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6p24.1

A chromosome band present on 6p
National Institutes of Health

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3 relations
Chromosome 6 Short ArmChromosomesEDN1 wt Allele

Papers overview

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2020
2020
Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection.
Importance Spontaneous coronary artery dissection (SCAD), an idiopathic disorder that predominantly affects young to middle-aged… 
2016
2016
Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population
Objectives To study the association of single nucleotide polymorphism (SNP) rs2076185 in chromosome 6p24.1 with the premature… 
2015
2015
Common Variants in Promoter of ADTRP Associate with Early-Onset Coronary Artery Disease in a Southern Han Chinese Population
The first genome-wide association study for coronary artery disease (CAD) in the Han Chinese population, we reported recently… 
2013
2013
Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population.
Highly Cited
2012
Highly Cited
2012
Early platelet activation, inflammation and acute brain injury after a subarachnoid hemorrhage: a pilot study
Mu¨nzel T, Zeller T, et al. A follow-up study of a genome-wide asso-ciation scan identifies a susceptibility locus for venous… 
2012
2012
Association of SNP Rs6903956 on Chromosome 6p24.1 with Angiographical Characteristics of Coronary Atherosclerosis in a Chinese Population
Objective To explore the association between rs6903956 and severity of coronary artery disease (CAD) in a Chinese population… 
Highly Cited
2011
Highly Cited
2011
Association of Genetic Variants and Incident Coronary Heart Disease in Multiethnic Cohorts: The PAGE Study
Background— Genome-wide association studies identified several single nucleotide polymorphisms (SNP) associated with prevalent… 
2009
2009
A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.
2008
2008
Subtelomeric 6p deletion: Clinical and array‐CGH characterization in two patients
We report on two patients with de novo subtelomeric terminal deletion of chromosome 6p. Patient 1 is an 8‐month‐old female born… 
2005
2005
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1‐22.3
Previously, the DFNA21 locus was positioned telomeric to the DFNA13 locus based on testing of candidate loci. One family member… 
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