C13orf31 (FAMIN) is a central regulator of immunometabolic function
Cader, M Zaeem, Boroviak, Katharina, Zhang, Qifeng, Assadi, Ghazaleh, Kempster, Sarah L, Sewell, Gavin W, Saveljeva, Svetlana, Ashcroft, Jonathan W, Clare, Simon, Mukhopadhyay, Subhankar, Brown, Karen P, Tschurtschenthaler, Markus, Raine, Tim, Doe, Brendan, Chilvers, Edwin R, Griffin, Jules L, Kaneider, Nicole C, Floto, R Andres, D'Amato, Mauro, Bradley, Allan, Wakelam, Michael J O, Dougan, Gordon, Kaser, Arthur
Published in Nature immunology (01.09.2016)
Published in Nature immunology (01.09.2016)
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Journal Article
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis
Ebers, George C, 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, Hudson, Thomas J
Published in Nature genetics (01.10.2005)
Published in Nature genetics (01.10.2005)
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Journal Article
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
Dyment, David A., Herrera, Blanca M., Cader, M. Zameel, Willer, Cristen J., Lincoln, Matthew R., Sadovnick, A. Dessa, Risch, Neil, Ebers, George C.
Published in Human molecular genetics (15.07.2005)
Published in Human molecular genetics (15.07.2005)
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Journal Article
OP0052 Use of ultrasound to predict persistence in patients with very early synovitis
Filer, A., Cader, M.Z., Abhishek, A., Allen, G., Buckley, C., de Pablo, P., Raza, K.
Published in Annals of the rheumatic diseases (01.06.2013)
Published in Annals of the rheumatic diseases (01.06.2013)
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Journal Article
SAT0107 Ultrasound defined tenosynovitis improves the prediction of rheumatoid arthritis and persistent disease in patients with very early synovitis
Filer, A., Cader, M.Z., Abhishek, A., Allen, G., Buckley, C., de Pablo, P., Raza, K.
Published in Annals of the rheumatic diseases (01.06.2013)
Published in Annals of the rheumatic diseases (01.06.2013)
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Journal Article
A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia
Cader, M Z, Steckley, J L, Dyment, D A, McLachlan, R S, Ebers, G C
Published in Neurology (12.07.2005)
Published in Neurology (12.07.2005)
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Journal Article
Multiple sclerosis susceptibility and the X chromosome
Herrera, BM, Cader, MZ, Dyment, DA, Bell, JT, DeLuca, GC, Willer, CJ, Lincoln, MR, Ramagopalan, SV, Chao, M., Orton, S-M., Sadovnick, AD, Ebers, GC
Published in Multiple sclerosis (01.08.2007)
Published in Multiple sclerosis (01.08.2007)
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Journal Article
Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13
Noble-Topham, S E, Dyment, D A, Cader, M Z, Ganapathy, R, Brown, J D, Rice, G P A, Ebers, G C
Published in Neurology (08.10.2002)
Published in Neurology (08.10.2002)
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Journal Article
A multigenerational family with multiple sclerosis
Dyment, D. A., Cader, M. Z., Willer, C. J., Risch, N., Sadovnick, A. D., Ebers, G. C.
Published in Brain (London, England : 1878) (01.07.2002)
Published in Brain (London, England : 1878) (01.07.2002)
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Journal Article
TCR β polymorphisms and multiple sclerosis
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
Published in Genes and immunity (01.07.2004)
Published in Genes and immunity (01.07.2004)
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Journal Article
Genetic loading in familial migraine with aura
Noble-Topham, S E, Cader, M Z, Dyment, D A, Rice, G P A, Brown, J D, Ebers, G C
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2003)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2003)
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Journal Article
Doctor’s knowledge of driving regulations: an interview-based survey
Kendall, Richard, Boyle, Adrian, Atkinson, Paul, McAuley, Duncan
Published in Clinical medicine (London, England) (01.03.2006)
Published in Clinical medicine (London, England) (01.03.2006)
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