Chromosomes, Human, Pair 15

Known as: 15 chromosome, Chromosome 15 
The designation for each member of the fifteenth largest human autosomal chromosome pair. Chromosome 15 spans about 106 million base pairs and… (More)
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Infertility is defined as a failure to conceive in a couple trying to reproduce for a period of two years without conception… (More)
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Highly Cited
2008
Highly Cited
2008
Twin studies indicate that additive genetic effects explain most of the variance in nicotine dependence (ND), a construct… (More)
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Highly Cited
2003
Highly Cited
2003
Genome-wide DNA hypomethylation occurs in many human cancers, but whether this epigenetic change is a cause or consequence of… (More)
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Highly Cited
2001
Highly Cited
2001
Prader-Willi syndrome (PWS) is a neurogenetic disorder that results from the lack of transcripts expressed from the paternal copy… (More)
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Highly Cited
1997
Highly Cited
1997
Inheritance of a defect in a neuronal mechanism that regulates response to auditory stimuli was studied in nine families with… (More)
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Highly Cited
1997
Highly Cited
1997
Duplications of proximal 15q have been found in individuals with autistic disorder (AD) and varying degrees of mental retardation… (More)
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Highly Cited
1995
Highly Cited
1995
A subset of patients with Angelman and Prader–Willi syndrome have apparently normal chromosomes of biparental origin, but… (More)
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Highly Cited
1990
Highly Cited
1990
A secreted inhibitor of angiogenesis that is controlled by a tumor suppressor gene in hamster cells has been found to be similar… (More)
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Highly Cited
1989
Highly Cited
1989
Many Prader-Willi syndrome (PWS) and Angelman syndrome (AS) patients have a cytogenetic deletion of 15q11q13. While AS and PWS… (More)
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Review
1979
Review
1979
Marfan syndrome is caused by a mutation of the fi brillin-1 gene located on chromosome 15. (1) Fibrillin-1 protein is an… (More)
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