkel, L., Chin-Yee, B., Deotare, U., Meybodi, A., Saini, L., Sadikovic, B., Chin-Yee, I.

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Double heterozygosity for germline mutations in BRCA1 and p53 in a woman with early onset breast cancer von Bell, K., Hodgson, N., Levine, M., Sadikovic, B., Zbuk, K.

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An aggressive multifocal primary CNS histiocytosis with PTPN11 (Shp2) mutation von Zhang, Q., Shibani, A., Sadikovic, B., Howlett, C. J., Ang, L.‐C.

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Inter-laboratory proficiency testing scheme for tumour next-generation sequencing in Ontario: a pilot study von Spence, T, Stickle, N, Yu, C, Chow, H, Feilotter, H, Lo, B, McCready, E, Sadikovic, B, Siu, L L, Bedard, P L, Stockley, T L

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OCTANE (Ontario-wide Cancer Targeted Nucleic Acid Evaluation): a platform for intraprovincial, national, and international clinical data-sharing von Malone, E R, Saleh, R R, Yu, C, Ahmed, L, Pugh, T, Torchia, J, Bartlett, J, Virtanen, C, Hotte, S J, Hilton, J, Welch, S, Robinson, A, McCready, E, Lo, B, Sadikovic, B, Feilotter, H, Hanna, T P, Kamel-Reid, S, Stockley, T L, Siu, L L, Bedard, P L

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P1019: A PREDICTION RULE TO GUIDE JAK2 MUTATION TESTING IN PATIENTS WITH SUSPECTED POLYCYTHEMIA VERA: RESULTS FROM THE JAK2 PREDICTION COHORT (JAKPOT) STUDY von Chin‐Yee, B., Bhai, P., Cheong, I., Matyashin, M., Hsia, C., Kawata, E., Ho, J., Levy, M., Stuart, A., Lin, H., Chin‐Yee, I., Kadour, M., Sadikovic, B., Lazo‐Langner, A.

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THU-450 - Next Generation Sequencing in the Study of Hyperferritinemia von Sadikovic, B., Levstik, A., Adams, P.

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Recurrent genomic alterations in sequential progressive leukoplakia and oral cancer: drivers of oral tumorigenesis? von Cervigne, Nilva K., Machado, Jerry, Goswami, Rashmi S., Sadikovic, Bekim, Bradley, Grace, Perez-Ordonez, Bayardo, Galloni, Natalie Naranjo, Gilbert, Ralph, Gullane, Patrick, Irish, Jonathan C., Jurisica, Igor, Reis, Patricia P., Kamel-Reid, Suzanne

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FP07.08 A Pan-Canadian Validation Study for the Detection of EGFR-T790M Mutations Using Circulating Tumour DNA (ctDNA) from Blood von Selvarajah, S., Plante, S., Speevak, M., Vaags, A., Mccready, E., Grafodatskaya, D., Blais, N., Tran-Thanh, D., Greer, W., Lo, B., Demetrick, D., Sadikovic, B., Walton, R., Stockley, T., Feilotter, H., Joubert, P.

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A191 NEXT GENERATION SEQUENCING IN THE INVESTIGATION OF HYPERFERRITINEMIA von Adams, P, Levstik, A, Sadikovic, B

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Benzopyrene exposure disrupts DNA methylation and growth dynamics in breast cancer cells von Sadikovic, Bekim, Rodenhiser, David I.

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Decitabine-Induced Demethylation of 5′ CpG Island in GADD45A Leads to Apoptosis in Osteosarcoma Cells von Al-Romaih, Khaldoun, Sadikovic, Bekim, Yoshimoto, Maisa, Wang, Yuzhuo, Zielenska, Maria, Squire, Jeremy A.

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P.077 Utility of a next generation sequencing in the diagnosis of Congenital Myasthenic Syndromes von Zapata-Aldana, E, Nguyen, CE, Nicolle, MW, Carere, DA, Stuart, A, Campbell, C, Sadikovic, B

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Sodium Bisulfite Analysis of the Methylation Status of DNA from Small Portions of Paraffin Slides von Anderson, A.E, Haines, T.R, Robinson, D.P, Butcher, D.T, Sadikovic, B, Rodenhiser, D.I

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A genome-wide DNA methylation signature for SETD1B-related syndrome von Krzyzewska, I. M, Maas, S. M, Henneman, Peter, Lip, K. V. D, Venema, A, Baranano, K, Chassevent, A, Aref-Eshghi, E, Essen, A. J. van, Fukuda, T, Ikeda, H, Jacquemont, M, Kim, H. G, Labalme, Audrey, Lewis, S. M, Lesca, Gaetan, Madrigal Bajo, Irene, Mahida, S, Matsumoto, N, Rabionet Janssen, Raquel, Rajcan-Separovic, E, Qiao, Y, Sadikovic, B, Saitsu, H, Sweetser, D. A, Alders, M, Mannens, M. M. A. M

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