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Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study
We performed variance components linkage analysis in nuclear families from the Framingham Heart Study on nine phenotypes derived from systolic blood pressure (SBP). The phenotypes were the maximum and mean SBP, and SBP at age 40, each analyzed either uncorrected, or corrected using two subsets of ep...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866475/ https://www.ncbi.nlm.nih.gov/pubmed/14975072 http://dx.doi.org/10.1186/1471-2156-4-S1-S4 |
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author | Byng, Martyn C Fisher, Sheila A Lewis, Cathryn M Whittaker, John C |
author_facet | Byng, Martyn C Fisher, Sheila A Lewis, Cathryn M Whittaker, John C |
author_sort | Byng, Martyn C |
collection | PubMed |
description | We performed variance components linkage analysis in nuclear families from the Framingham Heart Study on nine phenotypes derived from systolic blood pressure (SBP). The phenotypes were the maximum and mean SBP, and SBP at age 40, each analyzed either uncorrected, or corrected using two subsets of epidemiological/clinical factors. Evidence for linkage to chromosome 8p was detected with all phenotypes except the uncorrected maximum SBP, suggesting this region harbors a gene contributing to variation in SBP. |
format | Text |
id | pubmed-1866475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18664752007-05-11 Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study Byng, Martyn C Fisher, Sheila A Lewis, Cathryn M Whittaker, John C BMC Genet Proceedings We performed variance components linkage analysis in nuclear families from the Framingham Heart Study on nine phenotypes derived from systolic blood pressure (SBP). The phenotypes were the maximum and mean SBP, and SBP at age 40, each analyzed either uncorrected, or corrected using two subsets of epidemiological/clinical factors. Evidence for linkage to chromosome 8p was detected with all phenotypes except the uncorrected maximum SBP, suggesting this region harbors a gene contributing to variation in SBP. BioMed Central 2003-12-31 /pmc/articles/PMC1866475/ /pubmed/14975072 http://dx.doi.org/10.1186/1471-2156-4-S1-S4 Text en Copyright © 2003 Byng et al; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Proceedings Byng, Martyn C Fisher, Sheila A Lewis, Cathryn M Whittaker, John C Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title | Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title_full | Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title_fullStr | Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title_full_unstemmed | Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title_short | Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study |
title_sort | variance components linkage analysis for adjusted systolic blood pressure in the framingham heart study |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866475/ https://www.ncbi.nlm.nih.gov/pubmed/14975072 http://dx.doi.org/10.1186/1471-2156-4-S1-S4 |
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