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Tommaso Biagini
Tommaso Biagini
Unknown affiliation
Verified email at css-mendel.it
Title
Cited by
Cited by
Year
High-confidence assessment of functional impact of human mitochondrial non-synonymous genome variations by APOGEE
S Castellana, C Fusilli, G Mazzoccoli, T Biagini, D Capocefalo, M Carella, ...
PLoS computational biology 13 (6), e1005628, 2017
632017
Hypomorphic recessive variants in SUFU impair the sonic hedgehog pathway and cause Joubert syndrome with cranio-facial and skeletal defects
R De Mori, M Romani, S D’Arrigo, MS Zaki, E Lorefice, S Tardivo, ...
The American Journal of Human Genetics 101 (4), 552-563, 2017
512017
Genome assembly and transcriptome resource for river buffalo, Bubalus bubalis (2n = 50)
JL Williams, D Iamartino, KD Pruitt, T Sonstegard, TPL Smith, WY Low, ...
Gigascience 6 (10), gix088, 2017
482017
Hsa-miR-155-5p up-regulation in breast cancer and its relevance for treatment with poly [ADP-Ribose] polymerase 1 (PARP-1) inhibitors
B Pasculli, R Barbano, A Fontana, T Biagini, MP Di Viesti, M Rendina, ...
Frontiers in Oncology 10, 1415, 2020
362020
Insights from molecular characterization of adult patients of families with multigenerational diabetes
S Pezzilli, O Ludovico, T Biagini, L Mercuri, F Alberico, E Lauricella, ...
Diabetes 67 (1), 137-145, 2018
272018
Molecular dynamics recipes for genome research
T Biagini, G Chillemi, G Mazzoccoli, A Grottesi, C Fusilli, D Capocefalo, ...
Briefings in bioinformatics 19 (5), 853-862, 2018
252018
Between SCA5 and SCAR14: delineation of the SPTBN2 p.R480W-associated phenotype
S Nuovo, A Micalizzi, S D’Arrigo, M Ginevrino, T Biagini, T Mazza, ...
European Journal of Human Genetics 26 (7), 928-929, 2018
252018
Clinical significance of circulating miR-1273g-3p and miR-122-5p in pancreatic cancer
T Mazza, D Gioffreda, A Fontana, T Biagini, M Carella, O Palumbo, ...
Frontiers in oncology 10, 44, 2020
232020
MitImpact 3: modeling the residue interaction network of the Respiratory Chain subunits
S Castellana, T Biagini, F Petrizzelli, L Parca, N Panzironi, V Caputo, ...
Nucleic acids research 49 (D1), D1282-D1288, 2021
222021
Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation
A Frustaci, A De Luca, V Guida, T Biagini, T Mazza, C Gaudio, C Letizia, ...
Journal of the American Heart Association 7 (4), e008068, 2018
222018
Are gaming-enabled graphic processing unit cards convenient for molecular dynamics simulation?
T Biagini, F Petrizzelli, M Truglio, R Cespa, A Barbieri, D Capocefalo, ...
Evolutionary Bioinformatics 15, 1176934319850144, 2019
202019
Systematic analysis of mouse genome reveals distinct evolutionary and functional properties among circadian and ultradian genes
S Castellana, T Mazza, D Capocefalo, N Genov, T Biagini, C Fusilli, ...
Frontiers in physiology 9, 1178, 2018
202018
Early-onset diabetes as risk factor for pancreatic cancer: miRNA expression profiling in plasma uncovers a role for miR-20b-5p, miR-29a, and miR-18a-5p in diabetes of recent …
F Tavano, A Fontana, T Mazza, D Gioffreda, T Biagini, O Palumbo, ...
Frontiers in Oncology 10, 1567, 2020
182020
Multifaceted enrichment analysis of RNA–RNA crosstalk reveals cooperating micro-societies in human colorectal cancer
T Mazza, G Mazzoccoli, C Fusilli, D Capocefalo, A Panza, T Biagini, ...
Nucleic acids research 44 (9), 4025-4036, 2016
182016
Nociceptin/orphanin FQ opioid receptor (NOP) selective ligand MCOPPB links anxiolytic and senolytic effects
M Raffaele, K Kovacovicova, T Biagini, O Lo Re, J Frohlich, S Giallongo, ...
GeroScience, 1-21, 2022
162022
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2
R De Mori, M Severino, MM Mancardi, D Anello, S Tardivo, T Biagini, ...
Brain 142 (10), 2965-2978, 2019
162019
A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
P Palumbo, A Petracca, R Maggi, T Biagini, G Nardella, MC Sacco, ...
European Journal of Human Genetics 27 (7), 1113-1120, 2019
152019
Mutational spectrum and clinical signatures in 114 families with hereditary multiple osteochondromas: insights into molecular properties of selected exostosin variants
C Fusco, G Nardella, R Fischetto, M Copetti, A Petracca, F Annunziata, ...
Human Molecular Genetics 28 (13), 2133-2142, 2019
142019
A single‐center study on 140 patients with cerebral cavernous malformations: 28 new pathogenic variants and functional characterization of a PDCD10 large deletion
G Nardella, G Visci, V Guarnieri, S Castellana, T Biagini, L Bisceglia, ...
Human Mutation 39 (12), 1885-1900, 2018
142018
A primary tumor gene expression signature identifies a crucial role played by tumor stroma myofibroblasts in lymph node involvement in oral squamous cell carcinoma
G Mazzoccoli, S Castellana, M Carella, O Palumbo, C Tiberio, C Fusilli, ...
Oncotarget 8 (62), 104913, 2017
142017
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