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Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material.
Steeghs EMP, Kroeze LI, Tops BBJ, van Kempen LC, Ter Elst A, Kastner-van Raaij AWM, Hendriks-Cornelissen SJB, Hermsen MJW, Jansen EAM, Nederlof PM, Schuuring E, Ligtenberg MJL, Eijkelenboom A. Steeghs EMP, et al. Among authors: ligtenberg mjl. BMC Cancer. 2020 Apr 7;20(1):291. doi: 10.1186/s12885-020-06785-6. BMC Cancer. 2020. PMID: 32264863 Free PMC article.
Quality control in diagnostic molecular pathology in the Netherlands; proficiency testing for patient identification in tissue samples.
Thunnissen FB, Tilanus MG, Ligtenberg MJ, Nederlof PM, Dinjens WN, Meulemans E, Van den Brule AJ, van Noesel CJ, de Leeuw WJ, Schuuring E; Dutch Pathology Molecular Diagnostic Working Groups. Thunnissen FB, et al. J Clin Pathol. 2004 Jul;57(7):717-20. doi: 10.1136/jcp.2003.011973. J Clin Pathol. 2004. PMID: 15220364 Free PMC article.
A multiplex PCR predictor for aCGH success of FFPE samples.
van Beers EH, Joosse SA, Ligtenberg MJ, Fles R, Hogervorst FB, Verhoef S, Nederlof PM. van Beers EH, et al. Br J Cancer. 2006 Jan 30;94(2):333-7. doi: 10.1038/sj.bjc.6602889. Br J Cancer. 2006. PMID: 16333309 Free PMC article.
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.
Ligtenberg MJ, Kuiper RP, Chan TL, Goossens M, Hebeda KM, Voorendt M, Lee TY, Bodmer D, Hoenselaar E, Hendriks-Cornelissen SJ, Tsui WY, Kong CK, Brunner HG, van Kessel AG, Yuen ST, van Krieken JH, Leung SY, Hoogerbrugge N. Ligtenberg MJ, et al. Nat Genet. 2009 Jan;41(1):112-7. doi: 10.1038/ng.283. Epub 2008 Dec 21. Nat Genet. 2009. PMID: 19098912
270 results