Familial Ohtahara syndrome due to a novel ARX gene mutation by Giordano, L., Sartori, S., Russo, S., Accorsi, P., Galli, J., Tiberti, A., Bettella, E., Marchi, M., Vignoli, A., Darra, F., Murgia, A., Bernardina, B. Dalla

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Early-onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females by Bettella, E, Di Rosa, G, Polli, R, Leonardi, E, Tortorella, G, Sartori, S, Murgia, A

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Heavy metal inhibition of EROD activity in liver microsomes from the bass Dicentrarchus labrax exposed to organic xenobiotics: Role of GSH in the reduction of heavy metal effects by Viarengo, Aldo, Bettella, Elisa, Fabbri, Rita, Burlando, Bruno, Lafaurie, Marc

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Familial Ohtahara syndrome due to a novel ARX gene mutation by Giordano, L., Sartori, S., Russo, S., Accorsi, P., Galli, J., Tiberti, A., Bettella, E., Marchi, M., Vignoli, A., Darra, F., Murgia, A., Bernardina, B. Dalla

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Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk by Jansen, Iris E, Savage, Jeanne E, Watanabe, Kyoko, Bryois, Julien, Williams, Dylan M, Steinberg, Stacy, Sealock, Julia, Karlsson, Ida K, Hägg, Sara, Athanasiu, Lavinia, Voyle, Nicola, Proitsi, Petroula, Witoelar, Aree, Stringer, Sven, Aarsland, Dag, Almdahl, Ina Selseth, Andersen, Fred, Bergh, Sverre, Bettella, Francesco, Björnsson, Sigurbjörn, Brækhus, Anne, Bråthen, Geir, de Leeuw, Christiaan A, Desikan, Rahul S, Djurovic, Srdjan, Dumitrescu, Logan, Fladby, Tormod, Hohman, Timothy J, Jónsson, Pálmi V, Kiddle, Steven J, Rongve, Arvid, Saltvedt, Ingvild, Sando, Sigrid Botne, Selbæk, Geir, Shoai, Maryam, Skene, Nathan G, Snædal, Jón G, Stordal, Eystein, Ulstein, Ingun, Wang, Yunpeng, White, Linda Rosemary, Hardy, John, Hjerling-Leffler, Jens, Sullivan, Patrick, van der Flier, Wiesje M, Dobson, Richard, Davis, Lea K, Stefánsson, Hreinn, Stefánsson, Kári, Pedersen, Nancy L, Ripke, Stephan, Andreassen, Ole Andreas, Posthuma, Danielle

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Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence by Smeland, Olav B, Bahrami, Shahram, Frei, Oleksandr, Shadrin, Alexey, O'Connell, Kevin, Savage, Jeanne, Watanabe, Kyoko, Krull, Florian, Bettella, Francesco, Steen, Nils Eiel, Ueland, Torill, Posthuma, Danielle, Djurovic, Srdjan, Dale, Anders M, Andreassen, Ole A

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Identification of genetic loci jointly influencing schizophrenia risk and the cognitive traits of verbal-numerical reasoning, reaction time, and general cognitive function by Smeland, Olav Bjerkehagen, Frei, Oleksandr, Kauppi, Karolina, Hill, W. David, Li, Wen, Wang, Yunpeng, Krull, Florian, Bettella, Francesco, Eriksen, Jon Alm, Witoelar, Aree, Davies, Gail, Fan, Chun Chieh, Thompson, Wesley Kurt, Lam, Max, Lencz, Todd, Chen, Chi-Hua, Ueland, Torill, Jönsson, Erik Gunnar, Djurovic, Srdjan, Deary, Ian J, Dale, Anders, Andreassen, Ole Andreas

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Dependence of chick killing on nest density in a colony of yellow-legged gull (Larus cachinnans michaellis) by Marin, Guglielmo, Bettella, Elisa, Pilastro, Andrea, Amato, Stefano, Tiloca, Giovanni

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Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes by van der Meer, Dennis, Rokicki, Jaroslav, Kaufmann, Tobias, Córdova-Palomera, Aldo, Moberget, Torgeir, Alnæs, Dag, Bettella, Francesco, Frei, Oleksandr, Doan, Nhat Trung, Sønderby, Ida E, Smeland, Olav B, Agartz, Ingrid, Bertolino, Alessandro, Bralten, Janita, Brandt, Christine L, Buitelaar, Jan K, Djurovic, Srdjan, van Donkelaar, Marjolein, Dørum, Erlend S, Espeseth, Thomas, Faraone, Stephen V, Fernández, Guillén, Fisher, Simon E, Franke, Barbara, Haatveit, Beathe, Hartman, Catharina A, Hoekstra, Pieter J, Håberg, Asta K, Jönsson, Erik G, Kolskår, Knut K, Le Hellard, Stephanie, Lund, Martina J, Lundervold, Astri J, Lundervold, Arvid, Melle, Ingrid, Monereo Sánchez, Jennifer, Norbom, Linn C, Nordvik, Jan E, Nyberg, Lars, Oosterlaan, Jaap, Papalino, Marco, Papassotiropoulos, Andreas, Pergola, Giulio, de Quervain, Dominique J F, Richard, Geneviève, Sanders, Anne-Marthe, Selvaggi, Pierluigi, Shumskaya, Elena, Steen, Vidar M, Tønnesen, Siren, Ulrichsen, Kristine M, Zwiers, Marcel P, Andreassen, Ole A, Westlye, Lars T

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Machine Learning and Image Recognition Technologies to Identify Built Environment Barriers and Incentives to Walk by Trichês Lucchesi, Shanna, de Abreu e Silva, João, Margarita Larranaga, Ana, Zechin, Douglas, Beatriz Bettella Cybis, Helena

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Genome-wide Association Analysis of Parkinson’s Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci by Smeland, Olav B., Shadrin, Alexey, Bahrami, Shahram, Broce, Iris, Tesli, Martin, Frei, Oleksandr, Wirgenes, Katrine V., O’Connell, Kevin S., Krull, Florian, Bettella, Francesco, Steen, Nils Eiel, Sugrue, Leo, Wang, Yunpeng, Svenningsson, Per, Sharma, Manu, Pihlstrøm, Lasse, Toft, Mathias, O’Donovan, Michael, Djurovic, Srdjan, Desikan, Rahul, Dale, Anders M., Andreassen, Ole A.

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Indicated association between polygenic risk score and treatment-resistance in a naturalistic sample of patients with schizophrenia spectrum disorders by Werner, Maren Caroline Frogner, Wirgenes, Katrine Verena, Haram, Marit, Bettella, Francesco, Lunding, Synve Hoffart, Rødevand, Linn, Hjell, Gabriela, Agartz, Ingrid, Djurovic, Srdjan, Melle, Ingrid, Andreassen, Ole A., Steen, Nils Eiel

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Identification of shared genetic variants between schizophrenia and lung cancer by 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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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy by Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.

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Characterization of intellectual disability and autism comorbidity through gene panel sequencing by Aspromonte, Maria C., Bellini, Mariagrazia, Gasparini, Alessandra, Carraro, Marco, Bettella, Elisa, Polli, Roberta, Cesca, Federica, Bigoni, Stefania, Boni, Stefania, Carlet, Ombretta, Negrin, Susanna, Mammi, Isabella, Milani, Donatella, Peron, Angela, Sartori, Stefano, Toldo, Irene, Soli, Fiorenza, Turolla, Licia, Stanzial, Franco, Benedicenti, Francesco, Marino‐Buslje, Cristina, Tosatto, Silvio C. E., Murgia, Alessandra, Leonardi, Emanuela

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Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease by Creese, Byron, Vassos, Evangelos, Bergh, Sverre, Athanasiu, Lavinia, Johar, Iskandar, Rongve, Arvid, Medbøen, Ingrid Tøndel, Vasconcelos Da Silva, Miguel, Aakhus, Eivind, Andersen, Fred, Bettella, Francesco, Braekhus, Anne, Djurovic, Srdjan, Paroni, Giulia, Proitsi, Petroula, Saltvedt, Ingvild, Seripa, Davide, Stordal, Eystein, Fladby, Tormod, Aarsland, Dag, Andreassen, Ole A, Ballard, Clive, Selbaek, Geir

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Meta-analysis of Alzheimer's disease on 9,751 samples from Norway and IGAP study identifies four risk loci by Witoelar, Aree, Rongve, Arvid, Almdahl, Ina S, Ulstein, Ingun D, Engvig, Andreas, White, Linda R, Selbæk, Geir, Stordal, Eystein, Andersen, Fred, Brækhus, Anne, Saltvedt, Ingvild, Engedal, Knut, Hughes, Timothy, Bergh, Sverre, Bråthen, Geir, Bogdanovic, Nenad, Bettella, Francesco, Wang, Yunpeng, Athanasiu, Lavinia, Bahrami, Shahram, Le Hellard, Stephanie, Giddaluru, Sudheer, Dale, Anders M, Sando, Sigrid B, Steinberg, Stacy, Stefansson, Hreinn, Snaedal, Jon, Desikan, Rahul S, Stefansson, Kari, Aarsland, Dag, Djurovic, Srdjan, Fladby, Tormod, Andreassen, Ole A

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INFN muon tomography demonstrator: past and recent results with an eye to near-future activities by Checchia, P, Benettoni, M, Bettella, G, Conti, E, Cossutta, L, Furlan, M, Gonella, F, Klinger, J, Montecassiano, F, Nebbia, G, Pegoraro, M, Pesente, S, Rigoni Garola, A, Urbani, M, Viesti, G, Vanini, S, Zumerle, G

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Characterization of intellectual disability and autism comorbidity through gene panel sequencing by Aspromonte, Maria C., Bellini, Mariagrazia, Gasparini, Alessandra, Carraro, Marco, Bettella, Elisa, Polli, Roberta, Cesca, Federica, Bigoni, Stefania, Boni, Stefania, Carlet, Ombretta, Negrin, Susanna, Mammi, Isabella, Milani, Donatella, Peron, Angela, Sartori, Stefano, Toldo, Irene, Soli, Fiorenza, Turolla, Licia, Stanzial, Franco, Benedicenti, Francesco, Marino‐Buslje, Cristina, Tosatto, Silvio C.E., Murgia, Alessandra, Leonardi, Emanuela

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Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology by van der Meer, Dennis, Shadrin, Alexey A., O’Connell, Kevin, Bettella, Francesco, Djurovic, Srdjan, Wolfers, Thomas, Alnæs, Dag, Agartz, Ingrid, Smeland, Olav B., Melle, Ingrid, Sánchez, Jennifer Monereo, Linden, David E.J., Dale, Anders M., Westlye, Lars T., Andreassen, Ole A., Frei, Oleksandr, Kaufmann, Tobias

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