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Gianmauro Cuccuru
Gianmauro Cuccuru
Researcher, CRS4, Italy
Verified email at crs4.it - Homepage
Title
Cited by
Cited by
Year
Overexpression of the cytokine BAFF and autoimmunity risk
M Steri, V Orrů, ML Idda, M Pitzalis, M Pala, I Zara, C Sidore, V Faŕ, ...
New England Journal of Medicine 376 (17), 1615-1626, 2017
3672017
The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2022 update
Nucleic Acids Research 50 (W1), W345-W351, 2022
2422022
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
S Sanna, M Pitzalis, M Zoledziewska, I Zara, C Sidore, R Murru, ...
Nature genetics 42 (6), 495-497, 2010
2282010
Tools and data services registry: a community effort to document bioinformatics resources
J Ison, K Rapacki, H Ménager, M Kalaš, E Rydza, P Chmura, C Anthon, ...
Nucleic acids research 44 (D1), D38-D47, 2016
1672016
Orione, a web-based framework for NGS analysis in microbiology
G Cuccuru, M Orsini, A Pinna, A Sbardellati, N Soranzo, A Travaglione, ...
Bioinformatics 30 (13), 1928-1929, 2014
1652014
Buried in the Middle but Guilty: Intronic Mutations in the TCIRG1 Gene Cause Human Autosomal Recessive Osteopetrosis
E Palagano, HC Blair, A Pangrazio, I Tourkova, D Strina, A Angius, ...
Journal of Bone and Mineral Research 30 (10), 1814-1821, 2015
532015
Bi-allelic mutations in KLHL7 cause a Crisponi/CISS1-like phenotype associated with early-onset retinitis pigmentosa
A Angius, P Uva, I Buers, M Oppo, A Puddu, S Onano, I Persico, A Loi, ...
The American Journal of Human Genetics 99 (1), 236-245, 2016
422016
Fast low-memory streaming MLS reconstruction of point-sampled surfaces
R Pajarola, G Cuccuru, E Gobbetti, F Marton, R Pintus
University of Zurich, 2009
362009
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: a case report
RM Alves, P Uva, MF Veiga, M Oppo, FCR Zschaber, G Porcu, HP Porto, ...
BMC Medical Genetics 20, 1-7, 2019
212019
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP
A Angius, P Uva, M Oppo, I Persico, S Onano, S Olla, V Pes, C Perria, ...
American Journal of Medical Genetics Part A 179 (4), 634-638, 2019
192019
Genome-wide association study of susceptibility loci for breast cancer in Sardinian population
G Palomba, A Loi, E Porcu, A Cossu, I Zara, M Budroni, M Dei, S Lai, ...
BMC cancer 15 (1), 1-10, 2015
182015
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome
A Angius, S Cossu, P Uva, M Oppo, S Onano, I Persico, G Fotia, R Atzeni, ...
Clinical genetics 93 (6), 1245-1247, 2018
172018
BioBlend. objects: metacomputing with Galaxy
S Leo, L Pireddu, G Cuccuru, L Lianas, N Soranzo, E Afgan, G Zanetti
Bioinformatics 30 (19), 2816-2817, 2014
162014
An automated infrastructure to support high-throughput bioinformatics
G Cuccuru, S Leo, L Lianas, M Muggiri, A Pinna, L Pireddu, P Uva, ...
2014 International Conference on High Performance Computing & Simulation …, 2014
132014
Exome sequencing in Crisponi/cold‐induced sweating syndrome–like individuals reveals unpredicted alternative diagnoses
A Angius, P Uva, M Oppo, I Buers, I Persico, S Onano, G Cuccuru, ...
Clinical Genetics 95 (5), 607-614, 2019
92019
Training infrastructure as a service
H Rasche, C Hyde, J Davis, S Gladman, N Coraor, A Bretaudeau, ...
GigaScience 12, giad048, 2023
52023
Bacterial genomic data analysis in the next-generation sequencing era
M Orsini, G Cuccuru, P Uva, G Fotia
Data Mining Techniques for the Life Sciences, 407-422, 2016
52016
Expanding the Galaxy’s reference data
N VijayKrishna, J Joshi, N Coraor, J Hillman-Jackson, D Bouvier, ...
Bioinformatics Advances 2 (1), vbac030, 2022
22022
Simulating cardiac electrophysiology using unstructured all-hexahedra spectral elements
G Cuccuru, G Fotia, F Maggio, J Southern
BioMed research international 2015, 2015
22015
Automated and traceable processing for large-scale high-throughput sequencing facilities
L Pireddu, G Cuccuru, L Lianas, M Vocale, G Fotia, G Zanetti
EMBnet. journal 19 (A), 23-24, 2013
22013
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