FAQ

16p12

A chromosome band present on 16p
National Institutes of Health

Topic mentions per year

Topic mentions per year

1980-2018
0519802018

Related topics

Related topics

3 relations
Chromosome 16 Short ArmChromosomesGTF3C1 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
16p12
Chromosomes
Chromosome 16 Short Arm
GTF3C1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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… (More)
  • figure 1
  • table 1
Is this relevant?
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… (More)
Is this relevant?
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… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2004
2004
Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12
Age-related macular degeneration (AMD) is a complex disorder that is responsible for the majority of central vision loss in older… (More)
  • table 1
  • table 2
  • table 3
Is this relevant?
2003
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… (More)
Is this relevant?
2002
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… (More)
  • figure 1
  • table 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
2001
2001
Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.
BACKGROUND Autosomal-dominant medullary cystic kidney disease (MCKD) is an interstitial nephropathy characterized by structural… (More)
Is this relevant?
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… (More)
  • table 1
  • table 2
  • table 3
  • table 4
Is this relevant?
1999
1999
Identification of a new locus for medullary cystic disease, on chromosome 16p12.
Autosomal dominant medullary cystic disease (ADMCKD) is an interstitial nephropathy that has morphologic and clinical features… (More)
Is this relevant?
1999
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… (More)
Is this relevant?