Telemedicine for genetic and neurologic evaluation in the Neonatal Intensive Care Unit

Por Wenger, Tara L., Gerdes, Jeffrey, Taub, Katherine, Swarr, Daniel T., Deardorff, Matthew A., Abend, Nicholas S.
Publicado em 2014

Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage

Por Tully, Hannah M., Wenger, Tara L., Kukull, Walter A., Doherty, Dan, Dobyns, William B.
Publicado no Neurosurg Focus (2016)

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder

Por Wenger, Tara L., Kao, Charlly, McDonald-McGinn, Donna M., Zackai, Elaine H., Bailey, Alice, Schultz, Robert T., Morrow, Bernice E., Emanuel, Beverly S., Hakonarson, Hakon
Publicado no Sci Rep (2016)

22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

Por Wenger, Tara L., Miller, Judith S., DePolo, Lauren M., de Marchena, Ashley B., Clements, Caitlin C., Emanuel, Beverly S., Zackai, Elaine H., McDonald-McGinn, Donna M., Schultz, Robert T.
Publicado no Mol Autism (2016)

Erratum to: 22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screening

Por Wenger, Tara L., Miller, Judith S., DePolo, Lauren M., de Marchena, Ashley B., Clements, Caitlin C., Emanuel, Beverly S., Zackai, Elaine H., McDonald-McGinn, Donna M., Schultz, Robert T.
Publicado no Mol Autism (2016)

Tracheal cartilaginous sleeves in children with syndromic craniosynostosis

Por Wenger, Tara L., Dahl, John, Bhoj, Elizabeth J., Rosen, Anna, McDonald-McGinn, Donna, Zackai, Elaine, Jacobs, Ian, Heike, Carrie L., Hing, Anne, Santani, Avni, Inglis, Andrew F., Sie, Kathleen C.Y., Cunningham, Michael, Perkins, Jonathan
Publicado no Genet Med (2016)

Critical region within 22q11.2 linked to higher rate of autism spectrum disorder

Por Clements, Caitlin C., Wenger, Tara L., Zoltowski, Alisa R., Bertollo, Jennifer R., Miller, Judith S., de Marchena, Ashley B., Mitteer, Lauren M., Carey, John C., Yerys, Benjamin E., Zackai, Elaine H., Emanuel, Beverly S., McDonald-McGinn, Donna M., Schultz, Robert T.
Publicado no Mol Autism (2017)

Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients

Por Levin, Mark D., Saitta, Sulagna C., Gripp, Karen W., Wenger, Tara L., Ganesh, Jaya, Kalish, Jennifer M., Epstein, Michael R., Smith, Rosemarie, Czosek, Richard J., Ware, Stephanie M., Goldenberg, Paula, Myers, Angela, Chatfield, Kathryn C., Gillespie, Matthew J., Zackai, Elaine H., Lin, Angela E.
Publicado no Am J Med Genet A (2018)

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Por Li, Dong, Wenger, Tara L, Seiler, Christoph, March, Michael E, Gutierrez-Uzquiza, Alvaro, Kao, Charlly, Bhoj, Elizabeth, Tian, Lifeng, Rosenbach, Misha, Liu, Yichuan, Robinson, Nora, Behr, Mechenzie, Chiavacci, Rosetta, Hou, Cuiping, Wang, Tiancheng, Bakay, Marina, Pellegrino da Silva, Renata, Perkins, Jonathan A, Sleiman, Patrick, Levine, Michael A, Hicks, Patricia J, Itkin, Maxim, Dori, Yoav, Hakonarson, Hakon
Publicado no Hum Mol Genet (2018)