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Nagarajan Paramasivam
Nagarajan Paramasivam
Senior Bioinformatics Scientist, National Center for Tumor Diseases, German Cancer Research Center
Verified email at dkfz.de
Title
Cited by
Cited by
Year
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
2031*2020
The whole-genome landscape of medulloblastoma subtypes
PA Northcott, I Buchhalter, AS Morrissy, V Hovestadt, J Weischenfeldt, ...
Nature 547 (7663), 311-317, 2017
10722017
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
3412015
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
1692017
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
1612010
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), 1459, 2019
1382019
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), 4782, 2018
1222018
The genomic and transcriptional landscape of primary central nervous system lymphoma
J Radke, N Ishaque, R Koll, Z Gu, E Schumann, L Sieverling, S Uhrig, ...
Nature Communications 13 (1), 2558, 2022
902022
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma
N Paramasivam, D Hübschmann, UH Toprak, N Ishaque, M Neidert, ...
Acta neuropathologica 138, 295-308, 2019
852019
YAP1-fusions in pediatric NF2-wildtype meningioma
P Sievers, J Chiang, D Schrimpf, D Stichel, N Paramasivam, M Sill, ...
Acta neuropathologica 139, 215-218, 2020
672020
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
592017
Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas
D Hübschmann, K Kleinheinz, R Wagener, SH Bernhart, C López, ...
Leukemia 35 (7), 2002-2016, 2021
572021
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, 1-16, 2012
552012
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
522017
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples
MH Bailey, WU Meyerson, LJ Dursi, LB Wang, G Dong, WW Liang, ...
Nature communications 11 (1), 4748, 2020
462020
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
412017
Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers
A Jahn, A Rump, TJ Widmann, C Heining, P Horak, B Hutter, ...
Annals of Oncology 33 (11), 1186-1199, 2022
392022
Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity
L Möhrmann, M Werner, M Oleś, A Mock, S Uhrig, A Jahn, S Kreutzfeldt, ...
Nature Communications 13 (1), 4485, 2022
362022
Molecular profiling of pediatric meningiomas shows tumor characteristics distinct from adult meningiomas
E Kirches, F Sahm, A Korshunov, C Bluecher, N Waldt, S Kropf, ...
Acta neuropathologica 142, 873-886, 2021
352021
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
342017
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