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

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A genome-wide DNA methylation signature for SETD1B-related syndrome by 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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Next Generation Sequencing in the Study of Hyperferritinemia by 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 by 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 by 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 by Bell, K., Hodgson, N., Levine, M., Sadikovic, B., Zbuk, K.

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An aggressive multifocal primary CNS histiocytosis with PTPN11 (Shp2) mutation by 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 by 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 by 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 by 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 by Sadikovic, B., Levstik, A., Adams, P.

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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females by Radio, Francesca Clementina, Ciolfi, Andrea, Levy, Michael A., Hernández-García, Andrés, Pedace, Lucia, Pantaleoni, Francesca, Liu, Zhandong, de Boer, Elke, Jackson, Adam, Bruselles, Alessandro, McConkey, Haley, Stellacci, Emilia, Lo Cicero, Stefania, Motta, Marialetizia, Carrozzo, Rosalba, McWalter, Kirsty, Desai, Megha, Monaghan, Kristin G., Telegrafi, Aida, Philippe, Christophe, Vitobello, Antonio, Au, Margaret, Grand, Katheryn, Baez, Joanne, Lindstrom, Kristin, Kulch, Peggy, Sebastian, Jessica, Madan-Khetarpal, Suneeta, Roadhouse, Chelsea, MacKenzie, Jennifer J., Monteleone, Berrin, Saunders, Carol J., Jean Cuevas, July K., Zhou, Dihong, Sawyer, Sarah L., Monteiro, Fabíola Paoli, Secches, Tania Vertemati, Kok, Fernando, Schultz-Rogers, Laura E., Morava, Eva, Klee, Eric W., Kemppainen, Jennifer, Iascone, Maria, Selicorni, Angelo, Tenconi, Romano, Pais, Lynn, Gallacher, Lyndon, Turnpenny, Peter D., Stals, Karen, Ellard, Sian, Cabet, Sara, Lesca, Gaetan, Pascal, Joset, Steindl, Katharina, Weiss, Karin, Carter, Melissa T., Kalsner, Louisa, de Vries, Bert B.A., van Bon, Bregje W., Wevers, Marijke R., Pfundt, Rolph, Stegmann, Alexander P.A., Kerr, Bronwyn, Chandler, Kate E., Sheehan, Willow, Elias, Abdallah F., Shinde, Deepali N., Towne, Meghan C., Robin, Nathaniel H., Goodloe, Dana, Vanderver, Adeline, Sherbini, Omar, Bluske, Krista, Faletra, Flavio, Musante, Luciana, Kurtz-Nelson, Evangeline C., Earl, Rachel K., Anderlid, Britt-Marie, Morin, Gilles, van Slegtenhorst, Marjon, Diderich, Karin E.M., Brooks, Alice S., Gribnau, Joost, Boers, Ruben G., Finestra, Teresa Robert, Carter, Lauren B., Rauch, Anita, Gasparini, Paolo, Boycott, Kym M., Barakat, Tahsin Stefan, Graham, John M., Faivre, Laurence, Banka, Siddharth, Wang, Tianyun, Eichler, Evan E., Dallapiccola, Bruno, Vissers, Lisenka E.L.M., Sadikovic, Bekim, Holder, Jimmy Lloyd, Tartaglia, Marco

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Recurrent genomic alterations in sequential progressive leukoplakia and oral cancer: drivers of oral tumorigenesis? by 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 by 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 by Adams, P, Levstik, A, Sadikovic, B

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

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DNA Methylation Signature for JARID2-Neurodevelopmental Syndrome by Verberne, Eline A., van der Laan, Liselot, Haghshenas, Sadegheh, Rooney, Kathleen, Levy, Michael A., Alders, Mariëlle, Maas, Saskia M., Jansen, Sandra, Lieden, Agne, Anderlid, Britt-Marie, Rafael-Croes, Louise, Campeau, Philippe M., Chaudhry, Ayeshah, Koolen, David A., Pfundt, Rolph, Hurst, Anna C. E., Tran-Mau-Them, Frederic, Bruel, Ange-Line, Lambert, Laetitia, Isidor, Bertrand, Mannens, Marcel M. A. M., Sadikovic, Bekim, Henneman, Peter, van Haelst, Mieke M.

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Decitabine-Induced Demethylation of 5′ CpG Island in GADD45A Leads to Apoptosis in Osteosarcoma Cells by 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 by Zapata-Aldana, E, Nguyen, CE, Nicolle, MW, Carere, DA, Stuart, A, Campbell, C, Sadikovic, B

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SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females by Radio, FC, Pang, KF, Ciolfi, A, Levy, MA, Pedace, L, de Boer, E, Jackson, A, Stellacci, E, Lo Cicero, S, Dentici, ML, McWalter, K, Sanchez-Lara, PA, Lindstrom, K, Madan-Khetarpal, S, MacKenzie, JJ, Monteleone, B, Zhou, DH, Sawyer, SL, Monteiro, FP, Macke, EL, Iascone, M, Selicorni, A, Tenconi, R, Amor, DJ, Stals, K, Cabet, S, Steindl, K, Weiss, K, Castle, AMR, Kalsner, L, Chandler, KE, Sheehan, W, Shinde, DN, Goodloe, D, Bluske, K, Faletra, F, Kurtz-Nelson, EC, Anderlid, BM, Barakat, TS, Graham, JM, Faivre, L, Banka, S, Wang, TY, Priolo, M, Dallapiccola, B, Vissers, LELM, Sadikovic, B, Scott, DA, Holder, JL, Tartaglia, M

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