Search Results - Wenger, Tara L.

Telemedicine for genetic and neurologic evaluation in the Neonatal Intensive Care Unit by Wenger, Tara L., Gerdes, Jeffrey, Taub, Katherine, Swarr, Daniel T., Deardorff, Matthew A., Abend, Nicholas S.

Get full text Get full text Get full text

Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhage by Tully, Hannah M., Wenger, Tara L., Kukull, Walter A., Doherty, Dan, Dobyns, William B.

Get full text Get full text Get full text

Avoidance of surgery for head and neck infantile myofibromatosis using imatinib monotherapy by Pattisapu, Prasanth, Wenger, Tara L., Dahl, John P., Bly, Randall A., Bonilla‐Velez, Juliana, Wu, Natalie, Hall, Anurekha, Rudzinski, Erin R., Perkins, Jonathan A.

Get full text Get full text Get full text

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

Get full text Get full text Get full text

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

Get full text Get full text Get full text

Tracheal cartilaginous sleeves in children with syndromic craniosynostosis by 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

Get full text Get full text Get full text

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

Get full text Get full text Get full text

Perspectives from the Society for Pediatric Research: advice on sustaining science and mentoring during COVID-19 by Forster, Catherine S., Nguyen, Suong T., Powell, Weston T., Moore, Daniel J., Ho, Jacqueline, Heyman, Melvin B., Wenger, Tara L., Gonzalez, Fernando, Hostetter, Margaret, Nowalk, Andrew, Rassbach, Caroline E., Boyer, Debra, Weiss, Pnina, Blankenburg, Rebecca L., Orange, Jordan S., Ackerman, Kate G., Burns, Audrea M.

Get full text Get full text Get full text

Nonreentrant atrial tachycardia occurs independently of hypertrophic cardiomyopathy in RASopathy patients by 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.

Get full text Get full text Get full text

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly by 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

Get full text Get full text Get full text

A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants by Chawner, Samuel J.R.A., Doherty, Joanne L., Anney, Richard, Antshel, Kevin M., Kushan, Leila, Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Kochel, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., Hall, Jeremy, Owen, Michael J., van den Bree, Marianne B.M.

Get full text Get full text Get full text

Targeted long-read sequencing identifies missing disease-causing variation by Miller, Danny E., Sulovari, Arvis, Wang, Tianyun, Loucks, Hailey, Hoekzema, Kendra, Munson, Katherine M., Lewis, Alexandra P., Fuerte, Edith P. Almanza, Paschal, Catherine R., Walsh, Tom, Thies, Jenny, Bennett, James T., Glass, Ian, Dipple, Katrina M., Patterson, Karynne, Bonkowski, Emily S., Nelson, Zoe, Squire, Audrey, Sikes, Megan, Beckman, Erika, Bennett, Robin L., Earl, Dawn, Lee, Winston, Allikmets, Rando, Perlman, Seth J., Chow, Penny, Hing, Anne V., Wenger, Tara L., Adam, Margaret P., Sun, Angela, Lam, Christina, Chang, Irene, Zou, Xue, Austin, Stephanie L., Huggins, Erin, Safi, Alexias, Iyengar, Apoorva K., Reddy, Timothy E., Majoros, William H., Allen, Andrew S., Crawford, Gregory E., Kishnani, Priya S., King, Mary-Claire, Cherry, Tim, Chong, Jessica X., Bamshad, Michael J., Nickerson, Deborah A., Mefford, Heather C., Doherty, Dan, Eichler, Evan E.

Get full text Get full text Get full text