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Pedigree based DNA sequencing pipeline for germline genomes of cancer families.
Försti A, Kumar A, Paramasivam N, Schlesner M, Catalano C, Dymerska D, Lubinski J, Eils R, Hemminki K. Försti A, et al. Among authors: paramasivam n. Hered Cancer Clin Pract. 2016 Aug 9;14:16. doi: 10.1186/s13053-016-0058-1. eCollection 2016. Hered Cancer Clin Pract. 2016. PMID: 27508007 Free PMC article.
Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing.
Srivastava A, Giangiobbe S, Kumar A, Paramasivam N, Dymerska D, Behnisch W, Witzens-Harig M, Lubinski J, Hemminki K, Försti A, Bandapalli OR. Srivastava A, et al. Among authors: paramasivam n. Front Bioeng Biotechnol. 2020 Mar 6;8:179. doi: 10.3389/fbioe.2020.00179. eCollection 2020. Front Bioeng Biotechnol. 2020. PMID: 32211398 Free PMC article.
Cancer Predisposition Genes in Cancer-Free Families.
Zheng G, Catalano C, Bandapalli OR, Paramasivam N, Chattopadhyay S, Schlesner M, Sijmons R, Hemminki A, Dymerska D, Lubinski J, Hemminki K, Försti A. Zheng G, et al. Among authors: paramasivam n. Cancers (Basel). 2020 Sep 27;12(10):2770. doi: 10.3390/cancers12102770. Cancers (Basel). 2020. PMID: 32992489 Free PMC article.
A rare large duplication of MLH1 identified in Lynch syndrome.
Kumar A, Paramasivam N, Bandapalli OR, Schlesner M, Chen T, Sijmons R, Dymerska D, Golebiewska K, Kuswik M, Lubinski J, Hemminki K, Försti A. Kumar A, et al. Among authors: paramasivam n. Hered Cancer Clin Pract. 2021 Jan 19;19(1):10. doi: 10.1186/s13053-021-00167-0. Hered Cancer Clin Pract. 2021. PMID: 33468175 Free PMC article.
Characterization of rare germline variants in familial multiple myeloma.
Catalano C, Paramasivam N, Blocka J, Giangiobbe S, Huhn S, Schlesner M, Weinhold N, Sijmons R, de Jong M, Langer C, Preuss KD, Nilsson B, Durie B, Goldschmidt H, Bandapalli OR, Hemminki K, Försti A. Catalano C, et al. Among authors: paramasivam n. Blood Cancer J. 2021 Feb 13;11(2):33. doi: 10.1038/s41408-021-00422-6. Blood Cancer J. 2021. PMID: 33583942 Free PMC article. No abstract available.
Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer.
Srivastava A, Giangiobbe S, Skopelitou D, Miao B, Paramasivam N, Diquigiovanni C, Bonora E, Hemminki K, Försti A, Bandapalli OR. Srivastava A, et al. Among authors: paramasivam n. Front Endocrinol (Lausanne). 2021 Feb 22;12:600682. doi: 10.3389/fendo.2021.600682. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33692755 Free PMC article.
121 results