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Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
Smith, Andrew J P; Howard, Philip; Shah, Sonia; Eriksson, Per; Stender, Stefan; Giambartolomei, Claudia; Folkersen, Lasse; Tybjærg-Hansen, Anne; Kumari, Meena; Palmen, Jutta; Hingorani, Aroon D; Talmud, Philippa J; Humphries, Steve E.
Affiliation
  • Smith AJ; Centre for Cardiovascular Genetics, British Heart Foundation Laboratories, Institute of Cardiovascular Sciences, University College London, London, United Kingdom. Andrew.J.P.Smith@ucl.ac.uk
PLoS Genet ; 8(8): e1002908, 2012.
Article in En | MEDLINE | ID: mdl-22916038
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / White People / Alleles / Orphan Nuclear Receptors / Genotyping Techniques / Cholesterol, HDL Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2012 Document type: Article Affiliation country: United kingdom Country of publication: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cardiovascular Diseases / White People / Alleles / Orphan Nuclear Receptors / Genotyping Techniques / Cholesterol, HDL Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2012 Document type: Article Affiliation country: United kingdom Country of publication: United States