Autism genetics: opportunities and challenges for clinical translation von Vorstman, Jacob A. S., Parr, Jeremy R., Moreno-De-Luca, Daniel, Anney, Richard J. L., Nurnberger Jr, John I., Hallmayer, Joachim F.

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SHANK3 and IGF1 restore synaptic deficits in neurons from 22q13 deletion syndrome patients von Shcheglovitov, Aleksandr, Shcheglovitova, Olesya, Yazawa, Masayuki, Portmann, Thomas, Shu, Rui, Sebastiano, Vittorio, Krawisz, Anna, Froehlich, Wendy, Bernstein, Jonathan A., Hallmayer, Joachim F., Dolmetsch, Ricardo E.

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Assembly of functionally integrated human forebrain spheroids von Birey, Fikri, Andersen, Jimena, Makinson, Christopher D., Islam, Saiful, Wei, Wu, Huber, Nina, Fan, H. Christina, Metzler, Kimberly R. Cordes, Panagiotakos, Georgia, Thom, Nicholas, O’Rourke, Nancy A., Steinmetz, Lars M., Bernstein, Jonathan A., Hallmayer, Joachim, Huguenard, John R., Paşca, Sergiu P.

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Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder von Parker, Karen J., Garner, Joseph P., Libove, Robin A., Hyde, Shellie A., Hornbeak, Kirsten B., Carson, Dean S., Liao, Chun-Ping, Phillips, Jennifer M., Hallmayer, Joachim F., Hardan, Antonio Y.

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HPA Axis Reactivity: A Mechanism Underlying the Associations Among 5-HTTLPR, Stress, and Depression von Gotlib, Ian H, Joormann, Jutta, Minor, Kelly L, Hallmayer, Joachim

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Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome von Yazawa, Masayuki, Hsueh, Brian, Jia, Xiaolin, Pasca, Anca M., Bernstein, Jonathan A., Hallmayer, Joachim, Dolmetsch, Ricardo E.

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A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients von Sun, Yishan, Paşca, Sergiu P, Portmann, Thomas, Goold, Carleton, Worringer, Kathleen A, Guan, Wendy, Chan, Karen C, Gai, Hui, Vogt, Daniel, Chen, Ying-Jiun J, Mao, Rong, Chan, Karrie, Rubenstein, John Lr, Madison, Daniel V, Hallmayer, Joachim, Froehlich-Santino, Wendy M, Bernstein, Jonathan A, Dolmetsch, Ricardo E

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Functional impact of global rare copy number variation in autism spectrum disorders von Anney, Richard, Regan, Regina, Conroy, Judith, Magalhaes, Tiago R., Almeida, Joana, Berney, Tom, Bölte, Sven, Bolton, Patrick F., Bourgeron, Thomas, Brennan, Sean, Bryson, Susan E., Carson, Andrew R., Casey, Jillian, Crawford, Emily L., Cytrynbaum, Cheryl, Dawson, Geraldine, de Jonge, Maretha, Delorme, Richard, Duketis, Eftichia, Duque, Frederico, Estes, Annette, Farrar, Penny, Fernandez, Bridget A., Freitag, Christine M., Gilbert, John, Glessner, Joseph T., Goldberg, Jeremy, Green, Andrew, Green, Jonathan, Guter, Stephen J., Heron, Elizabeth A., Holt, Richard, Howe, Jennifer L., Hughes, Gillian, Klauck, Sabine M., Kolevzon, Alexander, Korvatska, Olena, Kustanovich, Vlad, Le Couteur, Ann, Leventhal, Bennett L., Lord, Catherine, Maestrini, Elena, Mahoney, William, McConachie, Helen, McDougle, Christopher J., Merikangas, Alison, Mirza, Ghazala K., Munson, Jeff, Nelson, Stanley F., Noor, Abdul, Nygren, Gudrun, Papanikolaou, Katerina, Parrini, Barbara, Paton, Tara, Piven, Joseph, Ponting, Chris P., Roberts, Wendy, Bierut, Laura J., Rice, John P., Salt, Jeff, Sansom, Katherine, Senman, Lili, Shah, Naisha, Sheffield, Val C., Soorya, Latha, Stein, Olaf, Sykes, Nuala, Stoppioni, Vera, Strawbridge, Christina, Thompson, Ann P., Tsiantis, John, Van Engeland, Herman, Volkmar, Fred, Wallace, Simon, Wang, Kai, Wang, Zhouzhi, Wassink, Thomas H., Webber, Caleb, Weksberg, Rosanna, Wood, Shawn, Wu, Jing, Yaspan, Brian L., Zwaigenbaum, Lonnie, Buxbaum, Joseph D., Cantor, Rita M., Cook, Edwin H., Cuccaro, Michael L., Devlin, Bernie, Ennis, Sean, Gallagher, Louise, Geschwind, Daniel H., Gill, Michael, Miller, Judith, Monaco, Anthony P., Szatmari, Peter, Vicente, Astrid M., Vieland, Veronica J., Scherer, Stephen W., Sutcliffe, James S., Betancur, Catalina

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Integrated systems analysis reveals a molecular network underlying autism spectrum disorders von Li, Jingjing, Shi, Minyi, Ma, Zhihai, Zhao, Shuchun, Euskirchen, Ghia, Ziskin, Jennifer, Urban, Alexander, Hallmayer, Joachim, Snyder, Michael

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Oxytocin receptor gene polymorphism (rs2254298) interacts with familial risk for psychopathology to predict symptoms of depression and anxiety in adolescent girls von Thompson, Renee J, Parker, Karen J, Hallmayer, Joachim F, Waugh, Christian E, Gotlib, Ian H

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Resolving the 22q11.2 deletion using CTLR-Seq reveals chromosomal rearrangement mechanisms and individual variance in breakpoints von Zhou, Bo, Purmann, Carolin, Guo, Hanmin, Shin, GiWon, Huang, Yiling, Pattni, Reenal, Meng, Qingxi, Greer, Stephanie U, Roychowdhury, Tanmoy, Wood, Raegan N, Ho, Marcus, Dohna, Heinrich Zu, Abyzov, Alexej, Hallmayer, Joachim F, Wong, Wing H, Ji, Hanlee P, Urban, Alexander E

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Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy von WINKELMANN, Juliane, LING LIN, POLI, Francesca, GRUBERT, Fabian, WIELAND, Thomas, GRAF, Elisabeth, HALLMAYER, Joachim, STROM, Tim M, MIGNOT, Emmanuel, SCHORMAIR, Barbara, KORNUM, Birgitte R, FARACO, Juliette, PLAZZI, Giuseppe, MELBERG, Atle, CORNELIO, Ferdinando, URBAN, Alexander E, PIZZA, Fabio

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Genetic and environmental influences on structural brain measures in twins with autism spectrum disorder von Hegarty, John P., Pegoraro, Luiz F. L., Lazzeroni, Laura C., Raman, Mira M., Hallmayer, Joachim F., Monterrey, Julio C., Cleveland, Sue C., Wolke, Olga N., Phillips, Jennifer M., Reiss, Allan L., Hardan, Antonio Y.

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ImmunoChip study implicates antigen presentation to T cells in narcolepsy von Faraco, Juliette, Lin, Ling, Kornum, Birgitte Rahbek, Kenny, Eimear E, Trynka, Gosia, Einen, Mali, Rico, Tom J, Lichtner, Peter, Dauvilliers, Yves, Arnulf, Isabelle, Lecendreux, Michel, Javidi, Sirous, Geisler, Peter, Mayer, Geert, Pizza, Fabio, Poli, Francesca, Plazzi, Giuseppe, Overeem, Sebastiaan, Lammers, Gert Jan, Kemlink, David, Sonka, Karel, Nevsimalova, Sona, Rouleau, Guy, Desautels, Alex, Montplaisir, Jacques, Frauscher, Birgit, Ehrmann, Laura, Högl, Birgit, Jennum, Poul, Bourgin, Patrice, Peraita-Adrados, Rosa, Iranzo, Alex, Bassetti, Claudio, Chen, Wei-Min, Concannon, Patrick, Thompson, Susan D, Damotte, Vincent, Fontaine, Bertrand, Breban, Maxime, Gieger, Christian, Klopp, Norman, Deloukas, Panos, Wijmenga, Cisca, Hallmayer, Joachim, Onengut-Gumuscu, Suna, Rich, Stephen S, Winkelmann, Juliane, Mignot, Emmanuel

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A Twin Study of Altered White Matter Heritability in Youth With Autism Spectrum Disorder von Hegarty, 2nd, John P, Monterrey, Julio C, Tian, Qiyuan, Cleveland, Sue C, Gong, Xinyi, Phillips, Jennifer M, Wolke, Olga N, McNab, Jennifer A, Hallmayer, Joachim F, Reiss, Allan L, Hardan, Antonio Y, Lazzeroni, Laura C

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Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human-Induced Neurons von Zhang, Siming, Zhang, Xianglong, Purmann, Carolin, Ma, Shining, Shrestha, Anima, Davis, Kasey N., Ho, Marcus, Huang, Yiling, Pattni, Reenal, Wong, Wing Hung, Bernstein, Jonathan A., Hallmayer, Joachim, Urban, Alexander E.

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Insulin resistance and hippocampal volume in women at risk for Alzheimer's disease von Rasgon, Natalie L, Kenna, Heather A, Wroolie, Tonita E, Kelley, Ryan, Silverman, Daniel, Brooks, John, Williams, Katherine E, Powers, Bevin N, Hallmayer, Joachim, Reiss, Allan

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Genetic and demographic predisposing factors associated with pediatric sleepwalking in the Philadelphia Neurodevelopmental Cohort von Chiba, Yuhei, Phillips, Owen R., Takenoshita, Shinichi, Ollila, Hanna M., Hallmayer, Joachim F., Nishino, Seiji, Singh, Manpreet K.

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Increased activation product of complement 4 protein in plasma of individuals with schizophrenia von Kalinowski, Agnieszka, Liliental, Joanna, Anker, Lauren A., Linkovski, Omer, Culbertson, Collin, Hall, Jacob N., Pattni, Reenal, Sabatti, Chiara, Noordsy, Douglas, Hallmayer, Joachim F., Mellins, Elizabeth D., Ballon, Jacob S., O’Hara, Ruth, Levinson, Douglas F., Urban, Alexander E.

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Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders von Zhou, Bo, Arthur, Joseph G., Guo, Hanmin, Kim, Taeyoung, Huang, Yiling, Pattni, Reenal, Wang, Tao, Kundu, Soumya, Luo, Jay X.J., Lee, HoJoon, Nachun, Daniel C., Purmann, Carolin, Monte, Emma M., Weimer, Annika K., Qu, Ping-Ping, Shi, Minyi, Jiang, Lixia, Yang, Xinqiong, Fullard, John F., Bendl, Jaroslav, Girdhar, Kiran, Kim, Minsu, Chen, Xi, Greenleaf, William J., Duncan, Laramie, Ji, Hanlee P., Zhu, Xiang, Song, Giltae, Montgomery, Stephen B., Palejev, Dean, zu Dohna, Heinrich, Roussos, Panos, Kundaje, Anshul, Hallmayer, Joachim F., Snyder, Michael P., Wong, Wing H., Urban, Alexander E.

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