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

Year Number of Results
1945 1
1990 1
2013 1
2014 2
2015 3
2016 2
2017 1
2018 2
2019 2
2020 4
2021 4
2022 5
2023 1
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26 results
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Page 1
Response to Tomao, Panici, and Tomao.
Vos JR, Ligtenberg MJL, Hoogerbrugge N. Vos JR, et al. J Natl Cancer Inst. 2020 Apr 1;112(4):425. doi: 10.1093/jnci/djz140. J Natl Cancer Inst. 2020. PMID: 31287552 Free PMC article. No abstract available.
A review on age-related cancer risks in PTEN hamartoma tumor syndrome.
Hendricks LAJ, Hoogerbrugge N, Schuurs-Hoeijmakers JHM, Vos JR. Hendricks LAJ, et al. Among authors: vos jr. Clin Genet. 2021 Feb;99(2):219-225. doi: 10.1111/cge.13875. Epub 2020 Nov 16. Clin Genet. 2021. PMID: 33140411 Free PMC article. Review.
Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort.
Hendricks LAJ, Hoogerbrugge N, Venselaar H, Aretz S, Spier I, Legius E, Brems H, de Putter R, Claes KBM, Evans DG, Woodward ER, Genuardi M, Brugnoletti F, van Ierland Y, Dijke K, Tham E, Tesi B, Schuurs-Hoeijmakers JHM, Branchaud M, Salvador H, Jahn A, Schnaiter S, Anastasiadou VC, Brunet J, Oliveira C, Roht L, Blatnik A, Irmejs A; PTEN Study Group; Mensenkamp AR, Vos JR. Hendricks LAJ, et al. Among authors: vos jr. Eur J Med Genet. 2022 Dec;65(12):104632. doi: 10.1016/j.ejmg.2022.104632. Epub 2022 Oct 18. Eur J Med Genet. 2022. PMID: 36270489 Free article.
Catch them if you are aware: PTEN postzygotic mosaicism in clinically suspicious patients with PTEN Hamartoma Tumour Syndrome and literature review.
Hendricks LAJ, Schuurs-Hoeijmakers J, Spier I, Haadsma ML, Eijkelenboom A, Cremer K, Mensenkamp AR, Aretz S, Vos JR, Hoogerbrugge N. Hendricks LAJ, et al. Among authors: vos jr. Eur J Med Genet. 2022 Jul;65(7):104533. doi: 10.1016/j.ejmg.2022.104533. Epub 2022 May 28. Eur J Med Genet. 2022. PMID: 35640862 Free article. Review.
The BRCA1/2 Parent-of-Origin Effect on Breast Cancer Risk-Response.
Vos JR, Oosterwijk JC, Rookus MA, van der Hout AH, Mourits MJ, de Bock GH; all authors. Vos JR, et al. Cancer Epidemiol Biomarkers Prev. 2017 Feb;26(2):285. doi: 10.1158/1055-9965.EPI-16-0947. Cancer Epidemiol Biomarkers Prev. 2017. PMID: 28167645 No abstract available.
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype.
Grolleman JE, de Voer RM, Elsayed FA, Nielsen M, Weren RDA, Palles C, Ligtenberg MJL, Vos JR, Ten Broeke SW, de Miranda NFCC, Kuiper RA, Kamping EJ, Jansen EAM, Vink-Börger ME, Popp I, Lang A, Spier I, Hüneburg R, James PA, Li N, Staninova M, Lindsay H, Cockburn D, Spasic-Boskovic O, Clendenning M, Sweet K, Capellá G, Sjursen W, Høberg-Vetti H, Jongmans MC, Neveling K, Geurts van Kessel A, Morreau H, Hes FJ, Sijmons RH, Schackert HK, Ruiz-Ponte C, Dymerska D, Lubinski J, Rivera B, Foulkes WD, Tomlinson IP, Valle L, Buchanan DD, Kenwrick S, Adlard J, Dimovski AJ, Campbell IG, Aretz S, Schindler D, van Wezel T, Hoogerbrugge N, Kuiper RP. Grolleman JE, et al. Among authors: vos jr. Cancer Cell. 2019 Feb 11;35(2):256-266.e5. doi: 10.1016/j.ccell.2018.12.011. Cancer Cell. 2019. PMID: 30753826 Free article.
26 results