متابعة
Nagarajan Paramasivam
Nagarajan Paramasivam
Senior Bioinformatics Scientist, National Center for Tumor Diseases, German Cancer Research Center
بريد إلكتروني تم التحقق منه على dkfz.de
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
1718*2020
The whole-genome landscape of medulloblastoma subtypes
PA Northcott, I Buchhalter, AS Morrissy, V Hovestadt, J Weischenfeldt, ...
Nature 547 (7663), 311-317, 2017
9642017
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
3232015
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
1582010
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
1452017
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
1152019
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
1152018
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
762019
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
632022
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
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
512021
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
502020
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
382017
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
312017
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
302018
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
292020
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
292018
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
282015
يتعذر على النظام إجراء العملية في الوقت الحالي. عاود المحاولة لاحقًا.
مقالات 1–20