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1q41

A chromosome band present on 1q
National Institutes of Health

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5 relations
ChromosomesDUSP10 wt AlleleMIR215 wt AlleleTGFB2 wt Allele

Papers overview

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2016
2016
Association of the genetic markers for myocardial infarction with sudden cardiac death
2013
2013
Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.
Genome-wide association studies of colorectal cancer (CRC) in Europeans and Asians have identified 21 risk susceptibility regions… 
Highly Cited
2011
Highly Cited
2011
Association of SNP rs17465637 on Chromosome 1q41 and rs599839 on 1p13.3 with Myocardial Infarction in an American Caucasian Population
Recent genome‐wide single nucleotide polymorphism (SNP) association studies (GWAS) have identified a number of SNPs that were… 
Highly Cited
2000
Highly Cited
2000
Comparative genomic hybridization reveals complex genetic changes in primary breast cancer tumors and their cell lines.
Highly Cited
1999
Highly Cited
1999
Confirmation of genetic linkage between human systemic lupus erythematosus and chromosome 1q41.
OBJECTIVE Genetic susceptibility to systemic lupus erythematosus (SLE) is undoubtedly complex and, presumably, involves multiple… 
1998
1998
Further refinement of the Usher 2A locus at 1q41.
Usher syndrome (USH) is characterised by congenital sensorineural hearing loss and progressive pigmentary retinopathy. All three… 
1997
1997
Assignment of STK6 to human chromosome 20q13.2-->q13.3 and a pseudogene STK6P to 1q41-->q42.
Fluorescence in situ hybridization analysis of human STK6 encoding a mitotic centrosomal protein kinase, Aik, revealed two… 
1996
1996
The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41.
The gene for Usher syndrome type II (USH2A), an autosomal recessive syndromic deafness, has been mapped to a region of 1q41… 
1996
1996
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families.
1995
1995
New heritable fragile site with spontaneous expression at 1q41.
The report presents a family ascertained through recurrent spontaneous abortions in which a new heritable fragile site located at… 
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