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Results by year

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

Year Number of Results
1983 1
1984 1
1988 3
1989 1
1990 1
1991 1
1992 3
1993 1
1994 6
1995 6
1996 6
1997 1
1998 3
1999 8
2000 2
2001 5
2002 5
2003 6
2004 6
2005 4
2006 6
2007 10
2008 5
2009 5
2010 9
2011 8
2012 7
2013 9
2014 12
2015 6
2016 8
2017 2
2018 2
2019 3
2020 2
2021 1
2022 2
2023 2
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Search Results

152 results
Results by year
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Page 1
Birt-Hogg-Dubé syndrome: diagnosis and management.
Menko FH, van Steensel MA, Giraud S, Friis-Hansen L, Richard S, Ungari S, Nordenskjöld M, Hansen TV, Solly J, Maher ER; European BHD Consortium. Menko FH, et al. Lancet Oncol. 2009 Dec;10(12):1199-206. doi: 10.1016/S1470-2045(09)70188-3. Lancet Oncol. 2009. PMID: 19959076 Review.
Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study.
Schrijver LH, Antoniou AC, Olsson H, Mooij TM, Roos-Blom MJ, Azarang L, Adlard J, Ahmed M, Barrowdale D, Davidson R, Donaldson A, Eeles R, Evans DG, Frost D, Henderson A, Izatt L, Ong KR, Bonadona V, Coupier I, Faivre L, Fricker JP, Gesta P, van Engelen K, Jager A, Menko FH, Mourits MJE, Singer CF, Tan YY, Foretova L, Navratilova M, Schmutzler RK, Ellberg C, Gerdes AM, Caldes T, Simard J, Olah E, Jakubowska A, Rantala J, Osorio A, Hopper JL, Phillips KA, Milne RL, Beth Terry M, Noguès C, Engel C, Kast K, Goldgar DE, van Leeuwen FE, Easton DF, Andrieu N, Rookus MA; Epidemiological Study of Familial Breast Cancer, Gene Etude Prospective Sein Ovaire Sein, Hereditary Breast and Ovarian Cancer Research Group Netherlands, and International BRCA1/2 Carrier Cohort Study. Schrijver LH, et al. Among authors: menko fh. Am J Obstet Gynecol. 2021 Jul;225(1):51.e1-51.e17. doi: 10.1016/j.ajog.2021.01.014. Epub 2021 Jan 22. Am J Obstet Gynecol. 2021. PMID: 33493488 Free PMC article.
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes.
Ruijs MW, Verhoef S, Rookus MA, Pruntel R, van der Hout AH, Hogervorst FB, Kluijt I, Sijmons RH, Aalfs CM, Wagner A, Ausems MG, Hoogerbrugge N, van Asperen CJ, Gomez Garcia EB, Meijers-Heijboer H, Ten Kate LP, Menko FH, van 't Veer LJ. Ruijs MW, et al. Among authors: menko fh. J Med Genet. 2010 Jun;47(6):421-8. doi: 10.1136/jmg.2009.073429. J Med Genet. 2010. PMID: 20522432 Free article.
European collaboration on genetic tumour risk syndromes.
Vetti HH, Blanco I, Menko FH. Vetti HH, et al. Among authors: menko fh. Eur J Med Genet. 2023 Feb;66(2):104691. doi: 10.1016/j.ejmg.2022.104691. Epub 2022 Dec 26. Eur J Med Genet. 2023. PMID: 36581153 No abstract available.
[Familial ovarian carcinoma].
Verheijen RH, Menko FH, Kenemans P. Verheijen RH, et al. Among authors: menko fh. Ned Tijdschr Geneeskd. 1994 Jan 8;138(2):63-6. Ned Tijdschr Geneeskd. 1994. PMID: 8107904 Review. Dutch. No abstract available.
Constitutional rearrangements of chromosome 22 as a cause of neurofibromatosis 2.
Tsilchorozidou T, Menko FH, Lalloo F, Kidd A, De Silva R, Thomas H, Smith P, Malcolmson A, Dore J, Madan K, Brown A, Yovos JG, Tsaligopoulos M, Vogiatzis N, Baser ME, Wallace AJ, Evans DG. Tsilchorozidou T, et al. Among authors: menko fh. J Med Genet. 2004 Jul;41(7):529-34. doi: 10.1136/jmg.2003.016774. J Med Genet. 2004. PMID: 15235024 Free PMC article. Review. No abstract available.
152 results