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2q36.1

A chromosome band present on 2q
National Institutes of Health

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3 relations
ChromosomesEPHA4 wt AlleleFARSB wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.
Highly Cited
2015
Highly Cited
2015
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Adolescent idiopathic scoliosis (AIS) is a structural deformity of the spine affecting millions of children. As a complex disease… 
2015
2015
ADP-ribosylation factor-like 4C (ARL4C), a novel ovarian cancer metastasis suppressor, identified by integrated genomics.
Understanding the molecular mechanisms involving the initiation, progression, and metastasis of ovarian cancer is important for… 
2014
2014
PAX3 gene deletion detected by microarray analysis in a girl with hearing loss
Deletions of the PAX3 gene have been rarely reported in the literature. Mutations of this gene are a common cause of Waardenburg… 
2012
2012
Use of germline polymorphisms in predicting concurrent chemoradiotherapy response in esophageal cancer.
2012
2012
A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state.
2011
2011
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family‐based, Arab‐Israeli sample
While the use of population‐based samples is a common strategy in genome‐wide association studies (GWASs), family‐based samples… 
2011
2011
Genome-wide association study of allergic diseases in Russians of West Siberia
Genome-wide association studies are currently considered as one of the most powerful tools for establishing the genetic basis of… 
2009
2009
Association of chromosome 2q36.1–36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families
Background: Ankylosing spondylitis (AS) is a chronic, potentially crippling, spondyloarthropathy with strong genetic components… 
2008
2008
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity
We previously reported a Vietnamese-American family with isolated autosomal dominant occipital cephalocele. Upon further… 
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