Alessandro Bruselles
Alessandro Bruselles
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Use of massively parallel ultradeep pyrosequencing to characterize the genetic diversity of hepatitis B virus in drug-resistant and drug-naive patients and to detect minorá…
M Solmone, D Vincenti, MCF Prosperi, A Bruselles, G Ippolito, ...
Journal of virology 83 (4), 1718-1726, 2009
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ...
European Journal of Human Genetics 28 (11), 1602-1614, 2020
Massively parallel pyrosequencing highlights minority variants in the HIV-1 env quasispecies deriving from lymphomonocyte sub-populations
G Rozera, I Abbate, A Bruselles, C Vlassi, G D'Offizi, P Narciso, G Chillemi, ...
Retrovirology 6 (1), 1-13, 2009
A specific mutational signature associated with DNA 8-oxoguanine persistence in MUTYH-defective colorectal cancer
A Viel, A Bruselles, E Meccia, M Fornasarig, M Quaia, V Canzonieri, ...
EBioMedicine 20, 39-49, 2017
p. Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas
V Pinna, V Lanari, P Daniele, F Consoli, E Agolini, K Margiotti, I Bottillo, ...
European Journal of Human Genetics 23 (8), 1068-1071, 2015
Single mutation in the linker domain confers protein flexibility and camptothecin resistance to human topoisomerase I
P Fiorani, A Bruselles, M Falconi, G Chillemi, A Desideri, P Benedetti
Journal of Biological Chemistry 278 (44), 43268-43275, 2003
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies
M Niceta, E Stellacci, KW Gripp, G Zampino, M Kousi, M Anselmi, ...
The American Journal of Human Genetics 96 (5), 816-825, 2015
Combinatorial analysis and algorithms for quasispecies reconstruction using next-generation sequencing
MCF Prosperi, L Prosperi, A Bruselles, I Abbate, G Rozera, D Vincenti, ...
BMC bioinformatics 12 (1), 1-13, 2011
Activating mutations affecting the Dbl homology domain of SOS2 cause Noonan syndrome
V Cordeddu, JC Yin, C Gunnarsson, C Virtanen, S Drunat, F Lepri, ...
Human mutation 36 (11), 1080-1087, 2015
Effect on DNA relaxation of the single Thr718Ala mutation in human topoisomerase I: a functional and molecular dynamics study
G Chillemi, P Fiorani, S Castelli, A Bruselles, P Benedetti, A Desideri
Nucleic acids research 33 (10), 3339-3350, 2005
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
L Grassi, R Alfonsi, F Francescangeli, M Signore, ML De Angelis, ...
Cell death & disease 10 (3), 1-15, 2019
Mutations in KCNK4 that affect gating cause a recognizable neurodevelopmental syndrome
CK Bauer, P Calligari, FC Radio, V Caputo, ML Dentici, N Falah, F High, ...
The American Journal of Human Genetics 103 (4), 621-630, 2018
Detection of quasispecies variants predicted to use CXCR4 by ultra-deep pyrosequencing during early HIV infection
I Abbate, C Vlassi, G Rozera, A Bruselles, B Bartolini, E Giombini, ...
Aids 25 (5), 611-617, 2011
Cancer stem cell‐based models of colorectal cancer reveal molecular determinants of therapy resistance
ML De Angelis, A Zeuner, E Policicchio, G Russo, A Bruselles, M Signore, ...
Stem cells translational medicine 5 (4), 511-523, 2016
Analysis of co‐receptor usage of circulating viral and proviral HIV genome quasispecies by ultra‐deep pyrosequencing in patients who are candidates for CCR5 antagonist treatment
I Abbate, G Rozera, C Tommasi, A Bruselles, B Bartolini, G Chillemi, ...
Clinical microbiology and infection 17 (5), 725-731, 2011
Aberrant function of the C-terminal tail of HIST1H1E accelerates cellular senescence and causes premature aging
E Flex, S Martinelli, A Van Dijck, A Ciolfi, S Cecchetti, E Coluzzi, ...
The American Journal of Human Genetics 105 (3), 493-508, 2019
Use of massive parallel pyrosequencing for near full-length characterization of a unique HIV Type 1 BF recombinant associated with a fatal primary infection
A Bruselles, G Rozera, B Bartolini, M Prosperi, F Del Nonno, P Narciso, ...
AIDS research and human retroviruses 25 (9), 937-942, 2009
Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia
S Barresi, M Niceta, P Alfieri, V Brankovic, G Piccini, A Bruselles, ...
Clinical genetics 91 (1), 86-91, 2017
Role of the linker domain and the 203–214 N-terminal residues in the human topoisomerase I DNA complex dynamics
G Chillemi, M Redinbo, A Bruselles, A Desideri
Biophysical journal 87 (6), 4087-4097, 2004
Specific combinations of biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome
S Paolacci, Y Li, E Agolini, E Bellacchio, CE Arboleda-Bustos, D Carrero, ...
Journal of medical genetics 55 (12), 837-846, 2018
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