Communicating new knowledge on previously reported genetic variants

Por Aronson, Samuel J., Clark, Eugene H., Varugheese, Matthew, Baxter, Samantha, Babb, Lawrence J., Rehm, Heidi L.
Publicado em 2012

Usability of a Novel Clinician Interface for Genetic Results

Por Neri, Pamela M., Pollard, Stephanie E., Volk, Lynn A., Newmark, Lisa, Varugheese, Matthew, Baxter, Samantha, Aronson, Samuel J., Rehm, Heidi L., Bates, David W.
Publicado em 2012

A novel clinician interface to improve clinician access to up-to-date genetic results

Por Wilcox, Allison R, Neri, Pamela M, Volk, Lynn A, Newmark, Lisa P, Clark, Eugene H, Babb, Lawrence J, Varugheese, Matthew, Aronson, Samuel J, Rehm, Heidi L, Bates, David W
Publicado em 2014

Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates

Por Klinkenberg-Ramirez, Stephanie, Neri, Pamela M., Volk, Lynn A., Samaha, Sara J., Newmark, Lisa P., Pollard, Stephanie, Varugheese, Matthew, Baxter, Samantha, Aronson, Samuel J., Rehm, Heidi L., Bates, David W.
Publicado no Appl Clin Inform (2016)

The GeneInsight Suite: A Platform to Support Laboratory and Provider Use of DNA based Genetic Testing

Por Aronson, Samuel J., Clark, Eugene H., Babb, Lawrence J, Baxter, Samantha, Farwell, Lisa M., Funke, Birgit H., Hernandez, Amy Lovelette, Joshi, Victoria A., Lyon, Elaine, Parthum, Andrew R., Russell, Franklin J., Varugheese, Matthew, Venman, Thomas C., Rehm, Heidi L.
Publicado em 2011