Year |
Citation |
Score |
2023 |
Alexandrov LB, Kim J, Haradhvala NJ, Huang MN, Tian Ng AW, Wu Y, Boot A, Covington KR, Gordenin DA, Bergstrom EN, Islam SMA, Lopez-Bigas N, Klimczak LJ, McPherson JR, Morganella S, et al. Author Correction: The repertoire of mutational signatures in human cancer. Nature. PMID 36697836 DOI: 10.1038/s41586-022-05600-5 |
0.348 |
|
2021 |
De Marco C, Zoppoli P, Rinaldo N, Morganella S, Morello M, Zuccalà V, Carriero MV, Malanga D, Chirillo R, Bruni P, Malzoni C, Di Vizio D, Venturella R, Zullo F, Rizzuto A, et al. Genome-wide analysis of copy number alterations led to the characterisation of PDCD10 as oncogene in ovarian cancer. Translational Oncology. 14: 101013. PMID 33516089 DOI: 10.1016/j.tranon.2021.101013 |
0.359 |
|
2020 |
Degasperi A, Amarante TD, Czarnecki J, Shooter S, Zou X, Glodzik D, Morganella S, Nanda AS, Badja C, Koh G, Momen SE, Georgakopoulos-Soares I, Dias JML, Young J, Memari Y, et al. A practical framework and online tool for mutational signature analyses show inter-tissue variation and driver dependencies. Nature Cancer. 1: 249-263. PMID 32118208 DOI: 10.1038/s43018-020-0027-5 |
0.441 |
|
2020 |
Alexandrov LB, Kim J, Haradhvala NJ, Huang MN, Tian Ng AW, Wu Y, Boot A, Covington KR, Gordenin DA, Bergstrom EN, Islam SMA, Lopez-Bigas N, Klimczak LJ, McPherson JR, Morganella S, et al. The repertoire of mutational signatures in human cancer. Nature. 578: 94-101. PMID 32025018 DOI: 10.1038/S41586-020-1943-3 |
0.559 |
|
2019 |
De Mattos-Arruda L, Sammut SJ, Ross EM, Bashford-Rogers R, Greenstein E, Markus H, Morganella S, Teng Y, Maruvka Y, Pereira B, Rueda OM, Chin SF, Contente-Cuomo T, Mayor R, Arias A, et al. The Genomic and Immune Landscapes of Lethal Metastatic Breast Cancer. Cell Reports. 27: 2690-2708.e10. PMID 31141692 DOI: 10.1016/J.Celrep.2019.04.098 |
0.451 |
|
2019 |
Brinkman AB, Nik-Zainal S, Simmer F, Rodríguez-González FG, Smid M, Alexandrov LB, Butler A, Martin S, Davies H, Glodzik D, Zou X, Ramakrishna M, Staaf J, Ringnér M, Sieuwerts A, ... ... Morganella S, et al. Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation. Nature Communications. 10: 1749. PMID 30988298 DOI: 10.1038/S41467-019-09828-0 |
0.408 |
|
2019 |
Kucab JE, Zou X, Morganella S, Joel M, Nanda AS, Nagy E, Gomez C, Degasperi A, Harris R, Jackson SP, Arlt VM, Phillips DH, Nik-Zainal S. A Compendium of Mutational Signatures of Environmental Agents. Cell. PMID 30982602 DOI: 10.1016/J.Cell.2019.03.001 |
0.462 |
|
2019 |
Iotchkova V, Ritchie GRS, Geihs M, Morganella S, Min JL, Walter K, Timpson NJ, Dunham I, Birney E, Soranzo N. GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals. Nature Genetics. PMID 30692680 DOI: 10.1038/S41588-018-0322-6 |
0.427 |
|
2019 |
Nik-Zainal S, Davies H, Staaf J, Ramakrishna M, Glodzik D, Zou X, Martincorena I, Alexandrov LB, Martin S, Wedge DC, Van Loo P, Ju YS, Smid M, Brinkman AB, Morganella S, et al. Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences. Nature. PMID 30659290 DOI: 10.1038/S41586-019-0883-2 |
0.497 |
|
2018 |
Georgakopoulos-Soares I, Morganella S, Jain N, Hemberg M, Nik-Zainal S. Noncanonical secondary structures arising from non-B DNA motifs are determinants of mutagenesis. Genome Research. PMID 30104284 DOI: 10.1101/Gr.231688.117 |
0.476 |
|
2018 |
Barton C, Morganella S, Ødegård-Fougner Ø, Alexander S, Ries J, Fitzgerald T, Ellenberg J, Birney E. ChromoTrace: Computational reconstruction of 3D chromosome configurations for super-resolution microscopy. Plos Computational Biology. 14: e1006002. PMID 29522506 DOI: 10.1371/Journal.Pcbi.1006002 |
0.388 |
|
2018 |
De Mattos-Arruda L, Sammut S, Ross EM, Bashford-Rogers R, Greenstein E, Morganella S, Rueda OM, Martinez-Saez E, Peg V, Cortés J, Nik-Zainal S, Murtaza M, Friedman N, Markowetz F, Seoane J, et al. The integrated genomic and immune landscapes of lethal metastatic breast cancer (MBC). Journal of Clinical Oncology. 36: 1009-1009. DOI: 10.1200/Jco.2018.36.15_Suppl.1009 |
0.424 |
|
2017 |
Glodzik D, Morganella S, Davies H, Simpson PT, Li Y, Zou X, Diez-Perez J, Staaf J, Alexandrov LB, Smid M, Brinkman AB, Rye IH, Russnes H, Raine K, Purdie CA, et al. Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers. Nature Genetics. 49: 1661. PMID 29074948 DOI: 10.1038/ng1117-1661a |
0.383 |
|
2017 |
Zou X, Morganella S, Glodzik D, Davies H, Li Y, Stratton MR, Nik-Zainal S. Short inverted repeats contribute to localized mutability in human somatic cells. Nucleic Acids Research. PMID 28977645 DOI: 10.1093/Nar/Gkx731 |
0.414 |
|
2017 |
Davies H, Morganella S, Purdie CA, Jang SJ, Borgen E, Russnes H, Glodzik D, Zou X, Viari A, Richardson AL, Børresen-Dale AL, Thompson A, Eyfjord JE, Kong G, Stratton MR, et al. Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency. Cancer Research. PMID 28904067 DOI: 10.1158/0008-5472.Can-17-1083 |
0.52 |
|
2017 |
Nik-Zainal S, Morganella S. Mutational Signatures in Breast Cancer: The Problem at the DNA Level Clinical Cancer Research. 23: 2617-2629. PMID 28572256 DOI: 10.1158/1078-0432.Ccr-16-2810 |
0.497 |
|
2017 |
Davies H, Glodzik D, Morganella S, Yates LR, Staaf J, Zou X, Ramakrishna M, Martin S, Boyault S, Sieuwerts AM, Simpson PT, King TA, Raine K, Eyfjord JE, Kong G, et al. HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. Nature Medicine. PMID 28288110 DOI: 10.1038/nm.4292 |
0.404 |
|
2017 |
Glodzik D, Morganella S, Davies H, Simpson PT, Li Y, Zou X, Diez-Perez J, Staaf J, Alexandrov LB, Smid M, Brinkman AB, Rye IH, Russnes H, Raine K, Purdie CA, et al. A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers. Nature Genetics. PMID 28112740 DOI: 10.1038/Ng.3771 |
0.521 |
|
2017 |
Glodzik D, Morganella S, Davies H, Nik-Zainal S. Abstract LB-262: A somatic-mutational process in breast cancer genomes recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers Cancer Research. 77. DOI: 10.1158/1538-7445.Am2017-Lb-262 |
0.548 |
|
2016 |
Morganella S, Alexandrov LB, Glodzik D, Zou X, Davies H, Staaf J, Sieuwerts AM, Brinkman AB, Martin S, Ramakrishna M, Butler A, Kim HY, Borg Å, Sotiriou C, Futreal PA, et al. The topography of mutational processes in breast cancer genomes. Nature Communications. 7: 11383. PMID 27136393 DOI: 10.1038/Ncomms11383 |
0.56 |
|
2016 |
Nik-Zainal S, Davies H, Staaf J, Ramakrishna M, Glodzik D, Zou X, Martincorena I, Alexandrov LB, Martin S, Wedge DC, Van Loo P, Ju YS, Smid M, Brinkman AB, Morganella S, et al. Landscape of somatic mutations in 560 breast cancer whole-genome sequences. Nature. PMID 27135926 DOI: 10.1038/Nature17676 |
0.534 |
|
2015 |
Nik-Zainal S, Kucab JE, Morganella S, Glodzik D, Alexandrov LB, Arlt VM, Weninger A, Hollstein M, Stratton MR, Phillips DH. The genome as a record of environmental exposure. Mutagenesis. 30: 763-70. PMID 26443852 DOI: 10.1093/Mutage/Gev073 |
0.508 |
|
2015 |
Anjum S, Morganella S, D'Angelo F, Iavarone A, Ceccarelli M. VEGAWES: variational segmentation on whole exome sequencing for copy number detection. Bmc Bioinformatics. 16: 315. PMID 26416038 DOI: 10.1186/S12859-015-0748-0 |
0.383 |
|
2015 |
Dunham I, Kulesha E, Iotchkova V, Morganella S, Birney E. FORGE: A tool to discover cell specific enrichments of GWAS associated SNPs in regulatory regions F1000research. 4: 18. DOI: 10.12688/F1000Research.6032.1 |
0.353 |
|
2012 |
Morganella S, Ceccarelli M. VegaMC: a R/bioconductor package for fast downstream analysis of large array comparative genomic hybridization datasets. Bioinformatics (Oxford, England). 28: 2512-4. PMID 22815357 DOI: 10.1093/Bioinformatics/Bts453 |
0.419 |
|
2011 |
Morganella S, Pagnotta SM, Ceccarelli M. Finding recurrent copy number alterations preserving within-sample homogeneity. Bioinformatics (Oxford, England). 27: 2949-56. PMID 21873327 DOI: 10.1093/Bioinformatics/Btr488 |
0.414 |
|
2010 |
Morganella S, Cerulo L, Viglietto G, Ceccarelli M. VEGA: variational segmentation for copy number detection. Bioinformatics (Oxford, England). 26: 3020-7. PMID 20959380 DOI: 10.1093/Bioinformatics/Btq586 |
0.374 |
|
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