ArticleAmerican journal of human genetics2004
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia.
Article in American journal of human genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.
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Who cites it
21 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.
- Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.PloS one · 2016Pooled it
- GENLIB: new function to simulate haplotype transmission in large complex genealogies.Bioinformatics (Oxford, England) · 2023Article
- Complete mitochondrial sequences from Mesolithic Sardinia.Scientific reports · 2017Article
- Path-counting formulas for generalized kinship coefficients and condensed identity coefficients.Computational and mathematical methods in medicine · 2014Article
- A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.Bioinformatics (Oxford, England) · 2013Article
- Environmental and genetic contribution to hypertension prevalence: data from an epidemiological survey on Sardinian genetic isolates.PloS one · 2013Article
- Efficient path-based computations on pedigree graphs with compact encodings.BMC bioinformatics · 2012Article
- A two-step genetic study on quantitative precursors of coronary artery disease in a homogeneous Indian population: case-control association discovery and validation by transmission-disequilibrium test.Journal of biosciences · 2011Article
- Identity by descent estimation with dense genome-wide genotype data.Genetic epidemiology · 2011Article
- Genetics of VEGF serum variation in human isolated populations of cilento: importance of VEGF polymorphisms.PloS one · 2011Article
- Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.PLoS genetics · 2011Article
- Comparing population structure as inferred from genealogical versus genetic information.European journal of human genetics : EJHG · 2009Article
- Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.Human molecular genetics · 2009Article
- Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations.BMC medical genetics · 2009Article
- A multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12.Genetic epidemiology · 2009Article
- Linkage analysis with dense SNP maps in isolated populations.Human heredity · 2009Article
- Linkage mapping of CVD risk traits in the isolated Norfolk Island population.Human genetics · 2008Article
- Identity-by-descent estimation and mapping of qualitative traits in large, complex pedigrees.Genetics · 2008Article
- A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.American journal of human genetics · 2007Article
- The genetic study of three population microisolates in South Tyrol (MICROS): study design and epidemiological perspectives.BMC medical genetics · 2007Article
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Authors and funding
10 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A powerful approach to mapping the genes for complex traits is to study isolated founder populations, in which genetic heterogeneity and environmental noise are likely to be reduced and in which extended genealogical data are often available. Using graph theory, we applied an approach that involved sampling from the large number of pairwise relationships present in an extended genealogy to reconstruct sets of subpedigrees that maximize the useful information for linkage mapping while minimizing calculation burden. We investigated, through simulation, the properties of the different sets in terms of bias in identity-by-descent (IBD) estimation and power decrease under various genetic models. We applied this approach to a small isolated population from Sardinia, the village of Talana, consisting of a unique large and complex pedigree, and performed a genomewide search through variance-components linkage analysis for serum lipid levels. We identified a region of significant linkage on chromosome 2 for total serum cholesterol and low-density lipoprotein (LDL) cholesterol. Through higher-density mapping, we obtained an increased linkage for both traits on 2q21.2-q24.1, with a LOD score of 4.3 for total serum cholesterol and of 3.9 for LDL cholesterol. A replication study was performed in an independent and larger set from a genetically differentiated isolated population of the same region of Sardinia, the village of Perdasdefogu. We obtained consistent linkage to the region for total serum cholesterol (LOD score 1.4) and LDL cholesterol (LOD score 2.2), with a level of concordance uncommon for complex traits, and refined the location of the quantitative-trait locus. Interestingly, the 2q21.1-22 region has also been linked to premature coronary heart disease in Finns, and, in the adjacent 2q14 region, significant linkage with triglycerides has been reported in Hutterites.
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