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9q21

A chromosome band present on 9q
National Institutes of Health

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2 relations
ChromosomesGNAQ wt Allele

Papers overview

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2015
2015
Detection of a Distinctive Genomic Signature in Rhabdoid Glioblastoma, A Rare Disease Entity Identified by Whole Exome Sequencing and Whole Transcriptome Sequencing
2006
2006
Maternal Segmental Disomy in Leigh Syndrome with Cytochrome c Oxidase Deficiency Caused by Homozygous SURF1 Mutation
SURF1 SURF1 
2004
2004
Loss of heterozygosity on chromosome 4q32–35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes
Background:  Studies on basal cell carcinoma (BCC) have demonstrated that patched gene and p53 gene located at 9q22.3 and 17p13… 
Highly Cited
2003
Highly Cited
2003
Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees
2003
2003
Two genome-wide linkage disequilibrium screens in Scandinavian multiple sclerosis patients
2003
2003
Tau and neurofilaments in a family with frontotemporal dementia unlinked to chromosome 17q21–22
2001
2001
Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types.
Highly Cited
2001
Highly Cited
2001
Mapping genes that regulate density of dopamine transporters and correlated behaviors in recombinant inbred mice.
Binding of 3beta-(4-iodophenyl) tropane-2beta-carboxylic acid methyl ester ([125I]RTI-55) to the dopamine transporter (DAT) in… 
2000
2000
Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer.
Highly Cited
1996
Highly Cited
1996
Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
The most common genetic alteration identified to date in bladder cancer is loss of heterozygosity (LOH) of chromosome 9… 
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