(Q34137411)

English

A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study

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scholarly article

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Europe PubMed Central

31 July 2017

A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study (English)

1 reference

Europe PubMed Central

31 July 2017

coronary artery disease

1 reference

based on heuristic

inferred from title

1

object named as

Nilesh J Samani

1 reference

Europe PubMed Central

31 July 2017

Massimo Mangino

3

object named as

Massimo Mangino

1 reference

Europe PubMed Central

31 July 2017

author name string

Paul Burton

2

1 reference

Europe PubMed Central

31 July 2017

Stephen G Ball

4

1 reference

Europe PubMed Central

31 July 2017

Anthony J Balmforth

5

1 reference

Europe PubMed Central

31 July 2017

Jenny Barrett

6

1 reference

Europe PubMed Central

31 July 2017

Timothy Bishop

7

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Europe PubMed Central

31 July 2017

Alistair Hall

8

1 reference

Europe PubMed Central

31 July 2017

BHF Family Heart Study Research Group

9

1 reference

Europe PubMed Central

31 July 2017

language of work or name

0 references

publication date

25 October 2005

1 reference

Europe PubMed Central

31 July 2017

American Journal of Human Genetics

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Europe PubMed Central

31 July 2017

77

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Europe PubMed Central

31 July 2017

1011-1020

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Europe PubMed Central

31 July 2017

6

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Europe PubMed Central

31 July 2017

describes a project that uses

1 reference

Europe PubMed Central

26 June 2022

https://europepmc.org/article/PMC/PMC1285159

based on heuristic

inferred from PubMed Central ID database lookup

Whole-genome patterns of common DNA variation in three human populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

A combined linkage-physical map of the human genome

1 reference

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5 July 2018

Genetics of atherosclerosis

1 reference

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5 July 2018

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

1 reference

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5 July 2018

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

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Genomewide linkage analysis for internal carotid artery intimal medial thickness: evidence for linkage to chromosome 12.

1 reference

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Mutation of MEF2A in an inherited disorder with features of coronary artery disease

1 reference

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A high-resolution recombination map of the human genome

1 reference

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5 July 2018

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

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5 July 2018

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Allegro, a new computer program for multipoint linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Replication of linkage studies of complex traits: an examination of variation in location estimates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Allele-sharing models: LOD scores and accurate linkage tests

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Construction of multilocus genetic linkage maps in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

5 July 2018

Polymorphisms of the interleukin-1beta gene affect the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to stimulation in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

MAP-O-MAT: internet-based linkage mapping.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

Bias toward the null hypothesis in model-free linkage analysis is highly dependent on the test statistic used

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

Relationship estimation in affected sib pair analysis of late-onset diseases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

A class of tests for linkage using affected pedigree members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1285159

28 October 2018

GRR: graphical representation of relationship errors

1 reference

https://pubmed.ncbi.nlm.nih.gov/16380912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ordered subset analysis in genetic linkage mapping of complex traits

1 reference

https://pubmed.ncbi.nlm.nih.gov/16380912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic susceptibility to death from coronary heart disease in a study of twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/16380912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of coronary artery disease: measuring the phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16380912

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

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