The SickKids Genome Clinic: developing and evaluating a pediatric model for individualized genomic medicine von Bowdin, S.C., Hayeems, R.Z., Monfared, N., Cohn, R.D., Meyn, M.S.

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Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines von Anderson, J.A., Hayeems, R.Z., Shuman, C., Szego, M.J., Monfared, N., Bowdin, S., Zlotnik Shaul, R., Meyn, M.S.

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Ataxia-telangiectasia and cellular responses to DNA damage von MEYN, M. S

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Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma von Xu, Y, Ashley, T, Brainerd, E E, Bronson, R T, Meyn, M S, Baltimore, D

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Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene von Meyn, M. Stephen

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The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testing von Hayeems, R. Z., Luca, S., Ungar, W. J., Bhatt, A., Chad, L., Pullenayegum, E., Meyn, M. S.

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Parents perspectives on whole genome sequencing for their children: qualified enthusiasm? von Anderson, J A, Meyn, M S, Shuman, C, Zlotnik Shaul, R, Mantella, L E, Szego, M J, Bowdin, S, Monfared, N, Hayeems, R Z

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High Spontaneous Intrachromosomal Recombination Rates in Ataxia-Telangiectasia von Meyn, M. Stephen

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Response to Rubanovich et al von Hayeems, R. Z., Luca, S., Ungar, W. J., Bhatt, A., Chad, L., Pullenayegum, E., Meyn, M. S.

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Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics von Szego, M.J., Meyn, M.S., Shuman, C., Zlotnik Shaul, R., Anderson, J.A., Bowdin, S., Monfared, N., Hayeems, R.Z.

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Interaction of the Fanconi Anemia Proteins and BRCA1 in a Common Pathway von Garcia-Higuera, Irene, Taniguchi, Toshiyasu, Ganesan, Shridar, Meyn, M.Stephen, Timmers, Cynthia, Hejna, James, Grompe, Markus, D'Andrea, Alan D

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WRN or telomerase constructs reverse 4-nitroquinoline 1-oxide sensitivity in transformed Werner syndrome fibroblasts von HISAMA, F. M, CHEN, Y.-H, MEYN, M. S, OSHIMA, J, WEISSMAN, S. M

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Testing the Role of p53 in the Expression of Genetic Instability and Apoptosis in Ataxia-telangiectasia von Meyn, M.S., Strasfeld, L., Allen, C.

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The yeast TEL1 gene partially substitutes for human ATM in suppressing hyperrecombination, radiation-induced apoptosis and telomere shortening in A-T cells von Fritz, E, Friedl, A A, Zwacka, R M, Eckardt-Schupp, F, Meyn, M S

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MOLECULAR DEFINITION OF THE SMALLEST REGION OF DELETION OVERLAP IN THE WOLF-HIRSCHHORN SYNDROME von GANDELMAN, KY, GIBSON, L, MEYN, MS, YANGFENG, TL

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The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes von Keegan, K S, Holtzman, D A, Plug, A W, Christenson, E R, Brainerd, E E, Flaggs, G, Bentley, N J, Taylor, E M, Meyn, M S, Moss, S B, Carr, A M, Ashley, T, Hoekstra, M F

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Adenovirus-mediated expression of hepatic lipase in LCAT transgenic mice von Dugi, K A, Vaisman, B L, Sakai, N, Knapper, C L, Meyn, S M, Brewer, Jr, H B, Santamarina-Fojo, S

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The biochemical effect of Ser167 phosphorylation on Chlamydomonas reinhardtii centrin von Meyn, Susan M., Seda, Christina, Campbell, Muriel, Weiss, Kevin L., Hu, Haitao, Pastrana-Rios, Belinda, Chazin, Walter J.

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Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers von Shlien, Adam, Campbell, Brittany B, de Borja, Richard, Alexandrov, Ludmil B, Merico, Daniele, Wedge, David, Van Loo, Peter, Tarpey, Patrick S, Coupland, Paul, Behjati, Sam, Pollett, Aaron, Lipman, Tatiana, Heidari, Abolfazl, Deshmukh, Shriya, Avitzur, Na'ama, Meier, Bettina, Gerstung, Moritz, Hong, Ye, Merino, Diana M, Ramakrishna, Manasa, Remke, Marc, Arnold, Roland, Panigrahi, Gagan B, Thakkar, Neha P, Hodel, Karl P, Henninger, Erin E, Göksenin, A Yasemin, Bakry, Doua, Charames, George S, Druker, Harriet, Lerner-Ellis, Jordan, Mistry, Matthew, Dvir, Rina, Grant, Ronald, Elhasid, Ronit, Farah, Roula, Taylor, Glenn P, Nathan, Paul C, Alexander, Sarah, Ben-Shachar, Shay, Ling, Simon C, Gallinger, Steven, Constantini, Shlomi, Dirks, Peter, Huang, Annie, Scherer, Stephen W, Grundy, Richard G, Durno, Carol, Aronson, Melyssa, Gartner, Anton, Meyn, M Stephen, Taylor, Michael D, Pursell, Zachary F, Pearson, Christopher E, Malkin, David, Futreal, P Andrew, Stratton, Michael R, Bouffet, Eric, Hawkins, Cynthia, Campbell, Peter J, Tabori, Uri

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Commentary on the development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) Response von Hayeems, R. Z., Luca, S., Ungar, W. J., Bhatt, A., Chad, L., Pullenayegum, E., Meyn, M. S.

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