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Results: 1 to 20 of 125

Similar articles for PubMed (Select 22570697)

1.

Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.

Matesanz F, González-Pérez A, Lucas M, Sanna S, Gayán J, Urcelay E, Zara I, Pitzalis M, Cavanillas ML, Arroyo R, Zoledziewska M, Marrosu M, Fernández O, Leyva L, Alcina A, Fedetz M, Moreno-Rey C, Velasco J, Real LM, Ruiz-Peña JL, Cucca F, Ruiz A, Izquierdo G.

PLoS One. 2012;7(5):e36140. doi: 10.1371/journal.pone.0036140. Epub 2012 May 3.

2.

GWAS-identified multiple sclerosis risk loci involved in immune response: validation in Russians.

Bashinskaya VV, Kulakova OG, Kiselev IS, Baulina NM, Favorov AV, Boyko AN, Tsareva EY, Favorova OO.

J Neuroimmunol. 2015 May 15;282:85-91. doi: 10.1016/j.jneuroim.2015.03.015. Epub 2015 Mar 17.

PMID:
25903733
3.

Multiple sclerosis genetics is dead.

Hawkes CH.

Mult Scler Relat Disord. 2013 Jul;2(3):156-61. doi: 10.1016/j.msard.2012.12.006. Epub 2013 Feb 16. Review.

PMID:
25877721
4.

[Genome-wide association study as a method for genetic architecture analysis in polygenic diseases (by the example of multiple sclerosis)].

Favorova OO, Bashinskaia VV, Kulakova OG, Favorov AV, Boĭko AN.

Mol Biol (Mosk). 2014 Jul-Aug;48(4):573-86. Review. Russian.

PMID:
25842843
5.

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
6.

Anti-inflammatory genes associated with multiple sclerosis: a gene expression study.

Perga S, Montarolo F, Martire S, Berchialla P, Malucchi S, Bertolotto A.

J Neuroimmunol. 2015 Feb 15;279:75-8. doi: 10.1016/j.jneuroim.2015.01.004. Epub 2015 Jan 21.

PMID:
25670004
7.

MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene.

Nischwitz S, Wolf C, Andlauer TF, Czamara D, Zettl UK, Rieckmann P, Buck D, Ising M, Bettecken T, Mueller-Myhsok B, Weber F.

J Neuroimmunol. 2015 Feb 15;279:46-9. doi: 10.1016/j.jneuroim.2015.01.008. Epub 2015 Jan 23.

PMID:
25670000
8.

Genomewide admixture study in Mexican Mestizos with multiple sclerosis.

Ordoñez G, Romero S, Orozco L, Pineda B, Jiménez-Morales S, Nieto A, García-Ortiz H, Sotelo J.

Clin Neurol Neurosurg. 2015 Mar;130:55-60. doi: 10.1016/j.clineuro.2014.11.026. Epub 2014 Dec 24.

PMID:
25577161
9.

Profile of differential promoter activity by nucleotide substitution at GWAS signals for multiple sclerosis.

Ryu J, Woo J, Shin J, Ryoo H, Kim Y, Lee C.

Medicine (Baltimore). 2014 Dec;93(28):e281. doi: 10.1097/MD.0000000000000281.

PMID:
25526461
10.

Complex approaches to study complex trait genetics in multiple sclerosis.

Kálmán B.

Ideggyogy Sz. 2014 Sep 30;67(9-10):309-21. Review.

PMID:
25518259
11.

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
12.

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.

Cerhan JR, Berndt SI, Vijai J, Ghesquières H, McKay J, Wang SS, Wang Z, Yeager M, Conde L, de Bakker PI, Nieters A, Cox D, Burdett L, Monnereau A, Flowers CR, De Roos AJ, Brooks-Wilson AR, Lan Q, Severi G, Melbye M, Gu J, Jackson RD, Kane E, Teras LR, Purdue MP, Vajdic CM, Spinelli JJ, Giles GG, Albanes D, Kelly RS, Zucca M, Bertrand KA, Zeleniuch-Jacquotte A, Lawrence C, Hutchinson A, Zhi D, Habermann TM, Link BK, Novak AJ, Dogan A, Asmann YW, Liebow M, Thompson CA, Ansell SM, Witzig TE, Weiner GJ, Veron AS, Zelenika D, Tilly H, Haioun C, Molina TJ, Hjalgrim H, Glimelius B, Adami HO, Bracci PM, Riby J, Smith MT, Holly EA, Cozen W, Hartge P, Morton LM, Severson RK, Tinker LF, North KE, Becker N, Benavente Y, Boffetta P, Brennan P, Foretova L, Maynadie M, Staines A, Lightfoot T, Crouch S, Smith A, Roman E, Diver WR, Offit K, Zelenetz A, Klein RJ, Villano DJ, Zheng T, Zhang Y, Holford TR, Kricker A, Turner J, Southey MC, Clavel J, Virtamo J, Weinstein S, Riboli E, Vineis P, Kaaks R, Trichopoulos D, Vermeulen RC, Boeing H, Tjonneland A, Angelucci E, Di Lollo S, Rais M, Birmann BM, Laden F, Giovannucci E, Kraft P, Huang J, Ma B, Ye Y, Chiu BC, Sampson J, Liang L, Park JH, Chung CC, Weisenburger DD, Chatterjee N, Fraumeni JF Jr, Slager SL, Wu X, de Sanjose S, Smedby KE, Salles G, Skibola CF, Rothman N, Chanock SJ.

Nat Genet. 2014 Nov;46(11):1233-8. doi: 10.1038/ng.3105. Epub 2014 Sep 28.

13.

The impact of the human genome project on complex disease.

Bailey JN, Pericak-Vance MA, Haines JL.

Genes (Basel). 2014 Jul 16;5(3):518-35. doi: 10.3390/genes5030518.

14.

A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis.

Real LM, Ruiz A, Gayán J, González-Pérez A, Sáez ME, Ramírez-Lorca R, Morón FJ, Velasco J, Marginet-Flinch R, Musulén E, Carrasco JM, Moreno-Rey C, Vázquez E, Chaves-Conde M, Moreno-Nogueira JA, Hidalgo-Pascual M, Ferrero-Herrero E, Castellví-Bel S, Castells A, Fernandez-Rozadilla C, Ruiz-Ponte C, Carracedo A, González B, Alonso S, Perucho M.

PLoS One. 2014 Jun 30;9(6):e101178. doi: 10.1371/journal.pone.0101178. eCollection 2014.

15.

The refinement of genetic predictors of multiple sclerosis.

Disanto G, Dobson R, Pakpoor J, Elangovan RI, Adiutori R, Kuhle J, Giovannoni G.

PLoS One. 2014 May 2;9(5):e96578. doi: 10.1371/journal.pone.0096578. eCollection 2014.

16.

Regulatory genomic regions active in immune cell types explain a large proportion of the genetic risk of multiple sclerosis.

Elangovan RI, Disanto G, Berlanga-Taylor AJ, Ramagopalan SV, Handunnetthi L.

J Hum Genet. 2014 Apr;59(4):211-5. doi: 10.1038/jhg.2014.3. Epub 2014 Feb 13.

PMID:
24522295
17.

A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility.

Damotte V, Guillot-Noel L, Patsopoulos NA, Madireddy L, El Behi M; International Multiple Sclerosis Genetics Consortium; Wellcome Trust Case Control Consortium 2, De Jager PL, Baranzini SE, Cournu-Rebeix I, Fontaine B.

Genes Immun. 2014 Mar;15(2):126-32. doi: 10.1038/gene.2013.70. Epub 2014 Jan 16.

PMID:
24430173
18.

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.

19.

Similar genetics of adult and pediatric MS: age is just a number.

Disanto G, Ramagopalan SV.

Neurology. 2013 Dec 3;81(23):1974-5. doi: 10.1212/01.wnl.0000436947.85775.5c. Epub 2013 Nov 6.

PMID:
24198289
20.

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.

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