Relationship Between Cortical Gyrification, White Matter Connectivity, and Autism Spectrum Disorder von Ecker, C, Andrews, D, Dell'Acqua, F, Daly, E, Murphy, C, Catani, M, Thiebaut de Schotten, M, Baron-Cohen, S, Lai, M C, Lombardo, M V, Bullmore, E T, Suckling, J, Williams, S, Jones, D K, Chiocchetti, A, Murphy, D G M

Volltext

A combination of LCPUFAs regulates the expression of miRNA-146a-5p in a murine asthma model and human alveolar cells von Fussbroich, D., Kohnle, C., Schwenger, T., Driessler, C., Dücker, R.P., Eickmeier, O., Gottwald, G., Jerkic, S.P., Zielen, S., Kreyenberg, H., Beermann, C., Chiocchetti, A.G., Schubert, R.

Volltext

Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach von Chiocchetti, A G, Kopp, M, Waltes, R, Haslinger, D, Duketis, E, Jarczok, T A, Poustka, F, Voran, A, Graab, U, Meyer, J, Klauck, S M, Fulda, S, Freitag, C M

Volltext

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder von Lim, Elaine T, Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S, Zhang, Xiaochang, D'Gama, Alissa M, Kim, Sonia N, Hill, Robert Sean, Goldberg, Arthur P, Poultney, Christopher, Minshew, Nancy J, Kushima, Itaru, Aleksic, Branko, Ozaki, Norio, Parellada, Mara, Arango, Celso, Penzol, Maria J, Carracedo, Angel, Kolevzon, Alexander, Hultman, Christina M, Weiss, Lauren A, Fromer, Menachem, Chiocchetti, Andreas G, Freitag, Christine M, Church, George M, Scherer, Stephen W, Buxbaum, Joseph D, Walsh, Christopher A

Volltext

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism von Klauck, S M, Felder, B, Kolb-Kokocinski, A, Schuster, C, Chiocchetti, A, Schupp, I, Wellenreuther, R, Schmötzer, G, Poustka, F, Breitenbach-Koller, L, Poustka, A

Volltext

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders von Chiocchetti, A G, Haslinger, D, Stein, J L, de la Torre-Ubieta, L, Cocchi, E, Rothämel, T, Lindlar, S, Waltes, R, Fulda, S, Geschwind, D H, Freitag, C M

Volltext

Corrigendum to “Generation of human induced pluripotent stem cell lines (hiPSC) from one bipolar disorder patient carrier of a DGKH risk haplotype and one non-risk-variant-carrier... von Palladino, V.S., Subrata, N.O.C., Geburtig-Chiocchetti, A., McNeill, R., Hoffmann, P., Reif, A., Kittel-Schneider, S.

Volltext

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism von Satterstrom, F. Kyle, Breen, Michael S., Grove, Jakob, Klei, Lambertus, Xu, Xinyi, Norman, Utku, Brand, Harrison, Schwartz, Grace, Barbosa, Mafalda, Bybjerg-Grauholm, Jonas, Carracedo, Angel, Chiocchetti, Andreas G., Chung, Brian H.Y., Coon, Hilary, Cuccaro, Michael L., Dalla Bernardina, Bernardo, Domenici, Enrico, Dong, Shan, Freitag, Christine M., González-Peñas, Javier, Guter, Stephen, He, Xin, Herman, Gail E., Hertz-Picciotto, Irva, Hougaard, David M., Ionita-Laza, Iuliana, Jacob, Suma, Jamison, Jesslyn, Jugessur, Astanand, Kolevzon, Alexander, Kushima, Itaru, Lee, So Lun, Lehtimäki, Terho, Lim, Elaine T., Lipkin, W. Ian, Lopergolo, Diego, Lopes, Fátima, Ludena, Yunin, Maciel, Patricia, Meiri, Gal, Menashe, Idan, Miller, Judith, Montenegro, Eduarda M.S., Muglia, Pierandrea, Nordentoft, Merete, Ozaki, Norio, Palotie, Aarno, Parellada, Mara, Passos-Bueno, Maria Rita, Persico, Antonio M., Pessah, Isaac, Puura, Kaija, Renieri, Alessandra, Riberi, Evelise, Robinson, Elise B., Samocha, Kaitlin E., Sandin, Sven, Santangelo, Susan L., Schellenberg, Gerry, Scherer, Stephen W., Schmitt, Lauren, Silva, Isabela M.W., Singh, Tarjinder, Siper, Paige M., Soares, Gabriela, Susser, Ezra, Szatmari, Peter, Tang, Lara, Tassone, Flora, Teufel, Karoline, Trelles, Maria del Pilar, Werge, Thomas, Werling, Donna M., Wigdor, Emilie M., Yu, Mullin H.C., Zachi, Elaine, Agerbo, Esben, Als, Thomas Damm, Bækvad-Hansen, Marie, Belliveau, Rich, Cerrato, Felecia, Chambert, Kimberly, Churchhouse, Claire, Dumont, Ashley, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Howrigan, Daniel P., Maller, Julian, Mattheisen, Manuel, Moran, Jennifer, Pallesen, Jonatan, Poulsen, Jesper Buchhave, Ripke, Stephan, Gallagher, Louise, Gill, Michael, Zwick, Michael E., State, Matthew W., Daly, Mark J., Buxbaum, Joseph D.

Volltext

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism von Fu, Jack M., Satterstrom, F. Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L., Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P., Stevens, Christine R., Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B., Gauthier, Laura, Lee, Samuel K., Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N., Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian H. Y., Cook, Edwin H., Cuccaro, Michael L., Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J. Jay, Herman, Gail E., Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S., Passos-Bueno, Maria Rita, Persico, Antonio M., Renieri, Alessandra, Sutcliffe, James S., Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus C. Y., Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N., Schmidt, Rebecca J., Smith, Moyra, Costa, Claudia I. S., Trajkova, Slavica, Wang, Jaqueline Y. T., Yu, Mullin H. C., Cutler, David J., De Rubeis, Silvia, Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Talkowski, Michael E.

Volltext

Solid lipid nanoparticles of cholesteryl butyrate inhibit the proliferation of cancer cells in vitro and in vivo models von Minelli, R, Occhipinti, S, Gigliotti, C L, Barrera, G, Gasco, P, Conti, L, Chiocchetti, A, Zara, G P, Fantozzi, R, Giovarelli, M, Dianzani, U, Dianzani, C

Volltext

Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder von Chiocchetti, A., Pakalapati, G., Duketis, E., Wiemann, S., Poustka, A., Poustka, F., Klauck, S. M.

Volltext

A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation von Clemente, N, Boggio, E, Gigliotti, C L, Orilieri, E, Cappellano, G, Toth, E, Valletti, P A, Santoro, C, Quinti, I, Pignata, C, Notarangelo, L D, Dianzani, C, Dianzani, I, Ramenghi, U, Dianzani, U, Chiocchetti, A

Volltext

High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation von Chiocchetti, Annalisa, Indelicato, Manuela, Bensi, Thea, Mesturini, Riccardo, Giordano, Mara, Sametti, Selina, Castelli, Luca, Bottarel, Flavia, Mazzarino, Maria Clorinda, Garbarini, Letizia, Giacopelli, Francesca, Valesini, Guido, Santoro, Claudio, Dianzani, Irma, Ramenghi, Ugo, Dianzani, Umberto

Volltext

1266 COMPLEX ROLE OF OSTEOPONTIN IN THE PROGRESSION OF NONALCOHOLIC STEATOHEPATITIS (NASH) von Jindal, A, Sutti, S, Locatelli, I, Chiocchetti, A, Soluri, M.F.F, Vacchiano, M, Maldi, E, Bozzola, C, Dianzani, U, Albano, E

Volltext

Determinants of long COVID among adults hospitalized for SARS-CoV-2 infection: A prospective cohort study von Bellan, Mattia, Apostolo, Daria, Albè, Alice, Crevola, Martina, Errica, Nicolò, Ratano, Giacomo, Tonello, Stelvio, Minisini, Rosalba, D'Onghia, Davide, Baricich, Alessio, Patrucco, Filippo, Zeppegno, Patrizia, Gramaglia, Carla, Balbo, Piero Emilio, Cappellano, Giuseppe, Casella, Sara, Chiocchetti, Annalisa, Clivati, Elisa, Giordano, Mara, Manfredi, Marcello, Patti, Giuseppe, Pinato, David James, Puricelli, Chiara, Raineri, Davide, Rolla, Roberta, Sainaghi, Pier Paolo, Pirisi, Mario

Volltext

Variations of the perforin gene in patients with multiple sclerosis von Cappellano, G, Orilieri, E, Comi, C, Chiocchetti, A, Bocca, S, Boggio, E, Bernardone, I S, Cometa, A, Clementi, R, Barizzone, N, D'Alfonso, S, Corrado, L, Galimberti, D, Scarpini, E, Guerini, F R, Caputo, D, Paolicelli, D, Trojano, M, Figà-Talamanca, L, Salvetti, M, Perla, F, Leone, M, Monaco, F, Dianzani, U

Volltext

Defective T cell Fas function in patients with multiple sclerosis von COMI, C, LEONE, M, BONISSONI, S, DEFRANCO, S, BOTTAREL, F, MEZZATESTA, C, CHIOCCHETTI, A, PERLA, F, MONACO, F, DIANZANI, U

Volltext

Training approaches for the dissemination of clinical guidelines for NSSI: a quasi-experimental trial von Koenig, Elisa, Hoffmann, Ulrike, Fegert, Jörg M, Keller, Ferdinand, Sicorello, Maurizio, Spohrs, Jennifer, Kraus, Laura, Nickel, Sandra, Schmahl, Christian, Abler, Birgit, In-Albon, Tina, Koenig, Julian, Ougrin, Dennis, Kaess, Michael, Plener, Paul L

Volltext

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism von Hadley, Dexter, Wu, Zhi-liang, Kao, Charlly, Kini, Akshata, Mohamed-Hadley, Alisha, Thomas, Kelly, Vazquez, Lyam, Qiu, Haijun, Mentch, Frank, Pellegrino, Renata, Kim, Cecilia, Connolly, John, Glessner, Joseph, Hakonarson, Hakon

Volltext

The Osteopontin Gene +1239A/C Single Nucleotide Polymorphism is Associated with Type 1 Diabetes Mellitus in the Italian Population von Chiocchetti, A., Orilieri, E., Cappellano, G., Barizzone, N., D'Alfonso, S., D'Annunzio, G., Lorini, R., Ravazzolo, R., Cadario, F., Martinetti, M., Calcaterra, V., Cerutti, F., Bruno, G., Larizza, D., Dianzani, U.

Volltext