Selection of safe artemisinin derivatives using a machine learning-based cardiotoxicity platform and in vitro and in vivo validation

von Kadioglu, Onat, Klauck, Sabine M., Fleischer, Edmond, Shan, Letian, Efferth, Thomas
Veröffentlicht in Arch Toxicol (2021)

Genetics of autistic disorders: review and clinical implications

von Freitag, Christine M., Staal, Wouter, Klauck, Sabine M., Duketis, Eftichia, Waltes, Regina
Veröffentlicht 2009

Genome-Based Classification and Therapy of Prostate Cancer

von Angeles, Arlou Kristina, Bauer, Simone, Ratz, Leonie, Klauck, Sabine M., Sültmann, Holger
Veröffentlicht in Diagnostics (Basel) (2018)

A Mutation Hot Spot for Nonspecific X-Linked Mental Retardation in the MECP2 Gene Causes the PPM-X Syndrome

von Klauck, Sabine M., Lindsay, Susan, Beyer, Kim S., Splitt, Miranda, Burn, John, Poustka, Annemarie
Veröffentlicht 2002

Novel RNA Markers in Prostate Cancer: Functional Considerations and Clinical Translation

von Pickl, Julia M. A., Heckmann, Doreen, Ratz, Leonie, Klauck, Sabine M., Sültmann, Holger
Veröffentlicht 2014

Cytotoxicity of nimbolide towards multidrug-resistant tumor cells and hypersensitivity via cellular metabolic modulation

von Mahmoud, Nuha, Saeed, Mohamed E.M., Sugimoto, Yoshikazu, Klauck, Sabine M., Greten, Henry J., Efferth, Thomas
Veröffentlicht in Oncotarget (2018)

TMPRSS2:ERG gene fusion variants induce TGF-β signaling and epithelial to mesenchymal transition in human prostate cancer cells

von Ratz, Leonie, Laible, Mark, Kacprzyk, Lukasz A, Wittig-Blaich, Stephanie M, Tolstov, Yanis, Duensing, Stefan, Altevogt, Peter, Klauck, Sabine M, Sültmann, Holger
Veröffentlicht in Oncotarget (2017)

miR-449a Repression Leads to Enhanced NOTCH Signaling in TMPRSS2:ERG Fusion Positive Prostate Cancer Cells

von Bauer, Simone, Ratz, Leonie, Heckmann-Nötzel, Doreen, Kaczorowski, Adam, Hohenfellner, Markus, Kristiansen, Glen, Duensing, Stefan, Altevogt, Peter, Klauck, Sabine M., Sültmann, Holger
Veröffentlicht in Cancers (Basel) (2021)

Inhibition of c-MYC with involvement of ERK/JNK/MAPK and AKT pathways as a novel mechanism for shikonin and its derivatives in killing leukemia cells

von Zhao, Qiaoli, Assimopoulou, Andreana N., Klauck, Sabine M., Damianakos, Harilaos, Chinou, Ioanna, Kretschmer, Nadine, Rios, José-Luis, Papageorgiou, Vassilios P., Bauer, Rudolf, Efferth, Thomas
Veröffentlicht in Oncotarget (2015)

The Chinese herbal formula Free and Easy Wanderer ameliorates oxidative stress through KEAP1-NRF2/HO-1 pathway

von Hong, Chunlan, Cao, Jingming, Wu, Ching-Fen, Kadioglu, Onat, Schüffler, Anja, Kauhl, Ulrich, Klauck, Sabine M., Opatz, Till, Thines, Eckhard, Paul, Norbert W., Efferth, Thomas
Veröffentlicht in Sci Rep (2017)

Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry

von Sousa, Inês, Clark, Taane G, Holt, Richard, Pagnamenta, Alistair T, Mulder, Erik J, Minderaa, Ruud B, Bailey, Anthony J, Battaglia, Agatino, Klauck, Sabine M, Poustka, Fritz, Monaco, Anthony P
Veröffentlicht 2010

Linkage and candidate gene studies of autism spectrum disorders in European populations

von Holt, Richard, Barnby, Gabrielle, Maestrini, Elena, Bacchelli, Elena, Brocklebank, Denise, Sousa, Inês, Mulder, Erik J, Kantojärvi, Katri, Järvelä, Irma, Klauck, Sabine M, Poustka, Fritz, Bailey, Anthony J, Monaco, Anthony P
Veröffentlicht 2010

Corrigendum to: Linkage and candidate gene studies of autism spectrum disorders in European populations

von Holt, Richard, Barnby, Gabrielle, Maestrini, Elena, Bacchelli, Elena, Brocklebank, Denise, Sousa, Inês, Mulder, Erik J, Kantojärvi, Katri, Järvelä, Irma, Klauck, Sabine M, Poustka, Fritz, Bailey, Anthony J, Monaco, Anthony P
Veröffentlicht 2010

A 15q13.3 microdeletion segregating with autism

von Pagnamenta, Alistair T, Wing, Kirsty, Akha, Elham Sadighi, Knight, Samantha JL, Bölte, Sven, Schmötzer, Gabriele, Duketis, Eftichia, Poustka, Fritz, Klauck, Sabine M, Poustka, Annemarie, Ragoussis, Jiannis, Bailey, Anthony J, Monaco, Anthony P
Veröffentlicht 2009

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

von 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.
Veröffentlicht in Transl Psychiatry (2020)

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

von 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
Veröffentlicht 2014

The role of rare compound heterozygous events in autism spectrum disorder

von 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
Veröffentlicht in Transl Psychiatry (2020)

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

von Buxbaum, Joseph D, Bolshakova, Nadia, Brownfeld, Jessica M, Anney, Richard JL, Bender, Patrick, Bernier, Raphael, Cook, Edwin H, Coon, Hilary, Cuccaro, Michael, Freitag, Christine M, Hallmayer, Joachim, Geschwind, Daniel, Klauck, Sabine M, Nurnberger, John I, Oliveira, Guiomar, Pinto, Dalila, Poustka, Fritz, Scherer, Stephen W, Shih, Andy, Sutcliffe, James S, Szatmari, Peter, Vicente, Astrid M, Vieland, Veronica, Gallagher, Louise
Veröffentlicht in Mol Autism (2014)

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

von Pagnamenta, Alistair T., Bacchelli, Elena, de Jonge, Maretha V., Mirza, Ghazala, Scerri, Thomas S., Minopoli, Fiorella, Chiocchetti, Andreas, Ludwig, Kerstin U., Hoffmann, Per, Paracchini, Silvia, Lowy, Ernesto, Harold, Denise H., Chapman, Jade A., Klauck, Sabine M., Poustka, Fritz, Houben, Renske H., Staal, Wouter G., Ophoff, Roel A., O'Donovan, Michael C., Williams, Julie, Nöthen, Markus M., Schulte-Körne, Gerd, Deloukas, Panos, Ragoussis, Jiannis, Bailey, Anthony J., Maestrini, Elena, Monaco, Anthony P.
Veröffentlicht 2010

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

von Leblond, Claire S., Heinrich, Jutta, Delorme, Richard, Proepper, Christian, Betancur, Catalina, Huguet, Guillaume, Konyukh, Marina, Chaste, Pauline, Ey, Elodie, Rastam, Maria, Anckarsäter, Henrik, Nygren, Gudrun, Gillberg, I. Carina, Melke, Jonas, Toro, Roberto, Regnault, Beatrice, Fauchereau, Fabien, Mercati, Oriane, Lemière, Nathalie, Skuse, David, Poot, Martin, Holt, Richard, Monaco, Anthony P., Järvelä, Irma, Kantojärvi, Katri, Vanhala, Raija, Curran, Sarah, Collier, David A., Bolton, Patrick, Chiocchetti, Andreas, Klauck, Sabine M., Poustka, Fritz, Freitag, Christine M., Waltes, Regina, Kopp, Marnie, Duketis, Eftichia, Bacchelli, Elena, Minopoli, Fiorella, Ruta, Liliana, Battaglia, Agatino, Mazzone, Luigi, Maestrini, Elena, Sequeira, Ana F., Oliveira, Barbara, Vicente, Astrid, Oliveira, Guiomar, Pinto, Dalila, Scherer, Stephen W., Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Bonneau, Dominique, Guinchat, Vincent, Devillard, Françoise, Assouline, Brigitte, Mouren, Marie-Christine, Leboyer, Marion, Gillberg, Christopher, Boeckers, Tobias M., Bourgeron, Thomas
Veröffentlicht 2012