Anterior Cingulate Cortex and Ventral Hippocampal Inputs to the Basolateral Amygdala Selectively Control Generalized Fear von Ortiz, Samantha, Latsko, Maeson S, Fouty, Julia L, Dutta, Sohini, Adkins, Jordan M, Jasnow, Aaron M

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A Novel Interaction between Tryptophan Hydroxylase 2 (TPH2) Gene Polymorphism (rs4570625) and BDNF Val66Met Predicts a High-Risk Emotional Phenotype in Healthy Subjects von Latsko, Maeson S, Gilman, T Lee, Matt, Lindsey M, Nylocks, K Maria, Coifman, Karin G, Jasnow, Aaron M

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Corticosterone after early adolescent stress prevents social avoidance, aversive behavior, and morphine-conditioned place preference in adulthood von Vanderhoof, Samantha O., Vincent, Carly J., Beaver, Jasmin N., Latsko, Maeson S., Aguilar-Alvarez, Ricardo, Jasnow, Aaron M.

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Aromatized testosterone attenuates contextual generalization of fear in male rats von Lynch, Joseph F., Vanderhoof, Tyler, Winiecki, Patrick, Latsko, Maeson S., Riccio, David C., Jasnow, Aaron M.

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Increased parasympathetic activity and ability to generate positive emotion: The influence of the BDNF Val66Met polymorphism on emotion flexibility von Nylocks, Karin Maria, Gilman, T. Lee, Latsko, Maeson S., Jasnow, Aaron M., Coifman, Karin G.

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Corticosterone may interact with peripubertal development to shape adult resistance to social defeat von Latsko, Maeson S., Farnbauch, Laure A., Gilman, T. Lee, Lynch, Joseph F., Jasnow, Aaron M.

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De novo missense variant in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy von Latsko, Maeson S., Koboldt, Daniel C., Franklin, Samuel J., Hickey, Scott E., Williamson, Rachel K., Garner, Shannon, Ostendorf, Adam P., Lee, Kristy, White, Peter, Wilson, Richard K.

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Phenotypic responses to social defeat are associated with differences in cued and contextual fear discrimination von Dulka, Brooke N., Lynch, Joseph F., Latsko, Maeson S., Mulvany, Jessica L., Jasnow, Aaron M.

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A Novel Interaction between Tryptophan Hydroxylase 2 von Latsko, Maeson S, Gilman, T. Lee, Matt, Lindsey M, Nylocks, K. Maria, Coifman, Karin G, Jasnow, Aaron M

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A Novel Interaction between Tryptophan Hydroxylase 2 and BDNF Val.sup.66Met Predicts a High-Risk Emotional Phenotype in Healthy Subjects von Latsko, Maeson S, Gilman, T. Lee, Matt, Lindsey M, Nylocks, K. Maria, Coifman, Karin G, Jasnow, Aaron M

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De novo missense mutation in GRIA2 in a patient with global developmental delay, autism spectrum disorder, and epileptic encephalopathy von Latsko, Maeson S, Koboldt, Daniel C, Franklin, Samuel J, Hickey, Scott E, Williamson, Rachel K, Garner, Shannon, Ostendorf, Adam P, Lee, Kristy, White, Peter, Wilson, Richard K

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Early adversity and insulin: neuroendocrine programming beyond glucocorticoids von Batra, Aashita, Latsko, Maeson, Portella, Andre Krumel, Silveira, Patricia P.

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Contextual Modulation of Vocal Behavior in Mouse: Newly Identified 12 kHz "Mid-Frequency" Vocalization Emitted during Restraint von Grimsley, Jasmine M S, Sheth, Saloni, Vallabh, Neil, Grimsley, Calum A, Bhattal, Jyoti, Latsko, Maeson, Jasnow, Aaron, Wenstrup, Jeffrey J

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Dominant-negative variants in CBX1 cause a neurodevelopmental disorder von Kuroda, Yukiko, Iwata-Otsubo, Aiko, Dias, Kerith-Rae, Temple, Suzanna E.L., Nagao, Koji, De Hayr, Lachlan, Zhu, Ying, Isobe, Shin-Ya, Nishibuchi, Gohei, Fiordaliso, Sarah K., Fujita, Yuki, Rippert, Alyssa L., Baker, Samuel W., Leung, Marco L., Koboldt, Daniel C., Harman, Adele, Keena, Beth A., Kazama, Izumi, Subramanian, Gopinath Musuwadi, Manickam, Kandamurugu, Schmalz, Betsy, Latsko, Maeson, Zackai, Elaine H., Edwards, Matt, Evans, Carey-Anne, Dulik, Matthew C., Buckley, Michael F., Yamashita, Toshihide, O'Brien, W. Timothy, Harvey, Robert J., Obuse, Chikashi, Roscioli, Tony, Izumi, Kosuke

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Variation of 5-HTTLPR and Deficits in Emotion Regulation: A Pathway to Risk? von Gilman, T. Lee, Latsko, Maeson, Matt, Lindsey, Flynn, Jessica, Cabrera, Omar de la Cruz, Douglas, Deborah, Jasnow, Aaron M., Coifman, Karin G.

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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition von Picketts, D, Mirzaa, G, Yan, K, Relator, R, Timpano, S, Yalcin, B, Collins, S, Ziegler, A, Pao, E, Oyama, N, Brischoux-Boucher, E, Piard, J, Monaghan, K, Sacoto, MG, Dobyns, W, Park, K, Fernández-Mayoralas, D, Fernández-Jaén, A, Jayakar, P, Brusco, A, Antona, V, Giorgio, E, Kvarnung, M, Isidor, B, Conrad, S, Cogné, B, Deb, W, Stuurman, KE, Sterbova, K, Smal, N, Weckhuysen, S, Oegema, R, Innes, M, Latsko, M, Ben-Omran, T, Yeh, R, Kruer, M, Bakhtiari, S, Papavasiliou, A, Moutton, S, Nambot, S, Chanprasert, S, Paolucci, S, Miller, K, Burton, B, Kim, K, O'Heir, E, Bruwer, Z, Donald, K, Kleefstra, T, Goldstein, A, Angle, B, Bontempo, K, Miny, P, Joset, P, Demurger, F, Hobson, E, Pang, L, Carpenter, L, Li, D, Bonneau, D, Sadikovic, B

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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition von Picketts, David, Mirzaa, Ghayda, Yan, Keqin, Relator, Raissa, Timpano, Sara, Yalcin, Binnaz, Collins, Stephan, Ziegler, Alban, Pao, Emily, Oyama, Nora, Brischoux-Boucher, Elise, Piard, Juliette, Monaghan, Kristin, Sacoto, Maria Guillen, Dobyns, William, Park, Kristen, Fernández-Mayoralas, Daniel, Fernández-Jaén, Alberto, Jayakar, Parul, Brusco, Alfredo, Antona, Vincenzo, Giorgio, Elisa, Kvarnung, Malin, Isidor, Bertrand, Conrad, Solène, Cogné, Benjamin, Deb, Wallid, Stuurman, K E, Sterbova, Katalin, Smal, Noor, Weckhuysen, Sarah, Oegema, Renske, Innes, Micheil, Latsko, Maeson, Ben-Omran, Tawfeg, Yeh, Rebecca, Kruer, Michael, Bakhtiari, Somayeh, Papavasiliou, Antigone, Moutton, Sébastien, Nambot, Sophie, Chanprasert, Sirisak, Paolucci, Sarah, Miller, Kait, Burton, Barbara, Kim, Katherine, O'Heir, Emily, Bruwer, Zandre, Donald, Kirsten, Kleefstra, Tjitske, Goldstein, Amy, Angle, Brad, Bontempo, Kelly, Miny, Peter, Joset, Pascal, Demurger, Florence, Hobson, Emma, Pang, Lewis, Carpenter, Lori, Li, Dong, Bonneau, Dominique, Sadikovic, Bekim

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