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5q35.2

A chromosome band present on 5q
National Institutes of Health

Papers overview

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2015
2015
Background and Purpose— The majority of genome-wide association studies (GWAS) of stroke have focused on European-ancestry… Expand
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2011
2011
We report on an infant with tetrasomy of 5q35.2‐5q35.3, an interstitial triplication on one chromosome and normal complement on… Expand
Highly Cited
2010
Highly Cited
2010
BACKGROUND A genetic contribution to smoking behavior is well-established. To identify loci that increase the risk for smoking… Expand
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Highly Cited
2009
Highly Cited
2009
Age at menarche and age at natural menopause are associated with causes of substantial morbidity and mortality such as breast… Expand
Highly Cited
2008
Highly Cited
2008
Silencing of multiple cancer-related genes is associated with de novo methylation of linked CpG islands. Additionally, bivalent… Expand
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Highly Cited
2005
Highly Cited
2005
We used array‐based comparative genomic hybridization (aCGH) to measure genomic copy number alterations (CNAs) in 42… Expand
Highly Cited
2004
Highly Cited
2004
The Ehlers–Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders characterized by skin… Expand
2004
2004
Linkage analysis is used routinely to map genes for human diseases and conditions. However, the existing linkage-analysis methods… Expand
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Highly Cited
2002
Highly Cited
2002
A genome scan of the hoarding phenotype (a component of obsessive-compulsive disorder) was conducted on 77 sib pairs collected by… Expand
1996
1996
Complementary DNA clones encoding human hexokinase III were isolated from a liver cDNA library. There was 84.7% identity between… Expand