Association between Polyunsaturated Fatty Acid Profile and Bronchial Inflammation in Bronchiolitis Obliterans

por Jerkic, Silvija P., Bächle, Laura, Duecker, Ruth Pia, Gronau, Lucia, Chiocchetti, Andreas G., Zielen, Stefan, Schubert, Ralf
Publicado 2023

Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and Treatment

por Vasic, Verica, Jones, Mattson S. O., Haslinger, Denise, Knaus, Lisa S., Schmeisser, Michael J., Novarino, Gaia, Chiocchetti, Andreas G.
Publicado 2021

Effects of Hypoxia on RNA Cargo in Extracellular Vesicles from Human Adipose-Derived Stromal/Stem Cells

por Koch, Benjamin, Geßner, Alec, Farmand, Samira, Fuhrmann, Dominik C., Chiocchetti, Andreas G., Schubert, Ralf, Baer, Patrick C.
Publicado 2022

Drug-Resistant Juvenile Myoclonic Epilepsy: Misdiagnosis of Progressive Myoclonus Epilepsy

por Martin, Sarah, Strzelczyk, Adam, Lindlar, Silvia, Krause, Kristina, Reif, Philipp S., Menzler, Katja, Chiocchetti, Andreas G., Rosenow, Felix, Knake, Susanne, Klein, Karl Martin
Publicado 2019

Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD

por Palladino, Viola Stella, Chiocchetti, Andreas G., Frank, Lukas, Haslinger, Denise, McNeill, Rhiannon, Radtke, Franziska, Till, Andreas, Haupt, Simone, Brüstle, Oliver, Günther, Katharina, Edenhofer, Frank, Hoffmann, Per, Reif, Andreas, Kittel-Schneider, Sarah
Publicado 2020

The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factors

por Chiocchetti, Andreas G., Yousaf, Afsheen, Waltes, Regina, Bernhard, Anka, Martinelli, Anne, Ackermann, Katharina, Haslinger, Denise, Rotter, Björn, Krezdorn, Nico, Konrad, Kerstin, Kohls, Gregor, Vetro, Agnes, Hervas, Amaia, Fernández-Rivas, Aranzazu, Freitag, Christine M.
Publicado 2022

Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder

por Yousaf, Afsheen, Waltes, Regina, Haslinger, Denise, Klauck, Sabine M., Duketis, Eftichia, Sachse, Michael, Voran, Anette, Biscaldi, Monica, Schulte-Rüther, Martin, Cichon, Sven, Nöthen, Markus, Ackermann, Jörg, Koch, Ina, Freitag, Christine M., Chiocchetti, Andreas G.
Publicado 2020

The MiR-320 Family Is Strongly Downregulated in Patients with COVID-19 Induced Severe Respiratory Failure

por Duecker, Ruth P., Adam, Elisabeth H., Wirtz, Sarah, Gronau, Lucia, Khodamoradi, Yascha, Eberhardt, Fabian J., Donath, Helena, Gutmann, Desiree, Vehreschild, Maria J. G. T., Zacharowski, Kai, Kreyenberg, Hermann, Chiocchetti, Andreas G., Zielen, Stefan, Schubert, Ralf
Publicado 2021

Protein signatures of oxidative stress response in a patient specific cell line model for autism

por Chiocchetti, Andreas G, Haslinger, Denise, Boesch, Maximilian, Karl, Thomas, Wiemann, Stefan, Freitag, Christine M, Poustka, Fritz, Scheibe, Burghardt, Bauer, Johann W, Hintner, Helmut, Breitenbach, Michael, Kellermann, Josef, Lottspeich, Friedrich, Klauck, Sabine M, Breitenbach-Koller, Lore
Publicado 2014

Risk Stratification for Bipolar Disorder Using Polygenic Risk Scores Among Young High-Risk Adults

por Biere, Silvia, Kranz, Thorsten M., Matura, Silke, Petrova, Kristiyana, Streit, Fabian, Chiocchetti, Andreas G., Grimm, Oliver, Brum, Murielle, Brunkhorst-Kanaan, Natalie, Oertel, Viola, Malyshau, Aliaksandr, Pfennig, Andrea, Bauer, Michael, Schulze, Thomas G., Kittel-Schneider, Sarah, Reif, Andreas
Publicado 2020

SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study

por Farrow, Elizabeth, Chiocchetti, Andreas G., Rogers, Jack C., Pauli, Ruth, Raschle, Nora M., Gonzalez-Madruga, Karen, Smaragdi, Areti, Martinelli, Anne, Kohls, Gregor, Stadler, Christina, Konrad, Kerstin, Fairchild, Graeme, Freitag, Christine M., Chechlacz, Magdalena, De Brito, Stephane A.
Publicado 2021

Correction: SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study

por Farrow, Elizabeth, Chiocchetti, Andreas G., Rogers, Jack C., Pauli, Ruth, Raschle, Nora M., Gonzalez-Madruga, Karen, Smaragdi, Areti, Martinelli, Anne, Kohls, Gregor, Stadler, Christina, Konrad, Kerstin, Fairchild, Graeme, Freitag, Christine M., Chechlacz, Magdalena, De Brito, Stephane A.
Publicado 2021

Recessive gene disruptions in autism spectrum disorder

por Doan, Ryan N, Lim, Elaine T., De Rubeis, Silvia, Betancur, Catalina, Cutler, David J., Chiocchetti, Andreas G., Overman, Lynne M., Soucy, Aubrie, Goetze, Susanne, Freitag, Christine M., Daly, Mark J., Walsh, Christopher A., Buxbaum, Joseph D., Yu, Timothy W.
Publicado 2019

Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model

por Haslinger, Denise, Waltes, Regina, Yousaf, Afsheen, Lindlar, Silvia, Schneider, Ines, Lim, Chai K., Tsai, Meng-Miao, Garvalov, Boyan K., Acker-Palmer, Amparo, Krezdorn, Nicolas, Rotter, Björn, Acker, Till, Guillemin, Gilles J., Fulda, Simone, Freitag, Christine M., Chiocchetti, Andreas G.
Publicado 2018

Association of polygenic risk scores and hair cortisol with mental health trajectories during COVID lockdown

por Ahrens, Kira F., Neumann, Rebecca J., von Werthern, Nina M., Kranz, Thorsten M., Kollmann, Bianca, Mattes, Björn, Puhlmann, Lara M. C., Weichert, Danuta, Lutz, Beat, Basten, Ulrike, Fiebach, Christian J., Wessa, Michèle, Kalisch, Raffael, Lieb, Klaus, Chiocchetti, Andreas G., Tüscher, Oliver, Reif, Andreas, Plichta, Michael M.
Publicado 2022

Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses

por Torrico, Bàrbara, Antón-Galindo, Ester, Fernàndez-Castillo, Noèlia, Rojo-Francàs, Eva, Ghorbani, Sadaf, Pineda-Cirera, Laura, Hervás, Amaia, Rueda, Isabel, Moreno, Estefanía, Fullerton, Janice M., Casadó, Vicent, Buitelaar, Jan K., Rommelse, Nanda, Franke, Barbara, Reif, Andreas, Chiocchetti, Andreas G., Freitag, Christine, Kleppe, Rune, Haavik, Jan, Toma, Claudio, Cormand, Bru
Publicado 2020

The role of rare compound heterozygous events in autism spectrum disorder

por Lin, Bochao Danae, Colas, Fabrice, Nijman, Isaac J., Medic, Jelena, Brands, William, Parr, Jeremy R., van Eijk, Kristel R., Klauck, Sabine M., Chiocchetti, Andreas G., Freitag, Christine M., Maestrini, Elena, Bacchelli, Elena, Coon, Hilary, Vicente, Astrid, Oliveira, Guiomar, Pagnamenta, Alistair T., Gallagher, Louise, Ennis, Sean, Anney, Richard, Bourgeron, Thomas, Luykx, Jurjen J., Vorstman, Jacob
Publicado 2020

Rates, Distribution, and Implications of Post-zygotic Mosaic Mutations in Autism Spectrum Disorder

por Lim, Elaine T., Uddin, Mohammed, De Rubeis, Silvia, Chan, Yingleong, Kamumbu, Anne S., Zhang, Xiaochang, D'Gama, Alissa, 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.
Publicado 2017

A point mutation in the Ncr1 signal peptide impairs the development of innate lymphoid cell subsets

por Almeida, Francisca F., Tognarelli, Sara, Marçais, Antoine, Kueh, Andrew J., Friede, Miriam E., Liao, Yang, Willis, Simon N., Luong, Kylie, Faure, Fabrice, Mercier, Francois E., Galluso, Justine, Firth, Matthew, Narni-Mancinelli, Emilie, Rais, Bushra, Scadden, David T., Spallotta, Francesco, Weil, Sandra, Giannattasio, Ariane, Kalensee, Franziska, Zöller, Tobias, Huntington, Nicholas D., Schleicher, Ulrike, Chiocchetti, Andreas G., Ugolini, Sophie, Herold, Marco J., Shi, Wei, Koch, Joachim, Steinle, Alexander, Vivier, Eric, Walzer, Thierry, Belz, Gabrielle T., Ullrich, Evelyn
Publicado 2018

DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

por van Dongen, Jenny, Hagenbeek, Fiona A., Suderman, Matthew, Roetman, Peter J., Sugden, Karen, Chiocchetti, Andreas G., Ismail, Khadeeja, Mulder, Rosa H., Hafferty, Jonathan D., Adams, Mark J., Walker, Rosie M., Morris, Stewart W., Lahti, Jari, Küpers, Leanne K., Escaramis, Georgia, Alemany, Silvia, Jan Bonder, Marc, Meijer, Mandy, Ip, Hill F., Jansen, Rick, Baselmans, Bart M. L., Parmar, Priyanka, Lowry, Estelle, Streit, Fabian, Sirignano, Lea, Send, Tabea S., Frank, Josef, Jylhävä, Juulia, Wang, Yunzhang, Mishra, Pashupati Prasad, Colins, Olivier F., Corcoran, David L., Poulton, Richie, Mill, Jonathan, Hannon, Eilis, Arseneault, Louise, Korhonen, Tellervo, Vuoksimaa, Eero, Felix, Janine F., Bakermans-Kranenburg, Marian J., Campbell, Archie, Czamara, Darina, Binder, Elisabeth, Corpeleijn, Eva, Gonzalez, Juan R., Grazuleviciene, Regina, Gutzkow, Kristine B., Evandt, Jorunn, Vafeiadi, Marina, Klein, Marieke, van der Meer, Dennis, Ligthart, Lannie, Kluft, Cornelis, Davies, Gareth E., Hakulinen, Christian, Keltikangas-Järvinen, Liisa, Franke, Barbara, Freitag, Christine M., Konrad, Kerstin, Hervas, Amaia, Fernández-Rivas, Aranzazu, Vetro, Agnes, Raitakari, Olli, Lehtimäki, Terho, Vermeiren, Robert, Strandberg, Timo, Räikkönen, Katri, Snieder, Harold, Witt, Stephanie H., Deuschle, Michael, Pedersen, Nancy L., Hägg, Sara, Sunyer, Jordi, Franke, Lude, Kaprio, Jaakko, Ollikainen, Miina, Moffitt, Terrie E., Tiemeier, Henning, van IJzendoorn, Marinus H., Relton, Caroline, Vrijheid, Martine, Sebert, Sylvain, Jarvelin, Marjo-Riitta, Caspi, Avshalom, Evans, Kathryn L., McIntosh, Andrew M., Bartels, Meike, Boomsma, Dorret I.
Publicado 2021