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Giulia Soldā
Giulia Soldā
Humanitas University
Verified email at hunimed.eu
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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
9042008
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
3732016
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, 1-17, 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
2462011
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
1202012
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
1192011
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
972017
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
952020
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
852014
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
772017
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
702017
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
682021
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
672015
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
662012
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
652019
The SPID-GBA study: sex distribution, penetrance, incidence, and dementia in GBA-PD
L Straniero, R Asselta, S Bonvegna, V Rimoldi, G Melistaccio, G Soldā, ...
Neurology: Genetics 6 (6), e523, 2020
452020
LINE1 are spliced in non-canonical transcript variants to regulate T cell quiescence and exhaustion
F Marasca, S Sinha, R Vadalā, B Polimeni, V Ranzani, EM Paraboschi, ...
Nature Genetics 54 (2), 180-193, 2022
412022
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
412016
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
392015
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
392001
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