Patient Decisions to Receive Secondary Pharmacogenomic Findings and Development of a Multidisciplinary Practice Model to Integrate Results Into Patient Care

por Hicks, J. Kevin, Shealy, Amy, Schreiber, Allison, Coleridge, Marissa, Noss, Ryan, Natowicz, Marvin, Moran, Rocio, Moss, Timothy, Erwin, Angelika, Eng, Charis
Publicado 2017

Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy

por Wagnon, Jacy L., Barker, Bryan S., Hounshell, James A., Haaxma, Charlotte A., Shealy, Amy, Moss, Timothy, Parikh, Sumit, Messer, Ricka D., Patel, Manoj K., Meisler, Miriam H.
Publicado 2015

Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices

por Heald, Brandie, Rybicki, Lisa, Clements, Diane, Marquard, Jessica, Mester, Jessica, Noss, Ryan, Nardini, Monica, Polk, Jill, Psensky, Brittany, Rigelsky, Christina, Schreiber, Allison, Shealy, Amy, Smith, Marissa, Eng, Charis
Publicado 2016