Literature DB >> 18319711

Primer: SNP-associated studies and what they can teach us.

Ryo Yamada1.   

Abstract

Single-nucleotide polymorphisms (SNPs) are single base-pair alterations in the DNA sequence that represent a major source of genetic heterogeneity. Well-developed and sophisticated technologies exist to measure and analyze the presence of SNPs, and SNP genotyping is an important tool with which to investigate other genetic variants. SNP-based, large-scale, genome-wide association studies are detecting many polymorphisms that can be used to evaluate the risk of various common traits, including rheumatic diseases. This increased knowledge of genetic risk could potentially be used to refine medical care in rheumatology clinics in the near future.

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Year:  2008        PMID: 18319711     DOI: 10.1038/ncprheum0757

Source DB:  PubMed          Journal:  Nat Clin Pract Rheumatol        ISSN: 1745-8382


  3 in total

1.  Evidence of uneven selective pressure on different subsets of the conserved human genome; implications for the significance of intronic and intergenic DNA.

Authors:  Scott Davidson; Andrew Starkey; Alasdair MacKenzie
Journal:  BMC Genomics       Date:  2009-12-16       Impact factor: 3.969

2.  Candidate single nucleotide polymorphism markers for arsenic responsiveness of protein targets.

Authors:  Raphael D Isokpehi; Hari H P Cohly; Matthew N Anyanwu; Rajendram V Rajnarayanan; Paul B Tchounwou; Udensi K Udensi; Barbara E Graham-Evans
Journal:  Bioinform Biol Insights       Date:  2010-10-11

3.  Effects of RHD gene polymorphisms on distinguishing weak D or DEL from RhD- in blood donation in a Chinese population.

Authors:  Jie Shi; Ying Luo
Journal:  Mol Genet Genomic Med       Date:  2019-04-05       Impact factor: 2.183

  3 in total

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