Nagarajan Paramasivam
Nagarajan Paramasivam
Senior Bioinformatics Scientist, National Center for Tumor Diseases, German Cancer Research Center
Bestätigte E-Mail-Adresse bei dkfz.de
Titel
Zitiert von
Zitiert von
Jahr
The whole-genome landscape of medulloblastoma subtypes
PA Northcott, I Buchhalter, AS Morrissy, V Hovestadt, J Weischenfeldt, ...
Nature 547 (7663), 311-317, 2017
4112017
Pan-cancer analysis of whole genomes
I The, TPCA of Whole, Genomes Consortium
Nature 578 (7793), 82, 2020
3182020
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
2282015
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
1162010
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
582017
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
382012
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
312018
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
312017
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
302019
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
272017
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
252019
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
242017
ClubSub-P: cluster-based subcellular localization prediction for Gram-negative bacteria and archaea
N Paramasivam, D Linke
Frontiers in microbiology 2, 218, 2011
232011
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
222015
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
192017
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
172015
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
162017
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
142020
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
142018
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
122016
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