Joseph G. Gleeson

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Christopher A WalshBoston Children's HospitalDirección de correo verificada de childrens.harvard.edu
lihadh al-gazaliProfessor in Clinical Genetics & PaediatricsDirección de correo verificada de uaeu.ac.ae
Eric Michael ScottUC San DiegoDirección de correo verificada de ucsd.edu
Francesco BrancatiProfessor, University of L'AquilaDirección de correo verificada de univaq.it
Stacey GabrielThe Broad Institute of Harvard and MITDirección de correo verificada de broadinstitute.org
Margaret Elizabeth RossWeill Cornell Medical CollegeDirección de correo verificada de med.cornell.edu
Hulya KayseriliProfessor of medical genetics, Koc university School of MedicineDirección de correo verificada de kuh.ku.edu.tr
ENRICO BERTINIHead of the Research Unit of Neuromuscular and Neurodegenerative Disorders, Ospedale PediatricoDirección de correo verificada de opbg.net
Murat GunelYale UniversityDirección de correo verificada de yale.edu
Martin BreussAssistant Professor, CU AnschutzDirección de correo verificada de cuanschutz.edu
Damir MusaevYale UniversityDirección de correo verificada de yale.edu
Bassam R AliProfessor of Molecular Genetics, College of Medicine, United Arab Emirates UniversityDirección de correo verificada de uaeu.ac.ae
Madeline LancasterMRC Laboratory of Molecular BiologyDirección de correo verificada de mrc-lmb.cam.ac.uk
Hiroyuki KoizumiAssistant professor, Dept. of Biol Sciences, Graduate School of Science, The University of TokyoDirección de correo verificada de bs.s.u-tokyo.ac.jp
majdi karaProfessorDirección de correo verificada de uot.edu.ly
Michaela FryeProfessor DKFZDirección de correo verificada de dkfz.de
Joon KimKAISTDirección de correo verificada de kaist.ac.kr
Alicia Guemez-GamboaNorthwestern UniversityDirección de correo verificada de northwestern.edu
Holden HigginbothamProfessor of Biology, Brigham Young University - IdahoDirección de correo verificada de byui.edu
Renzo GuerriniProfessore di Neuropsichiatria Infantile, Università di FirenzeDirección de correo verificada de meyer.it

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Joseph G. Gleeson

University of California, San Diego

Dirección de correo verificada de ucsd.edu - Página principal

Neurogenetics Novel therapeutics Gene-Environment interactions


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
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	1576	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	1165	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	723	2012
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	596	2014
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	586	1998
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	581	2014
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	575	2010
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	533	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	514	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	469	2004
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	436	2008
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	435	2012
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	434	2009
Nucleokinesis in neuronal migration LH Tsai, JG Gleeson Neuron 46 (3), 383-388, 2005	433	2005
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	419	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	416	2004
Neuronal migration disorders: from genetic diseases to developmental mechanisms JG Gleeson, CA Walsh Trends in neurosciences 23 (8), 352-359, 2000	404	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	398	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	379	2016
Mutations in BCKD-kinase Lead to a Potentially Treatable Form of Autism with Epilepsy G Novarino, P El-Fishawy, H Kayserili, NA Meguid, EM Scott, J Schroth, ... Science 338 (6105), 394-397, 2012	348	2012

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