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17q11

A chromosome band present on 17q
National Institutes of Health

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17qChromosomesRAD51D wt AlleleSARM1 wt Allele

Papers overview

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Highly Cited
2008
Highly Cited
2008
Genetic profiling of myeloproliferative disorders by single-nucleotide polymorphism oligonucleotide microarray.
2008
2008
Population-based association study and contrasting linkage disequilibrium pattern reveal genetic association of SLC6A4 with autism in the Indian population from West Bengal
2005
2005
Haplotypes within genes of β-chemokines in 17q11 are associated with multiple sclerosis: a second phase study
We previously defined haplotypes of single nucleotide polymorphisms (SNP) with possible relevance to multiple sclerosis (MS) in 2… 
Highly Cited
2005
Highly Cited
2005
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH
Background: Segmental duplications flanking the neurofibromatosis type 1 (NF1) gene locus on 17q11 mediate most gene deletions in… 
2005
2005
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma
Neurofibroma is a benign tumor originating from Schwann cells in peripheral nerve sheaths and may occur as a sporadic tumor or as… 
Highly Cited
2001
Highly Cited
2001
A meta-analysis of genomic screens in multiple sclerosis. The Transatlantic Multiple Sclerosis Genetics Cooperative.
We combined the raw genotyping data from three large multiple sclerosis genome screens and performed a global meta-analysis in… 
2000
2000
Multimarkerhaplotypes within the serotonin transporter gene suggest evidence of an association with bipolar disorder.
Previously we obtained modest linkage evidence implicating 17q11. 1-12 in bipolar disorder. A modified genome screen, based on… 
1999
1999
Physical mapping of the CC-chemokine gene cluster on the human 17q11. 2 region.
Chemokines are a family of small secreted proteins that are involved in the trafficking of leukocytes by acting on G-protein… 
1999
1999
Flotillin 2 is distinct from epidermal surface antigen (ESA) and is associated with filopodia formation
ECS‐1, a monoclonal antibody (MoAb) raised to cultured human keratinocytes, stains the intercellular glycocalyx with a pemphigus… 
Highly Cited
1995
Highly Cited
1995
Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.
Congenital cataracts constitute a morphologically and genetically heterogeneous group of diseases that are a major cause of… 
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