(Q33910046)

30 July 2017

title

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

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30 July 2017

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coronary artery disease

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32

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Margaret A. Pericak-Vance

30 July 2017

33

Margaret A Pericak-Vance

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Li-Ling Huang

Liling Huang

19

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Sheila E. Francis

Sheila Francis

16

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William E. Kraus

William E Kraus

34

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Christopher B. Granger

3

Christopher B Granger

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30 July 2017

4

Jonathan L Haines

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30 July 2017

Elizabeth R Hauser

1

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30 July 2017

David C Crossman

2

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30 July 2017

Christopher J H Jones

5

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30 July 2017

Vincent Mooser

6

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30 July 2017

Brendan McAdam

7

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30 July 2017

Bernhard R Winkelmann

8

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30 July 2017

Alan H Wiseman

9

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30 July 2017

J Brent Muhlestein

10

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30 July 2017

Alan G Bartel

11

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30 July 2017

Charles A Dennis

12

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30 July 2017

Elaine Dowdy

13

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30 July 2017

Susan Estabrooks

14

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30 July 2017

Karen Eggleston

15

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30 July 2017

Kath Roche

17

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30 July 2017

Paula W Clevenger

18

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30 July 2017

Bonnie Pedersen

20

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30 July 2017

Svati Shah

21

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30 July 2017

Silke Schmidt

22

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30 July 2017

Carol Haynes

23

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30 July 2017

Sandra West

24

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30 July 2017

Donny Asper

25

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30 July 2017

Michael Booze

26

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30 July 2017

Sanjay Sharma

27

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30 July 2017

Scott Sundseth

28

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30 July 2017

Lefkos Middleton

29

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30 July 2017

Allen D Roses

30

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30 July 2017

Michael A Hauser

31

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30 July 2017

language of work or name

English

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publication date

22 July 2004

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American Journal of Human Genetics

30 July 2017

published in

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30 July 2017

volume

75

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30 July 2017

issue

3

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30 July 2017

page(s)

436-447

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

30 July 2017

cites work

1 reference

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Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24.

28 July 2018

1 reference

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Evaluating the results of genomewide linkage scans of complex traits by locus counting

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Estimation of allele frequencies with data on sibships

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Genetics of lipoprotein abnormalities associated with coronary artery disease susceptibility

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Improved inference of relationship for pairs of individuals

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Association mapping in structured populations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Comprehensive human genetic maps: individual and sex-specific variation in recombination

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Allele-sharing models: LOD scores and accurate linkage tests

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Accurate inference of relationships in sib-pair linkage studies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Atherogenic dyslipidemia: lipoprotein abnormalities and implications for therapy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Familial occurrence of coronary heart disease: Effect of age at diagnosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Pedigree generation for analysis of genetic linkage and association.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Genome-wide search for type 2 diabetes/impaired glucose homeostasis susceptibility genes in the Chinese: significant linkage to chromosome 6q21-q23 and chromosome 1q21-q24.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Confirmed Locus on Chromosome 11p and Candidate Loci on 6q and 8p for the Triglyceride and Cholesterol Traits of Combined Hyperlipidemia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Meta-analysis of 4 coronary heart disease genome-wide linkage studies confirms a susceptibility locus on chromosome 3q.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

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.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Familial resemblance of plasma lipids, lipoproteins and postheparin lipoprotein and hepatic lipases in the HERITAGE Family Study.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182022

Ordered subset analysis in genetic linkage mapping of complex traits

29 October 2018

1 reference

12 December 2020

Familial resemblance for abdominal visceral fat: the HERITAGE family study

1 reference

12 December 2020

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

1 reference

12 December 2020

A genome search identifies major quantitative trait loci on human chromosomes 3 and 4 that influence cholesterol concentrations in small LDL particles

1 reference

12 December 2020

Contribution of major cardiovascular risk factors to familial premature coronary artery disease: the GENECARD project

1 reference

12 December 2020

A locus influencing total serum cholesterol on chromosome 19p: results from an autosomal genomic scan of serum lipid concentrations in Pima Indians

1 reference

12 December 2020

Familial Patterns of Covariation for Cardiovascular Risk Factors in Adults: The Victorian Family Heart Study

1 reference

12 December 2020

Familial resemblance in fatness and fat distribution

1 reference

12 December 2020

Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations

1 reference

12 December 2020

Confirmation of susceptibility gene loci on chromosome 1 in northern China Han families with type 2 diabetes

1 reference

12 December 2020

Family history as an independent risk factor for coronary artery disease

1 reference

12 December 2020

Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham Study

1 reference

12 December 2020

Identifiers

DOI

10.1086/423900

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30 July 2017

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30 July 2017

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