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A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants.
Wiik MU, Evans TJ, Belhadj S, Bolton KA, Dymerska D, Jagmohan-Changur S, Capellá G, Kurzawski G, Wijnen JT, Valle L, Vasen HFA, Lubinski J, Scott RJ, Talseth-Palmer BA. Wiik MU, et al. Among authors: jagmohan changur s. Sci Rep. 2021 May 31;11(1):11401. doi: 10.1038/s41598-021-90501-2. Sci Rep. 2021. PMID: 34059744 Free PMC article.
Genetic variant in the telomerase gene modifies cancer risk in Lynch syndrome.
Bellido F, Guinó E, Jagmohan-Changur S, Seguí N, Pineda M, Navarro M, Lázaro C, Blanco I, Vasen HF, Moreno V, Capellá G, Wijnen JT, Valle L. Bellido F, et al. Among authors: jagmohan changur s. Eur J Hum Genet. 2013 May;21(5):511-6. doi: 10.1038/ejhg.2012.204. Epub 2012 Sep 5. Eur J Hum Genet. 2013. PMID: 22948024 Free PMC article.
Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.
Talseth-Palmer BA, Wijnen JT, Brenne IS, Jagmohan-Changur S, Barker D, Ashton KA, Tops CM, Evans TJ, McPhillips M, Groombridge C, Suchy J, Kurzawski G; Dutch Cancer Genetics Group; Spigelman A, Møller P, Morreau HM, Van Wezel T, Lubinski J, Vasen HF, Scott RJ. Talseth-Palmer BA, et al. Among authors: jagmohan changur s. Int J Cancer. 2013 Apr 1;132(7):1556-64. doi: 10.1002/ijc.27843. Epub 2012 Oct 11. Int J Cancer. 2013. PMID: 22987364 Free article.
Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancer.
Middeldorp A, Jagmohan-Changur SC, van der Klift HM, van Puijenbroek M, Houwing-Duistermaat JJ, Webb E, Houlston R, Tops C, Vasen HF, Devilee P, Morreau H, van Wezel T, Wijnen J. Middeldorp A, et al. Among authors: jagmohan changur sc. Genes Chromosomes Cancer. 2010 Jun;49(6):539-48. doi: 10.1002/gcc.20763. Genes Chromosomes Cancer. 2010. PMID: 20222047
Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.
Jansen AM, Geilenkirchen MA, van Wezel T, Jagmohan-Changur SC, Ruano D, van der Klift HM, van den Akker BE, Laros JF, van Galen M, Wagner A, Letteboer TG, Gómez-García EB, Tops CM, Vasen HF, Devilee P, Hes FJ, Morreau H, Wijnen JT. Jansen AM, et al. Among authors: jagmohan changur sc. PLoS One. 2016 Jun 14;11(6):e0157381. doi: 10.1371/journal.pone.0157381. eCollection 2016. PLoS One. 2016. PMID: 27300758 Free PMC article.
Enrichment of low penetrance susceptibility loci in a Dutch familial colorectal cancer cohort.
Middeldorp A, Jagmohan-Changur S, van Eijk R, Tops C, Devilee P, Vasen HF, Hes FJ, Houlston R, Tomlinson I, Houwing-Duistermaat JJ, Wijnen JT, Morreau H, van Wezel T. Middeldorp A, et al. Among authors: jagmohan changur s. Cancer Epidemiol Biomarkers Prev. 2009 Nov;18(11):3062-7. doi: 10.1158/1055-9965.EPI-09-0601. Epub 2009 Oct 20. Cancer Epidemiol Biomarkers Prev. 2009. PMID: 19843678
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.
Talseth-Palmer BA, Wijnen JT, Andreassen EK, Barker D, Jagmohan-Changur S, Tops CM, Meldrum C; Dutch Cancer Genetics Group; Spigelman A, Hes FJ, Van Wezel T, Vasen HF, Scott RJ. Talseth-Palmer BA, et al. Among authors: jagmohan changur s. Hered Cancer Clin Pract. 2013 Dec 29;11(1):20. doi: 10.1186/1897-4287-11-20. Hered Cancer Clin Pract. 2013. PMID: 24373140 Free PMC article.
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers.
Ghorbanoghli Z, Nieuwenhuis MH, Houwing-Duistermaat JJ, Jagmohan-Changur S, Hes FJ, Tops CM, Wagner A, Aalfs CM, Verhoef S, Gómez García EB, Sijmons RH, Menko FH, Letteboer TG, Hoogerbrugge N, van Wezel T, Vasen HF, Wijnen JT. Ghorbanoghli Z, et al. Among authors: jagmohan changur s. Fam Cancer. 2016 Oct;15(4):563-70. doi: 10.1007/s10689-016-9877-5. Fam Cancer. 2016. PMID: 26880076 Free PMC article.
23 results