Ethnic differences in allele frequency of autoimmune-disease-associated SNPs
Top Cited Papers
- 10 May 2005
- journal article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 50 (5) , 264-266
- https://doi.org/10.1007/s10038-005-0246-8
Abstract
Journal of Human Genetics, official journal of the Japan Society of Human Genetics, publishes original articles and reviews on all aspects of human genetics, including medical genetics and genomicsKeywords
This publication has 15 references indexed in Scilit:
- SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian populationArthritis & Rheumatism, 2005
- A common inversion under selection in EuropeansNature Genetics, 2005
- Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn diseaseJournal of Human Genetics, 2004
- Genetic Association of the R620W Polymorphism of Protein Tyrosine Phosphatase PTPN22 with Human SLEAmerican Journal of Human Genetics, 2004
- A Missense Single-Nucleotide Polymorphism in a Gene Encoding a Protein Tyrosine Phosphatase (PTPN22) Is Associated with Rheumatoid ArthritisAmerican Journal of Human Genetics, 2004
- Functional variants of OCTN cation transporter genes are associated with Crohn diseaseNature Genetics, 2004
- A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetesNature Genetics, 2004
- An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritisNature Genetics, 2003
- A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humansNature Genetics, 2002
- Bayesian Haplotype Inference for Multiple Linked Single-Nucleotide PolymorphismsAmerican Journal of Human Genetics, 2002