Follow
Alberto Magi
Alberto Magi
Associate Professor of Bioengineering, Department of Information Engineering, University of Florence
Verified email at unifi.it
Title
Cited by
Cited by
Year
Detection of genomic structural variants from next-generation sequencing data
L Tattini, R D’Aurizio, A Magi
Frontiers in bioengineering and biotechnology 3, 92, 2015
3122015
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
A Magi, L Tattini, I Cifola, R D’Aurizio, M Benelli, E Mangano, C Battaglia, ...
Genome biology 14, 1-18, 2013
2522013
Nanopore sequencing data analysis: state of the art, applications and challenges
A Magi, R Semeraro, A Mingrino, B Giusti, R D’aurizio
Briefings in bioinformatics 19 (6), 1256-1272, 2018
1942018
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScript
M Benelli, C Pescucci, G Marseglia, M Severgnini, F Torricelli, A Magi
Bioinformatics 28 (24), 3232-3239, 2012
1942012
Bioinformatics for next generation sequencing data
A Magi, M Benelli, A Gozzini, F Girolami, F Torricelli, ML Brandi
Genes 1 (2), 294-307, 2010
1292010
H 3 M 2 : detection of runs of homozygosity from whole-exome sequencing data
A Magi, L Tattini, F Palombo, M Benelli, A Gialluisi, B Giusti, R Abbate, ...
Bioinformatics 30 (20), 2852-2859, 2014
1172014
Read count approach for DNA copy number variants detection
A Magi, L Tattini, T Pippucci, F Torricelli, M Benelli
Bioinformatics 28 (4), 470-478, 2012
1132012
Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm
A Magi, M Benelli, S Yoon, F Roviello, F Torricelli
Nucleic acids research 39 (10), e65-e65, 2011
912011
Enhanced copy number variants detection from whole-exome sequencing data using EXCAVATOR2
R D'Aurizio, T Pippucci, L Tattini, B Giusti, M Pellegrini, A Magi
Nucleic acids research 44 (20), e154-e154, 2016
892016
372 kb microdeletion in 18q12. 3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment
G Marseglia, MR Scordo, C Pescucci, G Nannetti, E Biagini, V Scandurra, ...
European journal of medical genetics 55 (3), 216-221, 2012
892012
Genetic bases of bicuspid aortic valve: the contribution of traditional and high-throughput sequencing approaches on research and diagnosis
B Giusti, E Sticchi, R De Cario, A Magi, S Nistri, G Pepe
Frontiers in physiology 8, 612, 2017
882017
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization
P Striano, A Coppola, R Paravidino, M Malacarne, S Gimelli, A Robbiano, ...
Archives of neurology 69 (3), 322-330, 2012
842012
Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm
B Giusti, C Saracini, P Bolli, A Magi, I Sestini, E Sticchi, G Pratesi, R Pulli, ...
Journal of Medical Genetics 45 (11), 721-730, 2008
822008
The antiangiogenic tissue kallikrein pattern of endothelial cells in systemic sclerosis
B Giusti, S Serratì, F Margheri, L Papucci, L Rossi, F Poggi, A Magi, ...
Arthritis & Rheumatism 52 (11), 3618-3628, 2005
762005
Characterization of MinION nanopore data for resequencing analyses
A Magi, B Giusti, L Tattini
Briefings in bioinformatics 18 (6), 940-953, 2017
702017
Acute kidney injury promotes development of papillary renal cell adenoma and carcinoma from renal progenitor cells
AJ Peired, G Antonelli, ML Angelotti, M Allinovi, F Guzzi, A Sisti, ...
Science translational medicine 12 (536), eaaw6003, 2020
672020
A model of anti-angiogenesis: differential transcriptosome profiling of microvascular endothelial cells from diffuse systemic sclerosis patients
B Giusti, G Fibbi, F Margheri, S Serratì, L Rossi, F Poggi, I Lapini, A Magi, ...
Arthritis research & therapy 8, 1-17, 2006
642006
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants
B Giusti, A Vestrini, C Poggi, A Magi, E Pasquini, R Abbate, C Dani
Free Radical Research, 1-24, 2012
632012
Epilepsy with auditory features: A heterogeneous clinico-molecular disease
T Pippucci, L Licchetta, S Baldassari, F Palombo, V Menghi, R D'Aurizio, ...
Neurology: Genetics 1 (1), e5, 2015
592015
Gene expression profiling of peripheral blood in patients with abdominal aortic aneurysm
B Giusti, L Rossi, I Lapini, A Magi, G Pratesi, M Lavitrano, GM Biasi, ...
European journal of vascular and endovascular surgery 38 (1), 104-112, 2009
492009
The system can't perform the operation now. Try again later.
Articles 1–20