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Where there is no genetic counselor: An online decision-aid supports the majority of parents' diagnostic genomic testing choices for their children Birch, Patricia; Beauchesne, Rhea; Bansback, Nick; Boelman, Cyrus; Connolly, Mary; Demos, Michelle; Friedman, Jan M.; Race, Simone; Stockler, Sylvia; Elliott, Alison M.; Adam, Shelin Share Save
Health Care Costs After Genome-Wide Sequencing for Children With Rare Diseases in England and Canada Weymann, Deirdre; Buckell, John; Fahr, Patrick; Loewen, Rosalie; Ehman, Morgan; Pollard, Samantha; Friedman, Jan M.; Stockler-Ipsiroglu, Sylvia; Elliott, Alison M.; Wordsworth, Sarah; Buchanan, James; Regier, Dean A. Share Save
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Real-world diagnostic outcomes and cost-effectiveness of genome-wide sequencing for developmental and seizure disorders: Evidence from Canada Regier, Dean A.; Loewen, Rosalie; Chan, Brandon; Ehman, Morgan; Pollard, Samantha; Friedman, Jan M.; Stockler-Ipsiroglu, Sylvia; van Karnebeek, Clara; Race, Simone; Elliott, Alison M.; Dragojlovic, Nick; Lynd, Larry D.; Weymann, Deirdre Share Save
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Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study Elliott, Alison M.; Adam, Shelin; du Souich, Christele; Lehman, Anna; Nelson, Tanya N.; van Karnebeek, Clara; Alderman, Emily; Armstrong, Linlea; Aubertin, Gudrun; Blood, Katherine; Boelman, Cyrus; Boerkoel, Cornelius; Bretherick, Karla; Brown, Lindsay; Chijiwa, Chieko; Clarke, Lorne; Couse, Madeline; Creighton, Susan; Watts-Dickens, Abby; Gibson, William T.; Gill, Harinder; Tarailo-Graovac, Maja; Hamilton, Sara; Heran, Harindar; Horvath, Gabriella; Huang, Lijia; Hulait, Gurdip K.; Koehn, David; Lee, Hyun Kyung; Lewis, Suzanne; Lopez, Elena; Louie, Kristal; Niederhoffer, Karen; Matthews, Allison; Meagher, Kirsten; Peng, Junran J.; Patel, Millan S.; Race, Simone; Richmond, Phillip; Rupps, Rosemarie; Salvarinova, Ramona; Seath, Kimberly; Selby, Kathryn; Steinraths, Michelle; Stockler, Sylvia; Tang, Kaoru; Tyson, Christine; van Allen, Margot; Wasserman, Wyeth; Mwenifumbo, Jill; Friedman, Jan M. Share Save
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Utilization and uptake of clinical genetics services in high-income countries: A scoping review Dragojlovic, Nick; Kopac, Nicola; Borle, Kennedy; Tandun, Rachel; Salmasi, Shahrzad; Ellis, Ursula; Birch, Patricia; Adam, Shelin; Friedman, Jan M.; Elliott, Alison M.; Lynd, Larry D. Share Save
Toward the diagnosis of rare childhood genetic diseases: what do parents value most? (Apr, 10.1038/s41431-021-00925-7, 2021) Pollard, Samantha; Weymann, Deirdre; Dunne, Jessica; Mayanloo, Fatemeh; Buckell, John; Buchanan, James; Wordsworth, Sarah; Friedman, Jan M.; Stockler-Ipsiroglu, Sylvia; Dragojlovic, Nick; Elliott, Alison M.; Harrison, Mark; Lynd, Larry D.; Regier, Dean A. Share Save
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder Szot, Justin O.; Slavotinek, Anne; Chong, Karen; Brandau, Oliver; Nezarati, Marjan; Cueto-Gonzalez, Anna M.; Patel, Millan S.; Devine, Walter P.; Rego, Shannon; Acyinena, Alicia P.; Shannon, Patrick; Myles-Reid, Diane; Blaser, Susan; Mieghem, Tim V.; Yavuz-Kienle, Halenur; Skladny, Heyko; Miller, Kristen; Riera, Miereia D. T.; Martinez, Silvia A.; Tizzano, Eduardo F.; Dupuis, Lucie; James Stavropoulos, Dimitri; McNiven, Vanda; Mendoza-Londono, Roberto; Elliott, Alison M.; Phillips, Robert S.; Chapman, Gavin; Dunwoodie, Sally L. Share Save
Toward the diagnosis of rare childhood genetic diseases: what do parents value most? Pollard, Samantha; Weymann, Deirdre; Dunne, Jessica; Mayanloo, Fatemeh; Buckell, John; Buchanan, James; Wordsworth, Sarah; Friedman, Jan M.; Stockler-Ipsiroglu, Sylvia; Dragojlovic, Nick; Elliott, Alison E.; Harrison, Mark; Lynd, Larry D.; Regier, Dean A. Share Save
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Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES Study Elliott, Alison M.; Dragojlovic, Nick; Campbell, Teresa; Adam, Shelin; Souich, Christele du; Fryer, Michele; Lehman, Anna; Karnebeek, Clara van; Lynd, Larry D.; Friedman, Jan M. Share Save
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