Fabio Vandin
Fabio Vandin
Professor, Department of Information Engineering, University of Padova
Geverifieerd e-mailadres voor unipd.it - Homepage
Geciteerd door
Geciteerd door
The cancer genome atlas pan-cancer analysis project
JN Weinstein, EA Collisson, GB Mills, KRM Shaw, BA Ozenberger, ...
Nature genetics 45 (10), 1113-1120, 2013
Integrated genomic analyses of ovarian carcinoma
Cancer Genome Atlas Research Network
Nature 474 (7353), 609, 2011
Mutational landscape and significance across 12 major cancer types
C Kandoth, MD McLellan, F Vandin, K Ye, B Niu, C Lu, M Xie, Q Zhang, ...
Nature 502 (7471), 333-339, 2013
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
Cancer Genome Atlas Research Network
New England Journal of Medicine 368 (22), 2059-2074, 2013
The mutational landscape of lethal castration-resistant prostate cancer
CS Grasso, YM Wu, DR Robinson, X Cao, SM Dhanasekaran, AP Khan, ...
Nature 487 (7406), 239-243, 2012
Comprehensive molecular characterization of clear cell renal cell carcinoma
Cancer Genome Atlas Research Network
Nature 499 (7456), 43, 2013
Integrated genomic characterization of papillary thyroid carcinoma.
CGAR Network.
Cell, 2014
Integrated genomic analyses of ovarian carcinoma
D Bell, A Berchuck, M Birrer, J Chien, DW Cramer, F Dao, R Dhir, ...
Nature Publishing Group, 2011
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin.
Cell 158 (4), 929-44, 2014
Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes
MDM Leiserson, F Vandin, HT Wu, JR Dobson, JV Eldridge, JL Thomas, ...
Nature genetics 47 (2), 106-114, 2015
De novo discovery of mutated driver pathways in cancer
F Vandin, E Upfal, BJ Raphael
Genome research 22 (2), 375-385, 2012
Algorithms for detecting significantly mutated pathways in cancer
F Vandin, E Upfal, BJ Raphael
Journal of Computational Biology 18 (3), 507-522, 2011
Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine
BJ Raphael, JR Dobson, L Oesper, F Vandin
Genome medicine 6 (1), 1-17, 2014
Computational pan-genomics: status, promises and challenges
Briefings in bioinformatics 19 (1), 118-135, 2018
CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer
MDM Leiserson, HT Wu, F Vandin, BJ Raphael
Genome biology 16 (1), 1-20, 2015
Discovery of mutated subnetworks associated with clinical data in cancer
F Vandin, P Clay, E Upfal, BJ Raphael
Biocomputing 2012, 55-66, 2012
An efficient rigorous approach for identifying statistically significant frequent itemsets
A Kirsch, M Mitzenmacher, A Pietracaprina, G Pucci, E Upfal, F Vandin
Journal of the ACM (JACM) 59 (3), 1-22, 2012
Algorithms on evolving graphs
A Anagnostopoulos, R Kumar, M Mahdian, E Upfal, F Vandin
Proceedings of the 3rd Innovations in Theoretical Computer Science …, 2012
De novo pathway-based biomarker identification
N Alcaraz, M List, R Batra, F Vandin, HJ Ditzel, J Baumbach
Nucleic acids research 45 (16), e151-e151, 2017
Mining top-K frequent itemsets through progressive sampling
A Pietracaprina, M Riondato, E Upfal, F Vandin
Data Mining and Knowledge Discovery 21 (2), 310-326, 2010
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Artikelen 1–20