| Innate immune memory in the brain shapes neurological disease hallmarks AC Wendeln, K Degenhardt, L Kaurani, M Gertig, T Ulas, G Jain, ... Nature 556 (7701), 332-338, 2018 | 735 | 2018 |
| Childhood trauma in schizophrenia: current findings and research perspectives D Popovic, A Schmitt, L Kaurani, F Senner, S Papiol, B Malchow, ... Frontiers in neuroscience 13, 422393, 2019 | 202 | 2019 |
| HDAC1 links early life stress to schizophrenia-like phenotypes S Bahari-Javan, H Varbanov, R Halder, E Benito, L Kaurani, S Burkhardt, ... Proceedings of the National Academy of Sciences 114 (23), E4686-E4694, 2017 | 100 | 2017 |
| KMT2A and KMT2B mediate memory function by affecting distinct genomic regions C Kerimoglu, MS Sakib, G Jain, E Benito, S Burkhardt, V Capece, ... Cell reports 20 (3), 538-548, 2017 | 93 | 2017 |
| A combined miRNA–piRNA signature to detect Alzheimer’s disease G Jain, A Stuendl, P Rao, T Berulava, T Pena Centeno, L Kaurani, ... Translational psychiatry 9 (1), 250, 2019 | 90 | 2019 |
| The diphenylpyrazole compound anle138b blocks Aβ channels and rescues disease phenotypes in a mouse model for amyloid pathology A Martinez Hernandez, H Urbanke, AL Gillman, J Lee, S Ryazanov, ... EMBO molecular medicine 10 (1), 32-47, 2018 | 79 | 2018 |
| A microRNA signature that correlates with cognition and is a target against cognitive decline MR Islam, L Kaurani, T Berulava, U Heilbronner, M Budde, TP Centeno, ... EMBO molecular medicine 13 (11), e13659, 2021 | 35 | 2021 |
| Conserved reduction of m6A RNA modifications during aging and neurodegeneration is linked to changes in synaptic transcripts R Castro-Hernández, T Berulava, M Metelova, R Epple, T Peña Centeno, ... Proceedings of the National Academy of Sciences 120 (9), e2204933120, 2023 | 24 | 2023 |
| Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma M Vishal, A Sharma, L Kaurani, G Alfano, S Mookherjee, K Narta, ... BMC medical genomics 9, 1-10, 2016 | 19 | 2016 |
| Engineered skeletal muscle recapitulates human muscle development, regeneration and dystrophy M Shahriyari, MR Islam, SM Sakib, M Rinn, A Rika, D Krüger, L Kaurani, ... Journal of Cachexia, Sarcopenia and Muscle 13 (6), 3106-3121, 2022 | 17 | 2022 |
| Neuronal extracellular vesicles and associated microRNAs induce circuit connectivity downstream BDNF A Antoniou, L Auderset, L Kaurani, E Sebastian, Y Zeng, M Allahham, ... Cell reports 42 (2), 2023 | 16 | 2023 |
| Interferon-driven brain phenotype in a mouse model of RNaseT2 deficient leukoencephalopathy M Kettwig, K Ternka, K Wendland, DM Krüger, S Zampar, C Schob, ... Nature Communications 12 (1), 6530, 2021 | 15 | 2021 |
| H3 acetylation selectively promotes basal progenitor proliferation and neocortex expansion C Kerimoglu, L Pham, AB Tonchev, MS Sakib, Y Xie, G Sokpor, PA Ulmke, ... Science advances 7 (38), eabc6792, 2021 | 15 | 2021 |
| TBK1 duplication is found in normal tension and not in high tension glaucoma patients of Indian origin L Kaurani, M Vishal, J Ray, A Sen, K Ray, A Mukhopadhyay Journal of genetics 95, 459-461, 2016 | 15 | 2016 |
| Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population M Vishal, A Sharma, L Kaurani, S Chakraborty, J Ray, A Sen, ... Scientific Reports 4 (1), 5115, 2014 | 13 | 2014 |
| Integrated multi-omics analysis reveals common and distinct dysregulated pathways for genetic subtypes of Frontotemporal Dementia K Menden, M Francescatto, T Nyima, C Blauwendraat, A Dhingra, ... bioRxiv, 2020.12. 01.405894, 2020 | 12 | 2020 |
| Fusion transcripts in normal human cortex increase with age and show distinct genomic features for single cells and tissues B Mehani, K Narta, D Paul, A Raj, D Kumar, A Sharma, L Kaurani, ... Scientific Reports 10 (1), 1368, 2020 | 11 | 2020 |
| Gene-rich large deletions are overrepresented in POAG patients of Indian and Caucasian origins L Kaurani, M Vishal, D Kumar, A Sharma, B Mehani, C Sharma, ... Investigative ophthalmology & visual science 55 (5), 3258-3264, 2014 | 10 | 2014 |
| Postnatal expression of the lysine methyltransferase SETD1B is essential for learning and the regulation of neuron‐enriched genes A Michurina, MS Sakib, C Kerimoglu, DM Krüger, L Kaurani, MR Islam, ... The EMBO journal 41 (1), e106459, 2022 | 9 | 2022 |
| Human engineered skeletal muscle of hypaxial origin from pluripotent stem cells with advanced function and regenerative capacity M Shahriyari, MR Islam, MS Sakib, A Rika, D Krüger, L Kaurani, ... bioRxiv, 2021.07. 12.452030, 2021 | 3 | 2021 |
Tonatiuh Peña CentenoGerman Center for Neurodegenerative DiseasesVerified email at dzne.de
