The need for polygenic score reporting standards in evidence-based practice: lipid genetics use case

por Wand, Hannah, Knowles, Joshua W., Clarke, Shoa L.
Publicado 2021

Differential Locus Expansion Distinguishes Toxoplasmatinae Species and Closely Related Strains of Toxoplasma gondii

por Adomako-Ankomah, Yaw, Wier, Gregory M., Borges, Adair L., Wand, Hannah E., Boyle, Jon P.
Publicado 2014

LitGen: Genetic Literature Recommendation Guided by Human Explanations

por Nie, Allen, Pineda, Arturo L., Wright, Matt W., Wand, Hannah, Wulf, Bryan, Costa, Helio, Patel, Ronak, Bustamante, Carlos D., Zou, James
Publicado 2020

Re-envisioning community genetics: community empowerment in preventive genomics

por Wand, Hannah, Martschenko, Daphne O., Smitherman, Annamaria, Michelson, Sheryl, Pun, Ting, Witte, John S., Scott, Stuart A., Cho, Mildred K., Ashley, Euan A.
Publicado 2023

Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents

por Landrum Peay, Holly, Fischer, Ryan, Tzeng, Janice P., Hesterlee, Sharon E., Morris, Carl, Strong Martin, Amy, Rensch, Colin, Smith, Edward, Ricotti, Valeria, Beaverson, Katherine, Wand, Hannah, Mansfield, Carol
Publicado 2019

Multiplex giant magnetoresistive biosensor microarrays identify interferon-associated autoantibodies in systemic lupus erythematosus

por Lee, Jung-Rok, Haddon, D. James, Wand, Hannah E., Price, Jordan V., Diep, Vivian K., Hall, Drew A., Petri, Michelle, Baechler, Emily C., Balboni, Imelda M., Utz, Paul J., Wang, Shan X.
Publicado 2016

Finding missed cases of familial hypercholesterolemia in health systems using machine learning

por Banda, Juan M., Sarraju, Ashish, Abbasi, Fahim, Parizo, Justin, Pariani, Mitchel, Ison, Hannah, Briskin, Elinor, Wand, Hannah, Dubois, Sebastien, Jung, Kenneth, Myers, Seth A., Rader, Daniel J., Leader, Joseph B., Murray, Michael F., Myers, Kelly D., Wilemon, Katherine, Shah, Nigam H., Knowles, Joshua W.
Publicado 2019

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

por 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.
Publicado 2020

Application of a framework to guide genetic testing communication across clinical indications

por Hallquist, Miranda L. G., Tricou, Eric P., Ormond, Kelly E., Savatt, Juliann M., Coughlin, Curtis R., Faucett, W. Andrew, Hercher, Laura, Levy, Howard P., O’Daniel, Julianne M., Peay, Holly L., Stosic, Melissa, Smith, Maureen, Uhlmann, Wendy R., Wand, Hannah, Wain, Karen E., Buchanan, Adam H.
Publicado 2021

ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines

por Preston, Christine G., Wright, Matt W., Madhavrao, Rao, Harrison, Steven M., Goldstein, Jennifer L., Luo, Xi, Wand, Hannah, Wulf, Bryan, Cheung, Gloria, Mandell, Mark E., Tong, Howard, Cheng, Shaung, Iacocca, Michael A., Pineda, Arturo Lopez, Popejoy, Alice B., Dalton, Karen, Zhen, Jimmy, Dwight, Selina S., Babb, Lawrence, DiStefano, Marina, O’Daniel, Julianne M., Lee, Kristy, Riggs, Erin R., Zastrow, Diane B., Mester, Jessica L., Ritter, Deborah I., Patel, Ronak Y., Subramanian, Sai Lakshmi, Milosavljevic, Aleksander, Berg, Jonathan S., Rehm, Heidi L., Plon, Sharon E., Cherry, J. Michael, Bustamante, Carlos D., Costa, Helio A.
Publicado 2022