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

Year Number of Results
1995 1
2007 2
2008 5
2009 3
2010 4
2011 2
2012 2
2018 3
2019 2
2020 5
2021 2
2022 0
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29 results
Results by year
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Page 1
Nevus anemicus and RASopathies.
Bulteel C, Morren MA, De Haes P, Denayer E, Legius E, Brems H. Bulteel C, et al. Among authors: denayer e. JAAD Case Rep. 2018 Apr 6;4(4):390-391. doi: 10.1016/j.jdcr.2017.09.037. eCollection 2018 May. JAAD Case Rep. 2018. PMID: 29693080 Free PMC article. No abstract available.
Cancer Surveillance in Healthy Carriers of Germline Pathogenic Variants in BRCA1/2: A Review of Secondary Prevention Guidelines.
Dullens B, de Putter R, Lambertini M, Toss A, Han S, Van Nieuwenhuysen E, Van Gorp T, Vanderstichele A, Van Ongeval C, Keupers M, Prevos R, Celis V, Dekervel J, Everaerts W, Wildiers H, Nevelsteen I, Neven P, Timmerman D, Smeets A, Denayer E, Van Buggenhout G, Legius E, Punie K. Dullens B, et al. Among authors: denayer e. J Oncol. 2020 Jun 20;2020:9873954. doi: 10.1155/2020/9873954. eCollection 2020. J Oncol. 2020. PMID: 32655641 Free PMC article. Review.
Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation.
Tšuiko O, Vanneste M, Melotte C, Ding J, Debrock S, Masset H, Peters M, Salumets A, De Leener A, Pirard C, Kluyskens C, Hostens K, van de Vijver A, Peeraer K, Denayer E, Vermeesch JR, Dimitriadou E. Tšuiko O, et al. Among authors: denayer e. NPJ Genom Med. 2021 Oct 7;6(1):81. doi: 10.1038/s41525-021-00246-0. NPJ Genom Med. 2021. PMID: 34620870 Free PMC article.
NRAS Mutations in Noonan Syndrome.
Denayer E, Peeters H, Sevenants L, Derbent M, Fryns JP, Legius E. Denayer E, et al. Mol Syndromol. 2012 Jun;3(1):34-38. doi: 10.1159/000338467. Epub 2012 May 3. Mol Syndromol. 2012. PMID: 22855653 Free PMC article.
Next-generation sequencing in prenatal setting: Some examples of unexpected variant association.
Rinaldi B, Race V, Corveleyn A, Van Hoof E, Bauters M, Van Den Bogaert K, Denayer E, de Ravel T, Legius E, Baldewijns M, Aertsen M, Lewi L, De Catte L, Breckpot J, Devriendt K. Rinaldi B, et al. Among authors: denayer e. Eur J Med Genet. 2020 May;63(5):103875. doi: 10.1016/j.ejmg.2020.103875. Epub 2020 Feb 10. Eur J Med Genet. 2020. PMID: 32058062
29 results