Communicating new knowledge on previously reported genetic variants

по Aronson, Samuel J., Clark, Eugene H., Varugheese, Matthew, Baxter, Samantha, Babb, Lawrence J., Rehm, Heidi L.
Опубликовано 2012

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

по 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
Опубликовано 2014

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

по 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.
Опубликовано 2011

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

по 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.
Опубликовано в: J Mol Diagn (2017)