A study of elective genome sequencing and pharmacogenetic testing in an unselected population

por Cochran, Meagan, East, Kelly, Greve, Veronica, Kelly, Melissa, Kelley, Whitley, Moore, Troy, Myers, Richard M., Odom, Katherine, Schroeder, Molly C., Bick, David
Publicado 2021

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

por Malinowski, Jennifer, Miller, David T., Demmer, Laurie, Gannon, Jennifer, Pereira, Elaine Maria, Schroeder, Molly C., Scheuner, Maren T., Tsai, Anne Chun-Hui, Hickey, Scott E., Shen, Jun
Publicado 2020

Somatic mosaicism for a novel PDHA1 mutation in a male with severe pyruvate dehydrogenase complex deficiency

por Deeb, Kristin K., Bedoyan, Jirair K., Wang, Raymond, Sremba, Leighann, Schroeder, Molly C., Grahame, George J., Boyer, Monica, McCandless, Shawn E., Kerr, Douglas S., Zhang, Shulin
Publicado 2014

Training professional caregivers to screen for report of cognitive changes in persons with intellectual disability

por Walaszek, Art, Albrecht, Tammi, LeCaire, Tamara, Sayavedra, Noelia, Schroeder, Molly, Krainer, Jody, Prichett, Gregory, Wilcenski, Mickell, Endicott, Sarah, Russmann, Sydney, Carlsson, Cynthia M., Mahoney, Jane
Publicado 2022

Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations

por Starosta, Rodrigo Tzovenos, Hou, Ying-Chen Claire, Leestma, Katelyn, Singh, Prapti, Viehl, Luke, Manwaring, Linda, Granadillo, Jorge Luis, Schroeder, Molly C., Colombo, Jamie N., Whitehead, Halana, Dickson, Patricia Irene, Hulbert, Monica L., Nguyen, Hoanh Thi
Publicado 2022

Genomic landscape of TP53-mutated myeloid malignancies

por Abel, Haley J., Oetjen, Karolyn A., Miller, Christopher A., Ramakrishnan, Sai M., Day, Ryan B., Helton, Nichole M., Fronick, Catrina C., Fulton, Robert S., Heath, Sharon E., Tarnawsky, Stefan P., Nonavinkere Srivatsan, Sridhar, Duncavage, Eric J., Schroeder, Molly C., Payton, Jacqueline E., Spencer, David H., Walter, Matthew J., Westervelt, Peter, DiPersio, John F., Ley, Timothy J., Link, Daniel C.
Publicado 2023

Genomic landscape of TP53-mutated myeloid malignancies

por Abel, Haley J., Oetjen, Karolyn A., Miller, Christopher A., Ramakrishnan, Sai M., Day, Ryan B., Helton, Nichole M., Fronick, Catrina C., Fulton, Robert S., Heath, Sharon E., Tarnawsky, Stefan P., Srivatsan, Sridhar Nonavinkere, Duncavage, Eric J., Schroeder, Molly C., Payton, Jacqueline E., Spencer, David H., Walter, Matthew J., Westervelt, Peter, DiPersio, John F., Ley, Timothy J., Link, Daniel C.
Publicado 2023