Piera Pasinelli
Overview
Explore the profile of Piera Pasinelli including associated specialties, affiliations and a list of published articles.
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Articles
43
Citations
2730
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Recent Articles
1.
Loher P, Londin E, Ilieva H, Pasinelli P, Rigoutsos I
Mol Neurobiol
. 2025 Feb;
PMID: 39982687
Amyotrophic lateral sclerosis (ALS) is a highly heterogeneous disease for which accurate diagnostic and prognostic biomarkers are needed. Toward this goal, we reanalyzed two published collections of datasets generated from...
2.
Ghaffari L, Welebob E, Boehringer A, Cyliax K, Pasinelli P, Trotti D, et al.
bioRxiv
. 2025 Feb;
PMID: 39975241
The GGGGCC nucleotide repeat expansion (NRE) mutation in the (C9) gene is the most common cause of ALS and FTD. Neuronal activity plays an essential role in shaping biological processes...
3.
Pasinelli P, Meyer K, Ferraiuolo L, Culibrk R, Sattler R
Front Mol Med
. 2024 Aug;
3:1337286.
PMID: 39086672
No abstract available.
4.
Nelson A, Cicardi M, Markandaiah S, Han J, Philp N, Welebob E, et al.
EMBO Rep
. 2024 Apr;
25(5):2479-2510.
PMID: 38684907
The most prevalent genetic cause of both amyotrophic lateral sclerosis and frontotemporal dementia is a (GGGGCC) nucleotide repeat expansion (NRE) occurring in the first intron of the C9orf72 gene (C9)....
5.
Urban M, Charsar B, Heinsinger N, Markandaiah S, Sprimont L, Zhou W, et al.
Elife
. 2024 Jan;
12.
PMID: 38224498
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by motor neuron loss. Importantly, non-neuronal cell types such as astrocytes also play significant roles in disease pathogenesis. However, mechanisms of...
6.
Urban M, Charsar B, Heinsinger N, Markandaiah S, Sprimont L, Zhou W, et al.
bioRxiv
. 2023 May;
PMID: 37215009
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by motor neuron loss. Importantly, non-neuronal cell types such as astrocytes also play significant roles in disease pathogenesis. However, mechanisms of...
7.
Jensen B, McAvoy K, Heinsinger N, Lepore A, Ilieva H, Haeusler A, et al.
Glia
. 2022 Apr;
70(7):1426-1449.
PMID: 35474517
Genetic mutations that cause amyotrophic lateral sclerosis (ALS), a progressively lethal motor neuron disease, are commonly found in ubiquitously expressed genes. In addition to direct defects within motor neurons, growing...
8.
Verdone B, Cicardi M, Wen X, Sriramoji S, Russell K, Markandaiah S, et al.
Sci Rep
. 2022 Apr;
12(1):5644.
PMID: 35379876
Translation of the hexanucleotide G4C2 expansion associated with C9orf72 amyotrophic lateral sclerosis and frontotemporal dementia (ALS/FTD) produces five different dipeptide repeat protein (DPR) species that can confer toxicity. There is...
9.
Krishnamurthy K, Trotti D, Pasinelli P, Jensen B
J Vis Exp
. 2021 Aug;
(173).
PMID: 34338673
Before neuronal degeneration, the cause of motor and cognitive deficits in patients with amyotrophic lateral sclerosis (ALS) and/or frontotemporal lobe dementia (FTLD) is dysfunction of communication between neurons and motor...
10.
Krishnamurthy K, Pasinelli P
J Neurosci Res
. 2021 Mar;
99(6):1499-1503.
PMID: 33729613
No abstract available.