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15q26.3

A chromosome band present on 15q
National Institutes of Health

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4 relations
15qChromosomesHSP90B2P wt AlleleIL16 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Novel fusion transcripts in bladder cancer identified by RNA-seq.
2013
2013
Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans
The following information was missing from the Funding section: "This work has been supported in part by grants to M. Lathrop… 
2012
2012
Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample
The majority of genetic risk factors for major depressive disorder (MDD) still await identification. Since copy number variants… 
Highly Cited
2012
Highly Cited
2012
Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations.
Central corneal thickness (CCT) is a highly heritable trait. Genes that significantly influence CCT can be candidate genes for… 
Review
2009
Review
2009
Two short children born small for gestational age with insulin-like growth factor 1 receptor haploinsufficiency illustrate the heterogeneity of its phenotype.
CONTEXT Small for gestational age (SGA)-born children comprise a heterogeneous group in which only few genetic causes have been… 
Highly Cited
2009
Highly Cited
2009
Phenotype–genotype correlation in a familial IGF1R microdeletion case
Background IGF1R (insulin-like growth factor 1 receptor) haploinsufficiency is a rare event causing difficulties in defining… 
Highly Cited
2007
Highly Cited
2007
Genome-Wide Scans for Diabetic Nephropathy and Albuminuria in Multiethnic Populations
The Family Investigation of Nephropathy and Diabetes (FIND) was initiated to map genes underlying susceptibility to diabetic… 
Review
2005
Review
2005
Advances in the genetic basis of coronary artery disease
Exciting advances have been made recently in genetic studies of coronary artery disease (CAD), myocardial infarction (MI), and… 
Highly Cited
2001
Highly Cited
2001
Human synemin gene generates splice variants encoding two distinct intermediate filament proteins.
Intermediate filament (IF) proteins are constituents of the cytoskeleton, conferring resistance to mechanical stress, and are… 
Highly Cited
1993
Highly Cited
1993
Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
An 11-year-old girl with de novo r(15) (p12q26.3) with a clinical diagnosis of Silver-Russell syndrome (SRS) is presented. She… 
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