Development of a storytelling communication facilitation tool (SCFT) to facilitate discussion of complex genetic diagnoses between parents and their children: A pilot study using 22q11.2 deletion syndrome as a model condition
Bogatan, Simina, Shugar, Andrea, Wasim, Syed, Ball, Susan, Schmidt, Cathryn, Chitayat, David, Shuman, Cheryl, Cytrynbaum, Cheryl
Published in PEC innovation (01.12.2023)
Published in PEC innovation (01.12.2023)
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Journal Article
The mental health and traumatic experiences of mothers of children with 22q11DS
Finless, Alexandra, Rideout, Andrea L, Xiong, Ting, Carbyn, Holly, Lingley-Pottie, Patricia, Palmer, Lisa D, Shugar, Andrea, McDonald-McGinn, Donna M, McGrath, Patrick J, Bassett, Anne S, Cytrynbaum, Cheryl, Orr, Matt, Swillen, Ann, Meier, Sandra
Published in European journal of psychotraumatology (2024)
Published in European journal of psychotraumatology (2024)
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Journal Article
Carrier Screening for Thalassemia and Hemoglobinopathies in Canada
Langlois, Sylvie, MD, Ford, Jason C., MD, Chitayat, David, MD, Désilets, Valerie A., MD, Farrell, Sandra A., MD, Geraghty, Michael, MD, Nelson, Tanya, PhD, Nikkel, Sarah M., MD, Shugar, Andrea, MSc, Skidmore, David, MD, Allen, Victoria M., MD, Audibert, François, MD, Blight, Claire, RN, Désilets, Valérie A., MD, Gagnon, Alain, MD, Johnson, Jo-Ann, MD, Douglas Wilson, R., MD, Wyatt, Philip, MD
Published in Journal of obstetrics and gynaecology Canada (01.10.2008)
Published in Journal of obstetrics and gynaecology Canada (01.10.2008)
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Journal Article
Prenatal screening for fetal aneuploidy
Summers, Anne M, Langlois, Sylvie, Wyatt, Phil, Douglas Wilson, R
Published in Journal of obstetrics and gynaecology Canada (01.02.2007)
Published in Journal of obstetrics and gynaecology Canada (01.02.2007)
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Journal Article
Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification
Stachon, Andrea C., Baskin, Berivan, Smith, Adam C., Shugar, Andrea, Cytrynbaum, Cheryl, Fishman, Leona, Mendoza-Londono, Roberto, Klatt, Regan, Teebi, Ahmed, Ray, Peter N., Weksberg, Rosanna
Published in American journal of medical genetics. Part A (15.12.2007)
Published in American journal of medical genetics. Part A (15.12.2007)
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Journal Article
Identification of SPRED1 deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR
Spencer, Emily, Davis, Julia, Mikhail, Fady, Fu, Chuanhua, Vijzelaar, Raymon, Zackai, Elaine H, Feret, Holly, Meyn, M Stephen, Shugar, Andrea, Bellus, Gary, Kocsis, Kristina, Kivirikko, Sirpa, Pöyhönen, Minna, Messiaen, Ludwine
Published in American journal of medical genetics. Part A (01.06.2011)
Published in American journal of medical genetics. Part A (01.06.2011)
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Journal Article
eP325 - Genetics simulation as a safe training tool for high-stakes conversations
Saleh, Maha, Shugar, Andrea, Bismilla, Zia
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Genetics simulation as a safe training tool for high-stakes conversations
Saleh, Maha, Shugar, Andrea, Bismilla, Zia
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Fragile X Testing in Obstetrics and Gynaecology in Canada
Chitayat, David, MD, Wyatt, Philip R., MD, Wilson, R. Douglas, Johnson, Jo-Ann, MD, Audibert, François, MD, Allen, Victoria, MD, Gagnon, Alain, MD, Langlois, Sylvie, MD, Blight, Claire, RN, Brock, Jo-Ann, MD, Désilets, Valerie, MD, Langlois, Sylvie, Désilets, Valerie A., MD, Farrell, Sandra A., MD, Geraghty, Michael, MD, Nelson, Tanya, PhD, Nikkel, Sarah M., MD, Skidmore, David, MD, Shugar, Andrea, MSc
Published in Journal of obstetrics and gynaecology Canada (01.09.2008)
Published in Journal of obstetrics and gynaecology Canada (01.09.2008)
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Journal Article
Practical guidelines for managing adults with 22q11.2 deletion syndrome
Fung, Wai Lun Alan, Butcher, Nancy J., Costain, Gregory, Andrade, Danielle M., Boot, Erik, Chow, Eva W.C., Chung, Brian, Cytrynbaum, Cheryl, Faghfoury, Hanna, Fishman, Leona, García-Miñaúr, Sixto, George, Susan, Lang, Anthony E., Repetto, Gabriela, Shugar, Andrea, Silversides, Candice, Swillen, Ann, van Amelsvoort, Therese, McDonald-McGinn, Donna M., Bassett, Anne S.
Published in Genetics in medicine (01.08.2015)
Published in Genetics in medicine (01.08.2015)
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Journal Article
Genetic simulation for high‐stakes conversations
Saleh, Maha, Shugar, Andrea, Dodds, Alison, Bismilla, Zia
Published in The clinical teacher (01.06.2022)
Published in The clinical teacher (01.06.2022)
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Journal Article
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
Koczkowska, Magdalena, Callens, Tom, Gomes, Alicia, Sharp, Angela, Chen, Yunjia, Hicks, Alesha D., Aylsworth, Arthur S., Azizi, Amedeo A., Basel, Donald G., Bellus, Gary, Bird, Lynne M., Blazo, Maria A., Burke, Leah W., Cannon, Ashley, Collins, Felicity, DeFilippo, Colette, Denayer, Ellen, Digilio, Maria C., Dills, Shelley K., Dosa, Laura, Greenwood, Robert S., Griffis, Cristin, Gupta, Punita, Hachen, Rachel K., Hernández-Chico, Concepción, Janssens, Sandra, Jones, Kristi J., Jordan, Justin T., Kannu, Peter, Korf, Bruce R., Lewis, Andrea M., Listernick, Robert H., Lonardo, Fortunato, Mahoney, Maurice J., Ojeda, Mayra Martinez, McDonald, Marie T., McDougall, Carey, Mendelsohn, Nancy, Miller, David T., Mori, Mari, Oostenbrink, Rianne, Perreault, Sebastién, Pierpont, Mary Ella, Piscopo, Carmelo, Pond, Dinel A., Randolph, Linda M., Rauen, Katherine A., Rednam, Surya, Rutledge, S. Lane, Saletti, Veronica, Schaefer, G. Bradley, Schorry, Elizabeth K., Scott, Daryl A., Shugar, Andrea, Siqveland, Elizabeth, Starr, Lois J., Syed, Ashraf, Trapane, Pamela L., Ullrich, Nicole J., Wakefield, Emily G., Walsh, Laurence E., Wangler, Michael F., Zackai, Elaine, Claes, Kathleen B. M., Wimmer, Katharina, van Minkelen, Rick, De Luca, Alessandro, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine M.
Published in Genetics in medicine (01.04.2019)
Published in Genetics in medicine (01.04.2019)
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Journal Article
A novel ENPP1 mutation identified in a multigenerational family affected by Cole disease
Gabaton, Niña, Kannu, Peter, Pope, Elena, Shugar, Andrea, Lara‐Corrales, Irene
Published in Pediatric dermatology (01.09.2020)
Published in Pediatric dermatology (01.09.2020)
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