A framework for the investigation of rare genetic disorders in neuropsychiatry

by Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.
Published 2021

Mapping cortical anatomy in preschool aged children with autism using surface-based morphometry☆

by Raznahan, Armin, Lenroot, Rhoshel, Thurm, Audrey, Gozzi, Marta, Hanley, Allison, Spence, Sarah J., Swedo, Susan E., Giedd, Jay N.
Published 2014

Practice guideline: Treatment for insomnia and disrupted sleep behavior in children and adolescents with autism spectrum disorder: Report of the Guideline Development, Disseminatio...

by Williams Buckley, Ashura, Hirtz, Deborah, Oskoui, Maryam, Armstrong, Melissa J, Batra, Anshu, Bridgemohan, Carolyn, Coury, Daniel, Dawson, Geraldine, Donley, Diane, Findling, Robert L, Gaughan, Thomas, Gloss, David, Gronseth, Gary, Kessler, Riley, Merillat, Shannon, Michelson, David, Owens, Judith, Pringsheim, Tamara, Sikich, Linmarie, Stahmer, Aubyn, Thurm, Audrey, Tuchman, Roberto, Warren, Zachary, Wetherby, Amy, Wiznitzer, Max, Ashwal, Stephen
Published 2020

A framework for the investigation of rare genetic disorders in neuropsychiatry

by Sanders, Stephan J., Sahin, Mustafa, Hostyk, Joseph, Thurm, Audrey, Jacquemont, Sebastien, Avillach, Paul, Douard, Elise, Martin, Christa L., Modi, Meera E., Moreno-De-Luca, Andres, Raznahan, Armin, Anticevic, Alan, Dolmetsch, Ricardo, Feng, Guoping, Geschwind, Daniel H., Glahn, David C., Goldstein, David B., Ledbetter, David H., Mulle, Jennifer G., Pasca, Sergiu P., Samaco, Rodney, Sebat, Jonathan, Pariser, Anne, Lehner, Thomas, Gur, Raquel E., Bearden, Carrie E.
Published 2022

Shifted phase of EEG cross-frequency coupling in individuals with Phelan-McDermid syndrome

by Mariscal, Michael G., Berry-Kravis, Elizabeth, Buxbaum, Joseph D., Ethridge, Lauren E., Filip-Dhima, Rajna, Foss-Feig, Jennifer H., Kolevzon, Alexander, Modi, Meera E., Mosconi, Matthew W., Nelson, Charles A., Powell, Craig M., Siper, Paige M., Soorya, Latha, Thaliath, Andrew, Thurm, Audrey, Zhang, Bo, Sahin, Mustafa, Levin, April R.
Published 2021

Functional genomics analysis of Phelan-McDermid syndrome 22q13 region during human neurodevelopment

by Ziats, Catherine A. (author), Grosvenor, Luke P. (author), Sarasua, Sara M. (author), Thurm, Audrey E. (author), Swedo, Susan E. (author), Mahfouz, A.M.E.T.A. (author), Rennert, Owen M. (author), Ziats, Mark N. (author)
Published 2019