A framework for an evidence-based gene list relevant to autism spectrum disorder von Schaaf, Christian P., Betancur, Catalina, Yuen, Ryan K. C., Parr, Jeremy R., Skuse, David H., Gallagher, Louise, Bernier, Raphael A., Buchanan, Janet A., Buxbaum, Joseph D., Chen, Chun-An, Dies, Kira A., Elsabbagh, Mayada, Firth, Helen V., Frazier, Thomas, Hoang, Ny, Howe, Jennifer, Marshall, Christian R., Michaud, Jacques L., Rennie, Olivia, Szatmari, Peter, Chung, Wendy K., Bolton, Patrick F., Cook, Edwin H., Scherer, Stephen W., Vorstman, Jacob A. S.

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Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder von C Yuen, Ryan K, Merico, Daniele, Bookman, Matt, L Howe, Jennifer, Thiruvahindrapuram, Bhooma, Patel, Rohan V, Whitney, Joe, Deflaux, Nicole, Bingham, Jonathan, Wang, Zhuozhi, Pellecchia, Giovanna, Buchanan, Janet A, Walker, Susan, Marshall, Christian R, Uddin, Mohammed, Zarrei, Mehdi, Deneault, Eric, D'Abate, Lia, Chan, Ada J S, Koyanagi, Stephanie, Paton, Tara, Pereira, Sergio L, Hoang, Ny, Engchuan, Worrawat, Higginbotham, Edward J, Ho, Karen, Lamoureux, Sylvia, Li, Weili, MacDonald, Jeffrey R, Nalpathamkalam, Thomas, Sung, Wilson W L, Tsoi, Fiona J, Wei, John, Xu, Lizhen, Tasse, Anne-Marie, Kirby, Emily, Van Etten, William, Twigger, Simon, Roberts, Wendy, Drmic, Irene, Jilderda, Sanne, Modi, Bonnie MacKinnon, Kellam, Barbara, Szego, Michael, Cytrynbaum, Cheryl, Weksberg, Rosanna, Zwaigenbaum, Lonnie, Woodbury-Smith, Marc, Brian, Jessica, Senman, Lili, Iaboni, Alana, Doyle-Thomas, Krissy, Thompson, Ann, Chrysler, Christina, Leef, Jonathan, Savion-Lemieux, Tal, Smith, Isabel M, Liu, Xudong, Nicolson, Rob, Seifer, Vicki, Fedele, Angie, Cook, Edwin H, Dager, Stephen, Estes, Annette, Gallagher, Louise, Malow, Beth A, Parr, Jeremy R, Spence, Sarah J, Vorstman, Jacob, Frey, Brendan J, Robinson, James T, Strug, Lisa J, Fernandez, Bridget A, Elsabbagh, Mayada, Carter, Melissa T, Hallmayer, Joachim, Knoppers, Bartha M, Anagnostou, Evdokia, Szatmari, Peter, Ring, Robert H, Glazer, David, Pletcher, Mathew T, Scherer, Stephen W

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Autism spectrum disorder: advances in evidence-based practice von Anagnostou, Evdokia, Zwaigenbaum, Lonnie, Szatmari, Peter, Fombonne, Eric, Fernandez, Bridget A, Woodbury-Smith, Marc, Brian, Jessica, Bryson, Susan, Smith, Isabel M, Drmic, Irene, Buchanan, Janet A, Roberts, Wendy, Scherer, Stephen W

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Research ethics recommendations for whole-genome research: consensus statement von Caulfield, Timothy, McGuire, Amy L, Cho, Mildred, Buchanan, Janet A, Burgess, Michael M, Danilczyk, Ursula, Diaz, Christina M, Fryer-Edwards, Kelly, Green, Shane K, Hodosh, Marc A, Juengst, Eric T, Kaye, Jane, Kedes, Laurence, Knoppers, Bartha Maria, Lemmens, Trudo, Meslin, Eric M, Murphy, Juli, Nussbaum, Robert L, Otlowski, Margaret, Pullman, Daryl, Ray, Peter N, Sugarman, Jeremy, Timmons, Michael

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A large data resource of genomic copy number variation across neurodevelopmental disorders von Zarrei, Mehdi, Burton, Christie L., Engchuan, Worrawat, Young, Edwin J., Higginbotham, Edward J., MacDonald, Jeffrey R., Trost, Brett, Chan, Ada J. S., Walker, Susan, Lamoureux, Sylvia, Heung, Tracy, Mojarad, Bahareh A., Kellam, Barbara, Paton, Tara, Faheem, Muhammad, Miron, Karin, Lu, Chao, Wang, Ting, Samler, Kozue, Wang, Xiaolin, Costain, Gregory, Hoang, Ny, Pellecchia, Giovanna, Wei, John, Patel, Rohan V., Thiruvahindrapuram, Bhooma, Roifman, Maian, Merico, Daniele, Goodale, Tara, Drmic, Irene, Speevak, Marsha, Howe, Jennifer L., Yuen, Ryan K. C., Buchanan, Janet A., Vorstman, Jacob A. S., Marshall, Christian R., Wintle, Richard F., Rosenberg, David R., Hanna, Gregory L., Woodbury-Smith, Marc, Cytrynbaum, Cheryl, Zwaigenbaum, Lonnie, Elsabbagh, Mayada, Flanagan, Janine, Fernandez, Bridget A., Carter, Melissa T., Szatmari, Peter, Roberts, Wendy, Lerch, Jason, Liu, Xudong, Nicolson, Rob, Georgiades, Stelios, Weksberg, Rosanna, Arnold, Paul D., Bassett, Anne S., Crosbie, Jennifer, Schachar, Russell, Stavropoulos, Dimitri J., Anagnostou, Evdokia, Scherer, Stephen W.

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Heterogeneity in clinical sequencing tests marketed for autism spectrum disorders von Hoang, Ny, Buchanan, Janet A., Scherer, Stephen W.

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Contemplating effects of genomic structural variation von Buchanan, Janet A., Scherer, Stephen W.

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Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay von Uddin, Mohammed, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, D’Abate, Lia, Merico, Daniele, Chan, Ada, Zarrei, Mehdi, Tammimies, Kristiina, Walker, Susan, Gazzellone, Matthew J., Nalpathamkalam, Thomas, Yuen, Ryan K. C., Devriendt, Koenraad, Mathonnet, Géraldine, Lemyre, Emmanuelle, Nizard, Sonia, Shago, Mary, Joseph-George, Ann M., Noor, Abdul, Carter, Melissa T., Yoon, Grace, Kannu, Peter, Tihy, Frédérique, Thorland, Erik C., Marshall, Christian R., Buchanan, Janet A., Speevak, Marsha, Stavropoulos, Dimitri J., Scherer, Stephen W.

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Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation von Gazzellone, Matthew J, Zarrei, Mehdi, Burton, Christie L, Walker, Susan, Uddin, Mohammed, Shaheen, S M, Coste, Julie, Rajendram, Rageen, Schachter, Reva J, Colasanto, Marlena, Hanna, Gregory L, Rosenberg, David R, Soreni, Noam, Fitzgerald, Kate D, Marshall, Christian R, Buchanan, Janet A, Merico, Daniele, Arnold, Paul D, Scherer, Stephen W

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Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes von Woodbury-Smith, Marc, Nicolson, Rob, Zarrei, Mehdi, Yuen, Ryan K. C., Walker, Susan, Howe, Jennifer, Uddin, Mohammed, Hoang, Ny, Buchanan, Janet A., Chrysler, Christina, Thompson, Ann, Szatmari, Peter, Scherer, Stephen W.

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Prenatal genomic microarray and sequencing in Canadian medical practice: towards consensus von Buchanan, Janet A, Chitayat, David, Kolomietz, Elena, Lee, Hin C, Scherer, Stephen W, Speevak, Marsha D, Sroka, Hana, Stavropoulos, Dimitri 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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Identification of the Cystic Fibrosis Gene: Genetic Analysis von Kerem, Bat-sheva, Rommens, Johanna M., Buchanan, Janet A., Markiewicz, Danuta, Cox, Tara K., Chakravarti, Aravinda, Buchwald, Manuel, Tsui, Lap-Chee

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Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders von Srivastava, Siddharth, Love-Nichols, Jamie A., Dies, Kira A., Ledbetter, David H., Martin, Christa L., Chung, Wendy K., Firth, Helen V., Frazier, Thomas, Hansen, Robin L., Prock, Lisa, Brunner, Han, Hoang, Ny, Scherer, Stephen W., Sahin, Mustafa, Miller, David T.

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De Novo Genome and Transcriptome Assembly of the Canadian Beaver ( Castor canadensis ) von Lok, Si, Paton, Tara A, Wang, Zhuozhi, Kaur, Gaganjot, Walker, Susan, Yuen, Ryan K C, Sung, Wilson W L, Whitney, Joseph, Buchanan, Janet A, Trost, Brett, Singh, Naina, Apresto, Beverly, Chen, Nan, Coole, Matthew, Dawson, Travis J, Ho, Karen, Hu, Zhizhou, Pullenayegum, Sanjeev, Samler, Kozue, Shipstone, Arun, Tsoi, Fiona, Wang, Ting, Pereira, Sergio L, Rostami, Pirooz, Ryan, Carol Ann, Tong, Amy Hin Yan, Ng, Karen, Sundaravadanam, Yogi, Simpson, Jared T, Lim, Burton K, Engstrom, Mark D, Dutton, Christopher J, Kerr, Kevin C R, Franke, Maria, Rapley, William, Wintle, Richard F, Scherer, Stephen W

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The cycle of genome-directed medicine von Buchanan, Janet A, Carson, Andrew R, Chitayat, David, Malkin, David, Meyn, M Stephen, Ray, Peter N, Shuman, Cheryl, Weksberg, Rosanna, Scherer, Stephen W

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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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Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay von Uddin, Mohammed, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, D'Abate, Lia, Merico, Daniele, Chan, Ada, Zarrei, Mehdi, Tammimies, Kristiina, Walker, Susan, Gazzellone, Matthew J, Nalpathamkalam, Thomas, Yuen, Ryan K.C, Devriendt, Koenraad, Mathonnet, Géraldine, Lemyre, Emmanuelle, Nizard, Sonia, Shago, Mary, Joseph-George, Ann M, Noor, Abdul, Carter, Melissa T, Yoon, Grace, Kannu, Peter, Tihy, Frédérique, Thorland, Erik C, Marshall, Christian R, Buchanan, Janet A, Speevak, Marsha, Stavropoulos, Dimitri J, Scherer, Stephen W

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Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population von Goldberg, Y.Paul, McMurray, Cynthia T., Zeisier, Jutta, Almqvist, Elisabeth, Sillence, David, Richards, Flona, Gacy, A.Marquis, Buchanan, Janet, Telenius, Hâkan, Hayden, Michael

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Mutations of the p53 gene do not occur in testis cancer von HONG-QI PENG, HOGG, D, MALKIN, D, BAILEY, D, GALLIE, B. L, MOHAMMED BULBUL, JEWETT, M, BUCHANAN, J, GOSS, P. E

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