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Items: 1 to 20 of 100

1.

From genetic associations to functional studies in multiple sclerosis.

Bos SD, Berge T, Celius EG, Harbo HF.

Eur J Neurol. 2016 May;23(5):847-53. doi: 10.1111/ene.12981. Epub 2016 Mar 7. Review.

PMID:
26948534
2.

SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approach.

McCauley JL, Kenealy SJ, Margulies EH, Schnetz-Boutaud N, Gregory SG, Hauser SL, Oksenberg JR, Pericak-Vance MA, Haines JL, Mortlock DP.

BMC Genomics. 2007 Aug 6;8:266.

3.

Estimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs.

Watson CT, Disanto G, Breden F, Giovannoni G, Ramagopalan SV.

Sci Rep. 2012;2:770. doi: 10.1038/srep00770. Epub 2012 Oct 25.

4.

Susceptibility variants in the CD58 gene locus point to a role of microRNA-548ac in the pathogenesis of multiple sclerosis.

Hecker M, Fitzner B, Blaschke J, Blaschke P, Zettl UK.

Mutat Res Rev Mutat Res. 2015 Jan-Mar;763:161-7. doi: 10.1016/j.mrrev.2014.10.002. Epub 2014 Oct 16. Review.

PMID:
25795118
5.

Annotation of functional variation within non-MHC MS susceptibility loci through bioinformatics analysis.

Briggs FB, Leung LJ, Barcellos LF.

Genes Immun. 2014 Oct;15(7):466-76. doi: 10.1038/gene.2014.37. Epub 2014 Jul 17.

PMID:
25030428
6.

Quantifying missing heritability at known GWAS loci.

Gusev A, Bhatia G, Zaitlen N, Vilhjalmsson BJ, Diogo D, Stahl EA, Gregersen PK, Worthington J, Klareskog L, Raychaudhuri S, Plenge RM, Pasaniuc B, Price AL.

PLoS Genet. 2013;9(12):e1003993. doi: 10.1371/journal.pgen.1003993. Epub 2013 Dec 26.

7.

Variants of ST8SIA1 are associated with risk of developing multiple sclerosis.

Husain S, Yildirim-Toruner C, Rubio JP, Field J; Southern MS Genetics Consortium, Schwalb M, Cook S, Devoto M, Vitale E.

PLoS One. 2008 Jul 9;3(7):e2653. doi: 10.1371/journal.pone.0002653.

8.

More CLEC16A gene variants associated with multiple sclerosis.

Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F.

Acta Neurol Scand. 2011 Jun;123(6):400-6. doi: 10.1111/j.1600-0404.2010.01421.x. Epub 2010 Sep 16.

PMID:
20849399
9.

Impact of genetic risk loci for multiple sclerosis on expression of proximal genes in patients.

James T, Lindén M, Morikawa H, Fernandes SJ, Ruhrmann S, Huss M, Brandi M, Piehl F, Jagodic M, Tegnér J, Khademi M, Olsson T, Gomez-Cabrero D, Kockum I.

Hum Mol Genet. 2018 Mar 1;27(5):912-928. doi: 10.1093/hmg/ddy001.

PMID:
29325110
10.

Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis.

Ragnedda G, Disanto G, Giovannoni G, Ebers GC, Sotgiu S, Ramagopalan SV.

PLoS One. 2012;7(10):e46730. doi: 10.1371/journal.pone.0046730. Epub 2012 Oct 18.

11.

Selecting SNPs for association studies based on population frequencies: a novel interactive tool and its application to polygenic diseases.

Möller S, Koczan D, Serrano-Fernandez P, Zettl UK, Thiesen HJ, Ibrahim SM.

In Silico Biol. 2004;4(4):417-27.

PMID:
15506992
12.

Functional relevance for multiple sclerosis-associated genetic variants.

Lin X, Deng FY, Mo XB, Wu LF, Lei SF.

Immunogenetics. 2015 Jan;67(1):7-14. doi: 10.1007/s00251-014-0803-4. Epub 2014 Oct 12.

PMID:
25308886
13.

Genetic variants of Complex I in multiple sclerosis.

Vyshkina T, Banisor I, Shugart YY, Leist TP, Kalman B.

J Neurol Sci. 2005 Jan 15;228(1):55-64.

PMID:
15607211
14.

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.

McCauley JL, Zuvich RL, Bradford Y, Kenealy SJ, Schnetz-Boutaud N, Gregory SG, Hauser SL, Oksenberg JR, Mortlock DP, Pericak-Vance MA, Haines JL.

Genes Immun. 2009 Oct;10(7):624-30. doi: 10.1038/gene.2009.53. Epub 2009 Jul 23.

15.

Linkage disequilibrium analyses within chromosome 19p in multiple sclerosis.

Vyshkina T, Kalman B.

Mult Scler. 2008 May;14(4):433-9. doi: 10.1177/1352458507084267. Epub 2008 Jan 21.

PMID:
18208878
16.

Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.

Alcina A, Fernández O, Gonzalez JR, Catalá-Rabasa A, Fedetz M, Ndagire D, Leyva L, Guerrero M, Arnal C, Delgado C, Lucas M, Izquierdo G, Matesanz F.

Eur J Hum Genet. 2010 Jul;18(7):827-31. doi: 10.1038/ejhg.2009.240. Epub 2010 Jan 20.

17.

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.

Zuvich RL, Bush WS, McCauley JL, Beecham AH, De Jager PL; International Multiple Sclerosis Genetics Consortium, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Sawcer SJ, Pericak-Vance MA, Barcellos LF, Mortlock DP, Haines JL.

Hum Mol Genet. 2011 Sep 1;20(17):3517-24. doi: 10.1093/hmg/ddr250. Epub 2011 Jun 8.

18.

Combinatorial effects of multiple enhancer variants in linkage disequilibrium dictate levels of gene expression to confer susceptibility to common traits.

Corradin O, Saiakhova A, Akhtar-Zaidi B, Myeroff L, Willis J, Cowper-Sal lari R, Lupien M, Markowitz S, Scacheri PC.

Genome Res. 2014 Jan;24(1):1-13. doi: 10.1101/gr.164079.113. Epub 2013 Nov 6.

19.

Where is the causal variant? On the advantage of the family design over the case-control design in genetic association studies.

Dandine-Roulland C, Perdry H.

Eur J Hum Genet. 2015 Oct;23(10):1357-63. doi: 10.1038/ejhg.2014.284. Epub 2015 Jan 14.

20.

Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.

Buck D, Albrecht E, Aslam M, Goris A, Hauenstein N, Jochim A; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium, Cepok S, Grummel V, Dubois B, Berthele A, Lichtner P, Gieger C, Winkelmann J, Hemmer B.

Ann Neurol. 2013 Jan;73(1):86-94. doi: 10.1002/ana.23749. Epub 2012 Dec 7.

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