Cader MZ - Search Results

1

A multigenerational family with multiple sclerosis.

Dyment DA, Cader MZ, Willer CJ, Risch N, Sadovnick AD, Ebers GC. Dyment DA, et al. Among authors: cader mz. Brain. 2002 Jul;125(Pt 7):1474-82. doi: 10.1093/brain/awf158. Brain. 2002. PMID: 12076998

2

Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance.

Dyment DA, Herrera BM, Cader MZ, Willer CJ, Lincoln MR, Sadovnick AD, Risch N, Ebers GC. Dyment DA, et al. Among authors: cader mz. Hum Mol Genet. 2005 Jul 15;14(14):2019-26. doi: 10.1093/hmg/ddi206. Epub 2005 Jun 1. Hum Mol Genet. 2005. PMID: 15930013

3

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis.

Lincoln MR, Montpetit A, Cader MZ, Saarela J, Dyment DA, Tiislar M, Ferretti V, Tienari PJ, Sadovnick AD, Peltonen L, Ebers GC, Hudson TJ. Lincoln MR, et al. Among authors: cader mz. Nat Genet. 2005 Oct;37(10):1108-12. doi: 10.1038/ng1647. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186814 Free article.

4

A first stage genome-wide screen for regions shared identical-by-descent in Hutterite families with multiple sclerosis.

Dyment DA, Cader MZ, Datta A, Broxholme SJ, Cherny SS, Willer CJ, Ramagopalan S, Herrera BM, Orton S, Chao M, Sadovnick AD, Hader M, Hader W, Ebers GC. Dyment DA, et al. Among authors: cader mz. Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):467-72. doi: 10.1002/ajmg.b.30620. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18081025

5

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. Among authors: cader mz. Ann Neurol. 2011 Dec;70(6):881-6. doi: 10.1002/ana.22678. Ann Neurol. 2011. PMID: 22190362

6

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. Among authors: cader mz. Neurology. 2012 Jul 31;79(5):406-11. doi: 10.1212/WNL.0b013e3182616fc4. Epub 2012 Jun 27. Neurology. 2012. PMID: 22744673 Free PMC article.

7

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

Steckley JL, Ebers GC, Cader MZ, McLachlan RS. Steckley JL, et al. Among authors: cader mz. Neurology. 2001 Oct 23;57(8):1499-502. doi: 10.1212/wnl.57.8.1499. Neurology. 2001. PMID: 11673600

8

Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13.

Noble-Topham SE, Dyment DA, Cader MZ, Ganapathy R, Brown JD, Rice GP, Ebers GC. Noble-Topham SE, et al. Among authors: cader mz. Neurology. 2002 Oct 8;59(7):1099-101. doi: 10.1212/wnl.59.7.1099. Neurology. 2002. PMID: 12370474

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. Among authors: cader mz. Genes Immun. 2004 Aug;5(5):337-42. doi: 10.1038/sj.gene.6364091. Genes Immun. 2004. PMID: 15175643

10

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.

Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC. Cader MZ, et al. Neurology. 2005 Jul 12;65(1):156-8. doi: 10.1212/01.wnl.0000167186.05465.7c. Neurology. 2005. PMID: 16009908

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