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

Year Number of Results
1959 1
1975 1
1983 2
1985 4
1986 1
1987 4
1988 3
1989 1
1990 3
1991 6
1992 3
1993 4
1994 7
1995 7
1996 8
1997 7
1998 7
1999 10
2000 10
2001 8
2002 11
2003 13
2004 11
2005 12
2006 11
2007 13
2008 25
2009 33
2010 21
2011 18
2012 20
2013 10
2014 18
2015 14
2016 10
2017 9
2018 15
2019 9
2020 8
2021 16
2022 7
2023 14
2024 7
2025 0

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383 results

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Page 1
Gene expression signature predicts rate of type 1 diabetes progression.
Suomi T, Starskaia I, Kalim UU, Rasool O, Jaakkola MK, Grönroos T, Välikangas T, Brorsson C, Mazzoni G, Bruggraber S, Overbergh L, Dunger D, Peakman M, Chmura P, Brunak S, Schulte AM, Mathieu C, Knip M, Lahesmaa R, Elo LL; INNODIA Consortium. Suomi T, et al. EBioMedicine. 2023 Jun;92:104625. doi: 10.1016/j.ebiom.2023.104625. Epub 2023 May 22. EBioMedicine. 2023. PMID: 37224769 Free PMC article.
Mouse models of fragile X-related disorders.
Willemsen R, Kooy RF. Willemsen R, et al. Dis Model Mech. 2023 Feb 1;16(2):dmm049485. doi: 10.1242/dmm.049485. Epub 2023 Jan 24. Dis Model Mech. 2023. PMID: 36692473 Free PMC article. Review.
Chest pain triage: gut feeling or protocol-based care?
Willemsen RTA, van 't Hof AWJ. Willemsen RTA, et al. Neth Heart J. 2021 Jun;29(6):309-310. doi: 10.1007/s12471-021-01589-0. Epub 2021 May 10. Neth Heart J. 2021. PMID: 33970437 Free PMC article. No abstract available.
[Fragile X syndrome: new therapeutic strategies].
Zeidler S, Dierckx B, Lubbers K, van Eeghen AM, Lincke CR, Kievit JA, Willemsen R, Rietman A. Zeidler S, et al. Among authors: willemsen r. Tijdschr Psychiatr. 2018;60(5):338-342. Tijdschr Psychiatr. 2018. PMID: 29766482 Free article. Review. Dutch.
Translational endpoints in fragile X syndrome.
de Esch CE, Zeidler S, Willemsen R. de Esch CE, et al. Among authors: willemsen r. Neurosci Biobehav Rev. 2014 Oct;46 Pt 2:256-69. doi: 10.1016/j.neubiorev.2013.10.012. Epub 2013 Oct 30. Neurosci Biobehav Rev. 2014. PMID: 24184744 Review.
Key features of puberty onset and progression can help distinguish self-limited delayed puberty from congenital hypogonadotrophic hypogonadism.
Aung Y, Kokotsis V, Yin KN, Banerjee K, Butler G, Dattani MT, Dimitri P, Dunkel L, Hughes C, McGuigan M, Korbonits M, Paltoglou G, Sakka S, Shah P, Storr HL, Willemsen RH, Howard SR. Aung Y, et al. Among authors: willemsen rh. Front Endocrinol (Lausanne). 2023 Aug 28;14:1226839. doi: 10.3389/fendo.2023.1226839. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37701896 Free PMC article.
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model.
Deng R, Medico-Salsench E, Nikoncuk A, Ramakrishnan R, Lanko K, Kühn NA, van der Linde HC, Lor-Zade S, Albuainain F, Shi Y, Yousefi S, Capo I, van den Herik EM, van Slegtenhorst M, van Minkelen R, Geeven G, Mulder MT, Ruijter GJG, Lütjohann D, Jacobs EH, Houlden H, Pagnamenta AT, Metcalfe K, Jackson A, Banka S, De Simone L, Schwaede A, Kuntz N, Palculict TB, Abbas S, Umair M, AlMuhaizea M, Colak D, AlQudairy H, Alsagob M, Pereira C, Trunzo R, Karageorgou V, Bertoli-Avella AM, Bauer P, Bouman A, Hoefsloot LH, van Ham TJ, Issa M, Zaki MS, Gleeson JG, Willemsen R, Kaya N, Arold ST, Maroofian R, Sanderson LE, Barakat TS. Deng R, et al. Among authors: willemsen r. Acta Neuropathol. 2023 Aug;146(2):353-368. doi: 10.1007/s00401-023-02579-9. Epub 2023 Apr 29. Acta Neuropathol. 2023. PMID: 37119330 Free PMC article.
[Integrated care: a necessity].
Willemsen RTA. Willemsen RTA. Ned Tijdschr Geneeskd. 2020 Nov 23;164:D5077. Ned Tijdschr Geneeskd. 2020. PMID: 33332049 Dutch.
FMR1: a gene with three faces.
Oostra BA, Willemsen R. Oostra BA, et al. Among authors: willemsen r. Biochim Biophys Acta. 2009 Jun;1790(6):467-77. doi: 10.1016/j.bbagen.2009.02.007. Epub 2009 Feb 21. Biochim Biophys Acta. 2009. PMID: 19233246 Free PMC article. Review.
383 results