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Muhammed Cader
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Research Profile (preview)
Physiology
Disorders
Chemicals & Drugs
Concepts & Ideas
Genes & Molecular Sequences
Activities & Behaviors
Procedures
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Network (preview)
12
Ebers, George
11
Dyment, David
8
Sadovnick, Dessa
5
Ramagopalan, Sreeram
5
Willer, Cristen
5
herrera, blanca
4
Risch, Neil
4
Lincoln, Matthew
4
Orton, Sarah
3
DeLuca, Gabriele
3
Steckley, JL
3
Talbot, Kevin
2
Noble-Topham, Sandra
2
Rice, G P A
2
Bell, Jordana Tzenova
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Geonetwork of Muhammed Cader (preview)
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All Publications
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2009: Achilli Francesca; Bros-Facer Virginie; Williams Hazel P; Banks Gareth T; AlQatari Mona; Chia Ruth; Tucci Valter; Groves Michael; Nickols Carole D; Seburn Kevin L; Kendall Rachel; Cader Muhammed Z; Talbot Kevin; van Minnen Jan; Burgess Robert W; Brandner Sebastian; Martin Joanne E; Koltzenburg Martin; Greensmith Linda; Nolan Patrick M; Fisher Elizabeth M C
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy.
Disease models & mechanisms 2009;2(7-8):359-73.
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2008: Dyment D A; Cader M Z; Herrera B M; Ramagopalan S V; Orton S M; Chao M; Willer C J; Sadovnick A D; Risch N; Ebers G C
A genome scan in a single pedigree with a high prevalence of multiple sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2008;79(2):158-62.
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2007: Ramagopalan S V; Ramscar N E; Cader M Z
Molecular mechanisms of migraine?
Journal of neurology 2007;254(12):1629-35.
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2007: DeLuca G C; Ramagopalan S V; Cader M Z; Dyment D A; Herrera B M; Orton S; Degenhardt A; Pugliatti M; Sadovnick A D; Sotgiu S; Ebers G C
The role of hereditary spastic paraplegia related genes in multiple sclerosis. A study of disease susceptibility and clinical outcome.
Journal of neurology 2007;254(9):1221-6.
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2007: Herrera B M; Cader M Z; Dyment D A; Bell J T; Deluca G C; Willer C J; Lincoln M R; Ramagopalan S V; Chao M; Orton S-M; Sadovnick A D; Ebers G C
Multiple sclerosis susceptibility and the X chromosome.
Multiple sclerosis (Houndmills, Basingstoke, England) 2007;13(7):856-64.
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2007: Cader Muhammed Z; Ren Jingshan; James Paul A; Bird Louise E; Talbot Kevin; Stammers David K
Crystal structure of human wildtype and S581L-mutant glycyl-tRNA synthetase, an enzyme underlying distal spinal muscular atrophy.
FEBS letters 2007;581(16):2959-64.
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2006: James P A; Cader M Z; Muntoni F; Childs A-M; Crow Y J; Talbot K
Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene.
Neurology 2006;67(9):1710-2.
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2006: Herrera B M; Cader M Z; Dyment D A; Bell J T; Ramagopalan S V; Lincoln M R; Orton S; Chao M J; Sadovnick A D; Ebers G C
Follow-up investigation of 12 proposed linkage regions in multiple sclerosis.
Genes and immunity 2006;7(5):366-71.
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2006: Irani S R; Cader Muhammed Z; Butterworth R J
Doctor's knowledge of driving regulations: an interview-based survey.
Clinical medicine (London, England) 2006;6(2):217-9.
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2005: Lincoln Matthew R; Montpetit Alexandre; Cader M Zameel; Saarela Janna; Dyment David A; Tiislar Milvi; Ferretti Vincent; Tienari Pentti J; Sadovnick A Dessa; Peltonen Leena; Ebers George C; Hudson Thomas J
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis.
Nature genetics 2005;37(10):1108-12.
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2005: Cader M Z; Steckley J L; Dyment D A; McLachlan R S; Ebers G C
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
Neurology 2005;65(1):156-8.
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2005: Dyment David A; Herrera Blanca M; Cader M Zameel; Willer Cristen J; Lincoln Matthew R; Sadovnick A Dessa; Risch Neil; Ebers George C
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance.
Human molecular genetics 2005;14(14):2019-26.
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2004: Dyment D A; Steckley J L; Morrison K; Willer C J; Cader M Z; DeLuca G C; Sadovnick A D; Risch N; Ebers G C;
TCR beta polymorphisms and multiple sclerosis.
Genes and immunity 2004;5(5):337-42.
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2003: Noble-Topham S E; Cader M Z; Dyment D A; Rice G P A; Brown J D; Ebers G C
Genetic loading in familial migraine with aura.
Journal of neurology, neurosurgery, and psychiatry 2003;74(8):1128-30.
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2002: Noble-Topham S E; Dyment D A; Cader M Z; Ganapathy R; Brown J D; Rice G P A; Ebers G C
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13.
Neurology 2002;59(7):1099-101.
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2002: Dyment D A; Cader M Z; Willer C J; Risch N; Sadovnick A D; Ebers G C
A multigenerational family with multiple sclerosis.
Brain : a journal of neurology 2002;125(Pt 7):1474-82.
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2001: Steckley J L; Ebers G C; Cader M Z; McLachlan R S
An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
Neurology 2001;57(8):1499-502.
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