Rare deleterious mutations of the gene EFR3A in autism spectrum disorders

by Gupta, Abha R, Pirruccello, Michelle, Cheng, Feng, Kang, Hyo Jung, Fernandez, Thomas V, Baskin, Jeremy M, Choi, Murim, Liu, Li, Ercan-Sencicek, Adife Gulhan, Murdoch, John D, Klei, Lambertus, Neale, Benjamin M, Franjic, Daniel, Daly, Mark J, Lifton, Richard P, De Camilli, Pietro, Zhao, Hongyu, Šestan, Nenad, State, Matthew W
Published 2014

No Evidence for Association of Autism with Rare Heterozygous Point Mutations in Contactin-Associated Protein-Like 2 (CNTNAP2), or in Other Contactin-Associated Proteins or Contacti...

by Murdoch, John D., Gupta, Abha R., Sanders, Stephan J., Walker, Michael F., Keaney, John, Fernandez, Thomas V., Murtha, Michael T., Anyanwu, Samuel, Ober, Gordon T., Raubeson, Melanie J., DiLullo, Nicholas M., Villa, Natalie, Waqar, Zainabdul, Sullivan, Catherine, Gonzalez, Luis, Willsey, A. Jeremy, Choe, So-Yeon, Neale, Benjamin M., Daly, Mark J., State, Matthew W.
Published 2015

Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons

by Griesi-Oliveira, Karina, Acab, Allan, Gupta, Abha R., Sunaga, Daniele Yumi, Chailangkarn, Thanathom, Nicol, Xavier, Nunez, Yanelli, Walker, Michael F., Murdoch, John D., Sanders, Stephan J., Fernandez, Thomas V., Ji, Weizhen, Lifton, Richard P., Vadasz, Estevão, Dietrich, Alexander, Pradhan, Dennis, Song, Hongjun, Ming, Guo-li, Guoe, Xiang, Haddad, Gabriel, Marchetto, Maria C. N., Spitzer, Nicholas, Passos-Bueno, Maria Rita, State, Matthew W., Muotri, Alysson R.
Published 2014