Assessment of Minimal Residual Disease in Ewing Sarcoma

por Wagner, Lars M., Smolarek, Teresa A., Sumegi, Janos, Marmer, Daniel
Publicado 2012

Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49–51 deletion phenotype

por Ulm, Elizabeth A., Nagaraj, Chinmayee B., Tian, Cuixia, Smolarek, Teresa A.
Publicado 2022

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing

por Tariq, Muhammad, Belmont, John W, Lalani, Seema, Smolarek, Teresa, Ware, Stephanie M
Publicado 2011

MON-249 Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome

por Alexandrou, Eirene, Cabrera-Salcedo, Catalina, Labilloy, Guillaume, Tyzinski, Leah, Smolarek, Teresa, Andrew, Melissa, Huang, Yongbo, Backeljauw, Philippe, Dauber, Andrew
Publicado 2019

Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disorders

por Hu, Xiaolin, Baker, Elizabeth K., Johnson, Jodie, Balow, Stephanie, Pena, Loren D. M., Conlin, Laura K., Guan, Qiaoning, Smolarek, Teresa A.
Publicado 2022

Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach

por Hinton, Robert B., McBride, Kim L., Bleyl, Steven B., Bowles, Neil E., Border, William L., Garg, Vidu, Smolarek, Teresa A., Lalani, Seema R., Ware, Stephanie M.
Publicado 2015

Further expansion and confirmation of phenotype in rare loss of YWHAE gene distinct from Miller–Dieker syndrome

por Baker, Elizabeth K., Brewer, Casey J., Ferreira, Leonardo, Schapiro, Mark, Tenney, Jeffrey, Wied, Heather M., Kline‐Fath, Beth M., Smolarek, Teresa A., Weaver, K. Nicole, Hopkin, Robert J.
Publicado 2022

Comparative Nonclinical Assessments of the Proposed Biosimilar PF-05280014 and Trastuzumab (Herceptin(®))

por Hurst, Susan, Ryan, Anne M., Ng, Chee-Keng, McNally, James M., Lorello, Leslie G., Finch, Gregory L., Leach, Michael W., Ploch, Stephen A., Fohey, Josh A., Smolarek, Teresa A.
Publicado 2014

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center

por Du, Xiaoli, Glass, Jennifer Elaine, Balow, Stephanie, Dyer, Lisa M., Rathbun, Pamela A., Guan, Qiaoning, Liu, Jie, Wu, Yaning, Dawson, D. Brian, Walters-Sen, Lauren, Smolarek, Teresa A., Zhang, Wenying
Publicado 2021

Nonclinical Evaluation of PF-06438179: A Potential Biosimilar to Remicade(®) (Infliximab)

por Derzi, Mazin, Johnson, Theodore R., Shoieb, Ahmed M., Conlon, Hugh D., Sharpe, Penny, Saati, Andrew, Koob, Sarah, Bolt, Michael W., Lorello, Leslie G., McNally, Jim, Kirchhoff, Carol F., Smolarek, Teresa A., Leach, Michael W.
Publicado 2016

TRLS-11. A PHASE 1 STUDY OF SAVOLITINIB IN RECURRENT, PROGRESSIVE, OR REFRACTORY MEDULLOBLASTOMA, HIGH-GRADE GLIOMA, DIFFUSE INTRINSIC PONTINE GLIOMA, AND CENTRAL NERVOUS SYSTEM (C...

por Salloum, Ralph, Huang, Jie, Stewart, Clinton F, Fuller, Christine, Smolarek, Teresa, Lenzen, Alicia, Waanders, Angela J, Baxter, Patiricia, Lindsay, Holly, Robison, Nathan, Pillay-Smiley, Natasha, Partap, Sonia, Fangusaro, Jason, Onar-Thomas, Arzu, Fouladi, Maryam, Dunkel, Ira J
Publicado 2023

Familial pulmonary alveolar proteinosis caused by mutations in CSF2RA

por Suzuki, Takuji, Sakagami, Takuro, Rubin, Bruce K., Nogee, Lawrence M., Wood, Robert E., Zimmerman, Sarah L., Smolarek, Teresa, Dishop, Megan K., Wert, Susan E., Whitsett, Jeffrey A., Grabowski, Gregory, Carey, Brenna C., Stevens, Carrie, van der Loo, Johannes C.M., Trapnell, Bruce C.
Publicado 2008

Characterizing temporal genomic heterogeneity in pediatric low-grade gliomas

por Lazow, Margot A., Hoffman, Lindsey, Schafer, Austin, Osorio, Diana S., Boué, Daniel R., Rush, Sarah, Wright, Erin, Lane, Adam, DeWire-Schottmiller, Mariko D., Smolarek, Teresa, Sipple, Jared, Taggert, Heather, Reuss, Jaime, Salloum, Ralph, Hummel, Trent R., de Blank, Peter, Pillay-Smiley, Natasha, Sutton, Mary E., Asher, Anthony, Stevenson, Charles B., Drissi, Rachid, Finlay, Jonathan L., Fouladi, Maryam, Fuller, Christine
Publicado 2020