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JG Gleeson, PT Lin, LA Flanagan, CA Walsh
Neuron 23 (2), 257-271, 1999
|Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein|
JG Gleeson, KM Allen, JW Fox, ED Lamperti, S Berkovic, I Scheffer, ...
Cell 92 (1), 63-72, 1998
|PAK3 mutation in nonsyndromic X-linked mental retardation|
KM Allen, JG Gleeson, S Bagrodia, MW Partington, JC MacMillan, ...
Nature genetics 20 (1), 25-30, 1998
|De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly|
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Nature genetics 44 (8), 941-945, 2012
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Nature 464 (7291), 1048-1051, 2010
|Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome|
EM Valente, JL Silhavy, F Brancati, G Barrano, SR Krishnaswami, ...
Nature genetics 38 (6), 623-625, 2006
|Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration|
T Tanaka, FF Serneo, C Higgins, MJ Gambello, A Wynshaw-Boris, ...
The Journal of cell biology 165 (5), 709-721, 2004
|Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders|
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T Shu, R Ayala, MD Nguyen, Z Xie, JG Gleeson, LH Tsai
Neuron 44 (2), 263-277, 2004
|Nucleokinesis in neuronal migration|
LH Tsai, JG Gleeson
Neuron 46 (3), 383-388, 2005
|Neuronal migration disorders: from genetic diseases to developmental mechanisms|
JG Gleeson, CA Walsh
Trends in neurosciences 23 (8), 352-359, 2000
|Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies|
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Nature genetics 41 (9), 1032, 2009
|LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation|
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Human molecular genetics 7 (13), 2029-2037, 1998
|TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum|
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Nature genetics 43 (3), 189-196, 2011
|Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome|
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The American Journal of Human Genetics 83 (2), 170-179, 2008
|Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling|
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Cell 150 (3), 533-548, 2012
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Cell reports 4 (2), 255-261, 2013
|Cdk5 phosphorylation of doublecortin ser297 regulates its effect on neuronal migration|
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Neuron 41 (2), 215-227, 2004
|Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria|
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The American Journal of Human Genetics 75 (6), 979-987, 2004
|CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium|
J Kim, SR Krishnaswami, JG Gleeson
Human molecular genetics 17 (23), 3796-3805, 2008