المؤلفون: Shashi, Vandana, Schoch, Kelly, Ganetzky, Rebecca, Kranz, Peter G., Sondheimer, Neal, Markert, M. Louise, Cope, Heidi, Sadeghpour, Azita, Roehrs, Philip, Arbogast, Thomas, Muraresku, Colleen, Tyndall, Amanda V., Esser, Michael J., Woodward, Kristine E., Ping-Yee Au, Billie, Parboosingh, Jillian S., Lamont, Ryan E., Bernier, Francois P., Wright, Nicola A.M., Benseler, Susa M., Parsons, Simon J., El-Dairi, Mays, Smith, Edward C., Valdez, Purnima, Tennison, Michael, Innes, A. Micheil, Davis, Erica E., Acosta, Maria T., Adam, Margaret, Adams, David R., Alvarez, Raquel L., Alvey, Justin, Amendola, Laura, Andrews, Ashley, Ashley, Euan A., Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Berg-Rood, Beverly

المساهمون: National Institutes of Health, Duke University, Duke University School of Medicine, Alberta Children's Hospital Foundation

المصدر: Genetics in Medicine ; volume 25, issue 9, page 100897 ; ISSN 1098-3600

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1016/j.gim.2023.100897Test
https://api.elsevier.com/content/article/PII:S1098360023009103?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1098360023009103?httpAccept=text/plainTest

المؤلفون: Werren, Elizabeth A., Guxholli, Alba, Jones, Natasha, Wagner, Matias, Hannibal, Iris, Granadillo, Jorge L., Tyndall, Amanda V., Moccia, Amanda, Kuehl, Ryan, Levandoski, Kristin M., Day-Salvatore, Debra L., Wheeler, Marsha, Chong, Jessica X., Bamshad, Michael J., Innes, A. Micheil, Pierson, Tyler Mark, Mackay, Joel P., Bielas, Stephanie L., Martin, Donna M.

المصدر: Human Genetics and Genomics Advances ; volume 4, issue 3, page 100198 ; ISSN 2666-2477

مصطلحات موضوعية: Genetics (clinical), Molecular Medicine

الإتاحة: https://doi.org/10.1016/j.xhgg.2023.100198Test
https://api.elsevier.com/content/article/PII:S2666247723000301?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2666247723000301?httpAccept=text/plainTest

المؤلفون: Vanden Broek, Kara, Ryu, Jae‐Ryeon, Perrier, Renee, Tyndall, Amanda V., Childs, Sarah J., Au, Ping Yee Billie

المصدر: Clinical Genetics; Apr2024, Vol. 105 Issue 4, p386-396, 11p

مصطلحات موضوعية: HYDROPS fetalis, PROTEIN-tyrosine kinases, MISSENSE mutation, EIGENFUNCTIONS, PROTEIN expression, FETUS

المؤلفون: Blackwell, Danielle L, Fraser, Sherri D, Caluseriu, Oana, Vivori, Claudia, Tyndall, Amanda V, Lamont, Ryan E, Parboosingh, Jillian S, Innes, A Micheil, Bernier, François P, Childs, Sarah J

المساهمون: McCallion, A, Canadian Institute of Health Research Institute of Genetics Rare Disease Models and Mechanisms, National Science and Engineering Research Council, Care4Rare Canada Consortium, Canadian Institutes of Health Research, Ontario Genomics Institute, Ontario Research Fund, Genome Alberta, Genome BC, Genome Quebec, Children’s Hospital of Eastern Ontario Foundation

المصدر: G3 Genes|Genomes|Genetics ; volume 12, issue 5 ; ISSN 2160-1836

مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Biology

الإتاحة: https://doi.org/10.1093/g3journal/jkac067Test
https://academic.oup.com/g3journal/article-pdf/12/5/jkac067/43583429/jkac067.pdfTest

المؤلفون: Weng, Patricia L., Majmundar, Amar J., Khan, Kamal, Lim, Tze Y., Shril, Shirlee, Jin, Gina, Musgrove, John, Wang, Minxian, Ahram, Dina F., Aggarwal, Vimla S., Bier, Louise E., Heinzen, Erin L., Onuchic-Whitford, Ana C., Mann, Nina, Buerger, Florian, Schneider, Ronen, Deutsch, Konstantin, Kitzler, Thomas M., Klämbt, Verena, Kolb, Amy, Mao, Youying, Moufawad El Achkar, Christelle, Mitrotti, Adele, Martino, Jeremiah, Beck, Bodo B., Altmüller, Janine, Benz, Marcus R., Yano, Shoji, Mikati, Mohamad A., Gunduz, Talha, Cope, Heidi, Shashi, Vandana, Trachtman, Howard, Bodria, Monica, Caridi, Gianluca, Pisani, Isabella, Fiaccadori, Enrico, AbuMaziad, Asmaa S., Martinez-Agosto, Julian A., Yadin, Ora, Zuckerman, Jonathan, Kim, Arang, John-Kroegel, Ulrike, Tyndall, Amanda V., Parboosingh, Jillian S., Innes, A. Micheil, Bierzynska, Agnieszka, Koziell, Ania B., Muorah, Mordi, Saleem, Moin A.

المساهمون: Manton Center for Orphan Disease Research, Boston Children's Hospital, Higher Education Commision, Pakistan, AstraZeneca, Alberta Children's Hospital Foundation, Alberta Children's Hospital Research Institute, American Society of Pediatric Nephrology, Kidney Research UK, National Institutes of Health, Medical Research Council, Canadian Institutes of Health Research, U.S. Department of Defense, Deutsche Forschungsgemeinschaft, National Center for Advancing Translational Sciences, Kidney Foundation of Canada, National Institute for Health Research, Canadian Society of Nephrology

المصدر: The American Journal of Human Genetics ; volume 108, issue 2, page 357-367 ; ISSN 0002-9297

مصطلحات موضوعية: Genetics (clinical), Genetics

الإتاحة: https://doi.org/10.1016/j.ajhg.2021.01.008Test
https://api.elsevier.com/content/article/PII:S0002929721000082?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0002929721000082?httpAccept=text/plainTest

المؤلفون: Ardila, Karen, Munro, Emily, Vega, Fernando, Mohite, Aashka, Curtis, Charlotte, Tyndall, Amanda V., Ethan MacDonald, M.

المصدر: 2023 IEEE 20th International Symposium on Biomedical Imaging (ISBI)

الإتاحة: https://doi.org/10.1109/isbi53787.2023.10230714Test
http://xplorestaging.ieee.org/ielx7/10230311/10230322/10230714.pdf?arnumber=10230714Test

المؤلفون: Tyndall, Amanda V., Longman, R. Stewart, Sajobi, Tolulope T., Parboosingh, Jillian S., Drogos, Lauren L., Davenport, Margie H., Eskes, Gail A., Hogan, David B., Hill, Michael D., Poulin, Marc J.

المصدر: Frontiers in Integrative Neuroscience ; volume 14 ; ISSN 1662-5145

مصطلحات موضوعية: Cellular and Molecular Neuroscience, Cognitive Neuroscience, Sensory Systems

الإتاحة: https://doi.org/10.3389/fnint.2020.571683Test

المؤلفون: Vanden Broek, Kara, Ryu, Jae‐Ryeon, Perrier, Renee, Tyndall, Amanda V., Childs, Sarah J., Au, Ping Yee Billie

المساهمون: Alberta Children's Hospital Foundation, Canadian Institutes of Health Research

المصدر: Clinical Genetics ; volume 105, issue 4, page 386-396 ; ISSN 0009-9163 1399-0004

الإتاحة: https://doi.org/10.1111/cge.14467Test

المؤلفون: HALL, SAMANTHA E., LAWAL, OLUWASEYI A., CLARK, CAMERON M., TYNDALL, AMANDA V., HILL, MICHAEL D., SAJOBI, TOLULOPE T., POULIN, MARC J.

المصدر: Medicine & Science in Sports & Exercise ; volume 51, issue 7, page 1506-1516 ; ISSN 1530-0315 0195-9131

الإتاحة: https://doi.org/10.1249/mss.0000000000001909Test
https://journals.lww.com/00005768-201907000-00019Test

المؤلفون: Tyndall, Amanda V., Argourd, Laurie, Sajobi, Tolulope T., Davenport, Margie H., Forbes, Scott C., Gill, Stephanie J., Parboosingh, Jillian S., Anderson, Todd J., Wilson, Ben J., Smith, Eric E., Hogan, David B., Hill, Michael D., Poulin, Marc J.

المساهمون: Alzheimer Society of Canada, Brenda Strafford Foundation Chair in Alzheimer Research, Alberta Innovates - Health Solutions, Heart and Stroke Foundation of Canada, Canadian Institutes of Health Research (CIHR) Focus-on-Stroke Postdoctoral Fellowship, University of Calgary Seed Grant Award, Brenda Strafford Centre for Aging, Canadian Institutes of Health Research

المصدر: Physiological Reports ; volume 4, issue 8, page e12733 ; ISSN 2051-817X

الإتاحة: https://doi.org/10.14814/phy2.12733Test