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Employment (2)

Istituto Superiore di Sanità: Roma, Lazio, IT

2011 to present | Ricercatore (Oncologia e Medicina Molecolare)
Employment
Source: Self-asserted source
Alessandro Bruselles

INMI Lazzaro Spallanzani IRCCS: Roma, Lazio, IT

2007 to 2010 | Ricercatore (Virology)
Employment
Source: Self-asserted source
Alessandro Bruselles

Education and qualifications (2)

Università degli Studi di Roma Tor Vergata: Roma, Lazio, IT

2002 to 2005 | Dottorato di ricerca Biologia Molecolare e Cellulare (Biologia)
Education
Source: Self-asserted source
Alessandro Bruselles

Università degli Studi di Roma Tor Vergata: Roma, Lazio, IT

1995 to 2002 | Laurea (Biologia)
Education
Source: Self-asserted source
Alessandro Bruselles

Works (50 of 76)

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Page 1 of 2

The Arg99Gln Substitution in HNRNPC Is Associated with a Distinctive Clinical Phenotype Characterized by Facial Dysmorphism and Ocular and Cochlear Anomalies

Genes
2025-02-01 | Journal article
DOI: 10.3390/genes16020176
Contributors: Luigi Chiriatti; Manuela Priolo; Roberta Onesimo; Mattia Carvetta; Chiara Leoni; Alessandro Bruselles; Francesca Clementina Radio; Camilla Cappelletti; Marco Ferilli; Daniela Ricci et al.
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Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency

International Journal of Molecular Sciences
2024-09 | Journal article | Author
DOI: 10.3390/ijms25179637
Contributors: Stefania Martino; Pietro D'Addabbo; Antonella Turchiano; Radio FC; Alessandro Bruselles; Viviana Cordeddu; Cecilia Mancini; Alessandro Stella; nicola laforgia; Donatella Capodiferro et al.
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Multidisciplinary Digital Publishing Institute

Whole Genome Sequencing Solves an Atypical Form of Bardet–Biedl Syndrome: Identification of Novel Pathogenic Variants of BBS9

International Journal of Molecular Sciences
2024-07-30 | Journal article
DOI: 10.3390/ijms25158313
Contributors: Emilia Stellacci; Marcello Niceta; Alessandro Bruselles; Emilio Straface; Massimo Tatti; Mattia Carvetta; Cecilia Mancini; Serena Cecchetti; Mariacristina Parravano; Lucilla Barbano et al.
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Male breast cancer risk associated with pathogenic variants in genes other than BRCA1/2: an Italian case-control study

European Journal of Cancer
2023-07 | Journal article
DOI: 10.1016/j.ejca.2023.04.022
Contributors: Agostino Bucalo; Giulia Conti; Virginia Valentini; Carlo Capalbo; Alessandro Bruselles; Marco Tartaglia; Bernardo Bonanni; Daniele Calistri; Anna Coppa; Laura Cortesi et al.
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Crossref

Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium

International Journal of Molecular Sciences
2022-11-24 | Journal article
DOI: 10.3390/ijms232314656
Contributors: Lucia Ziccardi; Marcello Niceta; Emilia Stellacci; Andrea Ciolfi; Massimo Tatti; Alessandro Bruselles; Cecilia Mancini; Lucilla Barbano; Serena Cecchetti; Eliana Costanzo et al.
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Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis

Journal of Medical Genetics
2022-02 | Journal article
DOI: 10.1136/jmedgenet-2020-107281
Contributors: Lisa Pavinato; Marina Villamor-Payà; Maria Sanchiz-Calvo; Cristina Andreoli; Marina Gay; Marta Vilaseca; Gianluca Arauz-Garofalo; Andrea Ciolfi; Alessandro Bruselles; Tommaso Pippucci et al.
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A rare case of brachyolmia with amelogenesis imperfecta caused by a new pathogenic splicing variant in ltbp3

Genes
2021 | Journal article
DOI: 10.3390/genes12091406
EID:

2-s2.0-85115204620

Part of ISSN: 20734425
Contributors: Flex, E.; Imperatore, V.; Carpentieri, G.; Bruselles, A.; Ciolfi, A.; Pizzi, S.; Tedesco, M.G.; Rogaia, D.; Mencarelli, A.; Di Cara, G. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

Broadening the phenotypic spectrum of Beta3GalT6-associated phenotypes

American Journal of Medical Genetics, Part A
2021 | Journal article
DOI: 10.1002/ajmg.a.62399
EID:

2-s2.0-85108317178

Part of ISSN: 15524833 15524825
Contributors: Leoni, C.; Tedesco, M.; Radio, F.C.; Chillemi, G.; Leone, A.; Bruselles, A.; Ciolfi, A.; Stellacci, E.; Pantaleoni, F.; Butera, G. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

Kcnk18 biallelic variants associated with intellectual disability and neurodevelopmental disorders alter tresk channel activity

International Journal of Molecular Sciences
2021 | Journal article
DOI: 10.3390/ijms22116064
EID:

2-s2.0-85107284344

Part of ISSN: 14220067 16616596
Contributors: Pavinato, L.; Nematian-Ardestani, E.; Zonta, A.; De Rubeis, S.; Buxbaum, J.; Mancini, C.; Bruselles, A.; Tartaglia, M.; Pessia, M.; Tucker, S.J. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

American Journal of Human Genetics
2021 | Journal article
DOI: 10.1016/j.ajhg.2021.01.015
EID:

2-s2.0-85101770406

Part of ISSN: 15376605 00029297
Contributors: Radio, F.C.; Pang, K.; Ciolfi, A.; Levy, M.A.; Hernández-García, A.; Pedace, L.; Pantaleoni, F.; Liu, Z.; de Boer, E.; Jackson, A. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

Expanding the clinical phenotype of the ultra‐rare Skraban‐Deardorff syndrome: Two novel individuals with WDR26 loss‐of‐function variants and a literature review

American Journal of Medical Genetics Part A
2021-06 | Journal article
DOI: 10.1002/ajmg.a.62157
Contributors: Lisa Pavinato; Slavica Trajkova; Enrico Grosso; Elisa Giorgio; Alessandro Bruselles; Francesca Clementina Radio; Tommaso Pippucci; Paola Dimartino; Marco Tartaglia; Aleksandar Petlichkovski et al.
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ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

European Journal of Human Genetics
2020 | Journal article
DOI: 10.1038/s41431-020-0691-z
EID:

2-s2.0-85088047712

Part of ISSN: 14765438 10184813
Contributors: Benetti, E.; Tita, R.; Spiga, O.; Ciolfi, A.; Birolo, G.; Bruselles, A.; Doddato, G.; Giliberti, A.; Marconi, C.; Musacchia, F. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment

American Journal of Human Genetics
2020 | Journal article
DOI: 10.1016/j.ajhg.2020.10.012
EID:

2-s2.0-85097099439

Part of ISSN: 15376605 00029297
Contributors: Rodger, C.; Flex, E.; Allison, R.J.; Sanchis-Juan, A.; Hasenahuer, M.A.; Cecchetti, S.; French, C.E.; Edgar, J.R.; Carpentieri, G.; Ciolfi, A. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum

American Journal of Human Genetics
2020 | Journal article
DOI: 10.1016/j.ajhg.2020.06.018
EID:

2-s2.0-85089385871

Part of ISSN: 15376605 00029297
Contributors: Motta, M.; Pannone, L.; Pantaleoni, F.; Bocchinfuso, G.; Radio, F.C.; Cecchetti, S.; Ciolfi, A.; Di Rocco, M.; Elting, M.W.; Brilstra, E.H. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

Refinement of the clinical and mutational spectrum of UBE2A deficiency syndrome

Clinical Genetics
2020 | Journal article
DOI: 10.1111/cge.13775
EID:

2-s2.0-85085871295

Part of ISSN: 13990004 00099163
Contributors: Cordeddu, V.; Macke, E.L.; Radio, F.C.; Lo Cicero, S.; Pantaleoni, F.; Tatti, M.; Bellacchio, E.; Ciolfi, A.; Agolini, E.; Bruselles, A. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

ACE2gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population

2020-04-06 | Other
DOI: 10.1101/2020.04.03.20047977
Contributors: Benetti Elisa; Tita Rossella; Spiga Ottavia; Ciolfi Andrea; Birolo Giovanni; Bruselles Alessandro; Doddato Gabriella; Giliberti Annarita; Marconi Caterina; Musacchia Francesco et al.
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Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging

The American Journal of Human Genetics
2019-09 | Journal article
DOI: 10.1016/j.ajhg.2019.07.007
Part of ISSN: 0002-9297
Source: Self-asserted source
Alessandro Bruselles
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The activating p.Ser466Arg change in STAT1 causes a peculiar phenotype with features of interferonopathies

Clinical Genetics
2019-09-04 | Journal article
DOI: 10.1111/cge.13632
Part of ISSN: 0009-9163
Part of ISSN: 1399-0004
Source: Self-asserted source
Alessandro Bruselles
grade
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A new bioavailable fenretinide formulation with antiproliferative, antimetabolic, and cytotoxic effects on solid tumors

Cell Death & Disease
2019-07 | Journal article
DOI: 10.1038/s41419-019-1775-y
Part of ISSN: 2041-4889
Source: Self-asserted source
Alessandro Bruselles
grade
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NBAS pathogenic variants: Defining the associated clinical and facial phenotype and genotype–phenotype correlations

Human Mutation
2019-06 | Journal article
DOI: 10.1002/humu.23734
Part of ISSN: 1059-7794
Part of ISSN: 1098-1004
Source: Self-asserted source
Alessandro Bruselles
grade
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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases

Cell Death & Disease
2019-03 | Journal article
DOI: 10.1038/s41419-019-1453-0
Part of ISSN: 2041-4889
Source: Self-asserted source
Alessandro Bruselles
grade
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Colorectal cancer spheroid biobanks: multi-level approaches to drug sensitivity studies

Cell Biology and Toxicology
2018-12 | Journal article
DOI: 10.1007/s10565-018-9423-3
Part of ISSN: 0742-2091
Part of ISSN: 1573-6822
Source: Self-asserted source
Alessandro Bruselles
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Specific combinations of biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome

Journal of Medical Genetics
2018-12 | Journal article
DOI: 10.1136/jmedgenet-2018-105528
Part of ISSN: 0022-2593
Part of ISSN: 1468-6244
Source: Self-asserted source
Alessandro Bruselles
grade
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VarGenius executes cohort-level DNA-seq variant calling and annotation and allows to manage the resulting data through a PostgreSQL database

BMC Bioinformatics
2018-12 | Journal article
DOI: 10.1186/s12859-018-2532-4
Part of ISSN: 1471-2105
Source: Self-asserted source
Alessandro Bruselles
grade
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Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental Syndrome

The American Journal of Human Genetics
2018-10 | Journal article
DOI: 10.1016/j.ajhg.2018.09.001
Part of ISSN: 0002-9297
Source: Self-asserted source
Alessandro Bruselles
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Defective kinesin binding of TUBB2A causes progressive spastic ataxia syndrome resembling sacsinopathy

Human Molecular Genetics
2018-06-01 | Journal article
DOI: 10.1093/hmg/ddy096
Part of ISSN: 0964-6906
Part of ISSN: 1460-2083
Source: Self-asserted source
Alessandro Bruselles
grade
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The impact of next-generation sequencing on the diagnosis of pediatric-onset hereditary spastic paraplegias: new genotype-phenotype correlations for rare HSP-related genes

neurogenetics
2018-05 | Journal article
DOI: 10.1007/s10048-018-0545-9
Part of ISSN: 1364-6745
Part of ISSN: 1364-6753
Source: Self-asserted source
Alessandro Bruselles
grade
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Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome

Clinical Genetics
2018-03 | Journal article
DOI: 10.1111/cge.13128
Part of ISSN: 0009-9163
Source: Self-asserted source
Alessandro Bruselles
grade
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A Specific Mutational Signature Associated with DNA 8-Oxoguanine Persistence in MUTYH-defective Colorectal Cancer

Ebiomedicine
2017 | Journal article
DOI: 10.1016/j.ebiom.2017.04.022
WOSUID:

WOS:000405719700012
Contributors: Viel, Alessandra; Bruselles, Alessandro; Meccia, Ettore; Fornasarig, Mara; Quaia, Michele; Canzonieri, Vincenzo; Policicchio, Eleonora; Urso, Emanuele Damiano; Agostini, Marco; Genuardi, Maurizio et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes

European Journal of Paediatric Neurology
2017 | Journal article
DOI: 10.1016/j.ejpn.2016.12.005
WOSUID:

WOS:000401209200009
Contributors: Giorgio, Elisa; Brussino, Alessandro; Biamino, Elisa; Belligni, Elga Fabia; Bruselles, Alessandro; Ciolfi, Andrea; Caputo, Viviana; Pizzi, Simone; Calcia, Alessandro; Di Gregorio, Eleonora et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Clinical Genetics
2017 | Journal article
DOI: 10.1111/cge.12783
WOSUID:

WOS:000393979600011
Contributors: Barresi, S.; Niceta, M.; Alfieri, P.; Brankovic, V.; Piccini, G.; Bruselles, A.; Barone, M. R.; Cusmai, R.; Tartaglia, M.; Bertini, E. et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Somatic mosaicism represents an underestimated event underlying collagen 6-related disorders

European Journal of Paediatric Neurology
2017 | Journal article
DOI: 10.1016/j.ejpn.2017.07.009
EID:

2-s2.0-85026287371

Part of ISSN: 15322130 10903798
Contributors: D'Amico, A.; Fattori, F.; Tasca, G.; Petrini, S.; Gualandi, F.; Bruselles, A.; D'Oria, V.; Verardo, M.; Carrozzo, R.; Niceta, M. et al.
Source: Self-asserted source
Alessandro Bruselles via Scopus - Elsevier

NovelSEC61G–EGFRFusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens

Cancer Research
2017-11-01 | Journal article
DOI: 10.1158/0008-5472.can-17-0790
Part of ISSN: 0008-5472
Part of ISSN: 1538-7445
Source: Self-asserted source
Alessandro Bruselles
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Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophy.

Brain : a journal of neurology
2017-10-01 | Journal article
DOI: 10.1093/brain/awx207
PMID: 28969374
Source: Self-asserted source
Alessandro Bruselles
grade
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Identification of novel and hotspot mutations in the channel domain of ITPR1 in two patients with Gillespie syndrome

Gene
2017-09 | Journal article
DOI: 10.1016/j.gene.2017.07.017
Part of ISSN: 0378-1119
Source: Self-asserted source
Alessandro Bruselles
grade
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A syndromic extreme insulin resistance caused by biallelic POC1A mutations in exon 10.

European journal of endocrinology
2017-08-17 | Journal article
DOI: 10.1530/eje-17-0431
PMID: 28819016
Source: Self-asserted source
Alessandro Bruselles
grade
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HIPK2-T566 autophosphorylation diversely contributes to UV- and doxorubicin-induced HIPK2 activation

Oncotarget
2017-03-07 | Journal article
DOI: 10.18632/oncotarget.14421
Part of ISSN: 1949-2553
Source: Self-asserted source
Alessandro Bruselles
grade
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A Follow-Up of the Multicenter Collaborative Study on HIV-1 Drug Resistance and Tropism Testing Using 454 Ultra Deep Pyrosequencing

Plos One
2016 | Journal article
DOI: 10.1371/journal.pone.0146687
WOSUID:

WOS:000367888800027
Contributors: St John, Elizabeth P.; Simen, Birgitte B.; Turenchalk, Gregory S.; Braverman, Michael S.; Abbate, Isabella; Aerssens, Jeroen; Bouchez, Olivier; Gabriel, Christian; Izopet, Jacques; Meixenberger, Karolin et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Cancer Stem Cell-Based Models of Colorectal Cancer Reveal Molecular Determinants of Therapy Resistance

Stem Cells Translational Medicine
2016 | Journal article
DOI: 10.5966/sctm.2015-0214
WOSUID:

WOS:000373523700011
Contributors: De Angelis, Maria Laura; Zeuner, Ann; Policicchio, Eleonora; Russo, Giorgio; Bruselles, Alessandro; Signore, Michele; Vitale, Sara; De Luca, Gabriele; Pilozzi, Emanuela; Boe, Alessandra et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Congenital Immunodeficiency in an Individual with Wiedemann-Steiner Syndrome Due to a Novel Missense Mutation in KMT2A

American Journal of Medical Genetics Part a
2016 | Journal article
DOI: 10.1002/ajmg.a.37681
WOSUID:

WOS:000383608700022
Contributors: Stellacci, Emilia; Onesimo, Roberta; Bruselles, Alessandro; Pizzi, Simone; Battaglia, Domenica; Leoni, Chiara; Zampino, Giuseppe; Tartaglia, Marco
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Cover Image, Volume 170A, Number 7, July 2016.

American journal of medical genetics. Part A
2016 | Journal article
DOI: 10.1002/ajmg.a.37790
WOSUID:

MEDLINE:27311422
Contributors: Giorgio, Elisa; Ciolfi, Andrea; Biamino, Elisa; Caputo, Viviana; Di Gregorio, Eleonora; Belligni, Elga Fabia; Calcia, Alessandro; Gaidolfi, Elena; Bruselles, Alessandro; Mancini, Cecilia et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Expanding the molecular diversity and phenotypic spectrum of glycerol 3-phosphate dehydrogenase 1 deficiency

Journal of Inherited Metabolic Disease
2016 | Journal article
DOI: 10.1007/s10545-016-9956-7
WOSUID:

WOS:000381986400009
Contributors: Dionisi-Vici, Carlo; Shteyer, Eyal; Niceta, Marcello; Rizzo, Cristiano; Pode-Shakked, Ben; Chillemi, Giovanni; Bruselles, Alessandro; Semeraro, Michela; Barel, Ortal; Eyal, Eran et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Whole Exome Sequencing Is Necessary to Clarify ID/DD Cases with De Novo Copy Number Variants of Uncertain Significance: Two Proof-of-Concept Examples

American Journal of Medical Genetics Part a
2016 | Journal article
DOI: 10.1002/ajmg.a.37649
WOSUID:

WOS:000379948000008
Contributors: Giorgio, Elisa; Ciolfi, Andrea; Biamino, Elisa; Caputo, Viviana; Di Gregorio, Eleonora; Belligni, Elga Fabia; Calcia, Alessandro; Gaidolfi, Elena; Bruselles, Alessandro; Mancini, Cecilia et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Activating Mutations Affecting the Dbl Homology Domain of SOS2 Cause Noonan Syndrome

Human Mutation
2015 | Journal article
DOI: 10.1002/humu.22834
WOSUID:

WOS:000362991400011
Contributors: Cordeddu, Viviana; Yin, Jiani C.; Gunnarsson, Cecilia; Virtanen, Carl; Drunat, Severine; Lepri, Francesca; De Luca, Alessandro; Rossi, Cesare; Ciolfi, Andrea; Pugh, Trevor J. et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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Mutations Impairing GSK3-Mediated MAF Phosphorylation Cause Cataract, Deafness, Intellectual Disability, Seizures, and a Down Syndrome-like Facies

American Journal of Human Genetics
2015 | Journal article
DOI: 10.1016/j.ajhg.2015.03.001
WOSUID:

WOS:000354189300012
Contributors: Niceta, Marcello; Stellacci, Emilia; Gripp, Karen W.; Zampino, Giuseppe; Kousi, Maria; Anselmi, Massimiliano; Traversa, Alice; Ciolfi, Andrea; Stabley, Deborah; Bruselles, Alessandro et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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p.Arg1809Cys substitution in neurofibromin is associated with a distinctive NF1 phenotype without neurofibromas

European Journal of Human Genetics
2015 | Journal article
DOI: 10.1038/ejhg.2014.243
WOSUID:

WOS:000358006100014
Contributors: Pinna, Valentina; Lanari, Valentina; Daniele, Paola; Consoli, Federica; Agolini, Emanuele; Margiotti, Katia; Bottillo, Irene; Torrente, Isabella; Bruselles, Alessandro; Fusilli, Caterina et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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An international multicenter study on HIV-1 drug resistance testing by 454 ultra-deep pyrosequencing

Journal of Virological Methods
2014 | Journal article
DOI: 10.1016/j.jviromet.2014.04.007
WOSUID:

WOS:000337649100006
Contributors: Simen, Birgitte B.; Braverman, Michael S.; Abbate, Isabella; Aerssens, Jeroen; Bidet, Yannick; Bouchez, Olivier; Gabriel, Christian; Izopet, Jacques; Kessler, Harald H.; Stelzl, Evelyn et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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The Genotypic False Positive Rate Determined by V3 Population Sequencing Can Predict the Burden of HIV-1 CXCR4-using Species Detected by Pyrosequencing

Plos One
2013 | Journal article
DOI: 10.1371/journal.pone.0053603
WOSUID:

WOS:000314759400052
Contributors: Svicher, Valentina; Cento, Valeria; Rozera, Gabriella; Abbate, Isabella; Santoro, Maria Mercedes; Armenia, Daniele; Fabeni, Lavinia; Bruselles, Alessandro; Latini, Alessandra; Palamara, Guido et al.
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Alessandro Bruselles via ResearcherID
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Ultra-deep sequencing reveals hidden HIV-1 minority lineages and shifts of viral population between the main cellular reservoirs of the infection after therapy interruption.

Journal of medical virology
2012 | Journal article
DOI: 10.1002/jmv.23292
WOSUID:

MEDLINE:22996031
Contributors: Rozera, Gabriella; Abbate, Isabella; Ciccozzi, Massimo; Lo Presti, Alessandra; Bruselles, Alessandro; Vlassi, Chrysoula; D'Offizi, Gianpiero; Narciso, Pasquale; Giombini, Emanuela; Bartolini, Barbara et al.
Source: Self-asserted source
Alessandro Bruselles via ResearcherID
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'Sentinel' mutations in standard population sequencing can predict the presence of HIV-1 reverse transcriptase major mutations detectable only by ultra-deep pyrosequencing

Journal of Antimicrobial Chemotherapy
2011 | Journal article
DOI: 10.1093/jac/dkr354
WOSUID:

WOS:000295989500028
Contributors: Alteri, Claudia; Santoro, Maria Mercedes; Abbate, Isabella; Rozera, Gabriella; Bruselles, Alessandro; Bartolini, Barbara; Gori, Caterina; Forbici, Federica; Orchi, Nicoletta; Tozzi, Valerio et al.
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Alessandro Bruselles via ResearcherID
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