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Clinical Actionability of Genetic Findings in Cerebral Palsy: A Systematic Review and Meta-Analysis Lewis, Sara A.; Chopra, Maya; Cohen, Julie S.; Bain, Jennifer M.; Aravamuthan, Bhooma; Carmel, Jason B.; Fahey, Michael C.; Segel, Reeval; Wintle, Richard F.; Zech, Michael; May, Halie; Haque, Nahla; Fehlings, Darcy; Srivastava, Siddharth; Kruer, Michael C. Share Save
Chromosomal-level reference genome assembly of muskox (Ovibos moschatus) from Banks Island in the Canadian Arctic, a resource for conservation genomics Lok, Si; Lau, Timothy N. H.; Trost, Brett; Tong, Amy H. Y.; Paton, Tara; Wintle, Richard F.; Engstrom, Mark D.; Gunn, Anne; Scherer, Stephen W. Share Save
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy Fehlings, Darcy L.; Zarrei, Mehdi; Engchuan, Worrawat; Sondheimer, Neal; Thiruvahindrapuram, Bhooma; MacDonald, Jeffrey R.; Higginbotham, Edward J.; Thapa, Ritesh; Behlim, Tarannum; Aimola, Sabrina; Switzer, Lauren; Ng, Pamela; Wei, John; Danthi, Prakroothi S.; Pellecchia, Giovanna; Lamoureux, Sylvia; Ho, Karen; Pereira, Sergio L.; de Rijke, Jill; Sung, Wilson W. L.; Mowjoodi, Alireza; Howe, Jennifer L.; Nalpathamkalam, Thomas; Manshaei, Roozbeh; Ghaffari, Siavash; Whitney, Joseph; Patel, Rohan V.; Hamdan, Omar; Shaath, Rulan; Trost, Brett; Knights, Shannon; Samdup, Dawa; McCormick, Anna; Hunt, Carolyn; Kirton, Adam; Kawamura, Anne; Mesterman, Ronit; Gorter, Jan Willem; Dlamini, Nomazulu; Merico, Daniele; Hilali, Murto; Hirschfeld, Kyle; Grover, Kritika; Bautista, Nelson X.; Han, Kara; Marshall, Christian R.; Yuen, Ryan K. C.; Subbarao, Padmaja; Azad, Meghan B.; Turvey, Stuart E.; Mandhane, Piush; Moraes, Theo J.; Simons, Elinor; Maxwell, George; Shevell, Michael; Costain, Gregory; Michaud, Jacques L.; Hamdan, Fadi F.; Gauthier, Julie; Uguen, Kevin; Stavropoulos, Dimitri J.; Wintle, Richard F.; Oskoui, Maryam; Scherer, Stephen W. Share Save
Gene copy number variation and pediatric mental health/neurodevelopment in a general population Zarrei, Mehdi; Burton, Christie L.; Engchuan, Worrawat; Higginbotham, Edward J.; Wei, John; Shaikh, Sabah; Roslin, Nicole M.; MacDonald, Jeffrey R.; Pellecchia, Giovanna; Nalpathamkalam, Thomas; Lamoureux, Sylvia; Manshaei, Roozbeh; Howe, Jennifer; Trost, Brett; Thiruvahindrapuram, Bhooma; Marshall, Christian R.; Yuen, Ryan K. C.; Wintle, Richard F.; Strug, Lisa J.; Stavropoulos, Dimitri J.; Vorstman, Jacob A. S.; Arnold, Paul; Merico, Daniele; Woodbury-Smith, Marc; Crosbie, Jennifer; Schachar, Russell J.; Scherer, Stephen W. Share Save
Whole Genome Sequencing to Resolve the Genomic Architecture of Cerebral Palsy in a Canadian Cohort Oskoui, Maryam; Zarrei, Mehdi; Engchuan, Worrawat; Sondheimer, Neal; Thiruv, Bhooma; Higginbotham, Edward; Thapa, Ritesh; Behlim, Tarannum; Aimola, Sabrina; Wei, John; Danthi, Prakroothi; Pellecchia, Giovanna; Ho, Karen; de Rijke, Jill; Howe, Jennifer; Nalpathamkalam, Thomas; Manshaei, Roozbeh; Whitney, Joseph; Patel, Rohan; Hamdan, Omar; Shaath, Rulan; Knights, Shannon; Trost, Brett; Samdup, Dawa; Mccormick, Anna; Hunt, Carolyn; Kirton, Adam; Kawamura, Anne; Mesterman, Ronit; Gorter, Jan Willem; Dlamini, Nomazulu; Merico, Daniele; Yuen, Ryan; Shevell, Michael; Stavropoulos, Dimitri; Wintle, Richard; Fehlings, Darcy; Scherer, Stephen Share Save
The development of the pediatric stroke neuroimaging platform (PEDSNIP) Domi, Trish; Robertson, Amanda; Lee, Wayne; Wintle, Richard F.; Stence, Nicholas; Bernard, Timothy; Kirton, Adam; Carlson, Helen; Andrade, Andrea; Rafay, Mubeen F.; Bjornson, Bruce; Kim, Danny; Dowling, Michael; Bonnett, Wilmot; Rivkin, Michael; Krishnan, Pradeep; Shroff, Manohar; Ertl-Wagner, Birgit; Strother, Stephen; Arnott, Steven; Wintermark, Max; Kassner, Andrea; Deveber, Gabrielle; Dlamini, Nomazulu Share Save
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants 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. Share Save
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy Zarrei, Mehdi; Fehlings, Darcy L.; Mawjee, Karizma; Switzer, Lauren; Thiruvahindrapuram, Bhooma; Walker, Susan; Merico, Daniele; Casallo, Guillermo; Uddin, Mohammed; MacDonald, Jeffrey R.; Gazzellone, Matthew J.; Higginbotham, Edward J.; Campbell, Craig; deVeber, Gabrielle; Frid, Pam; Gorter, Jan Willem; Hunt, Carolyn; Kawamura, Anne; Kim, Marie; McCormick, Anna; Mesterman, Ronit; Samdup, Dawa; Marshall, Christian R.; Stavropoulos, Dimitri J.; Wintle, Richard F.; Scherer, Stephen W. Share Save
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A high-resolution copy-number variation resource for clinical and population genetics Uddin, Mohammed; Thiruvahindrapuram, Bhooma; Walker, Susan; Wang, Zhuozhi; Hu, Pingzhao; Lamoureux, Sylvia; Wei, John; MacDonald, Jeffrey R.; Pellecchia, Giovanna; Lu, Chao; Lionel, Anath C.; Gazzellone, Matthew J.; McLaughlin, John R.; Brown, Catherine; Andrulis, Irene L.; Knight, Julia A.; Herbrick, Jo-Anne; Wintle, Richard F.; Ray, Peter; Stavropoulos, Dimitri J.; Marshall, Christian R.; Scherer, Stephen W. Share Save
Clinically relevant copy number variations detected in cerebral palsy Oskoui, Maryam; Gazzellone, Matthew J.; Thiruvahindrapuram, Bhooma; Zarrei, Mehdi; Andersen, John; Wei, John; Wang, Zhuozhi; Wintle, Richard F.; Marshall, Christian R.; Cohn, Ronald D.; Weksberg, Rosanna; Stavropoulos, Dimitri J.; Fehlings, Darcy; Shevell, Michael I.; Scherer, Stephen W. Share Save
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome Marshall, Christian R.; Farrell, Sandra A.; Cushing, Donna; Paton, Tara; Stockley, Tracy L.; Stavropoulos, Dimitri J.; Ray, Peter N.; Szego, Michael; Lau, Lynette; Pereira, Sergio L.; Cohn, Ronald D.; Wintle, Richard F.; Abuzenadah, Adel M.; Abu-Elmagd, Muhammad; Scherer, Stephen W. Share Save
FORGE Canada Consortium: Outcomes of a 2-Year National Rare-Disease Gene-Discovery Project Beaulieu, Chandree L.; Majewski, Jacek; Schwartzentruber, Jeremy; Samuels, Mark E.; Femandez, Bridget A.; Bernier, Francois P.; Brudno, Michael; Knoppers, Bartha; Marcadier, Janet; Dyment, David; Adam, Shelin; Bulman, Dennis E.; Jones, Steve J. M.; Avard, Denise; Minh Thu Nguyen; Rousseau, Francois; Marshall, Christian; Wintle, Richard F.; Shen, Yaoqing; Scherer, Stephen W.; Friedman, Jan M.; Michaud, Jacques L.; Boycott, Kym M. Share Save
A Genotype Resource for Postmortem Brain Samples From the Autism Tissue Program (vol 4, pg 89, 2011) Wintle, Richard F.; Lionel, Anath C.; Hu, Pingzhao; Ginsberg, Stephen D.; Pinto, Dalila; Thiruvahindrapduram, Bhooma; Wei, John; Marshall, Christian R.; Pickett, Jane; Cook, Edwin H.; Scherer, Stephen W. Share Save
A Genotype Resource for Postmortem Brain Samples from the Autism Tissue Program Wintle, Richard F.; Lionel, Anath C.; Hu, Pingzhao; Ginsberg, Stephen D.; Pinto, Dalila; Thiruvahindrapduram, Bhooma; Wei, John; Marshall, Christian R.; Pickett, Jane; Cook, Edwin H.; Scherer, Stephen W. Share Save
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