Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction von Ayalew, M, Le-Niculescu, H, Levey, D F, Jain, N, Changala, B, Patel, S D, Winiger, E, Breier, A, Shekhar, A, Amdur, R, Koller, D, Nurnberger, J I, Corvin, A, Geyer, M, Tsuang, M T, Salomon, D, Schork, N J, Fanous, A H, O'Donovan, M C, Niculescu, A B

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Uncovering the Hidden Risk Architecture of the Schizophrenias: Confirmation in Three Independent Genome-Wide Association Studies von Arnedo, Javier, Svrakic, Dragan M., del Val, Coral, Romero-Zaliz, Rocío, Hernández-Cuervo, Helena, Fanous, Ayman H., Pato, Michele T., Pato, Carlos N., de Erausquin, Gabriel A., Cloninger, C. Robert, Zwir, Igor

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Replication of association between schizophrenia and ZNF804A in the Irish Case–Control Study of Schizophrenia sample von Riley, B, Thiselton, D, Maher, B S, Bigdeli, T, Wormley, B, McMichael, G O, Fanous, A H, Vladimirov, V, O'Neill, F A, Walsh, D, Kendler, K S

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications von Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe'er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A., Gejman, Pablo V.

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Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia von Jia, Peilin, Wang, Lily, Fanous, Ayman H, Pato, Carlos N, Edwards, Todd L, Zhao, Zhongming

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Experimental validation of candidate schizophrenia gene ZNF804A as target for hsa-miR-137 von Kim, Albert H, Parker, Erin K, Williamson, Vernell, McMichael, Gowon O, Fanous, Ayman H, Vladimirov, Vladimir I

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Can genomics help usher schizophrenia into the age of RDoC and DSM-6? von Fanous, Ayman H

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Schizophrenia gene networks and pathways and their applications for novel candidate gene selection von Sun, Jingchun, Jia, Peilin, Fanous, Ayman H, van den Oord, Edwin, Chen, Xiangning, Riley, Brien P, Amdur, Richard L, Kendler, Kenneth S, Zhao, Zhongming

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Genetic heterogeneity, modifier genes, and quantitative phenotypes in psychiatric illness: searching for a framework von Fanous, A H, Kendler, K S

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Genome-Wide Association Study of Clinical Dimensions of Schizophrenia: Polygenic Effect on Disorganized Symptoms von Fanous, Ayman H., Zhou, Baiyu, Aggen, Steven H., Bergen, Sarah E., Amdur, Richard L., Duan, Jubao, Sanders, Alan R., Shi, Jianxin, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Dudbridge, Frank, Holmans, Peter A., Ripke, Stephan, Gejman, Pablo V., Kendler, Kenneth S., Levinson, Douglas F.

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A longitudinal study of personality and major depression in a population-based sample of male twins von FANOUS, AYMAN H., NEALE, MICHAEL C., AGGEN, STEVEN H., KENDLER, KENNETH S.

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DISTMIX: direct imputation of summary statistics for unmeasured SNPs from mixed ethnicity cohorts von Lee, Donghyung, Bigdeli, T Bernard, Williamson, Vernell S, Vladimirov, Vladimir I, Riley, Brien P, Fanous, Ayman H, Bacanu, Silviu-Alin

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Identification of shared genetic variants between schizophrenia and lung cancer von Zuber, Verena, Jönsson, Erik G., Frei, Oleksandr, Witoelar, Aree, Thompson, Wesley K., Schork, Andrew J., Bettella, Francesco, Wang, Yunpeng, Djurovic, Srdjan, Smeland, Olav B., Dieset, Ingrid, Fanous, Ayman H., Desikan, Rahul S., Küry, Sébastien, Bézieau, Stéphane, Dale, Anders M., Mills, Ian G., Andreassen, Ole A.

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Human–Artificial Intelligence Interaction Research Is Crucial for Medical Artificial Intelligence Implementation von Sams, Clarence M., Fanous, Aaron H., Daneshjou, Roxana

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Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia von Ruderfer, D M, Fanous, A H, Ripke, S, McQuillin, A, Amdur, R L, Gejman, P V, O'Donovan, M C, Andreassen, O A, Djurovic, S, Hultman, C M, Kelsoe, J R, Jamain, S, Landén, M, Leboyer, M, Nimgaonkar, V, Nurnberger, J, Smoller, J W, Craddock, N, Corvin, A, Sullivan, P F, Holmans, P, Sklar, P, Kendler, K S

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Genomewide Association Study of Movement-Related Adverse Antipsychotic Effects von Åberg, Karolina, Adkins, Daniel E, Bukszár, József, Webb, Bradley T, Caroff, Stanley N, Miller, Del D, Sebat, Jonathan, Stroup, Scott, Fanous, Ayman H, Vladimirov, Vladimir I, McClay, Joseph L, Lieberman, Jeffrey A, Sullivan, Patrick F, van den Oord, Edwin J.C.G

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Relationship Between a High-Risk Haplotype in the DTNBP1 (Dysbindin) Gene and Clinical Features of Schizophrenia von Fanous, Ayman H., van den Oord, Edwin J., Riley, Brien P., Aggen, Steven H., Neale, Michael C., O'Neill, F. Anthony, Walsh, Dermot, Kendler, Kenneth S.

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Significant correlation in linkage signals from genome-wide scans of schizophrenia and schizotypy von Fanous, A H, Neale, M C, Gardner, C O, Webb, B T, Straub, R E, O'Neill, F A, Walsh, D, Riley, B P, Kendler, K S

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Molecular Validation of the Schizophrenia Spectrum von BIGDELI, T. Bernard, BACANU, Silviu-Alin, WEBB, Bradley T, WALSH, Dermot, O'NEILL, F. Anthony, FANOUS, Ayman H, RILEY, Brien P, KENDLER, Kenneth S

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Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history von Bergen, Sarah E, O'Dushlaine, Colm T, Lee, Phil H, Fanous, Ayman H, Ruderfer, Douglas M, Ripke, Stephan, Sullivan, Patrick F, Smoller, Jordan W, Purcell, Shaun M, Corvin, Aiden

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