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48 peer-reviewed articles • 13,089 peer-reviewed citations • Sorted by year • Download PDF (PDF by citations)
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1SILVAN: Estimating Betweenness Centralities with Progressive Sampling and Non-uniform Rademacher Bounds2.813Citations (PDF)
2ALLSTAR: inference of reliAble causaL ruLes between Somatic muTAtions and canceR phenotypes.3.20Citations (PDF)
3Efficient Discovery of Significant Patterns with Few-Shot Resampling1.61Citations (PDF)
4Bounding the family-wise error rate in local causal discovery using Rademacher averages2.61Citations (PDF)
5caSPiTa: mining statistically significant paths in time series data from an unknown network1.91Citations (PDF)
6The Impact of Global Structural Information in Graph Neural Networks Applications
Data, 2022, 7, 10
1.66Citations (PDF)
7MCRapper: Monte-Carlo Rademacher Averages for Poset Families and Approximate Pattern Mining2.88Citations (PDF)
8SPRISS: approximating frequent k-mers by sampling reads, and applications.
Bioinformatics, 2022, 38, 3343-3350
3.23Citations (PDF)
9Technical perspective: Evaluating sampled metrics is challenging
Communications of the ACM, 2022, 65, 74-74
1.50Citations (PDF)
10gRosSo: mining statistically robust patterns from a sequence of datasets1.91Citations (PDF)
11Comparison of microbiome samples: methods and computational challenges4.126Citations (PDF)
12Attention-Based Deep Learning Framework for Human Activity Recognition With User Adaptation
IEEE Sensors Journal, 2021, 21, 13474-13483
3.070Citations (PDF)
13Fast Approximation of Frequent k-Mers and Applications to Metagenomics0.810Citations (PDF)
14Identifying Drug Sensitivity Subnetworks with NETPHIX
IScience, 2020, 23, 101619
2.56Citations (PDF)
15Efficient mining of the most significant patterns with permutation testing2.617Citations (PDF)
16Mining Sequential Patterns with VC-Dimension and Rademacher Complexity
Algorithms, 2020, 13, 123
1.512Citations (PDF)
17MiSoSouP: Mining Interesting Subgroups with Sampling and Pseudodimension2.85Citations (PDF)
18Enriched power of disease-concordant twin-case-only design in detecting interactions in genome-wide association studies2.15Citations (PDF)
19People also looked at
Frontiers in Genetics, 2019, 10, 437012
1.68Citations (PDF)
20Efficient algorithms to discover alterations with complementary functional association in cancer
PLoS Computational Biology, 2019, 15, e1006802
2.013Citations (PDF)
21Differentially mutated subnetworks discovery0.97Citations (PDF)
22Efficient detection of differentially methylated regions using DiMmeR.
Bioinformatics, 2017, 33, 549-551
3.29Citations (PDF)
23Disease-Concordant Twins Empower Genetic Association Studies
Annals of Human Genetics, 2017, 81, 20-26
1.051Citations (PDF)
24De novo pathway-based biomarker identification
Nucleic Acids Research, 2017, 45, e151
11.251Citations (PDF)
25HIT'nDRIVE: patient-specific multidriver gene prioritization for precision oncology
Genome Research, 2017, 27, 1573-1588
3.283Citations (PDF)
26Clustering uncertain graphs1.638Citations (PDF)
27People also looked at
Frontiers in Genetics, 2017, 8, 259369
1.631Citations (PDF)
28Differentially Methylated Genomic Regions in Birth-Weight Discordant Twin Pairs
Annals of Human Genetics, 2016, 80, 81-87
1.023Citations (PDF)
29Jllumina - A comprehensive Java-based API for statistical Illumina Infinium HumanMethylation450 and Infinium MethylationEPIC BeadChip data processing0.82Citations (PDF)
30On the Sample Complexity of Cancer Pathways Identification0.86Citations (PDF)
31CoMEt: a statistical approach to identify combinations of mutually exclusive alterations in cancer
Genome Biology, 2015, 16, 1-20
4.8205Citations (PDF)
32Simultaneous Inference of Cancer Pathways and Tumor Progression from Cross-Sectional Mutation Data0.833Citations (PDF)
33Accurate Computation of Survival Statistics in Genome-Wide Studies
PLoS Computational Biology, 2015, 11, e1004071
2.027Citations (PDF)
34Integrated Genomic Characterization of Papillary Thyroid Carcinoma
Cell, 2014, 159, 676-690
23.82,948Citations (PDF)
35Identifying driver mutations in sequenced cancer genomes: computational approaches to enable precision medicine
Genome Medicine, 2014, 6, 1-17
5.9218Citations (PDF)
36Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes
Nature Genetics, 2014, 47, 106-114
14.2970Citations (PDF)
37Mutational landscape and significance across 12 major cancer types
Nature, 2013, 502, 333-339
31.84,388Citations (PDF)
38Ballast: A Ball-based Algorithm for Structural Motifs0.85Citations (PDF)
39Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia24.44,921Citations (PDF)
40An Efficient Rigorous Approach for Identifying Statistically Significant Frequent Itemsets
Journal of the ACM, 2012, 59, 1-22
1.127Citations (PDF)
41The mutational landscape of lethal castration-resistant prostate cancer
Nature, 2012, 487, 239-243
31.82,449Citations (PDF)
42Finding driver pathways in cancer: models and algorithms0.919Citations (PDF)
43De novo discovery of mutated driver pathways in cancer
Genome Research, 2012, 22, 375-385
3.2428Citations (PDF)
44Algorithms and Genome Sequencing: Identifying Driver Pathways in Cancer
Computer, 2012, 45, 39-46
0.411Citations (PDF)
45Algorithms for Detecting Significantly Mutated Pathways in Cancer0.8454Citations (PDF)
46MADMX: A Strategy for Maximal Dense Motif Extraction0.816Citations (PDF)
47Mining top-K frequent itemsets through progressive sampling2.637Citations (PDF)
48General-purpose topology-aware embedding of tumor phylogenetic trees with graph neural networks0.90Citations (PDF)