FAQ

17q12

A chromosome band present on 17q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1981-2018
010203019812018

Related topics

Related topics

10 relations
17qASIC2 wt AlleleCCL1 wt AlleleCCL23 wt Allele
(More)

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
17q12
Chromosomes
17q
ASIC2 wt Allele
CCL1 wt Allele
CCL4 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
Autism spectrum disorders (ASD) and schizophrenia are neurodevelopmental disorders for which recent evidence indicates an… (More)
  • figure 1
  • table 1
  • figure 2
  • table 2
  • table 3
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis
We genotyped individuals with primary biliary cirrhosis and unaffected controls for suggestive risk loci (genome-wide association… (More)
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis
A genome-wide association screen for primary biliary cirrhosis risk alleles was performed in an Italian cohort. The results from… (More)
  • table 2
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Twenty bone mineral density loci identified by large-scale meta-analysis of genome-wide association studies
Bone mineral density (BMD) is a heritable complex trait used in the clinical diagnosis of osteoporosis and the assessment of… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2009
Highly Cited
2009
Common variants at ten loci influence QT interval duration in the QTGEN Study
QT interval duration, reflecting myocardial repolarization on the electrocardiogram, is a heritable risk factor for sudden… (More)
  • table 1
  • figure 1
  • figure 2
  • table 3
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Evidence for two independent prostate cancer risk–associated loci in the HNF1B gene at 17q12
We carried out a fine-mapping study in the HNF1B gene at 17q12 in two study populations and identified a second locus associated… (More)
  • figure 1
  • table 1
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.
Most studies of genomic disorders have focused on patients with cognitive disability and/or peripheral nervous system defects. In… (More)
Is this relevant?
Highly Cited
2006
Highly Cited
2006
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
Genomic disorders are characterized by the presence of flanking segmental duplications that predispose these regions to recurrent… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2006
Highly Cited
2006
Frequency, prognostic impact, and subtype association of 8p12, 8q24, 11q13, 12p13, 17q12, and 20q13 amplifications in breast cancers
Oncogene amplification and overexpression occur in tumor cells. Amplification status may provide diagnostic and prognostic… (More)
  • table 1
  • table 2
  • table 3
  • table 4
  • table 5
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization.
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?