Genomewide study of multiple sclerosis [3]

New England Journal of Medicine

Volumn 357, Issue 21, 2007, Pages 2199-2201

  Ramagopalan, Sreeram V ^a   Anderson, Carl ^a   Sadovnick, A Dessa ^b   Ebers, George C ^c  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^c UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE LINKAGE DISEQUILIBRIUM; GENOME; GENOTYPE; HUMAN; LETTER; MULTIPLE SCLEROSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 36348956793     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMc072836     Document Type: Letter

References (5)

1. The International Multiple Sclerosis Genetics Consortium. Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med 2007;357:851-62.
2. Peltonen L. Old suspects found guilty - the first genome profile of multiple sclerosis. N Engl J Med 2007;357:927-9.
3. Chanock SJ, Manolio T, Boehnke M, et al. Replicating genotype-phenotype associations. Nature 2007;447:655-60.
4. Howson JM, Barratt BJ, Todd JA, Cordell HJ. Comparison of population- and family-based methods for genetic association analysis in the presence of interacting loci. Genet Epidemiol 2005;29:51-67.
5. Li M, Boehnke M, Abecasis GR. Efficient study designs for test of genetic association using sibship data and unrelated cases and controls. Am J Hum Genet 2006;78:778-92.