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10q24.32

A chromosome band present on 10q.
National Institutes of Health

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5 relations
BTRC wt AlleleChromosomesMIR146B wt AlleleNT5C2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study
2019
2019
Identification of a functional 339 bp Alu insertion polymorphism in the schizophrenia-associated locus at 10q24.32
Genome-wide association studies (GWAS) have identified multiple single nucleotide polymorphisms (SNPs) or small indels robustly… 
2017
2017
Admixture mapping of uterine fibroid size and number in African American women.
2016
2016
Evidence of AS3MTd2d3-Associated Variants within 10q24.32-33 in the Genetic Risk of Major Affective Disorders
Genome-wide association studies suggest that 10q24.32-33 is a risk region for schizophrenia (SCZ). Considering the substantial… 
2015
2015
The Genetic Architecture of Arsenic Metabolism Efficiency:A SNP-Based Heritability Study of Bangladeshi Adults
Background Consumption of arsenic-contaminated drinking water adversely affects health. There is interindividual variation in… 
Highly Cited
2013
Highly Cited
2013
Macrocephaly as a Clinical Indicator of Genetic Subtypes in Autism
An association between autism and macrocephaly has been previously described. A subset of cases with extreme macrocephaly (>3… 
Highly Cited
2012
Highly Cited
2012
Association study of a new schizophrenia susceptibility locus of 10q24.32–33 in a Han Chinese population
2012
2012
Clinical improvement of the aggressive neurobehavioral phenotype in a patient with a deletion of PITX3 and the absence of L‐DOPA in the cerebrospinal fluid
The development of midbrain dopamine (DA) neurons is regulated by several transcription factors, including Nurr1, Wnt1, Lmx1a/1b… 
Highly Cited
2006
Highly Cited
2006
DNA copy number gains in head and neck squamous cell carcinoma
Gene amplification, a common mechanism for oncogene activation in cancer, has been used as a tag for the identification of novel… 
2005
2005
Identification of a Novel Homozygous Deletion Region at 6q23.1 in Medulloblastomas Using High-Resolution Array Comparative Genomic Hybridization Analysis
Purpose: The aim of this study is to comprehensively characterize genome copy number aberrations in medulloblastomas using high… 
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