Concepedia

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, Ganeshwaran H. Mochida, Mohammed S. Al‐Dosari, Jillian M. Felie, R. Sean Hill, Brenda J. Barry, Jennifer N. Partlow, Generoso G. Gascon,

The American Journal of Human Genetics · 2011 · 222 citations · 34 references

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34

A quantitative atlas of mitotic phosphorylation

Noah Dephoure, Chunshui Zhou, Judit Villén et al. · Proceedings of the National Academy of Sciences · 2008 · 1.6K citations · Full text

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doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox et al. · Cell · 1998 · 1.1K citations · Full text

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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

Susan E. Hong, Yin Yao Shugart, David T. Huang et al. · Nature Genetics · 2000 · 878 citations

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ASPM is a major determinant of cerebral cortical size

Jacquelyn Bond, Emma Roberts, Ganeshwaran H. Mochida et al. · Nature Genetics · 2002 · 569 citations

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A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

Jacquelyn Bond, Emma Roberts, Kelly Springell et al. · Nature Genetics · 2005 · 567 citations

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