Anne Grunewald
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Explore the profile of Anne Grunewald including associated specialties, affiliations and a list of published articles.
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83
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2565
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Recent Articles
1.
Chemla A, Arena G, Sacripanti G, Barmpa K, Zagare A, Garcia P, et al.
Brain
. 2025 Feb;
PMID: 39913247
The complex and heterogeneous nature of Parkinson's disease (PD) is still not fully understood, however, increasing evidence supports mitochondrial impairment as a major driver of neurodegeneration. Miro1, a mitochondrial GTPase...
2.
Andujar B, Pereira S, Busi S, Usnich T, Borsche M, Ertan S, et al.
Environ Int
. 2024 Nov;
194:109151.
PMID: 39571299
Pathogenic variants in the Leucine-rich repeat kinase 2 (LRRK2) gene are a primary monogenic cause of Parkinson's disease (PD). However, the likelihood of developing PD with inherited LRRK2 pathogenic variants...
3.
Scafidi A, Lind-Holm Mogensen F, Campus E, Pailas A, Neumann K, Legrave N, et al.
Heliyon
. 2024 Sep;
10(18):e37792.
PMID: 39315158
Background: Epidemiological studies suggest that metformin reduces the risk of developing several types of cancer, including gliomas, and improves the overall survival in cancer patients. Nevertheless, while the effect of...
4.
Lind-Holm Mogensen F, Sousa C, Ameli C, Badanjak K, Pereira S, Muller A, et al.
J Neuroinflammation
. 2024 Jul;
21(1):174.
PMID: 39014482
Background: Specific microglia responses are thought to contribute to the development and progression of neurodegenerative diseases, including Parkinson's disease (PD). However, the phenotypic acquisition of microglial cells and their role...
5.
Trinh J, Schymanski E, Smajic S, Kasten M, Sammler E, Grunewald A
Med Genet
. 2024 Jun;
34(2):103-116.
PMID: 38835904
Mutations in () are the most frequent cause of dominantly inherited Parkinson's disease (PD). mutations, among which p.G2019S is the most frequent, are inherited with reduced penetrance. Interestingly, the disease...
6.
Arena G, Landoulsi Z, Grossmann D, Payne T, Vitali A, Delcambre S, et al.
Ann Neurol
. 2024 May;
96(1):133-149.
PMID: 38767023
Objective: The aim of our study is to better understand the genetic architecture and pathological mechanisms underlying neurodegeneration in idiopathic Parkinson's disease (iPD). We hypothesized that a fraction of iPD...
7.
Diaw S, Delcambre S, Much C, Ott F, Kostic V, Gajos A, et al.
Neurogenetics
. 2024 Mar;
25(2):141-147.
PMID: 38498291
Dystonia due to pathogenic variants in the THAP1 gene (DYT-THAP1) shows variable expressivity and reduced penetrance of ~ 50%. Since THAP1 encodes a transcription factor, modifiers influencing this variability likely...
8.
Mulica P, Venegas C, Landoulsi Z, Badanjak K, Delcambre S, Tziortziou M, et al.
Biol Proced Online
. 2023 Sep;
25(1):26.
PMID: 37730545
Background: Astrocytes have recently gained attention as key contributors to the pathogenesis of neurodegenerative disorders including Parkinson's disease. To investigate human astrocytes in vitro, numerous differentiation protocols have been developed....
9.
Luth T, Gabbert C, Koch S, Konig I, Caliebe A, Laabs B, et al.
Mov Disord
. 2023 Jul;
38(10):1837-1849.
PMID: 37482924
Background: A mitochondrial polygenic score (MGS) is composed of genes related to mitochondrial function and found to be associated with Parkinson's disease (PD) risk. Objective: To investigate the impact of...
10.
Grossmann D, Malburg N, Glass H, Weeren V, Sondermann V, Pfeiffer J, et al.
Mov Disord
. 2023 Jul;
38(10):1822-1836.
PMID: 37449534
Background: It is generally believed that the pathogenesis of PINK1/parkin-related Parkinson's disease (PD) is due to a disturbance in mitochondrial quality control. However, recent studies have found that PINK1 and...