Search Results - David A. Dyment

Refine Results
  1. 1
    Multiple sclerosis in stepsiblings: recurrence risk and ascertainment

    Multiple sclerosis in stepsiblings: recurrence risk and ascertainment by David A. Dyment

    Published 2006
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  2. 2
    Genetics of multiple sclerosis

    Genetics of multiple sclerosis by David A. Dyment, George C. Ebers, A. Dessa Sadovnick

    Published 2004
    Get full text
    Revisão
    Save to List
    Saved in:
  3. 3
    Epilepsy genetics: Current knowledge, applications, and future directions

    Epilepsy genetics: Current knowledge, applications, and future directions by Kenneth A. Myers, Devon L. Johnstone, David A. Dyment

    Published 2018
    Get full text
    Revisão
    Save to List
    Saved in:
  4. 4
    Twin concordance and sibling recurrence rates in multiple sclerosis

    Twin concordance and sibling recurrence rates in multiple sclerosis by Cristen J. Willer, David A. Dyment, Neil Risch, A. Dessa Sadovnick, George C. Ebers

    Published 2003
    Get full text
    Artigo
    Save to List
    Saved in:
  5. 5
    Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature

    Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature by Stephanie M. Luco, Daniela Pohl, Erick Sell, Justin D. Wagner, David A. Dyment, Hussein Daoud

    Published 2016
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  6. 6
    Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative Study

    Effect of immigration on multiple sclerosis sex ratio in Canada: the Canadian Collaborative Study by S-M. Orton, S. V. Ramagopalan, Denise Brocklebank, Blanca Herrera, David A. Dyment, Irene M. Yee, A. Dessa Sadovnick, George C. Ebers

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  7. 7
    Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery

    Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery by Kym M. Boycott, Taila Hartley, Kristin D. Kernohan, David A. Dyment, Heather Howley, A. Micheil Innes, François Bernier, Michael Brudno

    Published 2022
    Get full text Get full text
    Revisão
    Save to List
    Saved in:
  8. 8
    Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance

    Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance by David A. Dyment, Blanca Herrera, M. Zameel Cader, Cristen J. Willer, Matthew R. Lincoln, A. Dessa Sadovnick, Neil Risch, George C. Ebers

    Published 2005
    Get full text
    Artigo
    Save to List
    Saved in:
  9. 9
    HLA class I alleles tag <i>HLA-DRB1</i> * <i>1501</i> haplotypes for differential risk in multiple sclerosis susceptibility

    HLA class I alleles tag <i>HLA-DRB1</i> * <i>1501</i> haplotypes for differential risk in multiple sclerosis susceptibility by Michael J. Chao, Martin Barnardo, Matthew R. Lincoln, Sreeram V. Ramagopalan, Blanca Herrera, David A. Dyment, Alexandre Montpetit, A. Dessa Sadovnick, Julian C. Knight, George C. Ebers

    Published 2008
    Get full text
    Artigo
    Save to List
    Saved in:
  10. 10
    Epistasis among<i>HLA-DRB1, HLA-DQA1,</i>and<i>HLA-DQB1</i>loci determines multiple sclerosis susceptibility

    Epistasis among<i>HLA-DRB1, HLA-DQA1,</i>and<i>HLA-DQB1</i>loci determines multiple sclerosis susceptibility by Matthew R. Lincoln, Sreeram V. Ramagopalan, Michael J. Chao, Blanca Herrera, Gabriele C. DeLuca, Sarah-Michelle Orton, David A. Dyment, A. Dessa Sadovnick, George C. Ebers

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  11. 11
    Homozygous mutations in<i>MFN2</i>cause multiple symmetric lipomatosis associated with neuropathy

    Homozygous mutations in<i>MFN2</i>cause multiple symmetric lipomatosis associated with neuropathy by Sarah L. Sawyer, Andy Cheuk‐Him Ng, A. Micheil Innes, Justin D. Wagner, David A. Dyment, Martine Tétreault, Jacek Majewski, Kym M. Boycott, Robert A. Screaton, Garth A. Nicholson

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  12. 12
    Biallelic Mutations in <i>BRCA1</i> Cause a New Fanconi Anemia Subtype

    Biallelic Mutations in <i>BRCA1</i> Cause a New Fanconi Anemia Subtype by Sarah L. Sawyer, Lei Tian, Marketta Kähkönen, Jeremy Schwartzentruber, Martin Kircher, Jacek Majewski, David A. Dyment, A. Micheil Innes, Kym M. Boycott, Lisa A. Moreau, Jukka S. Moilanen, Roger A. Greenberg

    Published 2014
    Get full text
    Artigo
    Save to List
    Saved in:
  13. 13
    A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

    A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis by Matthew R. Lincoln, Alexandre Montpetit, M. Zameel Cader, Janna Saarela, David A. Dyment, Milvi Tiislar, Vincent Ferretti, Pentti J. Tienari, A. Dessa Sadovnick, Leena Peltonen, George C. Ebers, Thomas J. Hudson

    Published 2005
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  14. 14
    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis

    Identification of Novel Mutations Confirms<i>Pde4d</i>as a Major Gene Causing Acrodysostosis by Danielle C. Lynch, David A. Dyment, Lijia Huang, Sarah M. Nikkel, Didier Lacombe, Philippe M. Campeau, Brendan Lee, Carlos A. Bacino, Jacques L. Michaud, François Bernier, FORGE Canada Consortium, Jillian S. Parboosingh, A. Micheil Innes

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  15. 15
    Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D

    Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D by Sreeram V Ramagopalan, Narelle Maugeri, Lahiru Handunnetthi, Matthew R. Lincoln, Sarah-Michelle Orton, David A. Dyment, Gabriele C. DeLuca, Blanca Herrera, Michael J. Chao, A. Dessa Sadovnick, George C. Ebers, Julian C. Knight

    Published 2009
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  16. 16
    An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the <i>HLA-DRB1</i> locus

    An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the <i>HLA-DRB1</i> locus by Gabriele C. DeLuca, S. V. Ramagopalan, Blanca Herrera, David A. Dyment, Matthew R. Lincoln, Alexandre Montpetit, Maura Pugliatti, Martin Barnardo, Neil Risch, A. Dessa Sadovnick, Melody Chao, Stefano Sotgiu, Thomas J. Hudson, George C. Ebers

    Published 2007
    Get full text
    Artigo
    Save to List
    Saved in:
  17. 17
    De novo substitutions of TRPM3 cause intellectual disability and epilepsy

    De novo substitutions of TRPM3 cause intellectual disability and epilepsy by David A. Dyment, Paulien A. Terhal, Cecilie F. Rustad, Kristian Tveten, Christopher Griffith, Parul Jayakar, Marwan Shinawi, Sara Ellingwood, Rosemarie Smith, Koen L.I. van Gassen, Kirsty McWalter, A. Micheil Innes, Matthew A. Lines

    Published 2019
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  18. 18
    Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the <i>TYK2</i> gene

    Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the <i>TYK2</i> gene by David A. Dyment, M. Zameel Cader, Michael J. Chao, Matthew R. Lincoln, Katie Morrison, Giulio Disanto, Julia M. Morahan, Gabriele C. DeLuca, A. Dessa Sadovnick, Pierre Lepage, Alexandre Montpetit, George C. Ebers, Sreeram V. Ramagopalan

    Published 2012
    Get full text
    Artigo
    Save to List
    Saved in:
  19. 19
    BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations

    BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations by Anindita Basak, Miroslava Hančárová, Jacob C. Ulirsch, Tuğçe B. Balcı, Marie Trková, Michal Pelisek, Markéta Vlčková, Kateřina Mužíková, Jaroslav Čermák, Jan Trka, David A. Dyment, Stuart H. Orkin, Mark J. Daly, Zdeněk Sedláček, Vijay G. Sankaran

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  20. 20
    DNM1L-related mitochondrial fission defect presenting as refractory epilepsy

    DNM1L-related mitochondrial fission defect presenting as refractory epilepsy by Jason Vanstone, Amanda M Smith, Skye McBride, Thierry Naas, Martin Holčı́k, Ghadi Antoun, Mary‐Ellen Harper, Jean Michaud, Erick Sell, Pranesh Chakraborty, Martine Tétreault, Jacek Majewski, Stephen Baird, Kym M. Boycott, David A. Dyment, Alex MacKenzie, Matthew A. Lines

    Published 2015
    Get full text Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: