Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
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ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFThe western and eastern roots of the Saami--the story of genetic "outliers" told by mitochondrial DNA and Y chromosomesGenetic markers and population history: Finland revisitedA haplotype map of the human genomeSearch for intracranial aneurysm susceptibility gene(s) using Finnish familiesExome sequencing and complex disease: practical aspects of rare variant association studiesGenome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern EuropeGenomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia studyGenetic basis of sitosterolemiaFine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communitiesGenotype imputation"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.Data mining applied to linkage disequilibrium mappingSimulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Fine mapping suggests that the goat Polled Intersex Syndrome and the human Blepharophimosis Ptosis Epicanthus Syndrome map to a 100-kb homologous region.Detecting population growth, selection and inherited fertility from haplotypic data in humans.Simulating association studies: a data-based resampling method for candidate regions or whole genome scans.Allele frequency matching between SNPs reveals an excess of linkage disequilibrium in genic regions of the human genome.Genetic susceptibility to non-polyposis colorectal cancer.On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.Mutation history of the roma/gypsies.Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1Distribution and medical impact of loss-of-function variants in the Finnish founder population.High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence.Worldwide mutation spectrum in cartilage-hair hypoplasia: ancient founder origin of the major70A-->G mutation of the untranslated RMRP.Haplotype fine mapping by evolutionary treesLinkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions2002 William Allen Award address. Introductory speech for Albert de la Chapelle.A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.Database for the mutations of the Finnish disease heritage.Nationwide registry-based analysis of cancer clustering detects strong familial occurrence of Kaposi sarcoma.Inferring linkage disequilibrium between a polymorphic marker locus and a trait locus in natural populationsModeling linkage disequilibrium between a polymorphic marker locus and a locus affecting complex dichotomous traits in natural populations.Precision and high-resolution mapping of quantitative trait loci by use of recurrent selection, backcross or intercross schemes.Linkage disequilibrium between microsatellite markers extends beyond 1 cM on chromosome 20 in Finns.Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population.Recurrent germline mutation in MSH2 arises frequently de novo.Nationwide prevalence of sporadic and familial idiopathic pulmonary fibrosis: evidence of founder effect among multiplex families in FinlandWill haplotype maps be useful for finding genes?
P2860
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P2860
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
description
1998 nî lūn-bûn
@nan
1998 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@ast
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@en
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@nl
type
label
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@ast
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@en
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@nl
prefLabel
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@ast
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@en
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@nl
P2860
P356
P1476
Linkage disequilibrium mapping in isolated populations: the example of Finland revisited.
@en
P2093
A de la Chapelle
F A Wright
P2860
P304
12416-12423
P356
10.1073/PNAS.95.21.12416
P407
P577
1998-10-01T00:00:00Z