Thèmes

• Pathologie moléculaire
• Hématologie

• 2005 - présent : Professeur associé, Faculté de médecine, Université McGill
• 2005 - présent : Membre, Commité aviseur du programme de technologies de laboratoire médicale, CEGEP Dawson
• 1999 - présent : Membre de l’Association for Molecular Pathology (AMP)
• 1998 - présent : Membre de Shevchenko Scientific Society, chapitre de Montréal

• Morin, R.D., S. Assouline, M. Alcaide, M. Alcaide, A. Mohajeri, R. Johnston, L. Chong, J. Grewal, S. Yu, D. Fornika, K. Bushell, T.H. Nielsen, T. Petrogiannis-Haliotis, M. Crump8, A. Tosikyan, B.M. Grande, D. MacDonald, C. Rousseau, M. Bayat, P. Sesques, R. Froment, M. Albuquerque, Y. Monczak, K. Klein Oros, C. Greenwood, Y. Riazalhosseini, M. Arseneault, E. Camlioglu, A. Constantin, R. Peng, Q. Pan-Hammarstrom, K.K.Mann, N. Johnson, 2016. Genetic landscapes of relapsed and refractory diffuse large B cell lymphomas.  Clinical Cancer Research 22 (9): 2290-2300
• Peltier, L,R. Brown, Y. Monczak, G. Propadi, J, Storring and P. Laneuville. 2014. Development of a New Third Party Unit for Adult Stem Cell Transplantation using Clinical-Grade Rejected Cord Blood Units. J. Genetic Syndromes & Gene Therapy 6 (1):1-11.
• Jarry, J, J-S Brunet, R. Laframboise, R. Drouin, J. Latreille, C. Richar, J. Gekas, B. Maranda, Y. Monczak, N. Wong, C. Pouchet, S. Zaor, L. Kasprzak, L. Palma, M.K. Wu, M. Tischkowitz, W.D. Foulkes, G. Chong. 2011. A Survey of APC Mutations in Quebec. Familial Cancer 10(4): 659-665.
• Mak, A, M.A. Miller, G. Chong and Y. Monczak. 2009. Comparison of PCR and culture for screening of vancomycin-resistant enterococci : highly disparate results for vanA and vanB. J. Clinical Microbiology 47(12): 4136-4137.
• Chong, G. J Jarry, V. Marcus, I. Thiffault, S. Winocour, Y. Monczak, R. Drouin, J. Latreille, K. Australie, B. Bapat, P.H. Gordon, Y. Giguère, A. Gologan, P. Galiatsatos, J.R. Jass, N. Wong, S. Zaor, L. Palma, L. Kasprzak, M. Tishchkowitz and W.D. Foulkes. 2009. High frequency of exon deletions and putative founder effects in French Canadian Lynch syndrome families. Human Mutation 30: E797-E812.
• Mercier, F, Y. Monczak, M François, J Prchal and Jacques Galipeau. Bone marrow mesenchymal stromal cells of patients with myeloproliferative disorders do not carry the JAK2 V617F mutation. 2009. Experimental Hematology 37: 416-420.