Giulia Soldā
Giulia Soldā
Humanitas University
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Cited by
Long noncoding RNAs in mouse embryonic stem cell pluripotency and differentiation
ME Dinger, PP Amaral, TR Mercer, KC Pang, SJ Bruce, BB Gardiner, ...
Genome research 18 (9), 1433-1445, 2008
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing
A Guffanti, M Iacono, P Pelucchi, N Kim, G Soldā, LJ Croft, RJ Taft, E Rizzi, ...
BMC genomics 10 (1), 1-17, 2009
Survival and dementia in GBA‐associated Parkinson's disease: The mutation matters
R Cilia, S Tunesi, G Marotta, E Cereda, C Siri, S Tesei, AL Zecchinelli, ...
Annals of neurology 80 (5), 662-673, 2016
Expression of distinct RNAs from 3′ untranslated regions
TR Mercer, D Wilhelm, ME Dinger, G Solda, DJ Korbie, EA Glazov, ...
Nucleic acids research 39 (6), 2393-2403, 2011
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
EM Paraboschi, G Soldā, D Gemmati, E Orioli, G Zeri, MD Benedetti, ...
International journal of molecular sciences 12 (12), 8695-8712, 2011
A novel mutation within the MIR96 gene causes non-syndromic inherited hearing loss in an Italian family by altering pre-miRNA processing
G Solda, M Robusto, P Primignani, P Castorina, E Benzoni, A Cesarani, ...
Human molecular genetics 21 (3), 577-585, 2012
Glucocerebrosidase mutations in primary parkinsonism
R Asselta, V Rimoldi, C Siri, R Cilia, I Guella, S Tesei, G Soldā, G Pezzoli, ...
Parkinsonism & related disorders 20 (11), 1215-1220, 2014
The characterization of GSDMB splicing and backsplicing profiles identifies novel isoforms and a circular RNA that are dysregulated in multiple sclerosis
G Cardamone, EM Paraboschi, V Rimoldi, S Duga, G Soldā, R Asselta
International Journal of Molecular Sciences 18 (3), 576, 2017
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
L Trotta, I Guella, G Soldā, F Sironi, S Tesei, M Canesi, G Pezzoli, ...
Parkinsonism & related disorders 18 (3), 257-262, 2012
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations
V Pensato, C Tiloca, L Corrado, C Bertolin, V Sardone, R Del Bo, D Calini, ...
Journal of neurology 262 (5), 1376-1378, 2015
Tumor-derived prostaglandin E2 promotes p50 NF-κB-dependent differentiation of monocytic MDSCs
C Porta, FM Consonni, S Morlacchi, S Sangaletti, A Bleve, MG Totaro, ...
Cancer Research 80 (13), 2874-2888, 2020
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
L Straniero, V Rimoldi, M Samarani, S Goldwurm, A Di Fonzo, R Krüger, ...
Scientific reports 7 (1), 1-13, 2017
DNAJC12 and dopa‐responsive nonprogressive parkinsonism
L Straniero, I Guella, R Cilia, L Parkkinen, V Rimoldi, A Young, R Asselta, ...
Annals of neurology 82 (4), 640-646, 2017
Not only cancer: the long non-coding RNA MALAT1 affects the repertoire of alternatively spliced transcripts and circular RNAs in multiple sclerosis
G Cardamone, EM Paraboschi, G Soldā, C Cantoni, D Supino, L Piccio, ...
Human molecular genetics 28 (9), 1414-1428, 2019
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic polymorphisms
S Duga, G Soldā, R Asselta, MT Bonati, L Dalprā, M Malcovati, ...
Journal of human genetics 46 (11), 640-648, 2001
Shedding light on the dark side of the genome: overlapping genes in higher eukaryotes
S Boi, G Solda, ML Tenchini
Current Genomics 5 (6), 509-524, 2004
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family
G Soldā, S Caccia, M Robusto, C Chiereghin, P Castorina, U Ambrosetti, ...
Journal of human genetics 61 (4), 295-300, 2016
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
R Asselta, M Platč, M Robusto, M Borhany, I Guella, G Soldā, A Afrasiabi, ...
Thrombosis and Haemostasis 113 (03), 567-576, 2015
An Ariadne's thread to the identification and annotation of noncoding RNAs in eukaryotes
G Soldā, IV Makunin, OU Sezerman, A Corradin, G Corti, A Guffanti
Briefings in bioinformatics 10 (5), 475-489, 2009
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis
EM Paraboschi, V Rimoldi, G Solda, T Tabaglio, C Dall'Osso, E Saba, ...
Human molecular genetics 23 (25), 6746-6761, 2014
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