Signaling Pathways and Sex Differential Processes in Autism Spectrum Disorder

por Enriquez, Kristen D., Gupta, Abha R., Hoffman, Ellen J.
Publicado 2021

Sex-dependent role for EPHB2 in brain development and autism-associated behavior

por Assali, Ahlem, Cho, Jennifer Y., Tsvetkov, Evgeny, Gupta, Abha R., Cowan, Christopher W.
Publicado 2021

Identification of amygdala-expressed genes associated with autism spectrum disorder

por Herrero, Maria Jesus, Velmeshev, Dmitry, Hernandez-Pineda, David, Sethi, Saarthak, Sorrells, Shawn, Banerjee, Payal, Sullivan, Catherine, Gupta, Abha R., Kriegstein, Arnold R., Corbin, Joshua G.
Publicado 2020

Engineering spatial-organized cardiac organoids for developmental toxicity testing

por Hoang, Plansky, Kowalczewski, Andrew, Sun, Shiyang, Winston, Tackla S., Archilla, Adriana M., Lemus, Stephanie M., Ercan-Sencicek, A. Gulhan, Gupta, Abha R., Liu, Wenzhong, Kontaridis, Maria I., Amack, Jeffrey D., Ma, Zhen
Publicado 2021

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene

por Fernandez, Thomas V., Williams, Zsanett P., Kline, Tina, Rajendran, Shreenath, Augustine, Farhan, Wright, Nicole, Sullivan, Catherine A. W., Olfson, Emily, Abdallah, Sarah B., Liu, Wenzhong, Hoffman, Ellen J., Gupta, Abha R., Singer, Harvey S.
Publicado 2023

A neurogenetic analysis of female autism

por Jack, Allison, Sullivan, Catherine A W, Aylward, Elizabeth, Bookheimer, Susan Y, Dapretto, Mirella, Gaab, Nadine, Van Horn, John D, Eilbott, Jeffrey, Jacokes, Zachary, Torgerson, Carinna M, Bernier, Raphael A, Geschwind, Daniel H, McPartland, James C, Nelson, Charles A, Webb, Sara J, Pelphrey, Kevin A, Gupta, Abha R
Publicado 2021

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders

por 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
Publicado 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...

por 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.
Publicado 2015

Neurogenetic analysis of childhood disintegrative disorder

por Gupta, Abha R., Westphal, Alexander, Yang, Daniel Y. J., Sullivan, Catherine A. W., Eilbott, Jeffrey, Zaidi, Samir, Voos, Avery, Vander Wyk, Brent C., Ventola, Pam, Waqar, Zainulabedin, Fernandez, Thomas V., Ercan-Sencicek, A. Gulhan, Walker, Michael F., Choi, Murim, Schneider, Allison, Hedderly, Tammy, Baird, Gillian, Friedman, Hannah, Cordeaux, Cara, Ristow, Alexandra, Shic, Frederick, Volkmar, Fred R., Pelphrey, Kevin A.
Publicado 2017

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

por 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.
Publicado 2014