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Year | Number of Results |
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2012 | 2 |
2013 | 3 |
2014 | 1 |
2019 | 1 |
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Page 1
Long non-coding RNAs in neurodevelopmental disorders.
Front Mol Neurosci. 2013 Dec 30;6:53. doi: 10.3389/fnmol.2013.00053.
Front Mol Neurosci. 2013.
PMID: 24415997
Free PMC article.
Review.
Converging evidence points towards a role of insulin signaling in regulating compulsive behavior.
van de Vondervoort IIGM, Amiri H, Bruchhage MMK, Oomen CA, Rustogi N, Cooper JD, van Asten JJA, Heerschap A, Bahn S, Williams SCR, Buitelaar JK, Poelmans G, Glennon JC.
van de Vondervoort IIGM, et al.
Transl Psychiatry. 2019 Sep 12;9(1):225. doi: 10.1038/s41398-019-0559-6.
Transl Psychiatry. 2019.
PMID: 31515486
Free PMC article.
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Serotonin transporter knockout rats show improved strategy set-shifting and reduced latent inhibition.
Nonkes LJ, van de Vondervoort II, de Leeuw MJ, Wijlaars LP, Maes JH, Homberg JR.
Nonkes LJ, et al. Among authors: van de vondervoort ii.
Learn Mem. 2012 Apr 13;19(5):190-3. doi: 10.1101/lm.025908.112.
Learn Mem. 2012.
PMID: 22505721
Free article.
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Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.
Schuurs-Hoeijmakers JH, Vulto-van Silfhout AT, Vissers LE, van de Vondervoort II, van Bon BW, de Ligt J, Gilissen C, Hehir-Kwa JY, Neveling K, del Rosario M, Hira G, Reitano S, Vitello A, Failla P, Greco D, Fichera M, Galesi O, Kleefstra T, Greally MT, Ockeloen CW, Willemsen MH, Bongers EM, Janssen IM, Pfundt R, Veltman JA, Romano C, Willemsen MA, van Bokhoven H, Brunner HG, de Vries BB, de Brouwer AP.
Schuurs-Hoeijmakers JH, et al. Among authors: van de vondervoort ii.
J Med Genet. 2013 Dec;50(12):802-11. doi: 10.1136/jmedgenet-2013-101644. Epub 2013 Oct 11.
J Med Genet. 2013.
PMID: 24123876
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The attribution of incentive salience to an appetitive conditioned cue is not affected by knockout of the serotonin transporter in rats.
Nonkes LJ, van de Vondervoort II, Homberg JR.
Nonkes LJ, et al. Among authors: van de vondervoort ii.
Behav Brain Res. 2014 Feb 1;259:268-73. doi: 10.1016/j.bbr.2013.11.017. Epub 2013 Nov 20.
Behav Brain Res. 2014.
PMID: 24269496
Free article.
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Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.
Schuurs-Hoeijmakers JH, Geraghty MT, Kamsteeg EJ, Ben-Salem S, de Bot ST, Nijhof B, van de Vondervoort II, van der Graaf M, Nobau AC, Otte-Höller I, Vermeer S, Smith AC, Humphreys P, Schwartzentruber J; FORGE Canada Consortium; Ali BR, Al-Yahyaee SA, Tariq S, Pramathan T, Bayoumi R, Kremer HP, van de Warrenburg BP, van den Akker WM, Gilissen C, Veltman JA, Janssen IM, Vulto-van Silfhout AT, van der Velde-Visser S, Lefeber DJ, Diekstra A, Erasmus CE, Willemsen MA, Vissers LE, Lammens M, van Bokhoven H, Brunner HG, Wevers RA, Schenck A, Al-Gazali L, de Vries BB, de Brouwer AP.
Schuurs-Hoeijmakers JH, et al. Among authors: van de vondervoort ii.
Am J Hum Genet. 2012 Dec 7;91(6):1073-81. doi: 10.1016/j.ajhg.2012.10.017. Epub 2012 Nov 21.
Am J Hum Genet. 2012.
PMID: 23176823
Free PMC article.
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