Bibliotecas PUC-SP - Busca Integrada

P133: CNS hemangioblastoma in pediatric patients with von Hippel–Lindau disease: When to start surveillance*

由 Yoshiko Nakano, Bailey Gallinger, Rosemarie Vnier, Abhaya Kulkarni, Peter Dirks, James Rutka, Jonathan Wasserman, Anita Villani, David Malkin
發表在 Genetics in Medicine Open (2024-01-01)

P080: Comprehensive overview and analysis of a longstanding pediatric cancer genetics program

由 Bailey Gallinger, Yoshiko Nakano, Kimberly Caswell, Harriet Drucker, Alexandria Mansfield, Jonathan Wasserman, Rosanna Weksberg, Rosemarie Venier, Yiming Wang, David Malkin, Anita Villani
發表在 Genetics in Medicine Open (2024-01-01)

P563: Adolescents’ experiences and perspectives of genetic testing and its personal utility

由 Daniel Assamad, Stephanie Luca, Elise Poole, Lucie Dupuis, Riyana Babul-Hirji, Kelsey Kalbfleisch, Rosemarie Venier, Bailey Gallinger, Laura Zahavich, Meredith Gillespie, Reem Rafei, Stella MacDonald, Tillie Chiu, Kelly Anderson, Connie Ens, Lauren Chad, Wendy Ungar, Tasha Wainstein, Alison Elliott, Robin Hayeems
發表在 Genetics in Medicine Open (2025-01-01)

P054: Creation of the Ontario Hereditary Cancer Research Network (OHCRN)

由 Lauren Hughes, Kirsten Farncombe, Michelle Brazas, Melyssa Aronson, Kathleen Bell, Brandon Chan, Andrea Eisen, Harriet Feilotter, Bailey Gallinger, Jordan Lerner-Ellis, David Malkin, Ellen MacDougall, Steven Narod, Karen Panabaker, Trevor Pugh, Sarah Sawyer, Alison Rusnak, Andrea Vaags, Laszlo Radvanyi, Lincoln Stein, Raymond Kim
發表在 Genetics in Medicine Open (2023-01-01)

P103: Operationalizing structured curated scientific literature (CIViC and Hypothesis) in developing gene-specific recommendations of the ClinGen VHL Variant Curation Expert Panel

由 Deborah Ritter, Chansonette Badduke, Michael Anderson, Arpad Danos, Kurston Doonanco, Kirsten Farncombe, Bailey Gallinger, Rachel Giles, Malachi Griffith, Obi Griffith, Carolyn Horton, Kathleen Hruska, Hio Chung Kang, Kilannin Krysiak, Minjie Luo, Jerry Machado, Eamonn Maher, Kelly McGoldrick, Tina Pesaran, Neta Pipko, Sarah Ridd, Jason Saliba, Clare Sheen, Raymond Kim
發表在 Genetics in Medicine Open (2024-01-01)

How does personal utility depend on clinical setting? Evidence from 3 cohorts

由 Elise Poole, Stephanie Luca, Daniel Assamad, Bowen Xiao, Joyce Yan, Yue Yin Xia, Lesleigh S. Abbott, Linlea Armstrong, Patricia Birch, Kym M. Boycott, June C. Carroll, Lauren Chad, David Chitayat, Avram Denburg, Rebecca J. Deyell, Alison M. Elliott, Catherine Goudie, Anne-Marie Laberge, Melissa Maio, Iskra T. Peltekova, Becky Quinlan, Sarah L. Sawyer, Rachel Silver, Maureen Smith, Ronni Teitelbaum, Anita Villani, Wendy J. Ungar, Robin Z. Hayeems, Andrea Staines, Bailey Gallinger, Claire Newman, Elisabeth Soubry, Grace Tam, Gregory Costain, Kimberly Seath, Kristal Louie, Nada Quercia, Nicole Gojska, Olivia M. Moran, Rosemarie E. Venier, Simina McDermott, Stephanie Hedges, Tami Uster, Tithi Paul
發表在 Genetics in Medicine Open (2025-01-01)

Development of the Ontario Hereditary Cancer Research Network, a unified registry as a resource for individuals with inherited cancer syndromes: an observational registry creation...

由 Vasily Giannakeas, Amanda Smith, Hong Wang, Harriet Feilotter, Melyssa Aronson, Andrea Eisen, Raymond H Kim, Jordan Lerner-Ellis, Steven A Narod, Laszlo Radvanyi, Kathleen Bell, Jane Bayani, Ian King, DAVID MALKIN, Kathy Chun, Irene L Andrulis, Bailey Gallinger, Anita Villani, George Charames, Lincoln Stein, Sarah Sawyer, Karen Panabaker, Philip Awadalla, Trevor Pugh, Mohammad Reza Akbari, Peter Goodhand, Brandon Chan, Yael Silberman, Jennifer Brooks, Melanie Spears, Kirsten M Farncombe, Lauren K Hughes, Elif Tuzlali, Michelle D Brazas, Melissa Cable-Cibula, Melanie Courtot, Jamie Harland, Katie Lark, Ellen MacDougall, Alison Rusnak, Christopher Deutschman, Chiquita Hessels, Brittney Johnstone, Talia Mancuso, Kelly McDonald, Meredith McLaren, Karen Ott, Stephen Parrott, Wendy Parulekar, Aaron Pollet, Laila Schenkel, Larissa Waldman, Martin Yaffe
發表在 BMJ Open (2024-11-01)