Morrison KME - Search Results

1

A genome-wide scan in forty large pedigrees with multiple sclerosis.

Willer CJ, Dyment DA, Cherny S, Ramagopalan SV, Herrera BM, Morrison KME, Sadovnick AD, Risch NJ, Ebers GC. Willer CJ, et al. Among authors: morrison kme. J Hum Genet. 2007;52(12):955-962. doi: 10.1007/s10038-007-0194-6. Epub 2007 Nov 15. J Hum Genet. 2007. PMID: 18000641

2

Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis.

Ramagopalan SV, Deluca GC, Morrison KM, Herrera BM, Dyment DA, Lincoln MR, Orton SM, Chao MJ, Degenhardt A, Pugliatti M, Sadovnick AD, Sotgiu S, Ebers GC. Ramagopalan SV, et al. J Neurol. 2008 Aug;255(8):1215-9. doi: 10.1007/s00415-008-0878-7. Epub 2008 Jun 20. J Neurol. 2008. PMID: 18563468

3

Methylation of class II transactivator gene promoter IV is not associated with susceptibility to multiple sclerosis.

Ramagopalan SV, Dyment DA, Morrison KM, Herrera BM, Deluca GC, Lincoln MR, Orton SM, Handunnetthi L, Chao MJ, Sadovnick AD, Ebers GC. Ramagopalan SV, et al. BMC Med Genet. 2008 Jul 7;9:63. doi: 10.1186/1471-2350-9-63. BMC Med Genet. 2008. PMID: 18606010 Free PMC article.

4

Variants in ST8SIA1 do not play a major role in susceptibility to multiple sclerosis in Canadian families.

Ramagopalan SV, Morrison KM, Para A, Handel A, Disanto G, Handunnetthi L, Orton SM, Sadovnick AD, Ebers GC. Ramagopalan SV, et al. J Neuroimmunol. 2009 Jul 25;212(1-2):142-4. doi: 10.1016/j.jneuroim.2009.04.017. Epub 2009 May 9. J Neuroimmunol. 2009. PMID: 19428123

5

Vitamin D metabolic pathway genes and risk of multiple sclerosis in Canadians.

Orton SM, Ramagopalan SV, Para AE, Lincoln MR, Handunnetthi L, Chao MJ, Morahan J, Morrison KM, Sadovnick AD, Ebers GC. Orton SM, et al. J Neurol Sci. 2011 Jun 15;305(1-2):116-20. doi: 10.1016/j.jns.2011.02.032. Epub 2011 Mar 26. J Neurol Sci. 2011. PMID: 21440908

6

Rare variants in the CYP27B1 gene are associated with multiple sclerosis.

Ramagopalan SV, Dyment DA, Cader MZ, Morrison KM, Disanto G, Morahan JM, Berlanga-Taylor AJ, Handel A, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC. Ramagopalan SV, et al. Ann Neurol. 2011 Dec;70(6):881-6. doi: 10.1002/ana.22678. Ann Neurol. 2011. PMID: 22190362

7

Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.

Dyment DA, Cader MZ, Chao MJ, Lincoln MR, Morrison KM, Disanto G, Morahan JM, De Luca GC, Sadovnick AD, Lepage P, Montpetit A, Ebers GC, Ramagopalan SV. Dyment DA, et al. Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27. Neurology. 2012. PMID: 22744673 Free PMC article.

8

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. D'Netto MJ, et al. Neurology. 2009 Jun 9;72(23):1984-8. doi: 10.1212/WNL.0b013e3181a92c25. Neurology. 2009. PMID: 19506219

9

TCR beta polymorphisms and multiple sclerosis.

Dyment DA, Steckley JL, Morrison K, Willer CJ, Cader MZ, DeLuca GC, Sadovnick AD, Risch N, Ebers GC; Canadian Collaborative Study Group. Dyment DA, et al. Genes Immun. 2004 Aug;5(5):337-42. doi: 10.1038/sj.gene.6364091. Genes Immun. 2004. PMID: 15175643

10

IGHV4-39 deletion polymorphism does not associate with risk or outcome of multiple sclerosis.

Watson CT, Ramagopalan SV, Morrison KM, Ebers GC, Breden F. Watson CT, et al. J Neuroimmunol. 2010 Aug 25;225(1-2):164-6. doi: 10.1016/j.jneuroim.2010.04.012. Epub 2010 May 15. J Neuroimmunol. 2010. PMID: 20471699

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