Brain Cell Type Specific Gene Expression and Co-expression Network Architectures von McKenzie, Andrew T., Wang, Minghui, Hauberg, Mads E., Fullard, John F., Kozlenkov, Alexey, Keenan, Alexandra, Hurd, Yasmin L., Dracheva, Stella, Casaccia, Patrizia, Roussos, Panos, Zhang, Bin

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Integration of Alzheimer’s disease genetics and myeloid genomics identifies disease risk regulatory elements and genes von Novikova, Gloriia, Kapoor, Manav, TCW, Julia, Abud, Edsel M., Efthymiou, Anastasia G., Chen, Steven X., Cheng, Haoxiang, Fullard, John F., Bendl, Jaroslav, Liu, Yiyuan, Roussos, Panos, Björkegren, Johan LM, Liu, Yunlong, Poon, Wayne W., Hao, Ke, Marcora, Edoardo, Goate, Alison M.

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Microvascular anomaly conditions in psychiatric disease. Schizophrenia – angiogenesis connection von Katsel, Pavel, Roussos, Panos, Pletnikov, Mikhail, Haroutunian, Vahram

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A Bayesian framework for multiple trait colocalization from summary association statistics von Giambartolomei, Claudia, Zhenli Liu, Jimmy, Zhang, Wen, Hauberg, Mads, Shi, Huwenbo, Boocock, James, Pickrell, Joe, Jaffe, Andrew E, Pasaniuc, Bogdan, Roussos, Panos

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Non-cell-autonomous disruption of nuclear architecture as a potential cause of COVID-19-induced anosmia von Zazhytska, Marianna, Kodra, Albana, Hoagland, Daisy A., Frere, Justin, Fullard, John F., Shayya, Hani, McArthur, Natalie G., Moeller, Rasmus, Uhl, Skyler, Omer, Arina D., Gottesman, Max E., Firestein, Stuart, Gong, Qizhi, Canoll, Peter D., Goldman, James E., Roussos, Panos, tenOever, Benjamin R., Jonathan B. Overdevest, Lomvardas, Stavros

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Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons von Hauberg, Mads E., Creus-Muncunill, Jordi, Bendl, Jaroslav, Kozlenkov, Alexey, Zeng, Biao, Corwin, Chuhyon, Chowdhury, Sarah, Kranz, Harald, Hurd, Yasmin L., Wegner, Michael, Børglum, Anders D., Dracheva, Stella, Ehrlich, Michelle E., Fullard, John F., Roussos, Panos

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An atlas of chromatin accessibility in the adult human brain von Fullard, John F, Hauberg, Mads E, Bendl, Jaroslav, Egervari, Gabor, Cirnaru, Maria-Daniela, Reach, Sarah M, Motl, Jan, Ehrlich, Michelle E, Hurd, Yasmin L, Roussos, Panos

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Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk von Rajarajan, Prashanth, Borrman, Tyler, Liao, Will, Schrode, Nadine, Flaherty, Erin, Casiño, Charlize, Powell, Samuel, Yashaswini, Chittampalli, LaMarca, Elizabeth A, Kassim, Bibi, Javidfar, Behnam, Espeso-Gil, Sergio, Li, Aiqun, Won, Hyejung, Geschwind, Daniel H, Ho, Seok-Man, MacDonald, Matthew, Hoffman, Gabriel E, Roussos, Panos, Zhang, Bin, Hahn, Chang-Gyu, Weng, Zhiping, Brennand, Kristen J, Akbarian, Schahram

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mGluR5 hypofunction is integral to glutamatergic dysregulation in schizophrenia von Wang, Hoau-Yan, MacDonald, Mathew L., Borgmann-Winter, Karin E., Banerjee, Anamika, Sleiman, Patrick, Tom, Andrew, Khan, Amber, Lee, Kuo-Chieh, Roussos, Panos, Siegel, Steven J., Hemby, Scott E., Bilker, Warren B., Gur, Raquel E., Hahn, Chang-Gyu

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Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants von Hauberg, Mads Engel, Roussos, Panos, Grove, Jakob, Børglum, Anders Dupont, Mattheisen, Manuel

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Transcription factor 4 as an important determinant of gating function in schizophrenia von Roussos, Panos

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Functional interpretation of genetic variants using deep learning predicts impact on chromatin accessibility and histone modification von Hoffman, Gabriel E, Bendl, Jaroslav, Girdhar, Kiran, Schadt, Eric E, Roussos, Panos

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Analysis of Transcriptional Variability in a Large Human iPSC Library Reveals Genetic and Non-genetic Determinants of Heterogeneity von Carcamo-Orive, Ivan, Hoffman, Gabriel E., Cundiff, Paige, Beckmann, Noam D., D’Souza, Sunita L., Knowles, Joshua W., Patel, Achchhe, Papatsenko, Dimitri, Abbasi, Fahim, Reaven, Gerald M., Whalen, Sean, Lee, Philip, Shahbazi, Mohammad, Henrion, Marc Y.R., Zhu, Kuixi, Wang, Sven, Roussos, Panos, Schadt, Eric E., Pandey, Gaurav, Chang, Rui, Quertermous, Thomas, Lemischka, Ihor

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Genetics of the human microglia regulome refines Alzheimer’s disease risk loci von Kosoy, Roman, Fullard, John F., Zeng, Biao, Bendl, Jaroslav, Dong, Pengfei, Rahman, Samir, Kleopoulos, Steven P., Shao, Zhiping, Girdhar, Kiran, Humphrey, Jack, de Paiva Lopes, Katia, Charney, Alexander W., Kopell, Brian H., Raj, Towfique, Bennett, David, Kellner, Christopher P., Haroutunian, Vahram, Hoffman, Gabriel E., Roussos, Panos

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The 3D Genome in Brain Development: An Exploration of Molecular Mechanisms and Experimental Methods von Rahman, Samir, Roussos, Panos

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Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits von Zhang, Wen, Voloudakis, Georgios, Rajagopal, Veera M., Readhead, Ben, Dudley, Joel T., Schadt, Eric E., Björkegren, Johan L. M., Kim, Yungil, Fullard, John F., Hoffman, Gabriel E., Roussos, Panos

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Differential gene regulatory pattern in the human brain from schizophrenia using transcriptomic-causal network von Yazdani, Akram, Mendez-Giraldez, Raul, Yazdani, Azam, Kosorok, Michael R, Roussos, Panos

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Meta-analysis on the association between genetic polymorphisms and prepulse inhibition of the acoustic startle response von Quednow, Boris B., Ejebe, Kenechi, Wagner, Michael, Giakoumaki, Stella G., Bitsios, Panos, Kumari, Veena, Roussos, Panos

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Substantial DNA methylation differences between two major neuronal subtypes in human brain von Kozlenkov, Alexey, Wang, Minghui, Roussos, Panos, Rudchenko, Sergei, Barbu, Mihaela, Bibikova, Marina, Klotzle, Brandy, Dwork, Andrew J, Zhang, Bin, Hurd, Yasmin L, Koonin, Eugene V, Wegner, Michael, Dracheva, Stella

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Chromatin accessibility mapping of the striatum identifies tyrosine kinase FYN as a therapeutic target for heroin use disorder von Egervari, Gabor, Akpoyibo, Diana, Rahman, Tanni, Fullard, John F., Callens, James E., Landry, Joseph A., Ly, Annie, Zhou, Xianxiao, Warren, Noël, Hauberg, Mads E., Hoffman, Gabriel, Ellis, Randy, Ferland, Jacqueline-Marie N., Miller, Michael L., Keller, Eva, Zhang, Bin, Roussos, Panos, Hurd, Yasmin L.

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