PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure

por Belyk, Michel, Kraft, Shelly Jo, Brown, Steven
Publicado 2014

Identifying developmental stuttering and associated comorbidities in electronic health records and creating a phenome risk classifier

por Pruett, Dillon G., Shaw, Douglas M., Chen, Hung-Hsin, Petty, Lauren E., Polikowsky, Hannah G., Kraft, Shelly Jo, Jones, Robin M., Below, Jennifer E.
Publicado 2021

Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering

por Shaw, Douglas M., Polikowsky, Hannah P., Pruett, Dillon G., Chen, Hung-Hsin, Petty, Lauren E., Viljoen, Kathryn Z., Beilby, Janet M., Jones, Robin M., Kraft, Shelly Jo, Below, Jennifer E.
Publicado 2021

Tools for standardized data collection: Speech, Language, and Hearing measurement protocols in the PhenX Toolkit

por Morton, Cynthia C., Marazita, Mary L., Peter, Beate, Rice, Mabel L., Kraft, Shelly Jo, Barkmeier‐Kraemer, Julie, Balaban, Carey, Phillips, Michael, Schoden, Jennifer, Maiese, Deborah, Hendershot, Tabitha, Hamilton, Carol M.
Publicado 2021

Population-based genetic effects for developmental stuttering

por Polikowsky, Hannah G., Shaw, Douglas M., Petty, Lauren E., Chen, Hung-Hsin, Pruett, Dillon G., Linklater, Jonathon P., Viljoen, Kathryn Z., Beilby, Janet M., Highland, Heather M., Levitt, Brandt, Avery, Christy L., Mullan Harris, Kathleen, Jones, Robin M., Below, Jennifer E., Kraft, Shelly Jo
Publicado 2021