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16q23.1

A chromosome band present on 16q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2016
02419842016

Related topics

Related topics

5 relations
16qBCAR1 wt AlleleCTRB1 wt AlleleChromosomes
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Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
16q23.1
Chromosomes
16q
BCAR1 wt Allele
CTRB1 wt Allele
TERF2IP wt Allele

Papers overview

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2015
2015
Hypermethylation of the 16q23.1 Tumor Suppressor Gene ADAMTS18 in Clear Cell Renal Cell Carcinoma
To identify tumor suppressor genes (TSGs) silenced by hypermethylation and discover new epigenetic biomarkers for early cancer… (More)
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2010
2010
Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.
To better understand the molecular mechanisms behind esophageal adenocarcinoma (EAC) tumorigenesis, we used high-density single… (More)
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Highly Cited
2008
Highly Cited
2008
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies
A genome-wide association (GWA) study with pooled DNA in adult attention-deficit/hyperactivity disorder (ADHD) employing ~500K… (More)
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2007
2007
Epigenetic identification of ADAMTS18 as a novel 16q23.1 tumor suppressor frequently silenced in esophageal, nasopharyngeal and multiple other carcinomas
Tumor suppressor genes (TSGs) often locate at chromosomal regions with frequent deletions in tumors. Loss of 16q23 occurs… (More)
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2006
2006
A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.
Congenital cataract, a clinically and genetically highly heterogeneous eye disorder, is one of the significant causes of visual… (More)
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2004
2004
Integration of high-resolution array comparative genomic hybridization analysis of chromosome 16q with expression array data refines common regions of loss at 16q23–qter and identifies underlying…
We have constructed a high-resolution genomic microarray of human chromosome 16q, and used it for comparative genomic… (More)
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Highly Cited
2000
Highly Cited
2000
Concurrent and independent genetic alterations in the stromal and epithelial cells of mammary carcinoma: implications for tumorigenesis.
The high frequency of loss of heterozygosity (LOH) in epithelial cells of mammary ductal carcinoma in situ (DCIS) and IDC is a… (More)
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Highly Cited
2000
Highly Cited
2000
Genetic abnormalities in mammary ductal intraepithelial neoplasia-flat type ("clinging ductal carcinoma in situ"): a simulator of normal mammary epithelium.
BACKGROUND Mammary ductal intraepithelial neoplasia (DIN)-flat type ("clinging ductal carcinoma in situ [DCIS]") generally is a… (More)
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1997
1997
A small deletion of 16q23.1-->16q24.2 [del(16)(q23.1q24.2).ish del(16)(q23.1q24.2)(D16S395+, D16S348-, P5432+)] in a boy with iris coloboma and minor anomalies.
We report on a 5-year-old boy with bilateral coloboma of iris, short stature, moderate developmental delay, and a few minor… (More)
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Highly Cited
1996
Highly Cited
1996
Promiscuous translocations into immunoglobulin heavy chain switch regions in multiple myeloma.
In multiple myeloma, karyotopic 14q32 translocations have been identified at a variable frequency (10-60% in different studies… (More)
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