ASPM gene

Known as: Asp (Abnormal Spindle) Homolog, Microcephaly Associated (Drosophila) Gene, Calmbp1, ASP, DROSOPHILA, HOMOLOG OF 
This gene plays a role in mitotic spindle regulation.
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Mutations in ASPM (abnormal spindle-like microcephaly associated) cause primary microcephaly in humans, a disorder characterized… (More)
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Highly Cited
2007
Highly Cited
2007
The correlations between interpopulation genetic and linguistic diversities are mostly noncausal (spurious), being due to… (More)
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Highly Cited
2006
Highly Cited
2006
The ASPM (abnormal spindle-like microcephaly-associated) protein has previously been implicated in the determination of human… (More)
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Highly Cited
2005
Highly Cited
2005
The gene ASPM (abnormal spindle-like microcephaly associated) is a specific regulator of brain size, and its evolution in the… (More)
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Highly Cited
2005
Highly Cited
2005
The most common cause of primary autosomal recessive microcephaly (MCPH) appears to be mutations in the ASPM gene which is… (More)
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Highly Cited
2004
Highly Cited
2004
Primary microcephaly (MCPH) is a neurodevelopmental disorder characterized by global reduction in cerebral cortical volume. The… (More)
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Highly Cited
2004
Highly Cited
2004
A prominent trend in the evolution of humans is the progressive enlargement of the cerebral cortex. The ASPM (Abnormal spindle… (More)
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Highly Cited
2003
Highly Cited
2003
Mutations in the ASPM gene at the MCPH5 locus are expected to be the most common cause of human autosomal recessive primary… (More)
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Highly Cited
2002
Highly Cited
2002
One of the most notable trends in mammalian evolution is the massive increase in size of the cerebral cortex, especially in… (More)
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Highly Cited
1997
Highly Cited
1997
Codon usage bias of 1,117 Drosophila melanogaster genes, as well as fewer D. pseudoobscura and D. virilis genes, was examined… (More)
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