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Gnocchi Matteo
Gnocchi Matteo
CNR - ITB
Verified email at itb.cnr.it
Title
Cited by
Cited by
Year
Durum wheat genome highlights past domestication signatures and future improvement targets
M Maccaferri, NS Harris, SO Twardziok, RK Pasam, H Gundlach, ...
Nature genetics 51 (5), 885-895, 2019
6112019
Classification and personalized prognostic assessment on the basis of clinical and genomic features in myelodysplastic syndromes
M Bersanelli, E Travaglino, M Meggendorfer, T Matteuzzi, C Sala, ...
Journal of Clinical Oncology 39 (11), 1223-1233, 2021
1672021
Multiclass HCV resistance to direct‐acting antiviral failure in real‐life patients advocates for tailored second‐line therapies
VC Di Maio, V Cento, I Lenci, M Aragri, P Rossi, S Barbaliscia, M Melis, ...
Liver international 37 (4), 514-528, 2017
1022017
An infrastructure for precision medicine through analysis of big data
M Moscatelli, A Manconi, M Pessina, G Fellegara, S Rampoldi, L Milanesi, ...
BMC bioinformatics 19, 51-61, 2018
332018
Network diffusion-based prioritization of autism risk genes identifies significantly connected gene modules
E Mosca, M Bersanelli, M Gnocchi, M Moscatelli, G Castellani, L Milanesi, ...
Frontiers in Genetics 8, 129, 2017
242017
A soft-voting ensemble classifier for detecting patients affected by COVID-19
A Manconi, G Armano, M Gnocchi, L Milanesi
Applied Sciences 12 (15), 7554, 2022
182022
HCV NS3 sequencing as a reliable and clinically useful tool for the assessment of genotype and resistance mutations for clinical samples with different HCV-RNA levels
VC Di Maio, V Cento, D Di Paolo, M Aragri, F De Leonardis, ...
Journal of Antimicrobial Chemotherapy 71 (3), 739-750, 2016
152016
Removing duplicate reads using graphics processing units
A Manconi, M Moscatelli, G Armano, M Gnocchi, A Orro, L Milanesi
BMC bioinformatics 17, 59-71, 2016
122016
Gene relevance based on multiple evidences in complex networks
N Di Nanni, M Gnocchi, M Moscatelli, L Milanesi, E Mosca
Bioinformatics 36 (3), 865-871, 2020
112020
A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study
G Maggioni, M Bersanelli, E Travaglino, AA Piérola, A Kasprzak, ...
The Lancet Haematology 10 (2), e117-e128, 2023
92023
isma: an R package for the integrative analysis of mutations detected by multiple pipelines
N Di Nanni, M Moscatelli, M Gnocchi, L Milanesi, E Mosca
BMC bioinformatics 20, 1-9, 2019
82019
G-CNV: a GPU-based tool for preparing data to detect CNVs with read-depth methods
A Manconi, E Manca, M Moscatelli, M Gnocchi, A Orro, G Armano, ...
Frontiers in Bioengineering and Biotechnology 3, 28, 2015
82015
A GPU-based high performance computing infrastructure for specialized NGS analyses
A Manconi, M Moscatelli, M Gnocchi, G Armano, L Milanesi
PeerJ Preprints, 2016
62016
Framing Apache Spark in life sciences
A Manconi, M Gnocchi, L Milanesi, O Marullo, G Armano
Heliyon 9 (2), 2023
22023
scMuffin: An R package to disentangle solid tumor heterogeneity by single-cell gene expression analysis
V Nale, A Chiodi, N Di Nanni, I Cifola, M Moscatelli, C Cocola, M Gnocchi, ...
BMC bioinformatics 24 (1), 445, 2023
12023
Network diffusion on multiple-layers: current approaches and integrative analysis of Rheumatoid Arthritis data.
N Di Nanni, M Gnocchi, M Moscatelli, L Milanesi, E Mosca
PeerJ Preprints 5, e3310v1, 2017
12017
Grid based genome wide studies on atrial flutter
A Calabria, D Di Pasquale, M Gnocchi, PA Cozzi, A Orro, GA Trombetti, ...
Journal of Grid Computing 8, 511-527, 2010
12010
A HPC and Grid enabling framework for genetic linkage analysis of SNPs
L Milanesi, A Calabria, D Di Pasquale, M Gnocchi, A Orro, G Trombetti
Il Nuovo Cimento 32, 249-253, 2009
12009
scMuffin: an R package for disentangling solid tumor heterogeneity from single-cell expression data
V Nale, A Chiodi, N Di Nanni, I Cifola, M Moscatelli, C Cocola, M Gnocchi, ...
bioRxiv, 2022.06. 01.494129, 2022
2022
Interactome-based multi-omics study of molecular networks implicated in disease activity in Multiple Sclerosis
V Nale, F Clarelli, N Di Nanni, L Ferre, E Mascia, S Santoro, M Gnocchi, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 317-318, 2022
2022
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