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

Year Number of Results
2001 1
2002 1
2003 1
2004 1
2007 1
2008 2
2009 1
2010 1
2011 2
2014 1
2015 1
2016 2
2017 9
2018 5
2019 4
2020 2
2021 1
2022 1
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32 results
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Page 1
The neuroinvasiveness, neurotropism, and neurovirulence of SARS-CoV-2.
Bauer L, Laksono BM, de Vrij FMS, Kushner SA, Harschnitz O, van Riel D. Bauer L, et al. Among authors: de vrij fms. Trends Neurosci. 2022 May;45(5):358-368. doi: 10.1016/j.tins.2022.02.006. Epub 2022 Mar 3. Trends Neurosci. 2022. PMID: 35279295 Free PMC article. Review.
Potential therapeutic interventions for fragile X syndrome.
Levenga J, de Vrij FM, Oostra BA, Willemsen R. Levenga J, et al. Among authors: de vrij fm. Trends Mol Med. 2010 Nov;16(11):516-27. doi: 10.1016/j.molmed.2010.08.005. Epub 2010 Sep 21. Trends Mol Med. 2010. PMID: 20864408 Free PMC article. Review.
Novel genetic loci affecting facial shape variation in humans.
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, de Jong MA, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, Xu SH, Jin L, Wang S, de Vrij FM, Lendemeijer B, Richmond S, Zhurov A, Lewis S, Sharp GC, Paternoster L, Thompson H, Gonzalez-Jose R, Bortolini MC, Canizales-Quinteros S, Gallo C, Poletti G, Bedoya G, Rothhammer F, Uitterlinden AG, Ikram MA, Wolvius E, Kushner SA, Nijsten TE, Palstra RT, Boehringer S, Medland SE, Tang K, Ruiz-Linares A, Martin NG, Spector TD, Stergiakouli E, Weinberg SM, Liu F, Kayser M; International Visible Trait Genetics (VisiGen) Consortium. Xiong Z, et al. Among authors: de vrij fm. Elife. 2019 Nov 26;8:e49898. doi: 10.7554/eLife.49898. Elife. 2019. PMID: 31763980 Free PMC article.
Hepatitis E Virus Infects Neurons and Brains.
Zhou X, Huang F, Xu L, Lin Z, de Vrij FMS, Ayo-Martin AC, van der Kroeg M, Zhao M, Yin Y, Wang W, Cao W, Wang Y, Kushner SA, Marie Peron J, Alric L, de Man RA, Jacobs BC, van Eijk JJ, Aronica EMA, Sprengers D, Metselaar HJ, de Zeeuw CI, Dalton HR, Kamar N, Peppelenbosch MP, Pan Q. Zhou X, et al. Among authors: de vrij fms. J Infect Dis. 2017 Apr 15;215(8):1197-1206. doi: 10.1093/infdis/jix079. J Infect Dis. 2017. PMID: 28199701
ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia.
Bouwkamp CG, Afawi Z, Fattal-Valevski A, Krabbendam IE, Rivetti S, Masalha R, Quadri M, Breedveld GJ, Mandel H, Tailakh MA, Beverloo HB, Stevanin G, Brice A, van IJcken WFJ, Vernooij MW, Dolga AM, de Vrij FMS, Bonifati V, Kushner SA. Bouwkamp CG, et al. Among authors: de vrij fms. Neurol Genet. 2018 Mar 21;4(2):e223. doi: 10.1212/NXG.0000000000000223. eCollection 2018 Apr. Neurol Genet. 2018. PMID: 29577077 Free PMC article.
A rare missense variant in RCL1 segregates with depression in extended families.
Amin N, de Vrij FMS, Baghdadi M, Brouwer RWW, van Rooij JGJ, Jovanova O, Uitterlinden AG, Hofman A, Janssen HLA, Darwish Murad S, Kraaij R, Stedehouder J, van den Hout MCGN, Kros JM, van IJcken WFJ, Tiemeier H, Kushner SA, van Duijn CM. Amin N, et al. Among authors: de vrij fms. Mol Psychiatry. 2018 May;23(5):1120-1126. doi: 10.1038/mp.2017.49. Epub 2017 Mar 21. Mol Psychiatry. 2018. PMID: 28322274 Free PMC article.
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders.
Tran Mau-Them F, Moutton S, Racine C, Vitobello A, Bruel AL, Nambot S, Kushner SA, de Vrij FMS, Lehalle D, Jean-Marçais N, Lecoquierre F, Delanne J, Thevenon J, Poe C, Jouan T, Chevarin M, Geneviève D, Willems M, Coubes C, Houcinat N, Masurel-Paulet A, Mosca-Boidron AL, Tisserant E, Callier P, Sorlin A, Duffourd Y, Faivre L, Philippe C, Thauvin-Robinet C. Tran Mau-Them F, et al. Among authors: de vrij fms. Hum Genet. 2020 Nov;139(11):1381-1390. doi: 10.1007/s00439-020-02178-8. Epub 2020 May 12. Hum Genet. 2020. PMID: 32399599
32 results