Neurophysiological differences between patients clinically at high risk for schizophrenia and neurotypical controls – first steps in development of a biomarker

por Duffy, Frank H., D’Angelo, Eugene, Rotenberg, Alexander, Gonzalez-Heydrich, Joseph
Publicado 2015

Young children with psychotic symptoms and risk for suicidal thoughts and behaviors: a research note

por Sinclair-McBride, Keneisha, Morelli, Nicholas, Tembulkar, Sahil, Graber, Kelsey, Gonzalez-Heydrich, Joseph, D’Angelo, Eugene J.
Publicado 2018

De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report

por Mavros, Chrystal F., Brownstein, Catherine A., Thyagrajan, Roshni, Genetti, Casie A., Tembulkar, Sahil, Graber, Kelsey, Murphy, Quinn, Cabral, Kristin, VanNoy, Grace E., Bainbridge, Matthew, Shi, Jiahai, Agrawal, Pankaj B., Beggs, Alan H., D’Angelo, Eugene, Gonzalez-Heydrich, Joseph
Publicado 2018

N100 Repetition Suppression Indexes Neuroplastic Defects in Clinical High Risk and Psychotic Youth

por Gonzalez-Heydrich, Joseph, Bosquet Enlow, Michelle, D'Angelo, Eugene, Seidman, Larry J., Gumlak, Sarah, Kim, April, Woodberry, Kristen A., Rober, Ashley, Tembulkar, Sahil, O'Donnell, Kyle, Hamoda, Hesham M., Kimball, Kara, Rotenberg, Alexander, Oberman, Lindsay M., Pascual-Leone, Alvaro, Keshavan, Matcheri S., Duffy, Frank H.
Publicado 2016

De novo ATP1A3 and compound heterozygous NLRP3 mutations in a child with autism spectrum disorder, episodic fatigue and somnolence, and muckle-wells syndrome

por Torres, Alcy, Brownstein, Catherine A., Tembulkar, Sahil K., Graber, Kelsey, Genetti, Casie, Kleiman, Robin J., Sweadner, Kathleen J., Mavros, Chrystal, Liu, Kevin X., Smedemark-Margulies, Niklas, Maski, Kiran, Yang, Edward, Agrawal, Pankaj B., Shi, Jiahai, Beggs, Alan H., D'Angelo, Eugene, Lincoln, Sarah Hope, Carroll, Devon, Dedeoglu, Fatma, Gahl, William A., Biggs, Catherine M., Swoboda, Kathryn J., Berry, Gerard T., Gonzalez-Heydrich, Joseph
Publicado 2018

RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes

por Brownstein, Catherine A., Smith, Richard S., Rodan, Lance H., Gorman, Mark P., Hojlo, Margaret A., Garvey, Emily A., Li, Jianqiao, Cabral, Kristin, Bowen, Joshua J., Rao, Abhijit S., Genetti, Casie A., Carroll, Devon, Deaso, Emma A., Agrawal, Pankaj B., Rosenfeld, Jill A., Bi, Weimin, Howe, Jennifer, Stavropoulos, Dimitri J., Hansen, Adam W., Hamoda, Hesham M., Pinard, Ferne, Caracansi, Annmarie, Walsh, Christopher A., D’Angelo, Eugene J., Beggs, Alan H., Zarrei, Mehdi, Gibbs, Richard A., Scherer, Stephen W., Glahn, David C., Gonzalez-Heydrich, Joseph
Publicado 2021