FAQ

12q24.13

A chromosome band present on 12q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2015
012319872015

Related topics

Related topics

4 relations
12qBCL7A wt AlleleChromosomesMAPKAPK5 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
12q24.13
Chromosomes
12q
MAPKAPK5 wt Allele
BCL7A wt Allele

Papers overview

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2015
2015
Common variation at 12q24.13 (OAS3) influences chronic lymphocytic leukemia risk
Chronic lymphocytic leukemia (CLL) is the most common form of lymphoid malignancy in Western countries. Recent multi-stage genome… (More)
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2013
2013
Copy Number Variation analysis in 98 individuals with PHACE syndrome
PHACE syndrome is the association of large segmental facial hemangiomas and congenital anomalies, such as posterior fossa… (More)
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Highly Cited
2011
Highly Cited
2011
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians
We conducted a meta-analysis of genome-wide association studies of systolic (SBP) and diastolic (DBP) blood pressure in 19,608… (More)
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Highly Cited
2011
Highly Cited
2011
Large-scale genome-wide association studies in east Asians identify new genetic loci influencing metabolic traits
To identify the genetic bases for nine metabolic traits, we conducted a meta-analysis combining Korean genome-wide association… (More)
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2009
2009
Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3–q14.1
A candidate gene study was conducted on 10 established type II diabetes genes and 45 genes associated with autoimmune diseases… (More)
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2009
2009
Genetic copy number variants in sib pairs both affected with schizophrenia
Schizophrenia is a complex disorder with involvement of multiple genes. In this study, genome-wide screening for DNA copy-number… (More)
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2009
2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndrome.
Noonan syndrome (NS) is a genetically heterogeneous disorder caused most commonly by activating mutations in PTPN11. We report a… (More)
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1998
1998
The BCL7 gene family: deletion of BCL7B in Williams syndrome.
The BCL7A gene, which maps to human chromosome 12q24.13, was cloned through its direct involvement with MYC and IGH in a three… (More)
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1993
1993
Unusual behaviour of a human autosome having two rare folate sensitive fragile sites.
A mother and daughter who have two rare folate sensitive fragile sites on the same homolog of chromosome 12 are recorded. This… (More)
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1987
1987
A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome
A fragile site on chromosome 12, at 12q24.13, was found in the lymphocytes of two members of a family during the study for… (More)
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