heiBIB: Paramasivam, Nagarajan

Paramasivam, NagarajanUniversität HeidelbergHeidelberg

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englisch (36)

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Publikationen in heiBIB

Liebers, Nora: Ex vivo drug response profiling for response and outcome prediction in hematologic malignancies : the prospective non-interventional SMARTrial / Nora Liebers, Peter-Martin Bruch, Tobias Terzer, Miguel Hernandez-Hernandez, Nagarajan Paramasivam, … , 02 October 2023. - 31 S.
In: Nature cancer, ISSN 2662-1347. 4(2023), 12, Seite 1648-1659, [1-15], 1-4
DOI: 10.1038/s43018-023-00645-5
Giesen, Nicola: Comprehensive genomic analysis of refractory multiple myeloma reveals a complex mutational landscape associated with drug resistance and novel therapeutic vulnerabilities / Nicola Giesen, Nagarajan Paramasivam, Umut H. Toprak, Daniel Huebschmann, Jing Xu, Sebastian Uhrig, … , August 2022. - 11 S.
In: Haematologica, ISSN 1592-8721. 107(2022), 8, Seite 1891-1901
DOI: 10.3324/haematol.2021.279360
Jahn, Arne: Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers / A. Jahn, A. Rump, T.J. Widmann, C. Heining, P. Horak, B. Hutter, N. Paramasivam, S. Uhrig, L. Gieldo… , 18 August 2022. - 14 S.
In: Annals of oncology, ISSN 1569-8041. 33(2022), 11, Seite 1186-1199
DOI: 10.1016/j.annonc.2022.07.008
Miao, Beiping: Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer / Beiping Miao, Diamanto Skopelitou, Aayushi Srivastava, Sara Giangiobbe, Dagmara Dymerska, Nagarajan … , 24 January 2022. - 20 S.
In: International journal of molecular sciences, ISSN 1422-0067. 23(2022), 3, Artikel-ID 1295, Seite 1-20
DOI: 10.3390/ijms23031295
Vick, Philipp: Identification of ZBTB26 as a novel risk factor for congenital hypothyroidism / Philipp Vick, Birgit Eberle, Daniela Choukair, Birgit Weiss, Ralph Roeth, Isabelle Schneider, Nagara… , 19 November 2021. - 1 Online-Ressource S. : Ilustrationen, Diagramme
In: Genes, ISSN 2073-4425. 12(2021), 12, Artikel-ID 1862, Seite 1-10
DOI: 10.3390/genes12121862
Hübschmann, Daniel: Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas / Daniel Hübschmann et al., 5 May 2021. - 15 S.
In: Leukemia, ISSN 1476-5551. 35(2021), 7, Seite 2002-2016
DOI: 10.1038/s41375-021-01251-z
Srivastava, Aayushi: Whole genome sequencing prioritizes CHEK2, EWSR1, and TIAM1 as possible predisposition genes for familial non-medullary thyroid cancer / Aayushi Srivastava, Sara Giangiobbe, Diamanto Skopelitou, Beiping Miao, Nagarajan Paramasivam, Chiar… , 22 February 2021. - 10 S.
In: Frontiers in endocrinology, ISSN 1664-2392. 12(2021) vom: 22. Feb., Artikel-ID 600682, Seite 1-10
DOI: 10.3389/fendo.2021.600682
Slater, Emily P.: Combinations of low-frequency genetic variants might predispose to familial pancreatic cancer / Emily P. Slater, Lisa M. Wilke, Lutz Benedikt Böhm, Konstantin Strauch, Manuel Lutz, Norman Gercke, … , 2 July 2021. - 14 S.
In: Journal of Personalized Medicine, ISSN 2075-4426. 11(2021), 7, Artikel-ID 631, Seite 1-14
DOI: 10.3390/jpm11070631
Skopelitou, Diamanto: Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer / Diamanto Skopelitou, Beiping Miao, Aayushi Srivastava, Abhishek Kumar, Magdalena Kuswick, Dagmara Dy… , 2 February 2021. - 21 S.
In: International journal of molecular sciences, ISSN 1422-0067. 22(2021), 4, Artikel-ID 1837, Seite 1-21
DOI: 10.3390/ijms22041837
Catalano, Calogerina: Characterization of rare germline variants in familial multiple myeloma / Calogerina Catalano, Nagarajan Paramasivam, Joanna Blocka, Sara Giangiobbe, Stefanie Huhn, Matthias … , 13 February 2021. - 4 S.
In: Blood cancer journal, ISSN 2044-5385. 11(2021), Artikel-ID 33, Seite 1-4
DOI: 10.1038/s41408-021-00422-6
Aslam, Muhammad: Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson’s disease / Muhammad Aslam, Nirosiya Kandasamy, Anwar Ullah, Nagarajan Paramasivam, Mehmet Ali Öztürk, Saima Nau… , 05 January 2021. - 10 S.
In: npj Genomic Medicine, ISSN 2056-7944. 6(2021,1) Artikel-Nummer 2, 10 Seiten
DOI: 10.1038/s41525-020-00163-8
Mederer, Tanja: A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease / Tanja Mederer, Stefanie Schmitteckert, Julia Volz, Cristina Martínez, Ralph Röth, Thomas Thumberger,… , November 5, 2020
In: PLoS Genetics, ISSN 1553-7404. 16(2020), 11, Seite e1009106
DOI: 10.1371/journal.pgen.1009106
Zheng, Guoqiao: Cancer predisposition genes in cancer-free families / Guoqiao Zheng, Calogerina Catalano, Obul Reddy Bandapalli, Nagarajan Paramasivam, Subhayan Chattopad… , 27 September 2020. - 13 S.
In: Cancers, ISSN 2072-6694. 12(2020,10) Artikel-Nummer 2770, 13 Seiten
DOI: 10.3390/cancers12102770
Choukair, Daniela: Identification of transient receptor potential channel 4-associated protein as a novel candidate gene causing congenital primary hypothyroidism / Daniela Choukair, Birgit Eberle, Philipp Vick, Pia Hermanns, Birgit Weiss, Nagarajan Paramasivam, Ma… , May 19, 2020. - 14 S.
In: Hormone research in paediatrics, ISSN 1663-2826. 93(2020), 1, Seite 16-29
DOI: 10.1159/000507114
Srivastava, Aayushi: Identification of familial Hodgkin lymphoma predisposing genes using whole genome sequencing / Aayushi Srivastava, Sara Giangiobbe, Abhishek Kumar, Nagarajan Paramasivam, Dagmara Dymerska, Wolfga… , 06 March 2020. - 11 S.
In: Frontiers in Bioengineering and Biotechnology, ISSN 2296-4185. 8(2020) Artikel-Nummer 179, 11 Seiten
DOI: 10.3389/fbioe.2020.00179
Sievers, Philipp: YAP1-fusions in pediatric NF2-wildtype meningioma / Philipp Sievers, Jason Chiang, Daniel Schrimpf, Damian Stichel, Nagarajan Paramasivam, Martin Sill, … , 2020. - 4 S.
In: Acta neuropathologica, ISSN 1432-0533. 139(2020), 1, Seite 215-218
DOI: 10.1007/s00401-019-02095-9
Paramasivam, Nagarajan: Mutational patterns and regulatory networks in epigenetic subgroups of meningioma / Nagarajan Paramasivam, Daniel Hübschmann, Umut H. Toprak, Naveed Ishaque, Marian Neidert, Daniel Sch… , 2019. - 14 S.
In: Acta neuropathologica, ISSN 1432-0533. 138(2019), 2, Seite 295-308
DOI: 10.1007/s00401-019-02008-w
Ott, Tim: The frog Xenopus as a model to study Joubert syndrome : the case of a human patient with compound heterozygous variants in PIBF1 / Tim Ott, Lilian Kaufmann, Martin Granzow, Katrin Hinderhofer, Claus R. Bartram, Susanne Theiß, Angel… , 25 February 2019. - 13 S.
In: Frontiers in physiology, ISSN 1664-042X. 10(2019) Artikel-Nummer 134, 13 Seiten
DOI: 10.3389/fphys.2019.00134
Dimitrov, Bianca: Cutis laxa, exocrine pancreatic insufficiency and altered cellular metabolomics as additional symptoms in a new patient with ATP6AP1-CDG / Bianca Dimitrov, Nastassja Himmelreich, Agnes L. Hipgrave Ederveen, Christian Lüchtenborg, Jürgen G.… , 2018. - 11 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 123(2018), 3, Seite 364-374
DOI: 10.1016/j.ymgme.2018.01.008
Bandapalli, Obul Reddy: Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma / Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Abhishek Kumar, Wolfgang Benisch, And… , 30 April 2018. - 3 S.
In: International journal of cancer, ISSN 1097-0215. 143(2018), 8, Seite 2076-2078
DOI: 10.1002/ijc.31576
Ishaque, Naveed: Whole genome sequencing puts forward hypotheses on metastasis evolution and therapy in colorectal cancer / Naveed Ishaque, Mohammed L. Abba, Christine Hauser, Nitin Patil, Nagarajan Paramasivam, Daniel Huebs… , 14 November 2018. - 14 S.
In: Nature Communications, ISSN 2041-1723. 9(2018) Artikel-Nummer 4782, 14 Seiten
DOI: 10.1038/s41467-018-07041-z
Kumar, Abhishek: Familial cancer variant prioritization pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family / Abhishek Kumar, Obul Reddy Bandapalli, Nagarajan Paramasivam, Sara Giangiobbe, Chiara Diquigiovanni,… , 02 August 2018. - 12 S.
In: Scientific reports, ISSN 2045-2322. 8(2018) Artikel-Nummer 11635, 12 Seiten
DOI: 10.1038/s41598-018-29952-z
Simm, Franziska: Identification of SLC20A1 and SLC15A4 among other genes as potential risk factors for combined pituitary hormone deficiency / Franziska Simm, Anne Griesbeck, Daniela Choukair, Birgit Weiß, Nagarajan Paramasivam, Jürgen Klammt,… , 2018. - 9 S.
In: Genetics in medicine, ISSN 1530-0366. 20(2018), 7, Seite 728-736
DOI: 10.1038/gim.2017.165
Küry, Sébastien: De Novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability / Sébastien Küry, Geeske M. van Woerden, Thomas Besnard, Martina Proietti Onori, Xénia Latypova, Megha… , November 2017. - 21 S.
In: The American journal of human genetics, ISSN 1537-6605. 101(2017), 5, Seite 768-788
DOI: 10.1016/j.ajhg.2017.10.003
Evers, Christina: Impact of clinical exomes in neurodevelopmental and neurometabolic disorders / Christina Evers, Christian Staufner, Martin Granzow, Nagarajan Paramasivam, Katrin Hinderhofer, Lili… , 30 June 2017. - 11 S.
In: Molecular genetics and metabolism, ISSN 1096-7206. 121(2017), 4, Seite 297-307
DOI: 10.1016/j.ymgme.2017.06.014
Evers, Christina: Diagnosis of CoPAN by whole exome sequencing : waking up a sleeping tiger's eye / Christina Evers, Angelika Seitz, Birgit Assmann, Thomas Opladen, Stephanie Karch, Katrin Hinderhofer… . - 9 S.
In: American journal of medical genetics, ISSN 1552-4833. 173(2017), 7, S. 1878-1886
DOI: 10.1002/ajmg.a.38252
Dikow, Nicola: DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome / Nicola Dikow, Martin Granzow, Luitgard M. Graul‐Neumann, Stephanie Karch, Katrin Hinderhofer, Nagara… , 29 March 2017. - 5 S.
In: American journal of medical genetics, ISSN 1552-4833. 173(2017), 5, Seite 1369-1373
DOI: 10.1002/ajmg.a.38164
Rafiullah, Rafiullah: A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity / Rafiullah Rafiullah, Alyssa B. Long, Anna A. Ivanova, Hazrat Ali, Simone Berkel, Ghulam Mustafa, Nag… . - 11 S.
In: European journal of human genetics, ISSN 1476-5438. 25(2017), 12, S. 1324-1334
DOI: 10.1038/s41431-017-0031-0
Ullah, Anwar: A report of whole-genome sequencing in neurologic Wilson's disease / Anwar Ullah, Nagarajan Paramasivam, Rashda Abbasi, Kafaitullah Khan, Aneesa Sultan, Matthias Schlesn… , 2017. - 3 S.
In: Neurology India, ISSN 1998-4022. 65(2017), 3, Seite 629-631
DOI: 10.4103/neuroindia.NI_1274_16
Gießler, Klara Monika: Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer / Klara M. Giessler, Kortine Kleinheinz, Daniel Huebschmann, Gnana Prakash Balasubramanian, Taronish D… , 2017. - 16 S.
In: Journal of experimental medicine, ISSN 1540-9538. 214(2017), 7, Seite 2073-2088
DOI: 10.1084/jem.20162017
Northcott, Paul A.: The whole-genome landscape of medulloblastoma subtypes / Paul A. Northcott, Ivo Buchhalter, A. Sorana Morrissy, Volker Hovestadt, Joachim Weischenfeldt, Tobi… , 19 July 2017. - 7 S.
In: Nature, ISSN 1476-4687. 547(2017), 7663, Seite 311-317
DOI: 10.1038/nature22973
Rafiullah, Rafiullah: Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family / Rafiullah Rafiullah, Muhammad Aslamkhan, Nagarajan Paramasivam, Christian Thiel, Ghulam Mustafa, Ste… , 2016. - 7 S.
In: Journal of medical genetics, ISSN 1468-6244. 53(2016), 2, Seite 138-144
DOI: 10.1136/jmedgenet-2015-103179
Evers, Christina: Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy / Christina Evers, Lilian Kaufmann, Angelika Seitz, Nagarajan Paramasivam, Martin Granzow, Stephanie K… , 7 March 2016. - 8 S.
In: American journal of medical genetics, ISSN 1552-4833. 170(2016), 6, Seite 1502-1509
DOI: 10.1002/ajmg.a.37632
Senís Herrero, Elena: TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus / Elena Senís, Stefan Mockenhaupt, Daniel Rupp, Tobias Bauer, Nagarajan Paramasivam, Bettina Knapp, Ja… , 2017. - 17 S.
In: Nucleic acids research, ISSN 1362-4962. 45(2017,1) Artikel-Nummer e3, 17 Seiten
DOI: 10.1093/nar/gkw805
Evers, Christina: SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract / Christina Evers, Nagarajan Paramasivam, Katrin Hinderhofer, Christine Fischer, Martin Granzow, Annet… , 25 March 2015. - 7 S.
In: European journal of human genetics, ISSN 1476-5438. 23(2015), 12, Seite 1627-1633
DOI: 10.1038/ejhg.2015.46
Granzow, Martin: 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, L. Kaufmann, C. Evers, U.… , October 2015. - 7 S.
In: Molecular and cellular probes, ISSN 1096-1194. 29(2015), 5, Seite 323-329
DOI: 10.1016/j.mcp.2015.05.012

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