Silvano Garnerone

Science for Life Laboratory — Sweden

Physics and Astronomy · Physical Sciences

17h-index1.5kcitations44works0.02yr avg
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Research Topics

Quantum many-body systems(13), Algebraic structures and combinatorial models(7), Cancer Genomics and Diagnostics(6), Quantum Information and Cryptography(5), DNA Repair Mechanisms(5)

Publications44 total

A recurrent chromosomal inversion suffices for driving escape from oncogene-induced senescence via subTAD reorganization
Molecular Cell·2021· 78 citedOpen Access
Genomic instability is an early event driving chromatin reorganization and escape from oncogene-induced senescence
2020· 2 citedOpen Access
Genome-wide detection of DNA double-strand breaks by in-suspension BLISS
Nature Protocols·2020· 46 cited
CUTseq is a versatile method for preparing multiplexed DNA sequencing libraries from low-input samples
2019Open Access
Breaks Labeling in situ and sequencing (BLISS)
2019· 2 citedOpen Access
CUTseq is a versatile method for preparing multiplexed DNA sequencing libraries from low-input samples
Nature Communications·2019· 21 citedOpen Access
CUTseq is a versatile method for preparing multiplexed DNA sequencing libraries from low-input samples
2019· 6 citedOpen Access
P2.01-66 Genomic Landscapes of DNA Copy Number Alterations in Primary Lung Cancers and Matched Brain Metastases
Journal of Thoracic Oncology·2019· 1 cited
CUTseq is a versatile method for preparing multiplexed DNA sequencing libraries from low-input samples
2019Open Access
Modeling double strand break susceptibility to interrogate structural variation in cancer
Genome biology·2019· 28 citedOpen Access
Data sets for modeling double strand break susceptibility and interrogating structural variation in cancer
2019Open Access
Data sets for modeling double strand break susceptibility and interrogating structural variation in cancer
Zenodo (CERN European Organization for Nuclear Research)·2019Open Access
Additional file 2: of Modeling double strand break susceptibility to interrogate structural variation in cancer
Figshare·2019Open Access
Modelling double strand break susceptibility to interrogate structural variation in cancer
2018· 1 citedOpen Access
Breaks Labeling in situ and sequencing (BLISS)
Protocol Exchange·2017· 5 citedOpen Access
BLISS is a versatile and quantitative method for genome-wide profiling of DNA double-strand breaks
Nature Communications·2017· 379 citedOpen Access
BLISS is a versatile and quantitative method for genome-wide profiling of DNA double-strand breaks
DSpace@MIT (Massachusetts Institute of Technology)·2017· 88 citedOpen Access
Quantification of HER2 and estrogen receptor heterogeneity in breast cancer by single-molecule RNA fluorescence in situ hybridization
Oncotarget·2017· 34 citedOpen Access
BLISS: quantitative and versatile genome-wide profiling of DNA breaks <i>in situ</i>
2016· 2 citedOpen Access
Quantum algorithms for topological and geometric analysis of data
Nature Communications·2016· 240 citedOpen Access
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Frequent Co-authors

Nicola Crosetto(19), Reza Mirzazadeh(17), Magda Bienko(11), Paolo Zanardi(10), Annalisa Marzuoli(8), Mario Rasetti(8), Erik Wernersson(6), Britta A. M. Bouwman(6), Winston X. Yan(5), Martin Schneider(5), Tomasz Kallas(5), Joaquín Custodio(5), Yinqing Li(5), Linyi Gao(5), Yana Federova(5), Bernd Zetsche(5), Stephan Haas(5), Michele Simonetti(5), Caterina Marchiò(5), Anna Sapino(5)