Il Museo Archeologico “S. Lauricella” e il parco archeologico di Monte Saraceno, Ravanusa (AG)

Por Elena Calafato
Publicado em 2017-06-01

Evaluating teacher multilingualism across contexts and multiple languages: validation and insights()

Por Calafato, Raees
Publicado no Heliyon (2020)

Chapter 11 Multilingual teacher identity in the Emirates

Por Calafato, Raees
Publicado em 2022

The interplay between genetics, cognition and schizophrenia

Por Calafato, Maria Stella, Bramon, Elvira
Publicado no Brain (2019)

Ricin: An Ancient Story for a Timeless Plant Toxin

Por Polito, Letizia, Bortolotti, Massimo, Battelli, Maria Giulia, Calafato, Giulia, Bolognesi, Andrea
Publicado no Toxins (Basel) (2019)

SU72. Abnormal Frontal Synaptic Gain Mediating the P300 in Patients With Psychosis and Their Unaffected Relatives

Por Diez, Alvaro, Ranlund, Siri, Pinotsis, Dimitris, Calafato, Stella, Shaikh, Madiha, Hall, Mei-Hua, Walshe, Muriel, Nevado, Ángel, Friston, Karl, Adams, Rick, Bramon, Elvira
Publicado no Schizophr Bull (2017)

Oxidative stress and cellular stress response in diabetic nephropathy

Por Calabrese, Vittorio, Mancuso, Cesare, Sapienza, Maria, Puleo, Eduardo, Calafato, Stella, Cornelius, Carolin, Finocchiaro, Manuela, Mangiameli, Andrea, Di Mauro, Maurizio, Stella, Anna Maria Giuffrida, Castellino, Pietro
Publicado em 2007

Abnormal frontoparietal synaptic gain mediating the P300 in patients with psychotic disorder and their unaffected relatives

Por Díez, Álvaro, Ranlund, Siri, Pinotsis, Dimitris, Calafato, Stella, Shaikh, Madiha, Hall, Mei‐Hua, Walshe, Muriel, Nevado, Ángel, Friston, Karl J., Adams, Rick A., Bramon, Elvira
Publicado no Hum Brain Mapp (2017)

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Por Kousi, Maria, Anttila, Verneri, Schulz, Angela, Calafato, Stella, Jakkula, Eveliina, Riesch, Erik, Myllykangas, Liisa, Kalimo, Hannu, Topcu, Meral, Gokben, Sarenur, Alehan, Fusun, Lemke, Johannes R, Alber, Michael, Palotie, Aarno, Kopra, Outi, Lehesjoki, Anna-Elina
Publicado em 2012

The GENCODE exome: sequencing the complete human exome

Por Coffey, Alison J, Kokocinski, Felix, Calafato, Maria S, Scott, Carol E, Palta, Priit, Drury, Eleanor, Joyce, Christopher J, LeProust, Emily M, Harrow, Jen, Hunt, Sarah, Lehesjoki, Anna-Elina, Turner, Daniel J, Hubbard, Tim J, Palotie, Aarno
Publicado em 2011

Use of schizophrenia and bipolar disorder polygenic risk scores to identify psychotic disorders

Por Calafato, Maria Stella, Thygesen, Johan H., Ranlund, Siri, Zartaloudi, Eirini, Cahn, Wiepke, Crespo-Facorro, Benedicto, Díez-Revuelta, Álvaro, Di Forti, Marta, Hall, Mei-Hua, Iyegbe, Conrad, Jablensky, Assen, Kahn, Rene, Kalaydjieva, Luba, Kravariti, Eugenia, Lin, Kuang, McDonald, Colm, McIntosh, Andrew M., McQuillin, Andrew, Picchioni, Marco, Rujescu, Dan, Shaikh, Madiha, Toulopoulou, Timothea, Os, Jim Van, Vassos, Evangelos, Walshe, Muriel, Powell, John, Lewis, Cathryn M., Murray, Robin M., Bramon, Elvira
Publicado no Br J Psychiatry (2018)

Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains

Por Blakey, R., Ranlund, S., Zartaloudi, E., Cahn, W., Calafato, S., Colizzi, M., Crespo-Facorro, B., Daniel, C., Díez-Revuelta, Á., Di Forti, M., Iyegbe, C., Jablensky, A., Jones, R., Hall, M.-H., Kahn, R., Kalaydjieva, L., Kravariti, E., Lin, K., McDonald, C., McIntosh, A. M., Picchioni, M., Powell, J., Presman, A., Rujescu, D., Schulze, K., Shaikh, M., Thygesen, J. H., Toulopoulou, T., Van Haren, N., Van Os, J., Walshe, M., Murray, R. M., Bramon, E.
Publicado no Psychol Med (2017)

A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains

Por Ranlund, Siri, Calafato, Stella, Thygesen, Johan H., Lin, Kuang, Cahn, Wiepke, Crespo‐Facorro, Benedicto, de Zwarte, Sonja M.C., Díez, Álvaro, Di Forti, Marta, Iyegbe, Conrad, Jablensky, Assen, Jones, Rebecca, Hall, Mei‐Hua, Kahn, Rene, Kalaydjieva, Luba, Kravariti, Eugenia, McDonald, Colm, McIntosh, Andrew M., McQuillin, Andrew, Picchioni, Marco, Prata, Diana P., Rujescu, Dan, Schulze, Katja, Shaikh, Madiha, Toulopoulou, Timothea, van Haren, Neeltje, van Os, Jim, Vassos, Evangelos, Walshe, Muriel, Lewis, Cathryn, Murray, Robin M., Powell, John, Bramon, Elvira
Publicado no Am J Med Genet B Neuropsychiatr Genet (2017)

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Por Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M, Calafato, M Stella, Nyholt, Dale R, Dimas, Antigone S, Freilinger, Tobias, Müller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A, Hämäläinen, Eija, de Vries, Boukje, Stam, Anine H, Weller, Claudia M, Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Göbel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Björnsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G, Hagen, Knut, Stovner, Lars, Wichmann, H-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S, Breteler, Monique M B, Uitterlinden, Andre G, Hofman, Albert, van Duijn, Cornelia M, Tikka-Kleemola, Päivi, Vepsäläinen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Färkkilä, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D, Olesen, Jes, Daly, Mark, Wessman, Maija, van den Maagdenberg, Arn M J M, Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T, Frants, Rune R, Palotie, Aarno
Publicado em 2010