Non-Genetic Healthcare Providers' Experiences and Perspectives with Rapid Genome-Wide Sequencing in Canadian Neonatal Intensive Care Units von Piers, Lauren, Wainstein, Tasha, Pelligra, Gustavo, Osiovich, Horacio, GenCOUNSEL Study, Elliott, Alison M

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P823: Insights and strategies for inclusive adolescent and young adult participation in genetics research von Wainstein, Tasha, Cook, Courtney, Assamad, Daniel, Heaton, Julia, Randhawa, Manraj, Yeung, David, Jennings, Lauren, Hayeems, Robin, Chhina, Harpreet, Cooper, Anthony, Study, GenCOUNSEL, Austin, Jehannine, Elliott, Alison

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P531: Developing the patient-reported Genetic testing Utility InDEx (P-GUIDE): Assessing value of genetic testing from patients’ perspectives in multiple clinical contexts von Poole, Elise, Luca, Stephanie, Assamad, Daniel, Xiao, Bowen, Yan, Joyce, Banglorewala, Pooja, Xia, Cheryl, Ungar, Wendy, Abbott, Lesleigh, Armstrong, Linlea, Birch, Patricia, Boycott, Kym, Carroll, June, Chad, Lauren, Chitayat, David, Denburg, Avram, Deyell, Rebecca, Elliott, Alison, Goudie, Catherine, Laberge, Anne-Marie, Maio, Melissa, Peltekova, Iskra, Quinlan, Becky, Sawyer, Sarah, Silver, Rachel, Smith, Maureen, Teitelbaum, Ronni, Villani, Anita, Wainstein, Tasha, Hayeems, Robin

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Far and wide: Exploring provider utilization of remote service provision for genome‐wide sequencing in Canada von Enns, Emily A., Wainstein, Tasha, Dragojlovic, Nick, Kopac, Nicola, Lynd, Larry D., Elliott, Alison M.

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Considerations for the use of qualitative methodologies in genetic counseling research von Wainstein, Tasha, Elliott, Alison M., Austin, Jehannine C.

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Adolescents' implicit and explicit attitudes toward their peers with genetic conditions von Wainstein, Tasha, Yeung, David, Jennings, Lauren, Elliott, Alison M.

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Promoting methodological integrity in qualitative genetic counseling research: Insights arising from the commentary by Lynch, Gillam, and Vears von Wainstein, Tasha, Elliott, Alison M., Austin, Jehannine C.

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Exploring genetic counselors' experiences with non-paternity in clinical settings von Cunningham, Emma, Hays, Stephen, Wainstein, Tasha, Zierhut, Heather, Virani, Alice, Tryon, Rebecca

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Review of 10 years of preimplantation genetic diagnosis in South Africa: implications for a low-to-middle-income country von Carzis, Bianca, Wainstein, Tasha, Gobetz, Lawrence, Krause, Amanda

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The experiences of adolescent siblings of children with rare genetic conditions: “It's made me who I am” von Heaton, Julia, Wainstein, Tasha, Elliott, Alison M., Austin, Jehannine

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Genetic counselors' research dissemination practices and attitudes von Blanche, Emma, Wainstein, Tasha, Dey, Alivia, Elliott, Alison M.

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Implementing genomics in the neonatal period: An assessment of parental decision making and anxiety von Wainstein, Tasha, Campbell, Teresa, Stojkova, Biljana J., Lavoie, Pascal M., Elliott, Alison M.

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Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia von Feben, Candice, Spencer, Careni, Lochan, Anneline, Laing, Nakita, Fieggen, Karen, Honey, Engela, Wainstein, Tasha, Krause, Amanda

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A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation von Macfadyen, Leah P., Austin, Jehannine, Cao, Ping, Cheng, John, Cremin, Carol, Duong, Linda, Elliott, Alison M., Guimond, Colleen, Lim, Shur, Race, Simone, Rajan‐Babu, Indhu‐Shree, Richardson, Anastasia, Wainstein, Tasha, Zahir, Farah, Birch, Patricia H.

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Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient? von Seymour, Heather Jessica, Wainstein, Tasha, Macaulay, Shelley, Haw, Tabitha, Krause, Amanda

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Testing for haemoglobinopathies in Johannesburg, South Africa: a 30-year review von Krause, Amanda, Wainstein, Tasha, Essop, Fahmida B, Goodyear, Quintin

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Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation von Wainstein, Tasha, Kerr, Robyn, Mitchell, Claire L, Madaree, Smita, Essop, Fahmida B, Vorster, Elana, Wainwright, Rosalind, Poole, Janet, Krause, Amanda

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