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Giulia Soldą
Giulia Soldą
Humanitas University
Verified email at hunimed.eu
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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
9112008
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
3942016
A transcriptional sketch of a primary human breast cancer by 454 deep sequencing
A Guffanti, M Iacono, P Pelucchi, N Kim, G Soldą, LJ Croft, RJ Taft, E Rizzi, ...
BMC genomics 10, 1-17, 2009
2902009
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
2492011
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
1262012
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients
EM Paraboschi, G Soldą, D Gemmati, E Orioli, G Zeri, MD Benedetti, ...
International journal of molecular sciences 12 (12), 8695-8712, 2011
1232011
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
1092020
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 Soldą, R Asselta
International journal of molecular sciences 18 (3), 576, 2017
1002017
Glucocerebrosidase mutations in primary parkinsonism
R Asselta, V Rimoldi, C Siri, R Cilia, I Guella, S Tesei, G Solda, G Pezzoli, ...
Parkinsonism & related disorders 20 (11), 1215-1220, 2014
862014
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), 12702, 2017
812017
Radiomics and gene expression profile to characterise the disease and predict outcome in patients with lung cancer
M Kirienko, M Sollini, M Corbetta, E Voulaz, N Gozzi, M Interlenghi, ...
European journal of nuclear medicine and molecular imaging 48, 3643-3655, 2021
762021
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
722017
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, 1376-1378, 2015
682015
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 Soldą, C Cantoni, D Supino, L Piccio, ...
Human molecular genetics 28 (9), 1414-1428, 2019
672019
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
L Trotta, I Guella, G Soldą, F Sironi, S Tesei, M Canesi, G Pezzoli, ...
Parkinsonism & related disorders 18 (3), 257-262, 2012
672012
The SPID-GBA study: sex distribution, penetrance, incidence, and dementia in GBA-PD
L Straniero, R Asselta, S Bonvegna, V Rimoldi, G Melistaccio, G Soldą, ...
Neurology: Genetics 6 (6), e523, 2020
562020
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion
F Marasca, S Sinha, R Vadalą, B Polimeni, V Ranzani, EM Paraboschi, ...
Nature genetics 54 (2), 180-193, 2022
542022
First independent replication of the involvement of LARS2 in Perrault syndrome by whole-exome sequencing of an Italian family
G Soldą, S Caccia, M Robusto, C Chiereghin, P Castorina, U Ambrosetti, ...
Journal of human genetics 61 (4), 295-300, 2016
432016
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
R Asselta, M Platč, M Robusto, M Borhany, I Guella, G Soldą, A Afrasiabi, ...
Thrombosis and Haemostasis 113 (03), 567-576, 2015
422015
Clinical relevance of clonal hematopoiesis in persons aged≥ 80 years
M Rossi, M Meggendorfer, M Zampini, M Tettamanti, E Riva, E Travaglino, ...
Blood, The Journal of the American Society of Hematology 138 (21), 2093-2105, 2021
392021
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