Literature DB >> 18563468

Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis.

Sreeram V Ramagopalan1, Gabriele C Deluca, Katie M Morrison, Blanca M Herrera, David A Dyment, Matthew R Lincoln, Sarah-Michelle Orton, Michael J Chao, Alexandra Degenhardt, Maura Pugliatti, A Dessa Sadovnick, Stefano Sotgiu, George C Ebers.   

Abstract

Multiple sclerosis (MS) is a common inflammatory disease of the central nervous system unsurpassed for its variability in disease outcome. As little is conclusively known about MS disease mechanisms, we have selected a variety of candidate genes that may influence the prognosis of the disease based on their function. A cohort of sporadic MS cases, taken from opposite extremes of the putative distribution of long-term outcome using the most stringent clinical criteria to date, was used to determine the role of on MS disease severity. The MS cases selected represent the prognostic best 5 % (benign MS) and worst 5 % (malignant MS) of cases in terms of clinical outcome assessed by the EDSS. Genotyping the two sets of MS patients (112 benign and 51 malignant) and a replication cohort from Sardinia provided no evidence to suggest that the genes selected have any outcome modifying activity, although small effects of these genes cannot be ruled out.

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Year:  2008        PMID: 18563468     DOI: 10.1007/s00415-008-0878-7

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  24 in total

1.  The structure of haplotype blocks in the human genome.

Authors:  Stacey B Gabriel; Stephen F Schaffner; Huy Nguyen; Jamie M Moore; Jessica Roy; Brendan Blumenstiel; John Higgins; Matthew DeFelice; Amy Lochner; Maura Faggart; Shau Neen Liu-Cordero; Charles Rotimi; Adebowale Adeyemo; Richard Cooper; Ryk Ward; Eric S Lander; Mark J Daly; David Altshuler
Journal:  Science       Date:  2002-05-23       Impact factor: 47.728

2.  HLA-DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation.

Authors:  O Olerup; H Zetterquist
Journal:  Tissue Antigens       Date:  1992-05

3.  Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits.

Authors:  S Purcell; S S Cherny; P C Sham
Journal:  Bioinformatics       Date:  2003-01       Impact factor: 6.937

4.  Multiple sclerosis in sibling pairs: an analysis of 250 families.

Authors:  J Chataway; A Mander; N Robertson; S Sawcer; J Deans; M Fraser; S Broadley; D Clayton; A Compston
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-12       Impact factor: 10.154

5.  Extreme discordant sib pairs for mapping quantitative trait loci in humans.

Authors:  N Risch; H Zhang
Journal:  Science       Date:  1995-06-16       Impact factor: 47.728

6.  Prognostic factors in a multiple sclerosis incidence cohort with twenty-five years of follow-up.

Authors:  B Runmarker; O Andersen
Journal:  Brain       Date:  1993-02       Impact factor: 13.501

7.  Familial factors influence disability in MS multiplex families. French Multiple Sclerosis Genetics Group.

Authors:  D Brassat; C Azais-Vuillemin; J Yaouanq; G Semana; J Reboul; I Cournu; C Mertens; G Edan; O Lyon-Caen; M Clanet; B Fontaine
Journal:  Neurology       Date:  1999-05-12       Impact factor: 9.910

8.  Autoimmune disease in families with multiple sclerosis: a population-based study.

Authors:  Sreeram Varadharajan Ramagopalan; David Alexandre Dyment; William Valdar; Blanca Marcela Herrera; Maria Criscuoli; Irene Mei Ling Yee; Adele Dessa Sadovnick; George Cornell Ebers
Journal:  Lancet Neurol       Date:  2007-07       Impact factor: 44.182

9.  Persistent functional deficit in multiple sclerosis and autosomal dominant cerebellar ataxia is associated with axon loss.

Authors:  C A Davie; G J Barker; S Webb; P S Tofts; A J Thompson; A E Harding; W I McDonald; D H Miller
Journal:  Brain       Date:  1995-12       Impact factor: 13.501

Review 10.  Neuropathology in multiple sclerosis: new concepts.

Authors:  H Lassmann
Journal:  Mult Scler       Date:  1998-06       Impact factor: 6.312

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  6 in total

Review 1.  Role of HLA class II genes in susceptibility and resistance to multiple sclerosis: studies using HLA transgenic mice.

Authors:  David Luckey; Dikshya Bastakoty; Ashutosh K Mangalam
Journal:  J Autoimmun       Date:  2011-05-31       Impact factor: 7.094

2.  Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.

Authors:  Cathy J Jensen; Jim Stankovich; Anneke Van der Walt; Melanie Bahlo; Bruce V Taylor; Ingrid A F van der Mei; Simon J Foote; Trevor J Kilpatrick; Laura J Johnson; Ella Wilkins; Judith Field; Patrick Danoy; Matthew A Brown; Justin P Rubio; Helmut Butzkueven
Journal:  PLoS One       Date:  2010-04-02       Impact factor: 3.240

3.  HLA-DQ8 (DQB1*0302)-restricted Th17 cells exacerbate experimental autoimmune encephalomyelitis in HLA-DR3-transgenic mice.

Authors:  Ashutosh Mangalam; David Luckey; Eati Basal; Megan Jackson; Michele Smart; Moses Rodriguez; Chella David
Journal:  J Immunol       Date:  2009-04-15       Impact factor: 5.422

Review 4.  The conundrum of iron in multiple sclerosis--time for an individualised approach.

Authors:  Susan J van Rensburg; Maritha J Kotze; Ronald van Toorn
Journal:  Metab Brain Dis       Date:  2012-03-17       Impact factor: 3.584

5.  Gene variants of adhesion molecules act as modifiers of disease severity in MS.

Authors:  Efthimios Dardiotis; Elena Panayiotou; Antonios Provatas; Kyproula Christodoulou; Andreas Hadjisavvas; Athos Antoniades; Athanasios Lourbopoulos; Marios Pantzaris; Nikolaos Grigoriadis; Georgios M Hadjigeorgiou; Theodoros Kyriakides
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2017-04-24

6.  Gene variants of adhesion molecules predispose to MS: A case-control study.

Authors:  Efthimios Dardiotis; Elena Panayiotou; Vasileios Siokas; Athina-Maria Aloizou; Kyproula Christodoulou; Andreas Hadjisavvas; Marios Pantzaris; Nikolaos Grigoriadis; Georgios M Hadjigeorgiou; Theodoros Kyriakides
Journal:  Neurol Genet       Date:  2019-01-16
  6 in total

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