(Q79966617)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15100713%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

title

Are common disease susceptibility alleles the same in outbred and founder populations? (English)

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27 December 2019

14

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27 December 2019

author name string

Dina L Newman

1

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27 December 2019

Sabine Hoffjan

2

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27 December 2019

Catherine Bourgain

3

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27 December 2019

Mark Abney

4

1 reference

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27 December 2019

Raluca I Nicolae

5

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27 December 2019

Elle T Profits

6

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27 December 2019

Michael A Grow

7

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27 December 2019

Karen Walker

8

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27 December 2019

Lori Steiner

9

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27 December 2019

Rodney Parry

10

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27 December 2019

Rebecca Reynolds

11

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27 December 2019

Mary Sara McPeek

12

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27 December 2019

Suzanne Cheng

13

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27 December 2019

publication date

1 July 2004

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European Journal of Human Genetics

27 December 2019

published in

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27 December 2019

volume

12

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27 December 2019

issue

7

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27 December 2019

page(s)

584-590

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201191

27 December 2019

exact match

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Positional cloning of disease genes: advantages of genetic isolates

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The genetic dissection of complex traits in a founder population

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THE DISTRIBUTION OF CERTAIN GENES IN THE OLD ORDER AMISH.

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7 January 2021

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7 January 2021

Database for the mutations of the Finnish disease heritage

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7 January 2021

The founder effect in a human isolate: Evolutionary implications

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7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

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7 January 2021

Estimation of variance components of quantitative traits in inbred populations

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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

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

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7 January 2021

Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree

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7 January 2021

A multilocus genotyping assay for candidate markers of cardiovascular disease risk

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7 January 2021

Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy

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7 January 2021

Genetic cholesteryl ester transfer protein deficiency caused by two prevalent mutations as a major determinant of increased levels of high density lipoprotein cholesterol

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7 January 2021

Inflammation in atherosclerosis

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7 January 2021

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

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7 January 2021

Cardiovascular Health in Childhood: A Statement for Health Professionals From the Committee on Atherosclerosis, Hypertension, and Obesity in the Young (AHOY) of the Council on Cardiovascular Disease in the Young, American Heart Association

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7 January 2021

The gene encoding atrial natriuretic peptide and the risk of human stroke

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7 January 2021

Assessing population differentiation and isolation from single-nucleotide polymorphism data

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7 January 2021

The apoAI-CIII-AIV gene cluster

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7 January 2021

Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review

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7 January 2021

LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis

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7 January 2021

Association of DNA-haplotypes in the human LDL-receptor gene with normal serum cholesterol levels

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7 January 2021

Association between common alleles of the low-density lipoprotein receptor gene region and interindividual variation in plasma lipid and apolipoprotein levels in a population-based sample from Rochester, Minnesota.

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Phenotypic variation in patients heterozygous for familial defective apolipoprotein B (FDB) in three European countries.

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Role of common genetic polymorphisms in the LDL receptor gene in affecting plasma cholesterol levels in the general population

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7 January 2021

Cholesteryl ester transfer protein: a novel target for raising HDL and inhibiting atherosclerosis

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7 January 2021

New functional promoter polymorphism, CETP/-629, in cholesteryl ester transfer protein (CETP) gene related to CETP mass and high density lipoprotein cholesterol levels: role of Sp1/Sp3 in transcriptional regulation

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7 January 2021

Haplotype analysis of the CETP gene: not TaqIB, but the closely linked -629C-->A polymorphism and a novel promoter variant are independently associated with CETP concentration

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Plasma lipoprotein(a) levels and expression of the apolipoprotein(a) gene are dependent on the nucleotide polymorphisms in its 5'-flanking region

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Detection of polymorphisms in the 5'-flanking region of the gene for apolipoprotein(a)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201191

7 January 2021

Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium

1 reference

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7 January 2021

Variation in the interleukin 4-receptor alpha gene confers susceptibility to asthma and atopy in ethnically diverse populations

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7 January 2021

Sequence variation in the promoter region of the cholinergic receptor muscarinic 3 gene and asthma and atopy

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7 January 2021

Variation in the HLA-G Promoter Region Influences Miscarriage Rates

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7 January 2021

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

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7 January 2021

Cost-effective designs for linkage disequilibrium mapping of complex traits

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7 January 2021

Best linear unbiased allele-frequency estimation in complex pedigrees.

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7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201191

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15100713%20AND%20SRC:MED&resulttype=core&format=json

27 December 2019

1 reference