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2q34

A chromosome band present on 2q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1977-2017
02419772017

Related topics

Related topics

4 relations
CREB1 wt AlleleChromosomesFN1 wt AlleleIKZF2 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
2q34
Chromosomes
IKZF2 wt Allele
FN1 wt Allele
CREB1 wt Allele

Papers overview

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2013
2013
A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability.
We report on a 15-year-old patient with hyperactivity, intellectual disability and severe speech developmental delay. An array… (More)
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2012
2012
Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
PURPOSE Genetic generalized epilepsies (GGEs) have a lifetime prevalence of 0.3% with heritability estimates of 80%. A… (More)
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Highly Cited
2011
Highly Cited
2011
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study
Although approximately 25 common genetic susceptibility loci have been identified to be independently associated with breast… (More)
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2003
2003
Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.
Alzheimer disease (AD) is a complex disorder characterized by a wide range, within and between families, of ages at onset of… (More)
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Highly Cited
2002
Highly Cited
2002
Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p.
The genetic background that predisposes the Japanese population to type 2 diabetes is largely unknown. Therefore, we conducted a… (More)
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2002
2002
Identification and characterization of a novel ABCA subfamily member, ABCA12, located in the lamellar ichthyosis region on 2q34.
The ABCA subfamily of ABC transporters includes ten members to date. In this study, we describe an additional gene, ABCA12. Four… (More)
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2002
2002
The genetics of systemic lupus erythematosus stratified by renal disease: linkage at 10q22.3 (SLEN1), 2q34-35 (SLEN2), and 11p15.6 (SLEN3)
Renal disease occurs in 40–75% of systemic lupus erythematosus (SLE) patients and significantly contributes to morbidity and… (More)
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1998
1998
The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.
We report that the Bjornstad syndrome gene maps to chromosome 2q34-36. The clinical association of sensorineural hearing loss… (More)
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1996
1996
Linkage of rheumatoid arthritis to the candidate gene NRAMP1 on 2q35.
The macrophage resistance gene NRAMP1 regulates priming/activation of macrophages for enhanced TNF alpha, IL 1 beta, and MHC… (More)
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Highly Cited
1986
Highly Cited
1986
Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.
We have previously identified a partial human cDNA for MAP2, and we now report the isolation of human cDNA clones for tau. The… (More)
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