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Nagarajan Paramasivam
Nagarajan Paramasivam
Senior Bioinformatics Scientist, National Center for Tumor Diseases, German Cancer Research Center
在 dkfz.de 的电子邮件经过验证
标题
引用次数
引用次数
年份
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
1782*2020
The whole-genome landscape of medulloblastoma subtypes
PA Northcott, I Buchhalter, AS Morrissy, V Hovestadt, J Weischenfeldt, ...
Nature 547 (7663), 311-317, 2017
9702017
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
3262015
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
1572010
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
1512017
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
1192019
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
1172018
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
782019
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
682022
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
562017
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
542012
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
522020
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
502021
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
492017
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
392017
Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family
A Kumar, OR Bandapalli, N Paramasivam, S Giangiobbe, ...
Scientific reports 8 (1), 11635, 2018
322018
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
322017
A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer
A Srivastava, B Miao, D Skopelitou, V Kumar, A Kumar, N Paramasivam, ...
Cancers 12 (6), 1441, 2020
302020
Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG
B Dimitrov, N Himmelreich, ALH Ederveen, C Lüchtenborg, JG Okun, ...
Molecular genetics and metabolism 123 (3), 364-374, 2018
302018
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
292022
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