Literature DB >> 15660514

Definition and clinical importance of haplotypes.

Dana C Crawford1, Deborah A Nickerson.   

Abstract

Advances in genotyping and sequencing technologies, coupled with the development of sophisticated statistical methods, have afforded investigators novel opportunities to define the role of sequence variation in the development of common human diseases. At the forefront of these investigations is the use of dense maps of single-nucleotide polymorphisms (SNPs) and the haplotypes derived from these polymorphisms. Here we review basic concepts of high-density genetic maps of SNPs and haplotypes and how they are typically generated and used in human genetic research. We also provide useful examples and tools available for researchers interested in incorporating haplotypes into their studies. Finally, we discuss the latest concepts for the analysis of haplotypes related to human disease, including haplotype blocks, the International HapMap Project, and the future directions of these resources.

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Year:  2005        PMID: 15660514     DOI: 10.1146/annurev.med.56.082103.104540

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  75 in total

1.  Genetic polymorphisms of the organic cation transporter 1 gene (SLC22A1) within the Cape Admixed population of South Africa.

Authors:  Morne Du Plessis; Brendon Pearce; Clifford Jacobs; Nisreen Hoosain; Mongi Benjeddou
Journal:  Mol Biol Rep       Date:  2014-11-15       Impact factor: 2.316

2.  Choline intake and genetic polymorphisms influence choline metabolite concentrations in human breast milk and plasma.

Authors:  Leslie M Fischer; Kerry Ann da Costa; Joseph Galanko; Wei Sha; Brigitte Stephenson; Julie Vick; Steven H Zeisel
Journal:  Am J Clin Nutr       Date:  2010-06-09       Impact factor: 7.045

3.  The value of molecular haplotypes in a family-based linkage study.

Authors:  E M Gillanders; J V Pearson; A J M Sorant; J M Trent; J R O'Connell; J E Bailey-Wilson
Journal:  Am J Hum Genet       Date:  2006-06-28       Impact factor: 11.025

4.  A novel strategy for defining haplotypes by selective depletion using restriction enzymes.

Authors:  Anna S Smirnova; Kátia C Ferreira-Silva; Karina L Mine; Vinicius Andrade-Oliveira; Natalia Shulzhenko; Maria Gerbase-DeLima; Andrey Morgun
Journal:  Immunogenetics       Date:  2006-12-05       Impact factor: 2.846

5.  Haplotype diversity in four genes (CLCNKA, CLCNKB, BSND, NEDD4L) involved in renal salt reabsorption.

Authors:  Saba Sile; Digna R Velez; Niloufar B Gillani; Charles A Alexander; Charles R Alexander; Alfred L George; Scott M Williams
Journal:  Hum Hered       Date:  2007-07-25       Impact factor: 0.444

6.  DNA: where to now?

Authors:  John Beilby
Journal:  Clin Biochem Rev       Date:  2007-05

7.  Endothelial nitric oxide synthase polymorphisms and haplotypes in genetic epidemiology and pharmacogenetics: remarks regarding a lack of association on the risk of myocardial infarction.

Authors:  Marcelo Rizzatti Luizon
Journal:  Mol Biol Rep       Date:  2014-01-07       Impact factor: 2.316

8.  Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.

Authors:  Shannon L Rhodes; Daniel D Buchanan; Ismaïl Ahmed; Kent D Taylor; Marie-Anne Loriot; Janet S Sinsheimer; Jeff M Bronstein; Alexis Elbaz; George D Mellick; Jerome I Rotter; Beate Ritz
Journal:  Neurobiol Dis       Date:  2013-10-08       Impact factor: 5.996

9.  Genetic basis for adverse events after smallpox vaccination.

Authors:  David M Reif; Brett A McKinney; Alison A Motsinger; Stephen J Chanock; Kathryn M Edwards; Michael T Rock; Jason H Moore; James E Crowe
Journal:  J Infect Dis       Date:  2008-07-01       Impact factor: 5.226

10.  Nutrigenomics and metabolomics will change clinical nutrition and public health practice: insights from studies on dietary requirements for choline.

Authors:  Steven H Zeisel
Journal:  Am J Clin Nutr       Date:  2007-09       Impact factor: 7.045

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