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Year Number of Results
2008 1
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2013 1
2014 1
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2017 3
2018 2
2020 1
2021 0
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Page 1
The recognition of the profession of Genetic Counsellors in Europe.
Cordier C, McAllister M, Serra-Juhe C, Bengoa J, Pasalodos S, Bjornevoll I, Feroce I, Moldovan R, Paneque M, Lambert D; All are member of the Board of the Genetic Nurses and Genetic Counsellors Professional Branch of the European Board of Medical Genetics. Cordier C, et al. Among authors: bjornevoll i. Eur J Hum Genet. 2018 Dec;26(12):1719-1720. doi: 10.1038/s41431-018-0260-x. Epub 2018 Sep 25. Eur J Hum Genet. 2018. PMID: 30254214 Free PMC article. No abstract available.
Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility.
Weren RDA, van der Post RS, Vogelaar IP, van Krieken JH, Spruijt L, Lubinski J, Jakubowska A, Teodorczyk U, Aalfs CM, van Hest LP, Oliveira C, Kamping EJ, Schackert HK, Ranzani GN, Gómez García EB, Hes FJ, Holinski-Feder E, Genuardi M, Ausems MGEM, Sijmons RH, Wagner A, van der Kolk LE, Cats A, Bjørnevoll I, Hoogerbrugge N, Ligtenberg MJL. Weren RDA, et al. Among authors: bjornevoll i. J Med Genet. 2018 Oct;55(10):669-674. doi: 10.1136/jmedgenet-2017-104962. Epub 2018 Jan 12. J Med Genet. 2018. PMID: 29330337 Free PMC article.
Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing.
Vogelaar IP, van der Post RS, van Krieken JHJ, Spruijt L, van Zelst-Stams WA, Kets CM, Lubinski J, Jakubowska A, Teodorczyk U, Aalfs CM, van Hest LP, Pinheiro H, Oliveira C, Jhangiani SN, Muzny DM, Gibbs RA, Lupski JR, de Ligt J, Vissers LELM, Hoischen A, Gilissen C, van de Vorst M, Goeman JJ, Schackert HK, Ranzani GN, Molinaro V, Gómez García EB, Hes FJ, Holinski-Feder E, Genuardi M, Ausems MGEM, Sijmons RH, Wagner A, van der Kolk LE, Bjørnevoll I, Høberg-Vetti H, van Kessel AG, Kuiper RP, Ligtenberg MJL, Hoogerbrugge N. Vogelaar IP, et al. Among authors: bjornevoll i. Eur J Hum Genet. 2017 Nov;25(11):1246-1252. doi: 10.1038/ejhg.2017.138. Epub 2017 Sep 6. Eur J Hum Genet. 2017. PMID: 28875981 Free PMC article.
The Norwegian PMS2 founder mutation c.989-1G > T shows high penetrance of microsatellite instable cancers with normal immunohistochemistry.
Grindedal EM, Aarset H, Bjørnevoll I, Røyset E, Mæhle L, Stormorken A, Heramb C, Medvik H, Møller P, Sjursen W. Grindedal EM, et al. Among authors: bjornevoll i. Hered Cancer Clin Pract. 2014 Apr 21;12(1):12. doi: 10.1186/1897-4287-12-12. eCollection 2014. Hered Cancer Clin Pract. 2014. PMID: 24790682 Free PMC article.
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