Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease
Stanley, Kaitlin J, Kalbfleisch, Kelsey J, Moran, Olivia M, Chaturvedi, Rajiv R, Roifman, Maian, Chen, Xin, Manshaei, Roozbeh, Martin, Nicole, McDermott, Simina, McNiven, Vanda, Myles-Reid, Diane, Nield, Lynne E, Reuter, Miriam S, Schwartz, Marci L B, Shannon, Patrick, Silver, Rachel, Somerville, Cherith, Teitelbaum, Ronni, Zahavich, Laura, Bassett, Anne S, Kim, Raymond H, Mital, Seema, Chitayat, David, Jobling, Rebekah K
Published in European journal of human genetics : EJHG (01.07.2024)
Published in European journal of human genetics : EJHG (01.07.2024)
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Journal Article
P218: SMAD6 variants in congenital heart disease
Schwartz, Marci, Moran, Olivia, Chen, Xin, Manshaei, Roozbeh, Kalbfleisch, Kelsey, Kim, Raymond, Jobling, Rebekah
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Challenges experienced by genetic counselors while they provided counseling about mosaic embryos
Moran, Olivia M, Flamenbaum, Kayla, Myles Reid, Diane, McCuaig, Jeanna M, Babul-Hirji, Riyana, Chitayat, David, Roifman, Maian
Published in F&S Reports (Online) (01.12.2023)
Published in F&S Reports (Online) (01.12.2023)
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Journal Article
Predictors of mammographic density among women with a strong family history of breast cancer
Moran, Olivia, Eisen, Andrea, Demsky, Rochelle, Blackmore, Kristina, Knight, Julia A, Panchal, Seema, Ginsburg, Ophira, Zbuk, Kevin, Yaffe, Martin, Metcalfe, Kelly A, Narod, Steven A, Kotsopoulos, Joanne
Published in BMC cancer (26.06.2019)
Published in BMC cancer (26.06.2019)
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Journal Article
P228: Molecular and clinical analyses of LRP1 and LRP2 variants in human congenital cardiac left-sided lesions
Chen, Xin, Ding, Qiliang, Manshaei, Roozbeh, Schwartz, Marci, Moran, Olivia, Stanley, Kaitlin, Kim, Raymond, Jobling, Rebekah
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P169: Characterizing the phenotypic spectrum and estimated penetrance of families with pathogenic loss of function variants in the FLT4 gene
Moran, Olivia, Somerville, Cherith, Reuter, Miriam, Kalbfleisch, Kelsey, Schwartz, Marci, Chen, Xin, Manshaei, Roozbeh, Kim, Raymond, Mital, Seema, Jobling, Rebekah
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P474: Precision child health: Integrating a consultative pharmacogenetics (PGx) program into clinical care at the Hospital for Sick Children
Cohn, Iris, Moran, Olivia, Stanley, Kaitlin, Scodellaro, Sierra, Kennedy, April, Manshaei, Roozbeh, Verstegen, Ruud, Ito, Shinya, Jobling, Rebekah, Lewis, Tamorah, Kim, Raymond
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P740: DMD or not DMD? Clinical genome sequencing in the interpretation of complex copy number gains
Higginbotham, Edward, Lau, Lynette, Thiruvahindrapuram, Bhooma, MacDonald, Jeffrey, Sung, Wilson, Moran, Olivia, Hasnain, Afia, Stavropoulos, Dimitri, Bergeron, Melanie Beaulieu, Boycott, Kym, McNiven, Vanda, Chun, Kathy
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P873: “If you look for a problem, you’ll find one”: A qualitative study to understand why parents/adult patients decline secondary findings
Hansen, Abigail, Luca, Stephanie, Moran, Olivia, Babul-Hirji, Riyana, Yan, Joyce, Fooks, Katharine, Venkataramanan, Viji, Ungar, Wendy, Hayeems, Robin, Study Team, Secondary Findings, Poole, Elise, Assamad, Daniel, Banglorewala, Pooja, Vermeer, Lydia, Marshall, Christian, Gillespie, Meredith, Szuto, Anna, Chisholm, Caitlin, Stavropoulos, James, Huang, Lijia, Jarinova, Olga, Lau, Lynette, Lee, Whiwon, Badalato, Lauren, Balci, Tugce, Chad, Lauren, Inglese, Cara, Ladouceur, Virginie, Mackley, Michael, Morel, Chantal, Richer, Julie, Tarnopolsky, Mark, Villani, Anita, Zahavich, Laura, Sawyer, Sarah, Mendoza-Londono, Roberto, Somerville, Martin, Boycott, Kym, Ungar, Wendy, Hayeems, Robin
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
P866: Exploring the impact of secondary findings in a cohort of patients and families receiving genome-wide sequencing
Fooks, Katharine, Vermeer, Lydia, Poole, Elise, Luca, Stephanie, Babul-Hirji, Riyana, Chad, Lauren, Chitayat, David, Mackley, Michael, Schwartz, Marci, Ungar, Wendy, Hayeems, Robin, Study Team, Secondary Findings, Yan, Joyce, Hansen, Abigail, Venkataramanan, Viji, Assamad, Daniel, Marshall, Christian, Gillespie, Meredith, Szuto, Anna, Chisholm, Caitlin, Stavropoulos, James, Huang, Lijia, Jarinova, Olga, Lau, Lynette, Lee, Whiwon, Badalato, Lauren, Balci, Tugce, Inglese, Cara, Ladouceur, Virginie Beausejour, Morel, Chantal, Richer, Julie, Tarnopolsky, Mark, Villani, Anita, Zahavich, Laura, Moran, Olivia, Sawyer, Sarah, Mendoza-Londono, Roberto, Somerville, Martin, Boycott, Kym
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Psychometric properties of the Metacognitive Awareness Inventory (MAI): standardization to an international spanish with 12 countries
Gutierrez de Blume, Antonio P., Montoya Londoño, Diana Marcela, Jiménez Rodríguez, Virginia, Morán Núñez, Olivia, Cuadro, Ariel, Daset, Lilián, Molina Delgado, Mauricio, García de la Cadena, Claudia, Beltrán Navarro, María Beatríz, Puente Ferreras, Aníbal, Urquijo, Sebastián, Arias, Walter Lizandro
Published in Metacognition and learning (24.06.2024)
Published in Metacognition and learning (24.06.2024)
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Normative data and standardization of an international protocol for the evaluation of metacognition in Spanish-speaking university students: A cross-cultural analysis
Gutierrez de Blume, Antonio P., Montoya Londoño, Diana Marcela, Daset, Lilián, Cuadro, Ariel, Molina Delgado, Mauricio, Morán Núñez, Olivia, García de la Cadena, Claudia, Beltrán Navarro, María Beatríz, Arias Trejo, Natalia, Ramirez Balmaceda, Ana, Jiménez Rodríguez, Virginia, Puente Ferreras, Aníbal, Urquijo, Sebastián, Arias, Walter Lizandro, Rivera, Laura Inés, Schulmeyer, Marion, Rivera-Sanchez, Jesus
Published in Metacognition and learning (01.08.2023)
Published in Metacognition and learning (01.08.2023)
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Journal Article
Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel
Moran, Olivia, Nikitina, Dina, Royer, Robert, Poll, Aletta, Metcalfe, Kelly, Narod, Steven A., Akbari, Mohammad R., Kotsopoulos, Joanne
Published in Breast cancer research and treatment (2017)
Published in Breast cancer research and treatment (2017)
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Journal Article
Inauthentic Newsfeeds and Agenda Setting in a Coordinated Inauthentic Information Operation
Ehrett, Carl, Linvill, Darren L., Smith, Hudson, Warren, Patrick L., Bellamy, Leya, Moawad, Marianna, Moran, Olivia, Moody, Monica
Published in Social science computer review (01.12.2022)
Published in Social science computer review (01.12.2022)
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Journal Article
Abstract B12: The effect of physical activity and body size on mammographic density in high-risk, BRCA mutation-negative women
Moran, Olivia M., Nikitina, Dina, Gunasekara, Anoma, Yaffe, Martin J., Metcalfe, Kelly A., Narod, Steven A., Kotsopoulos, Joanne
Published in Cancer epidemiology, biomarkers & prevention (01.05.2017)
Published in Cancer epidemiology, biomarkers & prevention (01.05.2017)
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Journal Article
Serum osteoprotegerin levels and mammographic density among high-risk women
Moran, Olivia, Zaman, Tasnim, Eisen, Andrea, Demsky, Rochelle, Blackmore, Kristina, Knight, Julia A., Elser, Christine, Ginsburg, Ophira, Zbuk, Kevin, Yaffe, Martin, Narod, Steven A., Salmena, Leonardo, Kotsopoulos, Joanne
Published in Cancer causes & control (01.06.2018)
Published in Cancer causes & control (01.06.2018)
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