Use of population isolates for mapping complex traits (Q34185425)

31 July 2017

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title

Use of population isolates for mapping complex traits (English)

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31 July 2017

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Peltonen L

1

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31 July 2017

Palotie A

series ordinal

2

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31 July 2017

Lange K

series ordinal

3

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31 July 2017

publication date

1 December 2000

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31 July 2017

published in

Nature Reviews Genetics

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31 July 2017

volume

1

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31 July 2017

issue

3

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31 July 2017

page(s)

182-190

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Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

31 July 2017

cites work

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A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

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Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

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Dual origins of Finns revealed by Y chromosome haplotype variation

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Linkage disequilibrium mapping in isolated populations: the example of Finland revisited

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Gene mapping in isolated populations: new roles for old friends?

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Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion

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Molecular genetics of the Finnish disease heritage.

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Population choice in mapping genes for complex diseases

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Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

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Genetic mapping of a locus predisposing to human colorectal cancer

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7 January 2021

Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

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7 January 2021

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

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7 January 2021

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Prospects for whole-genome linkage disequilibrium mapping of common disease genes

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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene

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The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

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Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

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The power to detect linkage in complex disease by means of simple LOD-score analyses

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Effects of misspecifying genetic parameters in lod score analysis.

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Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases

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The future of genetic studies of complex human diseases

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A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

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Sibling-based tests of linkage and association for quantitative traits

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Genetic association mapping based on discordant sib pairs: the discordant-alleles test

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A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

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Use of parents, sibs, and unrelated controls for detection of associations between genetic markers and disease

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Gamete-competition models

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Mapping a disease locus by allelic association

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Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium

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Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

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Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

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Multipoint oligogenic linkage analysis of quantitative traits.

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Extensions to multivariate normal models for pedigree analysis

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fw2.2: a quantitative trait locus key to the evolution of tomato fruit size

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Estimating Scandinavian and Gaelic ancestry in the male settlers of Iceland

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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

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A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

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7 January 2021

Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma

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7 January 2021

A genome-wide search for asthma susceptibility loci in ethnically diverse populations. The Collaborative Study on the Genetics of Asthma (CSGA)

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7 January 2021

A genome-wide search for type 2 diabetes susceptibility genes in Utah Caucasians

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7 January 2021

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

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7 January 2021

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

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7 January 2021

A putative vulnerability locus to multiple sclerosis maps to 5p14-p12 in a region syntenic to the murine locus Eae2

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7 January 2021

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

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7 January 2021

An international two–stage genome–wide search for schizophrenia susceptibility genes

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7 January 2021

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

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7 January 2021

Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search

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7 January 2021

Predisposing gene for early-onset prostate cancer, localized on chromosome 1q42.2-43

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7 January 2021

Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics

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7 January 2021

Identifiers

DOI

10.1038/35042049

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Dimensions Publication ID

31 July 2017

1025984469

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