Congenital disorders of glycosylation: new defects and still counting

由 Scott, Kyle, Gadomski, Therese, Kozicz, Tamas, Morava, Eva
出版 2014

Myocardial injury associated with coronavirus disease 2019 in pregnancy

由 Pachtman Shetty, Sarah L., Meirowitz, Natalie, Blitz, Matthew J., Gadomski, Therese, Weinberg, Catherine R.
發表在 Am J Obstet Gynecol (2021)

Implementation of a Standardized Post-Cesarean Delivery Order Set with Multimodal Combination Analgesia Reduces Inpatient Opioid Usage

由 Bornstein, Eran, Husk, Gregg, Lenchner, Erez, Grunebaum, Amos, Gadomski, Therese, Zottola, Cristina, Werner, Sarah, Hirsch, Jamie S., Chervenak, Frank A.
發表在 J Clin Med (2020)

Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects

由 Morelle, Willy, Potelle, Sven, Witters, Peter, Wong, Sunnie, Climer, Leslie, Lupashin, Vladimir, Matthijs, Gert, Gadomski, Therese, Jaeken, Jaak, Cassiman, David, Morava, Eva, Foulquier, François
發表在 J Clin Endocrinol Metab (2017)

Whole Genome Sequencing in Autism Identifies Hotspots for De Novo Germline Mutation

由 Michaelson, Jacob J., Shi, Yujian, Gujral, Madhusudan, Zheng, Hancheng, Malhotra, Dheeraj, Jin, Xin, Minghan, Jian, Liu, Guangming, Greer, Douglas, Bhandari, Abhishek, Wu, Wenting, Corominas, Roser, Peoples, Áine, Koren, Amnon, Gore, Athurva, Kang, Shuli, Lin, Guan Ning, Estabillo, Jasper, Gadomski, Therese, Singh, Balvindar, Zhang, Kun, Akshoomoff, Natacha, Corsello, Christina, McCarroll, Steven, Iakoucheva, Lilia M., Li, Yingrui, Wang, Jun, Sebat, Jonathan
出版 2012

ORAL D-GALACTOSE SUPPLEMENTATION IN PGM1-CDG

由 Wong, Sunnie Yan-Wai, Gadomski, Therese, van Scherpenzeel, Monique, Honzik, Tomas, Hansikova, Hana, Brocke Holmefjord, Katja S., Mork, Marit, Bowling, Francis, Cegielska, Jolanta Sykut, Koch, Dieter, Hertecant, Jozef, Preston, Graeme, Jaeken, Jaak, Peeters, Nicole, Perez, Stefanie, Nguyen, David Do, Crivelly, Kea, Emmerzaal, Tim, Gibson, K. Michael, Raymond, Kimiyo, Bakar, Nurulamin Abu, Foulquier, Francois, Poschet, Gernot, Ackermann, Amanda, He, Miao, Lefeber, Dirk, Thiel, Christian, Kozicz, Tamas, Morava, Eva
發表在 Genet Med (2017)

Frequency and Complexity of De Novo Structural Mutation in Autism

由 Brandler, William M., Antaki, Danny, Gujral, Madhusudan, Noor, Amina, Rosanio, Gabriel, Chapman, Timothy R., Barrera, Daniel J., Lin, Guan Ning, Malhotra, Dheeraj, Watts, Amanda C., Wong, Lawrence C., Estabillo, Jasper A., Gadomski, Therese E., Hong, Oanh, Fajardo, Karin V. Fuentes, Bhandari, Abhishek, Owen, Renius, Baughn, Michael, Yuan, Jeffrey, Solomon, Terry, Moyzis, Alexandra G., Maile, Michelle S., Sanders, Stephan J., Reiner, Gail E., Vaux, Keith K., Strom, Charles M., Zhang, Kang, Muotri, Alysson R., Akshoomoff, Natacha, Leal, Suzanne M., Pierce, Karen, Courchesne, Eric, Iakoucheva, Lilia M., Corsello, Christina, Sebat, Jonathan
發表在 Am J Hum Genet (2016)