Giulia Soldā
Giulia Soldā
Humanitas University
Verified email at hunimed.eu
Title
Cited by
Cited by
Year
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
7622008
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), 163, 2009
2602009
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
1872011
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
1412016
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
902012
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
902011
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
562014
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
542012
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
372015
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
352004
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
322017
Characterization of the genomic structure of the human neuronal nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster and identification of novel intragenic …
S Duga, G Soldā, R Asselta, MT Bonati, L Dalprā, M Malcovati, ...
Journal of human genetics 46 (11), 640-648, 2001
312001
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
302009
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
282017
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
282017
Molecular characterization of two novel mutations causing factor XI deficiency: a splicing defect and a missense mutation responsible for a CRM+ defect
I Guella, G Soldā, S Spena, R Asselta, R Ghiotto, ML Tenchini, ...
Thrombosis and haemostasis 99 (03), 523-530, 2008
272008
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
262016
In vivo RNA–RNA duplexes from human α3 and α5 nicotinic receptor subunit mRNAs
G Soldā, S Boi, S Duga, D Fornasari, R Benfante, M Malcovati, ...
Gene 345 (2), 155-164, 2005
262005
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
252015
Non-random retention of protein-coding overlapping genes in Metazoa
G Soldā, M Suyama, P Pelucchi, S Boi, A Guffanti, E Rizzi, P Bork, ...
Bmc Genomics 9 (1), 174, 2008
252008
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