Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate von Caulfield, Timothy, Evans, Jim, McGuire, Amy, McCabe, Christopher, Bubela, Tania, Cook-Deegan, Robert, Fishman, Jennifer, Hogarth, Stuart, Miller, Fiona A, Ravitsky, Vardit, Biesecker, Barbara, Borry, Pascal, Cho, Mildred K, Carroll, June C, Etchegary, Holly, Joly, Yann, Kato, Kazuto, Lee, Sandra Soo-Jin, Rothenberg, Karen, Sankar, Pamela, Szego, Michael J, Ossorio, Pilar, Pullman, Daryl, Rousseau, Francois, Ungar, Wendy J, Wilson, Brenda

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Please give me a copy of my child’s raw genomic data von Chad, Lauren, Szego, Michael J.

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Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration von Bramall, Alexa N, Szego, Michael J, Pacione, Laura R, Chang, Inik, Diez, Eduardo, D'Orleans-Juste, Pedro, Stewart, Duncan J, Hauswirth, William W, Yanagisawa, Masashi, McInnes, Roderick R

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Author Correction: Please give me a copy of my child’s raw genomic data von Chad, Lauren, Szego, Michael J.

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STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models von Jiang, Ke, Wright, Katherine L, Zhu, Ping, Szego, Michael J, Bramall, Alexa N, Hauswirth, William W, Li, Qiuhong, Egan, Sean E, McInnes, Roderick R

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Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility von Beauvais, Michael J S, Thorogood, Adrian M, Szego, Michael J, Sénécal, Karine, Zawati, M'an H, Knoppers, Bartha Maria

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Corrigendum: Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility von Beauvais, Michael J. S., Thorogood, Adrian M., Szego, Michael J., Sénécal, Karine, Zawati, Ma'n H., Knoppers, Bartha Maria

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Genomic architecture of autism from comprehensive whole-genome sequence annotation von Trost, Brett, Thiruvahindrapuram, Bhooma, Chan, Ada J.S., Engchuan, Worrawat, Higginbotham, Edward J., Howe, Jennifer L., Loureiro, Livia O., Reuter, Miriam S., Roshandel, Delnaz, Whitney, Joe, Zarrei, Mehdi, Bookman, Matthew, Somerville, Cherith, Shaath, Rulan, Abdi, Mona, Aliyev, Elbay, Patel, Rohan V., Pellecchia, Giovanna, Hamdan, Omar, Kaur, Gaganjot, Wang, Zhuozhi, MacDonald, Jeffrey R., Wei, John, Sung, Wilson W.L., Lamoureux, Sylvia, Hoang, Ny, Selvanayagam, Thanuja, Deflaux, Nicole, Geng, Melissa, Ghaffari, Siavash, Bates, John, Young, Edwin J., Ding, Qiliang, Shum, Carole, D'Abate, Lia, Bradley, Clarrisa A., Rutherford, Annabel, Aguda, Vernie, Apresto, Beverly, Chen, Nan, Desai, Sachin, Du, Xiaoyan, Fong, Matthew L.Y., Pullenayegum, Sanjeev, Samler, Kozue, Wang, Ting, Ho, Karen, Paton, Tara, Pereira, Sergio L., Herbrick, Jo-Anne, Fuerth, Jonathan, Noppornpitak, Juti, Ward, Heather, Magee, Patrick, Al Baz, Ayman, Kajendirarajah, Usanthan, Vlasblom, Jim, Valluri, Monica, Green, Joseph, Seifer, Vicki, Quirbach, Morgan, Rennie, Olivia, Kelley, Elizabeth, Masjedi, Nina, Lord, Catherine, Szego, Michael J., Zawati, Ma'n H., Lang, Michael, Strug, Lisa J., Marshall, Christian R., Costain, Gregory, Calli, Kristina, Iaboni, Alana, Yusuf, Afiqah, Ambrozewicz, Patricia, Gallagher, Louise, Amaral, David G., Brian, Jessica, Elsabbagh, Mayada, Georgiades, Stelios, Messinger, Daniel S., Ozonoff, Sally, Sebat, Jonathan, Sjaarda, Calvin, Smith, Isabel M., Szatmari, Peter, Zwaigenbaum, Lonnie, Kushki, Azadeh, Frazier, Thomas W., Vorstman, Jacob A.S., Fakhro, Khalid A., Fernandez, Bridget A., Lewis, M.E. Suzanne, Weksberg, Rosanna, Fiume, Marc, Yuen, Ryan K.C., Anagnostou, Evdokia, Sondheimer, Neal, Glazer, David, Hartley, Dean M.

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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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Revisiting code status in patients undergoing GI endoscopy with a “do not resuscitate” order von Wada, Kyoko, Szego, Michael J.

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Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations von PACIONE, Laura R, SZEGO, Michael J, IKEDA, Sakae, NISHINA, Patsy M, MCINNES, Roderick R

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Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine von Stavropoulos, Dimitri J, Merico, Daniele, Jobling, Rebekah, Bowdin, Sarah, Monfared, Nasim, Thiruvahindrapuram, Bhooma, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Yuen, Ryan K C, Szego, Michael J, Hayeems, Robin Z, Shaul, Randi Zlotnik, Brudno, Michael, Girdea, Marta, Frey, Brendan, Alipanahi, Babak, Ahmed, Sohnee, Babul-Hirji, Riyana, Porras, Ramses Badilla, Carter, Melissa T, Chad, Lauren, Chaudhry, Ayeshah, Chitayat, David, Doust, Soghra Jougheh, Cytrynbaum, Cheryl, Dupuis, Lucie, Ejaz, Resham, Fishman, Leona, Guerin, Andrea, Hashemi, Bita, Helal, Mayada, Hewson, Stacy, Inbar-Feigenberg, Michal, Kannu, Peter, Karp, Natalya, Kim, Raymond H, Kronick, Jonathan, Liston, Eriskay, MacDonald, Heather, Mercimek-Mahmutoglu, Saadet, Mendoza-Londono, Roberto, Nasr, Enas, Nimmo, Graeme, Parkinson, Nicole, Quercia, Nada, Raiman, Julian, Roifman, Maian, Schulze, Andreas, Shugar, Andrea, Shuman, Cheryl, Sinajon, Pierre, Siriwardena, Komudi, Weksberg, Rosanna, Yoon, Grace, Carew, Chris, Erickson, Raith, Leach, Richard A, Klein, Robert, Ray, Peter N, Meyn, M Stephen, Scherer, Stephen W, Cohn, Ronald D, Marshall, Christian R

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Ethics Debriefs and Moral Distress: What are we Doing? von de Bie, A. Lee, Abdool, Steve, Butler, Jeremy, Campbell, Alexandra, Hassanein, Maram, Hillman, Sean, Makkar, Juhee, Maurice, Rochelle, Robertson, Jamie, Szego, Michael J., Langlois, Dave

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The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants von Reuter, Miriam S, Walker, Susan, Thiruvahindrapuram, Bhooma, Whitney, Joe, Cohn, Iris, Sondheimer, Neal, Yuen, Ryan K C, Trost, Brett, Paton, Tara A, Pereira, Sergio L, Herbrick, Jo-Anne, Wintle, Richard F, Merico, Daniele, Howe, Jennifer, MacDonald, Jeffrey R, Lu, Chao, Nalpathamkalam, Thomas, Sung, Wilson W L, Wang, Zhuozhi, Patel, Rohan V, Pellecchia, Giovanna, Wei, John, Strug, Lisa J, Bell, Sherilyn, Kellam, Barbara, Mahtani, Melanie M, Bassett, Anne S, Bombard, Yvonne, Weksberg, Rosanna, Shuman, Cheryl, Cohn, Ronald D, Stavropoulos, Dimitri J, Bowdin, Sarah, Hildebrandt, Matthew R, Wei, Wei, Romm, Asli, Pasceri, Peter, Ellis, James, Ray, Peter, Meyn, M Stephen, Monfared, Nasim, Hosseini, S Mohsen, Joseph-George, Ann M, Keeley, Fred W, Cook, Ryan A, Fiume, Marc, Lee, Hin C, Marshall, Christian R, Davies, Jill, Hazell, Allison, Buchanan, Janet A, Szego, Michael J, Scherer, Stephen W

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Organelle Transplantation Should Be Legalized in Canada von Szego, Michael J., PhD, MHSc

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Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation von Hildebrandt, Matthew R., Reuter, Miriam S., Wei, Wei, Tayebi, Naeimeh, Liu, Jiajie, Sharmin, Sazia, Mulder, Jaap, Lesperance, L. Stephen, Brauer, Patrick M., Mok, Rebecca S.F., Kinnear, Caroline, Piekna, Alina, Romm, Asli, Howe, Jennifer, Pasceri, Peter, Meng, Guoliang, Rozycki, Matthew, Rodrigues, Deivid C., Martinez, Elisa C., Szego, Michael J., Zúñiga-Pflücker, Juan C., Anderson, Michele K., Prescott, Steven A., Rosenblum, Norman D., Kamath, Binita M., Mital, Seema, Scherer, Stephen W., Ellis, James

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Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again von Szego, Michael J, Zawati, Ma'n H

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Natural antisense transcripts associated with genes involved in eye development von Alfano, Giovanna, Vitiello, Carmen, Caccioppoli, Cristina, Caramico, Tiziana, Carola, Antonietta, Szego, Michael J., McInnes, Roderick R., Auricchio, Alberto, Banfi, Sandro

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Response von Wada, Kyoko, Szego, Michael J.

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Building Trust in 21st Century Genomics von Szego, Michael J, Buchanan, Janet A, Scherer, Stephen W

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