David Dyment
David Dyment
Verified email at
Cited by
Cited by
Genetics of multiple sclerosis
DA Dyment, GC Ebers, AD Sadovnick
The Lancet Neurology 3 (2), 104-110, 2004
Genetics of multiple sclerosis
DA Dyment, GC Ebers, AD Sadovnick
The Lancet Neurology 3 (2), 104-110, 2004
Twin concordance and sibling recurrence rates in multiple sclerosis
CJ Willer, DA Dyment, NJ Risch, AD Sadovnick, GC Ebers, ...
Proceedings of the National Academy of Sciences 100 (22), 12877-12882, 2003
Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D
SV Ramagopalan, NJ Maugeri, L Handunnetthi, MR Lincoln, SM Orton, ...
PLoS genetics 5 (2), e1000369, 2009
Timing of birth and risk of multiple sclerosis: population based study
CJ Willer, DA Dyment, AD Sadovnick, PM Rothwell, TJ Murray, GC Ebers
Bmj 330 (7483), 120, 2005
Evidence for genetic basis of multiple sclerosis
AD Sadovnick, DA Dyment, GC Ebers, NJ Risch, ...
The Lancet 347 (9017), 1728-1730, 1996
Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care
SL Sawyer, T Hartley, DA Dyment, CL Beaulieu, J Schwartzentruber, ...
Clinical genetics 89 (3), 275-284, 2016
A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis
MR Lincoln, A Montpetit, MZ Cader, J Saarela, DA Dyment, M Tiislar, ...
Nature genetics 37 (10), 1108-1112, 2005
Parent-of-origin effect in multiple sclerosis: observations in half-siblings
GC Ebers, AD Sadovnick, DA Dyment, IML Yee, CJ Willer, N Risch
The Lancet 363 (9423), 1773-1774, 2004
Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype
SL Sawyer, L Tian, M Kähkönen, J Schwartzentruber, M Kircher, ...
Cancer discovery 5 (2), 135-142, 2015
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
DA Dyment, BM Herrera, MZ Cader, CJ Willer, MR Lincoln, AD Sadovnick, ...
Human molecular genetics 14 (14), 2019-2026, 2005
Rare variants in the CYP27B1 gene are associated with multiple sclerosis
SV Ramagopalan, DA Dyment, MZ Cader, KM Morrison, G Disanto, ...
Annals of neurology 70 (6), 881-886, 2011
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project
CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ...
The American Journal of Human Genetics 94 (6), 809-817, 2014
XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia
NC Hoch, H Hanzlikova, SL Rulten, M Tétreault, E Komulainen, L Ju, ...
Nature 541 (7635), 87-91, 2017
Genetics of multiple sclerosis
DA Dyment, AD Sadnovich, GC Ebers
Human Molecular Genetics 6 (10), 1693-1698, 1997
Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility
MR Lincoln, SV Ramagopalan, MJ Chao, BM Herrera, GC DeLuca, ...
Proceedings of the National Academy of Sciences 106 (18), 7542-7547, 2009
The inheritance of resistance alleles in multiple sclerosis
SV Ramagopalan, AP Morris, DA Dyment, BM Herrera, GC DeLuca, ...
PLoS genetics 3 (9), e150, 2007
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
V Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ...
Nature communications 10 (1), 3094, 2019
Autoimmune disease in families with multiple sclerosis: a population-based study
SV Ramagopalan, DA Dyment, W Valdar, BM Herrera, M Criscuoli, ...
The Lancet Neurology 6 (7), 604-610, 2007
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked …
FJ Kaiser, M Ansari, D Braunholz, M Concepción Gil-Rodríguez, ...
Human molecular genetics 23 (11), 2888-2900, 2014
The system can't perform the operation now. Try again later.
Articles 1–20