Joseph Gleeson
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Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons
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
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
JH Lee, M Huynh, JL Silhavy, S Kim, T Dixon-Salazar, A Heiberg, E Scott, ...
Nature genetics 44 (8), 941-945, 2012
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
Functional genomic screen for modulators of ciliogenesis and cilium length
J Kim, JE Lee, S Heynen-Genel, E Suyama, K Ono, KY Lee, T Ideker, ...
Nature 464 (7291), 1048-1051, 2010
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders
G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ...
science 343 (6170), 506-511, 2014
Aberrant methylation of t RNA s links cellular stress to neuro‐developmental disorders
S Blanco, S Dietmann, JV Flores, S Hussain, C Kutter, P Humphreys, ...
The EMBO journal 33 (18), 2020-2039, 2014
NSun2-mediated cytosine-5 methylation of vault noncoding RNA determines its processing into regulatory small RNAs
S Hussain, AA Sajini, S Blanco, S Dietmann, P Lombard, Y Sugimoto, ...
Cell reports 4 (2), 255-261, 2013
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
Nucleokinesis in neuronal migration
LH Tsai, JG Gleeson
Neuron 46 (3), 383-388, 2005
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
V Cantagrel, JL Silhavy, SL Bielas, D Swistun, SE Marsh, JY Bertrand, ...
The American Journal of Human Genetics 83 (2), 170-179, 2008
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
SL Bielas, JL Silhavy, F Brancati, MV Kisseleva, L Al-Gazali, L Sztriha, ...
Nature genetics 41 (9), 1032-1036, 2009
Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling
M Chaki, R Airik, AK Ghosh, RH Giles, R Chen, GG Slaats, H Wang, ...
Cell 150 (3), 533-548, 2012
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
EE Davis, Q Zhang, Q Liu, BH Diplas, LM Davey, J Hartley, C Stoetzel, ...
Nature genetics 43 (3), 189-196, 2011
Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning
T Shu, R Ayala, MD Nguyen, Z Xie, JG Gleeson, LH Tsai
Neuron 44 (2), 263-277, 2004
Neuronal migration disorders: from genetic diseases to developmental mechanisms
JG Gleeson, CA Walsh
Trends in neurosciences 23 (8), 352-359, 2000
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
DT Pilz, N Matsumoto, S Minnerath, P Mills, JG Gleeson, KM Allen, ...
Human molecular genetics 7 (13), 2029-2037, 1998
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ...
Nature genetics 48 (9), 1071-1076, 2016
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
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