(Q36078055)

12 August 2017

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title

Complex trait mapping in isolated populations: Are specific statistical methods required? (English)

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12 August 2017

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Catherine Bourgain

1

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PubMed ID

15785775

12 August 2017

Emmanuelle Génin

series ordinal

2

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12 August 2017

1 June 2005

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European Journal of Human Genetics

12 August 2017

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12 August 2017

13

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12 August 2017

698-706

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12 August 2017

6

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201400

12 August 2017

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cites work

Gene finding in genetically isolated populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Positional cloning of disease genes: advantages of genetic isolates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Population isolates: their special value for locating genes for bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Population choice in mapping genes for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The role of linkage studies for common diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Anxiety with panic disorder linked to chromosome 9q in Iceland

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Familial Aggregation of Parkinson's Disease in Iceland

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genomewide Scan for Hand Osteoarthritis: A Novel Mutation in Matrilin-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Linkage of essential hypertension to chromosome 18q.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Linkage of osteoporosis to chromosome 20p12 and association to BMP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Localization of a gene for migraine without aura to chromosome 4q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Localization of a susceptibility gene for common forms of stroke to 5q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A major susceptibility gene for asthma maps to chromosome 14q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A susceptibility gene for late-onset idiopathic Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A susceptibility gene for psoriatic arthritis maps to chromosome 16q: evidence for imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Allegro, a new computer program for multipoint linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genome scanning for segments shared identical by descent among distant relatives in isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genomic mismatch scanning: a new approach to genetic linkage mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Estimation of the inbreeding coefficient through use of genomic data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Multipoint quantitative-trait linkage analysis in general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genes on chromosomes 1 and 13 have significant effects on Ascaris infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Estimation of variance components of quantitative traits in inbred populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Powerful regression-based quantitative-trait linkage analysis of general pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

An empirical test of the significance of an observed quantitative trait locus effect that preserves additive genetic variation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The importance of genealogy in determining genetic associations with complex traits

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Genomic control for association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Detecting association in a case-control study while correcting for population stratification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The power of genomic control

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

From genotypes to genes: doubling the sample size

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Transmission/disequilibrium tests for extended marker haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Family-based tests of association in the presence of linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A test for linkage and association in general pedigrees: the pedigree disequilibrium test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Transmission/disequilibrium tests using multiple tightly linked markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Transmission/disequilibrium test based on haplotype sharing for tightly linked markers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Use of closely related affected individuals for the genetic study of complex diseases in founder populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Association studies for quantitative traits in structured populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Impact of parental relationships in maximum lod score affected sib-pair method

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Properties of the transmission-disequilibrium test in the presence of inbreeding

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

Search for multifactorial disease susceptibility genes in founder populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

The value of isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

7 January 2021

Optimal allele-sharing statistics for genetic mapping using affected relatives

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

7 January 2021

Genomic mismatch scanning identifies human genomic DNA shared identical by descent

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

7 January 2021

Robust LOD scores for variance component-based linkage analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

7 January 2021

Tests for Linear Trends in Proportions and Frequencies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201400

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201400

1 reference

PubMed ID

15785775

Dimensions Publication ID

12 August 2017

0 references

1 reference

PubMed ID

15785775