Paola Forabosco
Overview
Explore the profile of Paola Forabosco including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
31
Citations
1047
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Forabosco P, Pala M, Crobu F, Diana M, Marongiu M, Cusano R, et al.
Front Immunol
. 2024 Apr;
15:1350111.
PMID: 38629067
Gene co-expression network analysis enables identification of biologically meaningful clusters of co-regulated genes (modules) in an unsupervised manner. We present here the largest study conducted thus far of co-expression networks...
2.
Busonero F, Steri M, Orru V, Sole G, Olla S, Marongiu M, et al.
Br J Haematol
. 2020 Nov;
191(5):e124-e128.
PMID: 33216977
No abstract available.
3.
Mencacci N, Reynolds R, Ruiz S, Vandrovcova J, Forabosco P, Sanchez-Ferrer A, et al.
Brain
. 2020 Sep;
143(9):2771-2787.
PMID: 32889528
Dystonia is a neurological disorder characterized by sustained or intermittent muscle contractions causing abnormal movements and postures, often occurring in absence of any structural brain abnormality. Psychiatric comorbidities, including anxiety,...
4.
Botia J, Vandrovcova J, Forabosco P, Guelfi S, DSa K, Hardy J, et al.
BMC Syst Biol
. 2017 Apr;
11(1):47.
PMID: 28403906
Background: Weighted Gene Co-expression Network Analysis (WGCNA) is a widely used R software package for the generation of gene co-expression networks (GCN). WGCNA generates both a GCN and a derived...
5.
Ferrari R, Forabosco P, Vandrovcova J, Botia J, Guelfi S, Warren J, et al.
Mol Neurodegener
. 2016 Feb;
11:21.
PMID: 26912063
Background: In frontotemporal dementia (FTD) there is a critical lack in the understanding of biological and molecular mechanisms involved in disease pathogenesis. The heterogeneous genetic features associated with FTD suggest...
6.
Bettencourt C, Forabosco P, Wiethoff S, Heidari M, Johnstone D, Botia J, et al.
Neurobiol Dis
. 2015 Dec;
87:59-68.
PMID: 26707700
Aberrant brain iron deposition is observed in both common and rare neurodegenerative disorders, including those categorized as Neurodegeneration with Brain Iron Accumulation (NBIA), which are characterized by focal iron accumulation...
7.
Mencacci N, Rubio-Agusti I, Zdebik A, Asmus F, Ludtmann M, Ryten M, et al.
Am J Hum Genet
. 2015 May;
96(6):938-47.
PMID: 25983243
Myoclonus-dystonia (M-D) is a rare movement disorder characterized by a combination of non-epileptic myoclonic jerks and dystonia. SGCE mutations represent a major cause for familial M-D being responsible for 30%-50%...
8.
Ramasamy A, Trabzuni D, Forabosco P, Smith C, Walker R, Dillman A, et al.
Mult Scler Relat Disord
. 2015 Jan;
3(2):211-219.
PMID: 25568836
Background: Multiple sclerosis (MS) is a common disease of the central nervous system and a major cause of disability amongst young adults. Genome-wide association studies have identified many novel susceptibility...
9.
Bettencourt C, Ryten M, Forabosco P, Schorge S, Hersheson J, Hardy J, et al.
JAMA Neurol
. 2014 May;
71(7):831-9.
PMID: 24862029
Importance: The core clinical and neuropathological feature of the autosomal dominant spinocerebellar ataxias (SCAs) is cerebellar degeneration. Mutations in the known genes explain only 50% to 60% of SCA cases....
10.
Cruchaga C, Karch C, Jin S, Benitez B, Cai Y, Guerreiro R, et al.
Nature
. 2013 Dec;
505(7484):550-554.
PMID: 24336208
Genome-wide association studies (GWAS) have identified several risk variants for late-onset Alzheimer's disease (LOAD). These common variants have replicable but small effects on LOAD risk and generally do not have...