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

Year Number of Results
1968 2
1970 1
1972 4
1973 3
1974 1
1975 1
1976 4
1978 1
1979 1
1981 3
1983 1
1984 2
1985 2
1986 2
1987 6
1988 5
1989 2
1990 3
1991 5
1992 5
1993 4
1994 6
1995 5
1996 9
1997 3
1998 3
1999 7
2000 7
2001 10
2002 7
2003 6
2004 2
2005 8
2006 5
2007 6
2008 1
2009 1
2010 4
2011 1
2012 8
2013 8
2014 4
2015 4
2016 5
2017 1
2018 3
2019 1
2020 3
2021 2
2022 5
2023 4
2024 3
2025 9

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201 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. 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.
Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome.
Drost M, Tiersma Y, Glubb D, Kathe S, van Hees S, Calléja F, Zonneveld JBM, Boucher KM, Ramlal RPE, Thompson BA, Rasmussen LJ, Greenblatt MS, Lee A, Spurdle AB, Tavtigian SV, de Wind N. Drost M, et al. Genet Med. 2020 May;22(5):847-856. doi: 10.1038/s41436-019-0736-2. Epub 2020 Jan 22. Genet Med. 2020. PMID: 31965077 Free PMC article.
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome.
van der Klift HM, Mensenkamp AR, Drost M, Bik EC, Vos YJ, Gille HJ, Redeker BE, Tiersma Y, Zonneveld JB, García EG, Letteboer TG, Olderode-Berends MJ, van Hest LP, van Os TA, Verhoef S, Wagner A, van Asperen CJ, Ten Broeke SW, Hes FJ, de Wind N, Nielsen M, Devilee P, Ligtenberg MJ, Wijnen JT, Tops CM. van der Klift HM, et al. Among authors: drost m. Hum Mutat. 2016 Nov;37(11):1162-1179. doi: 10.1002/humu.23052. Epub 2016 Aug 21. Hum Mutat. 2016. PMID: 27435373
DNA mismatch repair: from biophysics to bedside.
Lebbink JH, Drost M, de Wind N. Lebbink JH, et al. Among authors: drost m. DNA Repair (Amst). 2016 Feb;38:1-2. doi: 10.1016/j.dnarep.2015.11.007. Epub 2015 Dec 8. DNA Repair (Amst). 2016. PMID: 26777339 No abstract available.
Complications during gestation in the cow.
Drost M. Drost M. Theriogenology. 2007 Aug;68(3):487-91. doi: 10.1016/j.theriogenology.2007.04.023. Epub 2007 May 24. Theriogenology. 2007. PMID: 17531308 Review.
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders.
Smits DJ, Debuy C, Brooks AS, Schot R, Ferraro F, Rots D, Bouman A, Verhoeven VJM, Donker Kaat L, Kant SG, van Bever Y, Demirdas S, Zeidler S, van Dooren MF, Donze SH, Hoefsloot LH, van Slegtenhorst MA, Wilke M, Sleutels F, Drost M, Brüggenwirth HT, van Minkelen R, Goverde A, Hol JA, van de Laar IMBH, van Ierland Y, Kievit A, van der Schoot V, Stuurman KE, Mancini GMS, Wessels MW, van Ham TJ, Kleefstra T, Barakat TS. Smits DJ, et al. Among authors: drost m. Eur J Hum Genet. 2025 Oct;33(10):1281-1289. doi: 10.1038/s41431-025-01919-5. Epub 2025 Jul 29. Eur J Hum Genet. 2025. PMID: 40730689
Chorionic Villus Sampling for Rapid Confirmation of High-Risk NIPT Results for Trisomy 21, 18, and 13.
Srebniak MI, Weerts M, Joosten M, Drost M, Galjaard RJ, van der Schoot V, van den Born M, Knapen MFCM, Prinsen K, Cornette JMJ, DeKoninck PLJ, Papatsonis D, Spaan J, Dijkman A, de Weerd S, Go ATJI, Diderich KEM, Van Opstal D. Srebniak MI, et al. Among authors: drost m. Prenat Diagn. 2025 Jul;45(8):988-993. doi: 10.1002/pd.6837. Epub 2025 Jun 17. Prenat Diagn. 2025. PMID: 40528522 Free PMC article.
201 results