Publications of Anke Hoffmann

Journal Article (6)

2024
Journal Article
Raabe, F. J.; Hausruckinger, A.; Gagliardi, M.; Ahmad, R.; Almeida, V.; Galinski, S.; Hoffmann, A.; Weigert, L.; Rummel, C. K.; Murek, V. et al.; Trastulla, L.; Jiménez-Barrón, L.; Atella, A.; Maidl, S.; Menegaz, D.; Hauger, B.; Wagner, E.-M.; Gabellini, N.; Kauschat, B.; Riccardo, S.; Cesana, M.; Papiol, S.; Sportelli, V.; Rex-Haffner, M.; Stolte, S. J.; Wehr, M. C.; Salcedo, T. O.; Papazova, I.; Detera-Wadleigh, S.; McMahon, F. J.; Schmitt, A.; Falkai, P.; Hasan, A.; Cacchiarelli, D.; Dannlowski, U.; Nenadic, I.; Kircher, T.; Scheuss, V.; Eder, M.; Binder, E. B.; Spengler, D.; Rossner, M. J.; Ziller, M. J.: Polygenic risk for schizophrenia converges on alternative polyadenylation as molecular mechanism underlying synaptic impairment. bioRxiv: the preprint server for biology (2024)
2021
Journal Article
Hoffmann, A.; Spengler, D.: Single-Cell Transcriptomics Supports a Role of CHD8 in Autism. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 22 (6), 3261 (2021)
Journal Article
Hoffmann, A.; Spengler, D.: Chromatin Remodeler CHD8 in Autism and Brain Development. JOURNAL OF CLINICAL MEDICINE 10 (2), 366 (2021)
2020
Journal Article
Di Matteo, F.; Pipicelli, F.; Kyrousi, C.; Tovecci, I.; Penna, E.; Crispino, M.; Chambery, A.; Russo, R.; Ayo-Martin, A. C.; Giordano, M. et al.; Hoffmann, A.; Ciusani, E.; Canafoglia, L.; Goetz, M.; Di Giaimo, R.; Cappello, S.: Cystatin B is essential for proliferation and interneuron migration in individuals with EPM1 epilepsy. EMBO MOLECULAR MEDICINE 12 (6), e11419 (2020)
Journal Article
Hoffmann, A.; Ziller, M.; Spengler, D.: Focus on Causality in ESC/iPSC-Based Modeling of Psychiatric Disorders. CELLS 9 (2), 366 (2020)
2019
Journal Article
Hoffmann, A.; Ziller, M.; Spengler, D.: Progress in iPSC-Based Modeling of Psychiatric Disorders. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 20 (19), 4896 (2019)

Book Review (1)

2019
Book Review
Hoffmann, A.; Spengler, D.: Chromatin Remodeling Complex NuRD in Neurodevelopment and Neurodevelopmental Disorders. FRONTIERS IN GENETICS 10, 682 (2019)
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