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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 2
2004 4
2005 3
2006 3
2008 2
2009 6
2010 1
2011 1
2013 2
2014 4
2015 1
2016 4
2018 1
2019 3
2020 2
2021 1
2022 6
2023 2
2024 0

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45 results

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Page 1
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome.
Drost M, Tiersma Y, Thompson BA, Frederiksen JH, Keijzers G, Glubb D, Kathe S, Osinga J, Westers H, Pappas L, Boucher KM, Molenkamp S, Zonneveld JB, van Asperen CJ, Goldgar DE, Wallace SS, Sijmons RH, Spurdle AB, Rasmussen LJ, Greenblatt MS, de Wind N, Tavtigian SV. Drost M, et al. Among authors: westers h. Genet Med. 2019 Jul;21(7):1486-1496. doi: 10.1038/s41436-018-0372-2. Epub 2018 Dec 3. Genet Med. 2019. PMID: 30504929 Free PMC article.
SETD2: an epigenetic modifier with tumor suppressor functionality.
Li J, Duns G, Westers H, Sijmons R, van den Berg A, Kok K. Li J, et al. Among authors: westers h. Oncotarget. 2016 Aug 2;7(31):50719-50734. doi: 10.18632/oncotarget.9368. Oncotarget. 2016. PMID: 27191891 Free PMC article. Review.
Estrogens, MSI and Lynch syndrome-associated tumors.
Ferreira AM, Westers H, Albergaria A, Seruca R, Hofstra RM. Ferreira AM, et al. Among authors: westers h. Biochim Biophys Acta. 2009 Dec;1796(2):194-200. doi: 10.1016/j.bbcan.2009.06.004. Epub 2009 Jun 25. Biochim Biophys Acta. 2009. PMID: 19559756 Review.
Proteomics of protein secretion by Bacillus subtilis: separating the "secrets" of the secretome.
Tjalsma H, Antelmann H, Jongbloed JD, Braun PG, Darmon E, Dorenbos R, Dubois JY, Westers H, Zanen G, Quax WJ, Kuipers OP, Bron S, Hecker M, van Dijl JM. Tjalsma H, et al. Among authors: westers h. Microbiol Mol Biol Rev. 2004 Jun;68(2):207-33. doi: 10.1128/MMBR.68.2.207-233.2004. Microbiol Mol Biol Rev. 2004. PMID: 15187182 Free PMC article. Review.
Correspondence: SEMA4A variation and risk of colorectal cancer.
Kinnersley B, Chubb D, Dobbins SE, Frampton M, Buch S, Timofeeva MN, Castellví-Bel S, Farrington SM, Forsti A, Hampe J, Hemminki K, Hofstra RM, Northwood E, Palles C, Pinheiro M, Ruiz-Ponte C, Schafmayer C, Teixeira MR, Westers H, van Wezel T, Timothy Bishop D, Tomlinson I, Dunlop MG, Houlston RS. Kinnersley B, et al. Among authors: westers h. Nat Commun. 2016 Mar 10;7:10611. doi: 10.1038/ncomms10611. Nat Commun. 2016. PMID: 26961734 Free PMC article. No abstract available.
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance.
Ghorbani F, Alimohamed MZ, Vilacha JF, Van Dijk KK, De Boer-Bergsma J, Fokkens MR, Lemmink H, Sijmons RH, Sikkema-Raddatz B, Groves MR, Verschuuren-Bemelmans CC, Verbeek DS, Van Diemen CC, Westers H. Ghorbani F, et al. Among authors: westers h. Front Genet. 2022 Mar 25;13:782685. doi: 10.3389/fgene.2022.782685. eCollection 2022. Front Genet. 2022. PMID: 35401678 Free PMC article.
CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
Johansson LF, van Dijk F, de Boer EN, van Dijk-Bos KK, Jongbloed JD, van der Hout AH, Westers H, Sinke RJ, Swertz MA, Sijmons RH, Sikkema-Raddatz B. Johansson LF, et al. Among authors: westers h. Hum Mutat. 2016 May;37(5):457-64. doi: 10.1002/humu.22969. Epub 2016 Feb 24. Hum Mutat. 2016. PMID: 26864275
Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia.
Ghorbani F, de Boer-Bergsma J, Verschuuren-Bemelmans CC, Pennings M, de Boer EN, Kremer B, Vanhoutte EK, de Vries JJ, van de Berg R, Kamsteeg EJ, van Diemen CC, Westers H, van de Warrenburg BP, Verbeek DS. Ghorbani F, et al. Among authors: westers h. J Neurol. 2022 Nov;269(11):6086-6093. doi: 10.1007/s00415-022-11275-9. Epub 2022 Jul 21. J Neurol. 2022. PMID: 35864213 Free PMC article.
45 results