关注
Matteo Benelli
Matteo Benelli
Dept. of Experimental and Clinical Biomedical Sciences, University of Florence
在 unifi.it 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer
H Beltran, D Prandi, JM Mosquera, M Benelli, L Puca, J Cyrta, C Marotz, ...
Nature medicine 22 (3), 298-305, 2016
14532016
Genomic correlates of clinical outcome in advanced prostate cancer
W Abida, J Cyrta, G Heller, D Prandi, J Armenia, I Coleman, M Cieslik, ...
Proceedings of the National Academy of Sciences 116 (23), 11428-11436, 2019
10482019
SOX2 promotes lineage plasticity and antiandrogen resistance in TP53-and RB1-deficient prostate cancer
P Mu, Z Zhang, M Benelli, WR Karthaus, E Hoover, CC Chen, ...
Science 355 (6320), 84-88, 2017
9072017
N-Myc induces an EZH2-mediated transcriptional program driving neuroendocrine prostate cancer
E Dardenne, H Beltran, M Benelli, K Gayvert, A Berger, L Puca, J Cyrta, ...
Cancer cell 30 (4), 563-577, 2016
5132016
Patient derived organoids to model rare prostate cancer phenotypes
L Puca, R Bareja, D Prandi, R Shaw, M Benelli, WR Karthaus, J Hess, ...
Nature communications 9 (1), 2404, 2018
3032018
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
2552013
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
Circulating tumor DNA profile recognizes transformation to castration-resistant neuroendocrine prostate cancer
H Beltran, A Romanel, V Conteduca, N Casiraghi, M Sigouros, ...
The Journal of clinical investigation 130 (4), 1653-1668, 2020
1582020
Mechanisms of resistance to CDK4/6 inhibitors: potential implications and biomarkers for clinical practice
A McCartney, I Migliaccio, M Bonechi, C Biagioni, D Romagnoli, ...
Frontiers in oncology 9, 666, 2019
1392019
Bioinformatics for next generation sequencing data
A Magi, M Benelli, A Gozzini, F Girolami, F Torricelli, ML Brandi
Genes 1 (2), 294-307, 2010
1272010
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
1182014
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
1092012
Genomic and transcriptomic analyses of breast cancer primaries and matched metastases in AURORA, the Breast International Group (BIG) molecular screening initiative
P Aftimos, M Oliveira, A Irrthum, D Fumagalli, C Sotiriou, EN Gal-Yam, ...
Cancer discovery 11 (11), 2796-2811, 2021
1012021
Differential impact of RB status on E2F1 reprogramming in human cancer
C McNair, K Xu, AC Mandigo, M Benelli, B Leiby, D Rodrigues, J Lindberg, ...
The Journal of clinical investigation 128 (1), 341-358, 2018
1012018
Novel α-actinin 2 variant associated with familial hypertrophic cardiomyopathy and juvenile atrial arrhythmias: a massively parallel sequencing study
F Girolami, M Iascone, B Tomberli, S Bardi, M Benelli, G Marseglia, ...
Circulation: Cardiovascular Genetics 7 (6), 741-750, 2014
962014
Role of specialized composition of SWI/SNF complexes in prostate cancer lineage plasticity
J Cyrta, A Augspach, MR De Filippo, D Prandi, P Thienger, M Benelli, ...
Nature communications 11 (1), 5549, 2020
942020
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
902011
Cyclin E1 and Rb modulation as common events at time of resistance to palbociclib in hormone receptor-positive breast cancer
C Guarducci, M Bonechi, M Benelli, C Biagioni, G Boccalini, D Romagnoli, ...
NPJ breast cancer 4 (1), 38, 2018
892018
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
882012
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
832012
系统目前无法执行此操作,请稍后再试。
文章 1–20