| The whole-genome landscape of medulloblastoma subtypes PA Northcott, I Buchhalter, AS Morrissy, V Hovestadt, J Weischenfeldt, ... Nature 547 (7663), 311-317, 2017 | 411 | 2017 |
| Pan-cancer analysis of whole genomes I The, TPCA of Whole, Genomes Consortium Nature 578 (7793), 82, 2020 | 318 | 2020 |
| A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing TS Alioto, I Buchhalter, S Derdak, B Hutter, MD Eldridge, E Hovig, ... Nature communications 6 (1), 1-13, 2015 | 228 | 2015 |
| Efficient subfractionation of gram-negative bacteria for proteomics studies M Thein, G Sauer, N Paramasivam, I Grin, D Linke Journal of proteome research 9 (12), 6135-6147, 2010 | 116 | 2010 |
| De novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability S Küry, GM van Woerden, T Besnard, MP Onori, X Latypova, MC Towne, ... The American Journal of Human Genetics 101 (5), 768-788, 2017 | 58 | 2017 |
| Is the C-terminal insertional signal in Gram-negative bacterial outer membrane proteins species-specific or not? N Paramasivam, M Habeck, D Linke BMC genomics 13 (1), 1-16, 2012 | 38 | 2012 |
| Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer N Ishaque, ML Abba, C Hauser, N Patil, N Paramasivam, ... Nature communications 9 (1), 1-14, 2018 | 31 | 2018 |
| DDX3X mutations in two girls with a phenotype overlapping Toriello–Carey syndrome N Dikow, M Granzow, LM Graul‐Neumann, S Karch, K Hinderhofer, ... American journal of medical genetics Part A 173 (5), 1369-1373, 2017 | 31 | 2017 |
| Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma C López, K Kleinheinz, SM Aukema, M Rohde, SH Bernhart, ... Nature communications 10 (1), 1-19, 2019 | 30 | 2019 |
| Impact of clinical exomes in neurodevelopmental and neurometabolic disorders C Evers, C Staufner, M Granzow, N Paramasivam, K Hinderhofer, ... Molecular genetics and metabolism 121 (4), 297-307, 2017 | 27 | 2017 |
| Mutational patterns and regulatory networks in epigenetic subgroups of meningioma N Paramasivam, D Hübschmann, UH Toprak, N Ishaque, M Neidert, ... Acta neuropathologica 138 (2), 295-308, 2019 | 25 | 2019 |
| Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer KM Giessler, K Kleinheinz, D Huebschmann, GP Balasubramanian, ... Journal of Experimental Medicine 214 (7), 2073-2088, 2017 | 24 | 2017 |
| ClubSub-P: cluster-based subcellular localization prediction for Gram-negative bacteria and archaea N Paramasivam, D Linke Frontiers in microbiology 2, 218, 2011 | 23 | 2011 |
| Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline M Granzow, N Paramasivam, K Hinderhofer, C Fischer, S Chotewutmontri, ... Molecular and cellular probes 29 (5), 323-329, 2015 | 22 | 2015 |
| Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eye C Evers, A Seitz, B Assmann, T Opladen, S Karch, K Hinderhofer, ... American Journal of Medical Genetics Part A 173 (7), 1878-1886, 2017 | 19 | 2017 |
| SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract C Evers, N Paramasivam, K Hinderhofer, C Fischer, M Granzow, ... European Journal of Human Genetics 23 (12), 1627-1633, 2015 | 17 | 2015 |
| Large-scale uniform analysis of cancer whole genomes in multiple computing environments CK Yung, BD O’Connor, S Yakneen, J Zhang, K Ellrott, K Kleinheinz, ... BioRxiv, 161638, 2017 | 16 | 2017 |
| YAP1-fusions in pediatric NF2-wildtype meningioma P Sievers, J Chiang, D Schrimpf, D Stichel, N Paramasivam, M Sill, ... Acta neuropathologica 139 (1), 215-218, 2020 | 14 | 2020 |
| Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency F Simm, A Griesbeck, D Choukair, B Weiß, N Paramasivam, J Klammt, ... Genetics in Medicine 20 (7), 728-736, 2018 | 14 | 2018 |
| Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family R Rafiullah, M Aslamkhan, N Paramasivam, C Thiel, G Mustafa, ... Journal of medical genetics 53 (2), 138-144, 2016 | 12 | 2016 |
Matthias SchlesnerBiomedical Informatics, Data Mining and Data Analytics, Augsburg UniversityBestätigte E-Mail-Adresse bei informatik.uni-augsburg.de
