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Items: 1 to 20 of 92

1.

Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes.

Motsinger AA, Brassat D, Caillier SJ, Erlich HA, Walker K, Steiner LL, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD.

Neurogenetics. 2007 Jan;8(1):11-20. Epub 2006 Sep 22.

PMID:
17024427
2.

Multifactor dimensionality reduction reveals gene-gene interactions associated with multiple sclerosis susceptibility in African Americans.

Brassat D, Motsinger AA, Caillier SJ, Erlich HA, Walker K, Steiner LL, Cree BA, Barcellos LF, Pericak-Vance MA, Schmidt S, Gregory S, Hauser SL, Haines JL, Oksenberg JR, Ritchie MD.

Genes Immun. 2006 Jun;7(4):310-5. Epub 2006 Apr 20.

3.

Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses.

Wongseree W, Assawamakin A, Piroonratana T, Sinsomros S, Limwongse C, Chaiyaratana N.

BMC Bioinformatics. 2009 Sep 17;10:294. doi: 10.1186/1471-2105-10-294.

4.

Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.

Ashley-Koch AE, Jaworski J, Ma DQ, Mei H, Ritchie MD, Skaar DA, Robert Delong G, Worley G, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Martin ER, Pericak-Vance MA.

Psychiatr Genet. 2007 Aug;17(4):221-6.

PMID:
17621165
5.

Two-locus linkage analysis in multiple sclerosis (MS).

Tienari PJ, Terwilliger JD, Ott J, Palo J, Peltonen L.

Genomics. 1994 Jan 15;19(2):320-5.

PMID:
7514567
6.

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
7.

Aggregation of multiple sclerosis genetic risk variants in multiple and single case families.

Gourraud PA, McElroy JP, Caillier SJ, Johnson BA, Santaniello A, Hauser SL, Oksenberg JR.

Ann Neurol. 2011 Jan;69(1):65-74. doi: 10.1002/ana.22323.

8.

No evidence for association of multiple sclerosis with the complement factors C6 and C7.

Chataway J, Sawcer S, Sherman D, Hobart M, Fernie B, Coraddu F, Feakes R, Broadley S, Gray J, Jones HB, Clayton D, Goodfellow PN, Compston A.

J Neuroimmunol. 1999 Sep 1;99(1):150-6.

PMID:
10496188
9.

Risk alleles for multiple sclerosis in multiplex families.

D'Netto MJ, Ward H, Morrison KM, Ramagopalan SV, Dyment DA, DeLuca GC, Handunnetthi L, Sadovnick AD, Ebers GC.

Neurology. 2009 Jun 9;72(23):1984-8. doi: 10.1212/WNL.0b013e3181a92c25.

PMID:
19506219
10.

Chromosome 19 single-locus and multilocus haplotype associations with multiple sclerosis. Evidence of a new susceptibility locus in Caucasian and Chinese patients.

Barcellos LF, Thomson G, Carrington M, Schafer J, Begovich AB, Lin P, Xu XH, Min BQ, Marti D, Klitz W.

JAMA. 1997 Oct 15;278(15):1256-61.

PMID:
9333267
11.

Genetic association between polymorphisms in the ADAMTS14 gene and multiple sclerosis.

Goertsches R, Comabella M, Navarro A, Perkal H, Montalban X.

J Neuroimmunol. 2005 Jul;164(1-2):140-7.

PMID:
15913795
12.

Model-Based Multifactor Dimensionality Reduction to detect epistasis for quantitative traits in the presence of error-free and noisy data.

Mahachie John JM, Van Lishout F, Van Steen K.

Eur J Hum Genet. 2011 Jun;19(6):696-703. doi: 10.1038/ejhg.2011.17. Epub 2011 Mar 16.

13.

Weighted risk score-based multifactor dimensionality reduction to detect gene-gene interactions in nasopharyngeal carcinoma.

Li CF, Luo FT, Zeng YX, Jia WH.

Int J Mol Sci. 2014 Jun 13;15(6):10724-37. doi: 10.3390/ijms150610724.

14.

EVI5 is a risk gene for multiple sclerosis.

Hoppenbrouwers IA, Aulchenko YS, Ebers GC, Ramagopalan SV, Oostra BA, van Duijn CM, Hintzen RQ.

Genes Immun. 2008 Jun;9(4):334-7. doi: 10.1038/gene.2008.22. Epub 2008 Apr 10.

PMID:
18401352
15.

Pair-wise multifactor dimensionality reduction method to detect gene-gene interactions in a case-control study.

He H, Oetting WS, Brott MJ, Basu S.

Hum Hered. 2010;69(1):60-70. doi: 10.1159/000243155. Epub 2009 Oct 2.

16.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

Ma DQ, Whitehead PL, Menold MM, Martin ER, Ashley-Koch AE, Mei H, Ritchie MD, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Hussman JP, Gilbert JR, Pericak-Vance MA.

Am J Hum Genet. 2005 Sep;77(3):377-88. Epub 2005 Jul 15.

17.

Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.

Al Jumah M, Al Balwi M, Hussein M, Kojan S, Al Khathaami A, Al Fawaz M, Al Muzaini B, Jawhary A, Al Abdulkareem I.

Mult Scler. 2012 Oct;18(10):1395-400. Epub 2012 Apr 4.

PMID:
22492128
18.

Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis.

Cox MB, Bowden NA, Scott RJ, Lechner-Scott J.

Mult Scler. 2014 Apr;20(4):489-91. doi: 10.1177/1352458513498127. Epub 2013 Jul 29.

PMID:
23897640
19.

Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis.

Cox MB, Ban M, Bowden NA, Baker A, Scott RJ, Lechner-Scott J.

Mult Scler. 2012 Jan;18(1):16-22. doi: 10.1177/1352458511415562. Epub 2011 Aug 3.

PMID:
21816760

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