Multiple sclerosis in stepsiblings: recurrence risk and ascertainment

Por Dyment, D A, Yee, I M L, Ebers, G C, Sadovnick, A D
Publicado em 2006

Twin concordance and sibling recurrence rates in multiple sclerosis

Por Willer, C. J., Dyment, D. A., Risch, N. J., Sadovnick, A. D., Ebers, G. C.
Publicado em 2003

Parent-of-origin effect in multiple sclerosis: Observations from interracial matings

Por Ramagopalan, S V., Yee, I M., Dyment, D A., Orton, S -M., Marrie, R A., Sadovnick, A D., Ebers, G C.
Publicado em 2009

MHC transmission: Insights into gender bias in MS susceptibility

Por Chao, M.J., Ramagopalan, S.V., Herrera, B.M., Orton, S.M., Handunnetthi, L., Lincoln, M.R., Dyment, D.A., Sadovnick, A.D., Ebers, G.C.
Publicado em 2011

An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus

Por DeLuca, G. C., Ramagopalan, S. V., Herrera, B. M., Dyment, D. A., Lincoln, M. R., Montpetit, A., Pugliatti, M., Barnardo, M. C. N., Risch, N. J., Sadovnick, A. D., Chao, M., Sotgiu, S., Hudson, T. J., Ebers, G. C.
Publicado em 2007

Utility of whole‐exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care

Por Sawyer, S.L., Hartley, T., Dyment, D.A., Beaulieu, C.L., Schwartzentruber, J., Smith, A., Bedford, H.M., Bernard, G., Bernier, F.P., Brais, B., Bulman, D.E., Warman Chardon, J., Chitayat, D., Deladoëy, J., Fernandez, B.A., Frosk, P., Geraghty, M.T., Gerull, B., Gibson, W., Gow, R.M., Graham, G.E., Green, J.S., Heon, E., Horvath, G., Innes, A.M., Jabado, N., Kim, R.H., Koenekoop, R.K., Khan, A., Lehmann, O.J., Mendoza‐Londono, R., Michaud, J.L., Nikkel, S.M., Penney, L.S., Polychronakos, C., Richer, J., Rouleau, G.A., Samuels, M.E., Siu, V.M., Suchowersky, O., Tarnopolsky, M.A., Yoon, G., Zahir, F.R., Majewski, J., Boycott, K.M.
Publicado no Clin Genet (2015)