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Author Details

Nagarajan Paramasivam
National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
2009
58
19
PMIDPaper TitleJournal TitlePublished Year
36808802Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling.Mol Oncol2023
37783805Ex vivo drug response profiling for response and outcome prediction in hematologic malignancies: the prospective non-interventional SMARTrial.Nat Cancer2023
37037472PyOncoPrint: a python package for plotting OncoPrints.Genomics Inform2023
37368072A T-cell antigen atlas for meningioma: novel options for immunotherapy.Acta Neuropathol2023
35045690Comprehensive genomic analysis of refractory multiple myeloma reveals a complex mutational landscape associated with drug resistance and novel therapeutic vulnerabilities.Haematologica2022
35563565Recurrent Germline Variant in <i>RAD21</i> Predisposes Children to Lymphoblastic Leukemia or Lymphoma.Int J Mol Sci2022
35562597Whole exome sequencing identifies novel germline variants of SLC15A4 gene as potentially cancer predisposing in familial colorectal cancer.Mol Genet Genomics2022
36611892Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.Cells2022
35918329Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity.Nat Commun2022
35163215Whole-Exome Sequencing Identifies a Novel Germline Variant in <i>PTK7</i> Gene in Familial Colorectal Cancer.Int J Mol Sci2022
35158942Germline Variants of <i>CYBA</i> and <i>TRPM4</i> Predispose to Familial Colorectal Cancer.Cancers (Basel)2022
33468175A rare large duplication of MLH1 identified in Lynch syndrome.Hered Cancer Clin Pract2021
33673279Whole Exome Sequencing Identifies <i>APCDD1</i> and <i>HDAC5</i> Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer.Int J Mol Sci2021
33692755Whole Genome Sequencing Prioritizes <i>CHEK2, EWSR1</i>, and <i>TIAM1</i> as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer.Front Endocrinol (Lausanne)2021
33583942Characterization of rare germline variants in familial multiple myeloma.Blood Cancer J2021
33916261A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer.J Pers Med2021
34946811Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism.Genes (Basel)2021
34495383Molecular profiling of pediatric meningiomas shows tumor characteristics distinct from adult meningiomas.Acta Neuropathol2021
33953289Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas.Leukemia2021
34194391Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes.Front Endocrinol (Lausanne)2021
34357098Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer.J Pers Med2021
33402667Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson's disease.NPJ Genom Med2021
32428920Identification of Transient Receptor Potential Channel 4-Associated Protein as a Novel Candidate Gene Causing Congenital Primary Hypothyroidism.Horm Res Paediatr2020
31734728YAP1-fusions in pediatric NF2-wildtype meningioma.Acta Neuropathol2020
33151932A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease.PLoS Genet2020
32992489Cancer Predisposition Genes in Cancer-Free Families.Cancers (Basel)2020
32211398Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing.Front Bioeng Biotechnol2020
32492864A Germline Mutation in the <i>POT1</i> Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer.Cancers (Basel)2020
30858804The Frog <i>Xenopus</i> as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in <i>PIBF1</i>.Front Physiol2019
31537871Segregation and potential functional impact of a rare stop-gain PABPC4L variant in familial atypical Parkinsonism.Sci Rep2019
30926794Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma.Nat Commun2019
31069492Mutational patterns and regulatory networks in epigenetic subgroups of meningioma.Acta Neuropathol2019
29261175Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency.Genet Med2018
30072699Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family.Sci Rep2018
30429477Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer.Nat Commun2018
29708584Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma.Int J Cancer2018
29396028Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG.Mol Genet Metab2018
27614072TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus.Nucleic Acids Res2017
28489334Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eye.Am J Med Genet A2017
28488633A report of whole-genome sequencing in neurologic Wilson's disease.Neurol India2017
28371085DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.Am J Med Genet A2017
29255182A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity.Eur J Hum Genet2017
29100089De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.Am J Hum Genet2017
28572216Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer.J Exp Med2017
28726821The whole-genome landscape of medulloblastoma subtypes.Nature2017
28688840Impact of clinical exomes in neurodevelopmental and neurometabolic disorders.Mol Genet Metab2017
27016154Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy.Am J Med Genet A2016
26566883Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.J Med Genet2016
27508007Pedigree based DNA sequencing pipeline for germline genomes of cancer families.Hered Cancer Clin Pract2016
25804400SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract.Eur J Hum Genet2015
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Collaborators

Matthias Schlesner
University of Augsburg
Co-authored papers 37
Roland Eils
Berlin Institute of Health (BIH) and Charite
Co-authored papers 18
Daniel H??bschmann
Heidelberg Institute for Stem Cell Technology and Experimental Medicine (HI-STEM)
Co-authored papers 9
Jan Lubinski
Pomeranian Medical University
Co-authored papers 9
Benedikt Brors
German Cancer Research Center (DKFZ)
Co-authored papers 8
Stefan Wiemann
Co-authored papers 5
Kortine Kleinheinz
Co-authored papers 5
Peter Lichter
German Cancer Research Center (DKFZ)
Co-authored papers 5
Stefan M Pfister
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 5
Andrey Korshunov
Institute of Pathology, University Hospital Heidelberg
Co-authored papers 4
Barbara Hutter
National Center for Tumor Diseases (NCT) Heidelberg
Co-authored papers 4
Stefan Fr??hling
German Cancer Research Center (DKFZ), National Center for Tumor Diseases (NCT)
Co-authored papers 4
David T W Jones
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 4
Marc Zapatka
Co-authored papers 4
Felix Sahm
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers 4
Michael Weller
University Hospital and University of Zurich
Co-authored papers 3
Ivo Buchhalter
German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK)
Co-authored papers 3
Arndt Borkhardt
Hematology and Clinical Immunology, Heinrich Heine University Dusseldorf
Co-authored papers 3
Sebastian M Waszak
University of California san francisco
Co-authored papers 3
Christel Herold-Mende
Co-authored papers 3
Andreas von Deimling
Co-authored papers 3
Niels Weinhold
Co-authored papers 3
Jan O Korbel
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 3
Sebastian Uhrig
National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
Co-authored papers 3
Rebecca C Wade
Center for Molecular Biology (ZMBH), Heidelberg University
Co-authored papers 3
Lars Feuerbach
German Cancer Research Center (DKFZ)
Co-authored papers 2
Christian Mawrin
Co-authored papers 2
Reiner Siebert
Co-authored papers 2
Peter Horak
German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT)
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Chris Lawerenz
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Release 1.2