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

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

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

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings

Por Lubin, Ira M., Aziz, Nazneen, Babb, Lawrence J., Ballinger, Dennis, Bisht, Himani, Church, Deanna M., Cordes, Shaun, Eilbeck, Karen, Hyland, Fiona, Kalman, Lisa, Landrum, Melissa, Lockhart, Edward R., Maglott, Donna, Marth, Gabor, Pfeifer, John D., Rehm, Heidi L., Roy, Somak, Tezak, Zivana, Truty, Rebecca, Ullman-Cullere, Mollie, Voelkerding, Karl V., Worthey, Elizabeth A., Zaranek, Alexander W., Zook, Justin M.
Publicado no J Mol Diagn (2017)