Prenatal biochemical screening and long term risk of maternal cardiovascular disease: population based cohort study

por Ray, Joel G, Huang, Tianhua, Meschino, Wendy S, Cohen, Eyal, Park, Alison L
Publicado 2018

Prenatal Biochemical Screening and a Woman’s Long-Term Risk of Cancer: A Population-Based Cohort Study

por Park, Alison L, Huang, Tianhua, Meschino, Wendy S, Iqbal, Javaid, Ray, Joel G
Publicado 2019

Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray

por Soster, Erica, Tynan, John, Gibbons, Clare, Meschino, Wendy, Wardrop, Jenna, Almasri, Eyad, Schwartz, Stuart, McLennan, Graham
Publicado 2023

Feasibility of computerized working memory training in individuals with Huntington disease

por Sadeghi, Mahsa, Barlow-Krelina, Emily, Gibbons, Clare, Shaikh, Komal T., Fung, Wai Lun Alan, Meschino, Wendy S., Till, Christine
Publicado 2017

Prenatal screening for trisomy 21: a comparative performance and cost analysis of different screening strategies

por Huang, Tianhua, Gibbons, Clare, Rashid, Shamim, Priston, Megan K., Bedford, H. Melanie, Mak-Tam, Ellen, Meschino, Wendy S.
Publicado 2020

Genetic assessment wait time indicators in the High Risk Ontario Breast Screening Program

por Eisen, Andrea, Blackmore, Kristina M., Meschino, Wendy S., Muradali, Derek, Carroll, June C., Majpruz, Vicky, Warner, Ellen, Rabeneck, Linda, Chiarelli, Anna M.
Publicado 2018

Real-world health services utilisation and outcomes after BRCA1 and BRCA2 testing in Ontario, Canada: the What Comes Next Cohort Study protocol

por Dossa, Fahima, Cusimano, Maria C, Sutradhar, Rinku, Metcalfe, Kelly, Little, Tari, Lerner-Ellis, Jordan, Eisen, Andrea, Meschino, Wendy S, Baxter, Nancy N
Publicado 2018

Building the What Comes Next Cohort for BRCA1 and BRCA2 testing: a descriptive analysis

por Dossa, Fahima, Metcalfe, Kelly, Sutradhar, Rinku, Little, Tari, Eisen, Andrea, Chun, Kathy, Meschino, Wendy S., Velsher, Lea, Ellis, Jordan Lerner, Baxter, Nancy N.
Publicado 2021

Modified multiple marker aneuploidy screening as a primary screening test for preeclampsia

por Huang, Tianhua, Bedford, H. Melanie, Rashid, Shamim, Rasasakaram, Evasha, Priston, Megan, Mak-Tam, Ellen, Gibbons, Clare, Meschino, Wendy S., Cuckle, Howard, Mei-Dan, Elad
Publicado 2022

Development and validation of a brief screening instrument for psychosocial risk associated with genetic testing: a pan-Canadian cohort study

por Esplen, Mary Jane, Cappelli, Mario, Wong, Jiahui, Bottorff, Joan L, Hunter, Jon, Carroll, June, Dorval, Michel, Wilson, Brenda, Allanson, Judith, Semotiuk, Kara, Aronson, Melyssa, Bordeleau, Louise, Charlemagne, Nicole, Meschino, Wendy
Publicado 2013

Supporting genetics in primary care: investigating how theory can inform professional education

por Wilson, Brenda J, Islam, Rafat, Francis, Jill J, Grimshaw, Jeremy M, Permaul, Joanne A, Allanson, Judith E, Blaine, Sean, Graham, Ian D, Meschino, Wendy S, Ramsay, Craig R, Carroll, June C
Publicado 2016

International trends in the uptake of cancer risk reduction strategies in women with a BRCA1 or BRCA2 mutation

por Metcalfe, Kelly, Eisen, Andrea, Senter, Leigha, Armel, Susan, Bordeleau, Louise, Meschino, Wendy S., Pal, Tuya, Lynch, Henry T., Tung, Nadine M., Kwong, Ava, Ainsworth, Peter, Karlan, Beth, Moller, Pal, Eng, Charis, Weitzel, Jeffrey N., Sun, Ping, Lubinski, Jan, Narod, Steven A.
Publicado 2019

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap

por McCuaig, Jeanna M, Stockley, Tracy L, Shaw, Patricia, Fung-Kee-Fung, Michael, Altman, Alon D, Bentley, James, Bernardini, Marcus Q, Cormier, Beatrice, Hirte, Hal, Kieser, Katharina, MacMillan, Andree, Meschino, Wendy S, Panabaker, Karen, Perrier, Renee, Provencher, Diane, Schrader, Kasmintan A, Serfas, Kimberly, Tomiak, Eva, Wong, Nora, Young, Sean S, Gotlieb, Walter Henri, Hoskins, Paul, Kim, Raymond H
Publicado 2018

New insights into DNA methylation signatures: SMARCA2 variants in Nicolaides-Baraitser syndrome

por Chater-Diehl, Eric, Ejaz, Resham, Cytrynbaum, Cheryl, Siu, Michelle T., Turinsky, Andrei, Choufani, Sanaa, Goodman, Sarah J., Abdul-Rahman, Omar, Bedford, Melanie, Dorrani, Naghmeh, Engleman, Kendra, Flores-Daboub, Josue, Genevieve, David, Mendoza-Londono, Roberto, Meschino, Wendy, Perrin, Laurence, Safina, Nicole, Townshend, Sharron, Scherer, Stephen W., Anagnostou, Evdokia, Piton, Amelie, Deardorff, Matthew, Brudno, Michael, Chitayat, David, Weksberg, Rosanna
Publicado 2019

Mutations in Alström Protein Impair Terminal Differentiation of Cardiomyocytes

por Shenje, Lincoln T., Andersen, Peter, Halushka, Marc K., Lui, Cecillia, Fernandez, Laviel, Collin, Gayle B., Amat-Alarcon, Nuria, Meschino, Wendy, Cutz, Ernest, Chang, Kenneth, Yonescu, Raluca, Batista, Denise A. S., Chen, Yan, Chelko, Stephen, Crosson, Jane E., Scheel, Janet, Vricella, Luca, Craig, Brian D., Marosy, Beth A., Mohr, David W., Hetrick, Kurt N., Romm, Jane M., Scott, Alan F., Valle, David, Naggert, Jürgen K., Kwon, Chulan, Doheny, Kimberly F., Judge, Daniel P.
Publicado 2014

BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes

por Aref-Eshghi, Erfan, Bend, Eric G., Hood, Rebecca L., Schenkel, Laila C., Carere, Deanna Alexis, Chakrabarti, Rana, Nagamani, Sandesh C. S., Cheung, Sau Wai, Campeau, Philippe M., Prasad, Chitra, Siu, Victoria Mok, Brady, Lauren, Tarnopolsky, Mark A., Callen, David J., Innes, A. Micheil, White, Susan M., Meschino, Wendy S., Shuen, Andrew Y., Paré, Guillaume, Bulman, Dennis E., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Hennekam, Raoul C., Boycott, Kym M., Schwartz, Charles E., Sadikovic, Bekim
Publicado 2018

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

por Rivière, Jean-Baptiste, Mirzaa, Ghayda M., O’Roak, Brian J., Beddaoui, Margaret, Alcantara, Diana, Conway, Robert L., St-Onge, Judith, Schwartzentruber, Jeremy A., Gripp, Karen W., Nikkel, Sarah M., Worthylake, Thea, Sullivan, Christopher T., Ward, Thomas R., Butler, Hailly E., Kramer, Nancy A., Albrecht, Beate, Armour, Christine M., Armstrong, Linlea, Caluseriu, Oana, Cytrynbaum, Cheryl, Drolet, Beth A., Innes, A. Micheil, Lauzon, Julie L., Lin, Angela E., Mancini, Grazia M. S., Meschino, Wendy S., Reggin, James D., Saggar, Anand K., Lerman-Sagie, Tally, Uyanik, Gökhan, Weksberg, Rosanna, Zirn, Birgit, Beaulieu, Chandree L., Majewski, Jacek, Bulman, Dennis E., O’Driscoll, Mark, Shendure, Jay, Graham, John M., Boycott, Kym M., Dobyns, William B.
Publicado 2012