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16p12

A chromosome band present on 16p
National Institutes of Health

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3 relations
Chromosome 16 Short ArmChromosomesGTF3C1 wt Allele

Papers overview

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Highly Cited
2010
Highly Cited
2010
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.
We have performed a genome-wide association study (GWAS) of schizophrenia in a Norwegian discovery sample of 201 cases and 305… Expand
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Highly Cited
2010
Highly Cited
2010
Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases
Chronic kidney disease (CKD) is a worldwide public health problem that is associated with substantial morbidity and mortality. To… Expand
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Highly Cited
2009
Highly Cited
2009
Population analysis of large copy number variants and hotspots of human genetic disease.
Copy number variants (CNVs) contribute to human genetic and phenotypic diversity. However, the distribution of larger CNVs in the… Expand
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Highly Cited
2007
Highly Cited
2007
Integrated profiling of basal and luminal breast cancers.
Basal and luminal are two molecular subtypes of breast cancer with opposite histoclinical features. We report a combined, high… Expand
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Highly Cited
2003
Highly Cited
2003
Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.
We performed a genome-wide scan for susceptibility loci in bipolar disorder in a study sample colleted from the isolated Finnish… Expand
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Highly Cited
2003
Highly Cited
2003
A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.
Familial juvenile hyperuricemic nephropathy (FJHN [MIM 162000]) is an autosomal-dominant disorder characterized by abnormal… Expand
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Highly Cited
2002
Highly Cited
2002
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.
Hereditary predisposition to develop neuroblastoma (Online Mendelian Inheritance in Man 256700), a pediatric cancer of the… Expand
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Highly Cited
2000
Highly Cited
2000
A second-generation genomewide screen for asthma-susceptibility alleles in a founder population.
A genomewide screen for asthma- and atopy-susceptibility loci was conducted, using 563 markers, in 693 Hutterites who are members… Expand
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Highly Cited
1999
Highly Cited
1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2.
We describe a pedigree in which 3 members in the same generation are affected by Rolandic epilepsy (RE), paroxysmal exercise… Expand
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Highly Cited
1998
Highly Cited
1998
Chromosomal and gene amplification in diffuse large B-cell lymphoma.
Chromosomal translocations leading to deregulation of specific oncogenes characterize approximately 50% of cases of diffuse large… Expand
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