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GROSSMANN Dajana

Main Referenced Co-authors
KRÜGER, Rejko  (5)
ANTONY, Paul  (4)
GRÜNEWALD, Anne  (3)
BALLING, Rudolf  (2)
BAUMURATOV, Aidos  (2)
Main Referenced Keywords
Miro1 (2); mitochondria (2); Parkinson's disease (2); Parkinson’s disease (2); Cellular neuroscience (1);
Main Referenced Unit & Research Centers
Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) (2)
Luxembourg Centre for Systems Biomedicine (LCSB): Biomedical Data Science (Glaab Group) (2)
Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group) (2)
Hertie Institute for Clinical Brain Research, University of Tübingen, Germany (1)
Luxembourg Centre for Systems Biomedicine (LCSB) - Clinical and Experimental neuroscience (Krüger Group) (1)
Main Referenced Disciplines
Biochemistry, biophysics & molecular biology (4)
Genetics & genetic processes (3)
Neurology (2)
Human health sciences: Multidisciplinary, general & others (1)

Publications (total 6)

The most downloaded
94 downloads
NEUMANN, M. A.-C.* , GROSSMANN, D.* , Schimpf-Linzenbold, S., Dayan, D., Stingl, K., Ben-Menachem, R., Pines, O., MASSART, F., DELCAMBRE, S., GHELFI, J., BOHLER, J., Strom, T., Kessel, A., Azem, A., Schöls, L., GRÜNEWALD, A., Wissinger, B., & KRÜGER, R. (2020). Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophy. Scientific Reports. doi:10.1038/s41598-020-73557-4 https://hdl.handle.net/10993/44703

The most cited

69 citations (OpenAlex)

GROSSMANN, D., BERENGUER, C., Bellet, M. E., Scheibner, D., Bohler, J., MASSART, F., Rapaport, D., SKUPIN, A., FOUQUIER D'HÉROUËL, A., Sharma, M., GHELFI, J., Rakovic, A., Lichtner, P., ANTONY, P., GLAAB, E., MAY, P., Dimmer, K. S., Fitzgerald, J. C., GRÜNEWALD, A., & KRÜGER, R. (2019). Mutations in RHOT1 disrupt ER-mitochondria contact sites interfering with calcium homeostasis and mitochondrial dynamics in Parkinson's disease. Antioxidants and Redox Signaling. doi:10.1089/ars.2018.7718 https://hdl.handle.net/10993/39949

ARENA, G., LANDOULSI, Z., GROSSMANN, D., Payne, T., VITALI, A., DELCAMBRE, S., BARON, A., ANTONY, P., BOUSSAAD, I., BOBBILI, D. R., Sreelatha, A. A. K., PAVELKA, L., J Diederich, N., Klein, C., Seibler, P., GLAAB, E., Foltynie, T., Bandmann, O., Sharma, M., ... COURAGE‐PD Consortium. (2024). Polygenic Risk Scores Validated in Patient-Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's Disease. Annals of Neurology. doi:10.1002/ana.26949
Peer Reviewed verified by ORBi

Zanin, M., Santos, B. F. R., ANTONY, P., Berenguer-Escuder, C., Larsen, S. B., HANSS, Z., BARBUTI, P., BAUMURATOV, A., GROSSMANN, D., Capelle, C. M., Weber, J., BALLING, R., Ollert, M., KRÜGER, R., Diederich, N. J., & HE, F. (10 November 2020). Mitochondria interaction networks show altered topological patterns in Parkinson's disease. NPJ Systems Biology and Applications, 6 (1), 38. doi:10.1038/s41540-020-00156-4
Peer Reviewed verified by ORBi

NEUMANN, M. A.-C.* , GROSSMANN, D.* , Schimpf-Linzenbold, S., Dayan, D., Stingl, K., Ben-Menachem, R., Pines, O., MASSART, F., DELCAMBRE, S., GHELFI, J., BOHLER, J., Strom, T., Kessel, A., Azem, A., Schöls, L., GRÜNEWALD, A., Wissinger, B., & KRÜGER, R. (2020). Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophy. Scientific Reports. doi:10.1038/s41598-020-73557-4
Peer Reviewed verified by ORBi
* These authors have contributed equally to this work.

KRÜGER, R., BALLING, R., ANTONY, P., KONDRATYEVA, O., OSTASZEWSKI, M., BAUMURATOV, A., GROSSMANN, D., Mommaerts, K., Sokolowska, K., LONGHINO, L., Poulain, J. F., & Diederich, N. J. (2020). Fibroblast mitochondria in idiopathic Parkinson’s disease display morphological changes and enhanced resistance to depolarization. Scientific Reports. doi:10.1038/s41598-020-58505-6
Peer Reviewed verified by ORBi

GROSSMANN, D., BERENGUER, C., Bellet, M. E., Scheibner, D., Bohler, J., MASSART, F., Rapaport, D., SKUPIN, A., FOUQUIER D'HÉROUËL, A., Sharma, M., GHELFI, J., Rakovic, A., Lichtner, P., ANTONY, P., GLAAB, E., MAY, P., Dimmer, K. S., Fitzgerald, J. C., GRÜNEWALD, A., & KRÜGER, R. (2019). Mutations in RHOT1 disrupt ER-mitochondria contact sites interfering with calcium homeostasis and mitochondrial dynamics in Parkinson's disease. Antioxidants and Redox Signaling. doi:10.1089/ars.2018.7718
Peer reviewed

GROSSMANN, D. (2016). Functional characterization of novel RhoT1 variants, which are associated with Parkinson's disease [Doctoral thesis, Unilu - University of Luxembourg]. ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/27669

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