17q12

A chromosome band present on 17q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1981-2018
010203019812018

Papers overview

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Highly Cited
2010
Highly Cited
2010
Autism spectrum disorders (ASD) and schizophrenia are neurodevelopmental disorders for which recent evidence indicates an… (More)
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Highly Cited
2010
Highly Cited
2010
We genotyped individuals with primary biliary cirrhosis and unaffected controls for suggestive risk loci (genome-wide association… (More)
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Highly Cited
2010
Highly Cited
2010
A genome-wide association screen for primary biliary cirrhosis risk alleles was performed in an Italian cohort. The results from… (More)
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Highly Cited
2009
Highly Cited
2009
Bone mineral density (BMD) is a heritable complex trait used in the clinical diagnosis of osteoporosis and the assessment of… (More)
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Highly Cited
2009
Highly Cited
2009
QT interval duration, reflecting myocardial repolarization on the electrocardiogram, is a heritable risk factor for sudden… (More)
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Highly Cited
2008
Highly Cited
2008
We carried out a fine-mapping study in the HNF1B gene at 17q12 in two study populations and identified a second locus associated… (More)
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Highly Cited
2007
Highly Cited
2007
Most studies of genomic disorders have focused on patients with cognitive disability and/or peripheral nervous system defects. In… (More)
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Highly Cited
2006
Highly Cited
2006
Genomic disorders are characterized by the presence of flanking segmental duplications that predispose these regions to recurrent… (More)
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Highly Cited
2006
Highly Cited
2006
Oncogene amplification and overexpression occur in tumor cells. Amplification status may provide diagnostic and prognostic… (More)
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Highly Cited
1993
Highly Cited
1993
A Na(+)- and Cl(-)-coupled serotonin (5-hydroxytryptamine, 5HT) transporter is expressed on human neuronal, platelet, placental… (More)
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