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

Year Number of Results
1967 1
2005 1
2007 1
2008 1
2009 1
2010 4
2011 3
2012 5
2013 2
2014 1
2015 1
2016 1
2019 2
2020 3
2023 1
2024 0

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23 results

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Page 1
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
van Rheenen W, Shatunov A, Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U, de Jong S, Robinson MR, Yang J, Fogh I, van Doormaal PT, Tazelaar GH, Koppers M, Blokhuis AM, Sproviero W, Jones AR, Kenna KP, van Eijk KR, Harschnitz O, Schellevis RD, Brands WJ, Medic J, Menelaou A, Vajda A, Ticozzi N, Lin K, Rogelj B, Vrabec K, Ravnik-Glavač M, Koritnik B, Zidar J, Leonardis L, Grošelj LD, Millecamps S, Salachas F, Meininger V, de Carvalho M, Pinto S, Mora JS, Rojas-García R, Polak M, Chandran S, Colville S, Swingler R, Morrison KE, Shaw PJ, Hardy J, Orrell RW, Pittman A, Sidle K, Fratta P, Malaspina A, Topp S, Petri S, Abdulla S, Drepper C, Sendtner M, Meyer T, Ophoff RA, Staats KA, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin VM, Trojanowski JQ, Elman L, McCluskey L, Basak AN, Tunca C, Hamzeiy H, Parman Y, Meitinger T, Lichtner P, Radivojkov-Blagojevic M, Andres CR, Maurel C, Bensimon G, Landwehrmeyer B, Brice A, Payan CA, Saker-Delye S, Dürr A, Wood NW, Tittmann L, Lieb W, Franke A, Rietschel M, Cichon S, Nöthen MM, Amouyel P, Tzourio C, Dartigues JF, Uitterlinden AG, Rivadeneira F, Estrada K, Hofman A, Curtis C, Blauw HM, van der Kooi AJ, de Visser M, … See abstract for full author list ➔ van Rheenen W, et al. Among authors: medic j. Nat Genet. 2016 Sep;48(9):1043-8. doi: 10.1038/ng.3622. Epub 2016 Jul 25. Nat Genet. 2016. PMID: 27455348 Free PMC article.
Multivariate genome-wide analysis of stress-related quantitative phenotypes.
Schijven D, Geuze E, Vinkers CH, Pulit SL, Schür RR, Malgaz M, Bekema E, Medic J, van der Kust KE, Veldink JH, Boks MP, Vermetten E, Luykx JJ. Schijven D, et al. Among authors: medic j. Eur Neuropsychopharmacol. 2019 Dec;29(12):1354-1364. doi: 10.1016/j.euroneuro.2019.09.012. Epub 2019 Oct 9. Eur Neuropsychopharmacol. 2019. PMID: 31606302
The role of rare compound heterozygous events in autism spectrum disorder.
Lin BD, Colas F, Nijman IJ, Medic J, Brands W, Parr JR, van Eijk KR, Klauck SM, Chiocchetti AG, Freitag CM, Maestrini E, Bacchelli E, Coon H, Vicente A, Oliveira G, Pagnamenta AT, Gallagher L, Ennis S, Anney R, Bourgeron T, Luykx JJ, Vorstman J. Lin BD, et al. Among authors: medic j. Transl Psychiatry. 2020 Jun 22;10(1):204. doi: 10.1038/s41398-020-00866-7. Transl Psychiatry. 2020. PMID: 32572023 Free PMC article.
Pharmacokinetics of intravenous immunoglobulin in multifocal motor neuropathy.
Vlam L, Cats EA, Willemse E, Franssen H, Medic J, Piepers S, Veldink JH, van den Berg LH, van der Pol WL. Vlam L, et al. Among authors: medic j. J Neurol Neurosurg Psychiatry. 2014 Oct;85(10):1145-8. doi: 10.1136/jnnp-2013-306227. Epub 2013 Dec 11. J Neurol Neurosurg Psychiatry. 2014. PMID: 24336791 Clinical Trial.
Starch characterization and ethanol production of sorghum.
Ai Y, Medic J, Jiang H, Wang D, Jane JL. Ai Y, et al. Among authors: medic j. J Agric Food Chem. 2011 Jul 13;59(13):7385-92. doi: 10.1021/jf2007584. Epub 2011 Jun 3. J Agric Food Chem. 2011. PMID: 21604720
Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
van Blitterswijk M, van Es MA, Hennekam EA, Dooijes D, van Rheenen W, Medic J, Bourque PR, Schelhaas HJ, van der Kooi AJ, de Visser M, de Bakker PI, Veldink JH, van den Berg LH. van Blitterswijk M, et al. Among authors: medic j. Hum Mol Genet. 2012 Sep 1;21(17):3776-84. doi: 10.1093/hmg/dds199. Epub 2012 May 29. Hum Mol Genet. 2012. PMID: 22645277
Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy.
Wadman RI, Jansen MD, Curial CAD, Groen EJN, Stam M, Wijngaarde CA, Medic J, Sodaar P, van Eijk KR, Huibers MMH, van Kuik J, Lemmink HH, van Rheenen W, Veldink JH, van den Berg LH, van der Pol WL. Wadman RI, et al. Among authors: medic j. Neurol Genet. 2019 Jan 3;6(1):e386. doi: 10.1212/NXG.0000000000000386. eCollection 2020 Feb. Neurol Genet. 2019. PMID: 32042914 Free PMC article.
23 results