A Distinctive DNA Damage Response in Human Hematopoietic Stem Cells Reveals an Apoptosis-Independent Role for p53 in Self-Renewal von Milyavsky, Michael, Gan, Olga I., Trottier, Magan, Komosa, Martin, Tabach, Ofer, Notta, Faiyaz, Lechman, Eric, Hermans, Karin G., Eppert, Kolja, Konovalova, Zhanna, Ornatsky, Olga, Domany, Eytan, Meyn, M. Stephen, Dick, John E.

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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists von Boycott, Kym, Hartley, Taila, Adam, Shelin, Bernier, Francois, Chong, Karen, Fernandez, Bridget A, Friedman, Jan M, Geraghty, Michael T, Hume, Stacey, Knoppers, Bartha M, Laberge, Anne-Marie, Majewski, Jacek, Mendoza-Londono, Roberto, Meyn, M Stephen, Michaud, Jacques L, Nelson, Tanya N, Richer, Julie, Sadikovic, Bekim, Skidmore, David L, Stockley, Tracy, Taylor, Sherry, van Karnebeek, Clara, Zawati, Ma'n H, Lauzon, Julie, Armour, Christine M

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K63-Ubiquitylation of VHL by SOCS1 mediates DNA double-strand break repair von Metcalf, J L, Bradshaw, P S, Komosa, M, Greer, S N, Stephen Meyn, M, Ohh, M

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An oligogenic case of severe neonatal thrombocytopenia and a purportedly benign variant in GFI1B requiring reinterpretation von Frenkel, Max, Hall, April, Meyn, M Stephen, Diamond, Carol A

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Genome Diagnostics: Novel Strategies for Measuring Value von Hayeems, Robin Z., Luca, Stephanie, Pullenayegum, Eleanor, Meyn, M. Stephen, Ungar, Wendy J.

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Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice von Houghtaling, Scott, Timmers, Cynthia, Noll, Meenakshi, Finegold, Milton J, Jones, Stephen N, Meyn, M Stephen, Grompe, Markus

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Impaired telomere maintenance in Alazami syndrome patients with LARP7 deficiency von Holohan, Brody, Kim, Wanil, Lai, Tsung-Po, Hoshiyama, Hirotoshi, Zhang, Ning, Alazami, Anas M, Wright, Woodring E, Meyn, M Stephen, Alkuraya, Fowzan S, Shay, Jerry W

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Attenuated DNA damage responses and increased apoptosis characterize human hematopoietic stem cells exposed to irradiation von Biechonski, Shahar, Olender, Leonid, Zipin-Roitman, Adi, Yassin, Muhammad, Aqaqe, Nasma, Marcu-Malina, Victoria, Rall-Scharpf, Melanie, Trottier, Magan, Meyn, M. Stephen, Wiesmüller, Lisa, Beider, Katia, Raz, Yael, Grisaru, Dan, Nagler, Arnon, Milyavsky, Michael

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The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors von Kolomietz, Elena, Meyn, M. Stephen, Pandita, Ajay, Squire, Jeremy A.

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Comprehensive Analysis of Hypermutation in Human Cancer von Campbell, Brittany B., Light, Nicholas, Fabrizio, David, Zatzman, Matthew, Fuligni, Fabio, de Borja, Richard, Davidson, Scott, Edwards, Melissa, Elvin, Julia A., Hodel, Karl P., Zahurancik, Walter J., Suo, Zucai, Lipman, Tatiana, Wimmer, Katharina, Kratz, Christian P., Bowers, Daniel C., Laetsch, Theodore W., Dunn, Gavin P., Johanns, Tanner M., Grimmer, Matthew R., Smirnov, Ivan V., Larouche, Valérie, Samuel, David, Bronsema, Annika, Osborn, Michael, Stearns, Duncan, Raman, Pichai, Cole, Kristina A., Storm, Phillip B., Yalon, Michal, Opocher, Enrico, Mason, Gary, Thomas, Gregory A., Sabel, Magnus, George, Ben, Ziegler, David S., Lindhorst, Scott, Issai, Vanan Magimairajan, Constantini, Shlomi, Toledano, Helen, Elhasid, Ronit, Farah, Roula, Dvir, Rina, Dirks, Peter, Huang, Annie, Galati, Melissa A., Chung, Jiil, Ramaswamy, Vijay, Irwin, Meredith S., Aronson, Melyssa, Durno, Carol, Taylor, Michael D., Rechavi, Gideon, Maris, John M., Bouffet, Eric, Hawkins, Cynthia, Costello, Joseph F., Meyn, M. Stephen, Pursell, Zachary F., Malkin, David, Tabori, Uri, Shlien, Adam

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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test von Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Walker, Susan, Reuter, Miriam S, Hosseini, S Mohsen, Thiruvahindrapuram, Bhooma, Merico, Daniele, Jobling, Rebekah, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Sung, Wilson W L, Wang, Zhuozhi, Bikangaga, Peter, Boelman, Cyrus, Carter, Melissa T, Cordeiro, Dawn, Cytrynbaum, Cheryl, Dell, Sharon D, Dhir, Priya, Dowling, James J, Heon, Elise, Hewson, Stacy, Hiraki, Linda, Inbar-Feigenberg, Michal, Klatt, Regan, Kronick, Jonathan, Laxer, Ronald M, Licht, Christoph, MacDonald, Heather, Mercimek-Andrews, Saadet, Mendoza-Londono, Roberto, Piscione, Tino, Schneider, Rayfel, Schulze, Andreas, Silverman, Earl, Siriwardena, Komudi, Snead, O Carter, Sondheimer, Neal, Sutherland, Joanne, Vincent, Ajoy, Wasserman, Jonathan D, Weksberg, Rosanna, Shuman, Cheryl, Carew, Chris, Szego, Michael J, Hayeems, Robin Z, Basran, Raveen, Stavropoulos, Dimitri J, Ray, Peter N, Bowdin, Sarah, Meyn, M Stephen, Cohn, Ronald D, Scherer, Stephen W, Marshall, Christian R

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Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study von Cohn, Iris, Paton, Tara A., Marshall, Christian R., Basran, Raveen, Stavropoulos, Dimitri J., Ray, Peter N., Monfared, Nasim, Hayeems, Robin Z., Meyn, M. Stephen, Bowdin, Sarah, Scherer, Stephen W., Cohn, Ronald D., Ito, Shinya

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PhenoTips: Patient Phenotyping Software for Clinical and Research Use von Girdea, Marta, Dumitriu, Sergiu, Fiume, Marc, Bowdin, Sarah, Boycott, Kym M., Chénier, Sébastien, Chitayat, David, Faghfoury, Hanna, Meyn, M. Stephen, Ray, Peter N., So, Joyce, Stavropoulos, Dimitri J., Brudno, Michael

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DNA Damage-Induced Phosphorylation of the Human Telomere-Associated Protein TRF2 von Tanaka, Hiromi, Mendonca, Marc S., Paul S. Bradshaw, Derek J. Hoelz, Malkas, Linda H., Meyn, M. Stephen, Gilley, David

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FANCD2 limits BLM-dependent telomere instability in the alternative lengthening of telomeres pathway von Root, Heather, Larsen, Andrew, Komosa, Martin, Al-Azri, Fakhriya, Li, Ren, Bazett-Jones, David P., Stephen Meyn, M.

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Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing von Costain, Gregory, Jobling, Rebekah, Walker, Susan, Reuter, Miriam S, Snell, Meaghan, Bowdin, Sarah, Cohn, Ronald D, Dupuis, Lucie, Hewson, Stacy, Mercimek-Andrews, Saadet, Shuman, Cheryl, Sondheimer, Neal, Weksberg, Rosanna, Yoon, Grace, Meyn, M Stephen, Stavropoulos, Dimitri J, Scherer, Stephen W, Mendoza-Londono, Roberto, Marshall, Christian R

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FANCD2 limits BLM-dependent telomere instability in the alternative lengthening of telomeres pathway von Root, Heather, Larsen, Andrew, Komosa, Martin, Al-Azri, Fakhriya, Li, Ren, Bazett-Jones, David P, Stephen Meyn, M

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The point‐of‐care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning von Marwaha, Ashish, Chitayat, David, Meyn, M. Stephen, Mendoza‐Londono, Roberto, Chad, Lauren

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Visualization and quantitative analysis of extrachromosomal telomere-repeat DNA in individual human cells by Halo-FISH von Komosa, Martin, Root, Heather, Meyn, M Stephen

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Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability von Hayeems, Robin Z., Luca, Stephanie, Chad, Lauren, Quercia, Nada, Xiao, Bowen, Hossain, Alomgir, Meyn, M. Stephen, Pullenayegum, Eleanor, Ungar, Wendy J.

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