2181: Patient preferences and attitudes regarding next-generation sequencing results: scoping review of the literature

por Neu, Matthew, Knight, Sara
Publicado 2018

2443 Attitudes and preferences for return of results from next-generation sequencing

por Neu, Matthew, Richards, Jaimie, Knight, Sara J.
Publicado 2018

Endothelial progenitor dysfunction in the pathogenesis of diabetic retinopathy: treatment concept to correct diabetes-associated deficits

por Li Calzi, Sergio, Neu, Matthew B., Shaw, Lynn C., Grant, Maria B.
Publicado 2010

CUILESS2016: a clinical corpus applying compositional normalization of text mentions

por Osborne, John D., Neu, Matthew B., Danila, Maria I., Solorio, Thamar, Bethard, Steven J.
Publicado 2018

Per2 Mutation Recapitulates the Vascular Phenotype of Diabetes in the Retina and Bone Marrow

por Bhatwadekar, Ashay D., Yan, Yuanqing, Qi, Xiaoping, Thinschmidt, Jeffrey S., Neu, Matthew B., Li Calzi, Sergio, Shaw, Lynn C., Dominiguez, James M., Busik, Julia V., Lee, Choogon, Boulton, Michael E., Grant, Maria B.
Publicado 2013

Genomic sequencing identifies secondary findings in a cohort of parent study participants

por Thompson, Michelle L., Finnila, Candice R., Bowling, Kevin M., Brothers, Kyle B., Neu, Matthew B., Amaral, Michelle D., Hiatt, Susan M., East, Kelly M., Gray, David E., Lawlor, James M.J., Kelley, Whitley V., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Levy, Shawn E., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Publicado 2018

De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay

por Hiatt, Susan M., Neu, Matthew B., Ramaker, Ryne C., Hardigan, Andrew A., Prokop, Jeremy W., Hancarova, Miroslava, Prchalova, Darina, Havlovicova, Marketa, Prchal, Jan, Stranecky, Viktor, Yim, Dwight K. C., Powis, Zöe, Keren, Boris, Nava, Caroline, Mignot, Cyril, Rio, Marlene, Revah-Politi, Anya, Hemati, Parisa, Stong, Nicholas, Iglesias, Alejandro D., Suchy, Sharon F., Willaert, Rebecca, Wentzensen, Ingrid M., Wheeler, Patricia G., Brick, Lauren, Kozenko, Mariya, Hurst, Anna C. E., Wheless, James W., Lacassie, Yves, Myers, Richard M., Barsh, Gregory S., Sedlacek, Zdenek, Cooper, Gregory M.
Publicado 2018

Parents’ Perspectives on the Utility of Genomic Sequencing in the Neonatal Intensive Care Unit

por Lemke, Amy A., Thompson, Michelle L., Gimpel, Emily C., McNamara, Katelyn C., Rich, Carla A., Finnila, Candice R., Cochran, Meagan E., Lawlor, James M. J., East, Kelly M., Bowling, Kevin M., Latner, Donald R., Hiatt, Susan M., Amaral, Michelle D., Kelley, Whitley V., Greve, Veronica, Gray, David E., Felker, Stephanie A., Meddaugh, Hannah, Cannon, Ashley, Luedecke, Amanda, Jackson, Kelly E., Hendon, Laura G., Janani, Hillary M., Johnston, Marla, Merin, Lee Ann, Deans, Sarah L., Tuura, Carly, Hughes, Trent, Williams, Heather, Laborde, Kelly, Neu, Matthew B., Patrick-Esteve, Jessica, Hurst, Anna C. E., Kirmse, Brian M., Savich, Renate, Spedale, Steven B., Knight, Sara J., Barsh, Gregory S., Korf, Bruce R., Cooper, Gregory M., Brothers, Kyle B.
Publicado 2023