(Q24811421)

7

object named as

Patrick T Ellinor

0 references

Christopher J O'Donnell

2

object named as

Christopher J O'Donnell

0 references

author name string

Adrian F Low

1

0 references

Brendan Everett

4

0 references

Claudia U Chae

5

0 references

Stanley Y Shaw

6

0 references

Calum A MacRae

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

8

0 references

language of work or name

English

0 references

publication date

31 October 2005

0 references

published in

BMC Medical Genetics

0 references

volume

6

0 references

issue

1

0 references

page(s)

38

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Monogenic hypercholesterolemia: new insights in pathogenesis and treatment

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Association of human aging with a functional variant of klotho

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Initial sequencing and analysis of the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Assessing the impact of population stratification on genetic association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

The structure of haplotype blocks in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Life at the edge: the nuclear envelope and human disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Angiogenesis and vasculogenesis are impaired in the precocious-aging klotho mouse

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Lamin a truncation in Hutchinson-Gilford progeria.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

KLOTHO allele status and the risk of early-onset occult coronary artery disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Problems of reporting genetic associations with complex outcomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

A bias-ed assessment of the use of SNPs in human complex traits

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Association study designs for complex diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

The genesis of atherosclerosis and risk factors: a review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Population-based family study designs: an interdisciplinary research framework for genetic epidemiology

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1289285

Elevated serum C-reactive protein and free fatty acids among nondiabetic carriers of missense mutations in the gene encoding lamin A/C (LMNA) with partial lipodystrophy

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-6-38

Asymptotic power of chi square tests for linear trends in proportions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-6-38

Major risk factors as antecedents of fatal and nonfatal coronary heart disease events

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-6-38

SNP judgments and freedom of association

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16262891

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16262891

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Population–based family study designs: An interdisciplinary research framework for genetic epidemiology

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-6-38

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1186/1471-2350-6-38

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4768566

Dimensions Publication ID

1050831449

0 references

OpenCitations bibliographic resource ID

4768566

1 reference