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

Year Number of Results
2000 1
2003 1
2006 1
2007 4
2008 6
2009 15
2010 19
2011 14
2012 5
2013 12
2014 15
2015 7
2016 9
2017 8
2018 5
2019 8
2020 4
2021 3
2022 1
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111 results
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Page 1
Exome-wide rare variant analysis in familial essential tremor.
Diez-Fairen M, Houle G, Ortega-Cubero S, Bandres-Ciga S, Alvarez I, Carcel M, Ibañez L, Fernandez MV, Budde JP, Trotta JR, Tonda R, Chong JX, Bamshad MJ, Nickerson DA; University of Washington Center for Mendelian Genomics (UWCMG), Aguilar M, Tartari JP, Gironell A, García-Martín E, Agundez JA, Alonso-Navarro H, Jimenez-Jimenez FJ, Fernandez M, Valldeoriola F, Marti MJ, Tolosa E, Coria F, Pastor MA, Vilariño-Güell C, Rajput A, Dion PA, Cruchaga C, Rouleau GA, Pastor P. Diez-Fairen M, et al. Among authors: vilarino guell c. Parkinsonism Relat Disord. 2021 Jan;82:109-116. doi: 10.1016/j.parkreldis.2020.11.021. Epub 2020 Nov 24. Parkinsonism Relat Disord. 2021. PMID: 33279834 Free PMC article.
Analysis of galanin receptor GALR2 in multiple sclerosis.
Encarnacion M, Bernales CQ, Traboulsee AL, Sadovnick AD, Vilariño-Güell C. Encarnacion M, et al. Among authors: vilarino guell c. Pharmacogenomics J. 2019 Dec;19(6):499-500. doi: 10.1038/s41397-019-0100-6. Epub 2019 Oct 14. Pharmacogenomics J. 2019. PMID: 31611593 No abstract available.
Oligodendrocyte ARNT2 expression is altered in models of MS.
Becquart P, Johnston J, Vilariño-Güell C, Quandt JA. Becquart P, et al. Among authors: vilarino guell c. Neurol Neuroimmunol Neuroinflamm. 2020 May 21;7(4):e745. doi: 10.1212/NXI.0000000000000745. Print 2020 Jul. Neurol Neuroimmunol Neuroinflamm. 2020. PMID: 32439712 Free PMC article.
Whole-Exome Sequencing of an Exceptional Longevity Cohort.
Nygaard HB, Erson-Omay EZ, Wu X, Kent BA, Bernales CQ, Evans DM, Farrer MJ, Vilariño-Güell C, Strittmatter SM. Nygaard HB, et al. Among authors: vilarino guell c. J Gerontol A Biol Sci Med Sci. 2019 Aug 16;74(9):1386-1390. doi: 10.1093/gerona/gly098. J Gerontol A Biol Sci Med Sci. 2019. PMID: 29750252 Free PMC article.
Case-Control Studies Are Not Familial Studies.
Wang Z, Sadovnick AD, Traboulsee AL, Ross JP, Bernales CQ, Encarnacion M, Yee IM, de Lemos M, Greenwood T, Lee JD, Wright G, Ross CJ, Zhang S, Song W, Vilariño-Güell C. Wang Z, et al. Among authors: vilarino guell c. Neuron. 2016 Oct 19;92(2):339-341. doi: 10.1016/j.neuron.2016.09.053. Neuron. 2016. PMID: 27764669 Free article.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, Kreisler A, Ross OA, Nishioka K, Soto-Ortolaza AI, Cobb SA, Melrose HL, Behrouz B, Keeling BH, Bacon JA, Hentati E, Williams L, Yanagiya A, Sonenberg N, Lockhart PJ, Zubair AC, Uitti RJ, Aasly JO, Krygowska-Wajs A, Opala G, Wszolek ZK, Frigerio R, Maraganore DM, Gosal D, Lynch T, Hutchinson M, Bentivoglio AR, Valente EM, Nichols WC, Pankratz N, Foroud T, Gibson RA, Hentati F, Dickson DW, Destée A, Farrer MJ. Chartier-Harlin MC, et al. Among authors: vilarino guell c. Am J Hum Genet. 2011 Sep 9;89(3):398-406. doi: 10.1016/j.ajhg.2011.08.009. Am J Hum Genet. 2011. PMID: 21907011 Free PMC article.
Analysis of NOD-like receptor NLRP1 in multiple sclerosis families.
Bernales CQ, Encarnacion M, Criscuoli MG, Yee IM, Traboulsee AL, Sadovnick AD, Vilariño-Güell C. Bernales CQ, et al. Among authors: vilarino guell c. Immunogenetics. 2018 Mar;70(3):205-207. doi: 10.1007/s00251-017-1034-2. Epub 2017 Oct 7. Immunogenetics. 2018. PMID: 28988323
111 results