Benefits of effective multidisciplinary teamwork: catheter ablation of premature ventricular ectopics

由 Daveney, John, Nguyen, Thomas, Wright, Matt
發表在 BMJ Case Rep (2020)

Three-dimensional atrial wall thickness maps to inform catheter ablation procedures for atrial fibrillation

由 Bishop, Martin, Rajani, Ronak, Plank, Gernot, Gaddum, Nicholas, Carr-White, Gerry, Wright, Matt, O'Neill, Mark, Niederer, Steven
發表在 Europace (2016)

LitGen: Genetic Literature Recommendation Guided by Human Explanations

由 Nie, Allen, Pineda, Arturo L., Wright, Matt W., Wand, Hannah, Wulf, Bryan, Costa, Helio, Patel, Ronak, Bustamante, Carlos D., Zou, James
發表在 Pac Symp Biocomput (2020)

Quality of life and healthcare utilisation improvements after atrial fibrillation ablation

由 Gupta, Dhiraj, Vijgen, Johan, Potter, Tom De, Scherr, Daniel, Van Herendael, Hugo, Knecht, Sebastien, Kobza, Richard, Berte, Benjamin, Sandgaard, Niels, Albenque, Jean-Paul, Széplaki, Gábor, Stevenhagen, Yorick, Taghji, Philippe, Wright, Matt, Duytschaever, Mattias
發表在 Heart (2021)

OpenEP: A Cross-Platform Electroanatomic Mapping Data Format and Analysis Platform for Electrophysiology Research

由 Williams, Steven E., Roney, Caroline H., Connolly, Adam, Sim, Iain, Whitaker, John, O’Hare, Daniel, Kotadia, Irum, O’Neill, Louisa, Corrado, Cesare, Bishop, Martin, Niederer, Steven A., Wright, Matt, O’Neill, Mark, Linton, Nick W. F.
發表在 Front Physiol (2021)

ClinGen Allele Registry links information about genetic variants

由 Pawliczek, Piotr, Patel, Ronak Y., Ashmore, Lillian R., Jackson, Andrew R., Bizon, Chris, Nelson, Tristan, Powell, Bradford, Freimuth, Robert R., Strande, Natasha, Shah, Neethu, Paithankar, Sameer, Wright, Matt W., Dwight, Selina, Zhen, Jimmy, Landrum, Melissa, McGarvey, Peter, Babb, Larry, Plon, Sharon E., Milosavljevic, Aleksandar
發表在 Hum Mutat (2018)

Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

由 Brnich, Sarah E., Abou Tayoun, Ahmad N., Couch, Fergus J., Cutting, Garry R., Greenblatt, Marc S., Heinen, Christopher D., Kanavy, Dona M., Luo, Xi, McNulty, Shannon M., Starita, Lea M., Tavtigian, Sean V., Wright, Matt W., Harrison, Steven M., Biesecker, Leslie G., Berg, Jonathan S.
發表在 Genome Med (2019)

Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures

由 Popejoy, Alice B., Crooks, Kristy R., Fullerton, Stephanie M., Hindorff, Lucia A., Hooker, Gillian W., Koenig, Barbara A., Pino, Natalie, Ramos, Erin M., Ritter, Deborah I., Wand, Hannah, Wright, Matt W., Yudell, Michael, Zou, James Y., Plon, Sharon E., Bustamante, Carlos D., Ormond, Kelly E.
發表在 Am J Hum Genet (2020)

Unique Aspects of Sequence Variant Interpretation for Inborn Errors of Metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene

由 Zastrow, Diane B., Baudet, Heather, Shen, Wei, Thomas, Amanda, Si, Yue, Weaver, Meredith A., Lager, Angela, Liu, Jixia, Mangels, Rachel, Dwight, Selina S., Wright, Matt W., Dobrowolski, Steven F., Eilbeck, Karen, Enns, Gregory M., Feigenbaum, Annette, Lichter-Konecki, Uta, Lyon, Elaine, Pasquali, Marzia, Watson, Michael, Blau, Nenad, Steiner, Robert D., Craigen, William J., Mao, Rong
發表在 Hum Mutat (2018)

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource

由 Strande, Natasha T., Riggs, Erin Rooney, Buchanan, Adam H., Ceyhan-Birsoy, Ozge, DiStefano, Marina, Dwight, Selina S., Goldstein, Jenny, Ghosh, Rajarshi, Seifert, Bryce A., Sneddon, Tam P., Wright, Matt W., Milko, Laura V., Cherry, J. Michael, Giovanni, Monica A., Murray, Michael F., O’Daniel, Julianne M., Ramos, Erin M., Santani, Avni B., Scott, Alan F., Plon, Sharon E., Rehm, Heidi L., Martin, Christa L., Berg, Jonathan S.
發表在 Am J Hum Genet (2017)