Xavier Jaglin

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Gordon FishellProfessor of neuroscience Harvard Medical SchoolGeverifieerd e-mailadres voor hms.harvard.edu
Bahi BuissonNeuropediatre Hopital Necker Enfants Malades Université Paris DescartesGeverifieerd e-mailadres voor nck.aphp.fr
David KeaysProfessor of Neurobiology, LMU, Munich. Principal Research Associate, PDN, University of Cambridge.Geverifieerd e-mailadres voor bio.lmu.de
Renata Batista-BritoAlbert Einstein College of MedicineGeverifieerd e-mailadres voor einsteinmed.edu
edouard w khandjianprofesseur université lavalGeverifieerd e-mailadres voor crulrg.ulaval.ca
Christian MayerMax Planck Institute of NeurobiologyGeverifieerd e-mailadres voor neuro.mpg.de
Rachel Bandler, MD, PhDYale UniversityGeverifieerd e-mailadres voor yale.edu
Jonathan FlintUniversity of California, Los AngelesGeverifieerd e-mailadres voor well.ox.ac.uk
BOMONTNeuroMyogène institute-PGNM, Lyon, FranceGeverifieerd e-mailadres voor inserm.fr
Emilia FavuzziYale UniversityGeverifieerd e-mailadres voor yale.edu
Brie WamsleyPostdoctoral Scholar in Department of Neurology, UCLAGeverifieerd e-mailadres voor mednet.ucla.edu
Barbara BardoniResearch Director INSERMGeverifieerd e-mailadres voor ipmc.cnrs.fr
Christoph HafemeisterPostdoctoral Research Associate, St. Anna Children's Cancer Research InstituteGeverifieerd e-mailadres voor ccri.at
Rahul SatijaCore Faculty Member, New York Genome Center. Department of Biology, NYUGeverifieerd e-mailadres voor nygenome.org
GENEVIEVEHead of clinical genetic unit and of the Medical Genetic Departement, Rare Diseases and PersonalizedGeverifieerd e-mailadres voor chu-montpellier.fr
Rima Nabboutcentre de refrence epilepsies rares, Necker enfants Malades, Imagine instituteGeverifieerd e-mailadres voor aphp.fr
Theofanis KarayannisBrain Research Institute, University of ZurichGeverifieerd e-mailadres voor hifo.uzh.ch
Bernardo RudyProfessor of Neuroscience and Physiology, NYU School of MedicineGeverifieerd e-mailadres voor nyumc.org
Maximiliano Jose NigroAssociate Professor, NTNUGeverifieerd e-mailadres voor ntnu.no
Giulia QuattrocoloAssociate Professor, NTNU, Kavli Institute for Systems NeuroscienceGeverifieerd e-mailadres voor ntnu.no

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Xavier Jaglin

Harvard Medical School

Geverifieerd e-mailadres voor hms.harvard.edu - Homepage

Developmental neurobiology - Interneuron development - Autism and Intellectual disability


Titel Sorteren op citaties Sorteren op jaar Sorteren op titel	Geciteerd door Geciteerd door	Jaar
Developmental diversification of cortical inhibitory interneurons C Mayer, C Hafemeister, RC Bandler, R Machold, R Batista Brito, X Jaglin, ... Nature 555 (7697), 457-462, 2018	496	2018
Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria XH Jaglin, K Poirier, Y Saillour, E Buhler, G Tian, N Bahi-Buisson, ... Nature genetics 41 (6), 746-752, 2009	394	2009
Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects K Poirier, Y Saillour, N Bahi-Buisson, XH Jaglin, C Fallet-Bianco, ... Human molecular genetics 19 (22), 4462-4473, 2010	313	2010
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities M Breuss, JIT Heng, K Poirier, G Tian, XH Jaglin, Z Qu, A Braun, T Gstrein, ... Cell reports 2 (6), 1554-1562, 2012	208	2012
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects XH Jaglin, J Chelly Trends in Genetics 25 (12), 555-566, 2009	200	2009
The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules L Davidovic, XH Jaglin, AM Lepagnol-Bestel, S Tremblay, M Simonneau, ... Human molecular genetics 16 (24), 3047-3058, 2007	179	2007
Clonally related forebrain interneurons disperse broadly across both functional areas and structural boundaries C Mayer, XH Jaglin, LV Cobbs, RC Bandler, C Streicher, CL Cepko, ... Neuron 87 (5), 989-998, 2015	125	2015
Tracking the fragile X mental retardation protein in a highly ordered neuronal ribonucleoparticles population: a link between stalled polyribosomes and RNA granules R El Fatimy, L Davidovic, S Tremblay, X Jaglin, A Dury, C Robert, ... PLoS genetics 12 (7), e1006192, 2016	121	2016
Activity regulates cell death within cortical interneurons through a calcineurin-dependent mechanism R Priya, MF Paredes, T Karayannis, N Yusuf, X Liu, X Jaglin, I Graef, ... Cell reports 22 (7), 1695-1709, 2018	106	2018
Rbfox1 mediates cell-type-specific splicing in cortical interneurons B Wamsley, XH Jaglin, E Favuzzi, G Quattrocolo, MJ Nigro, N Yusuf, ... Neuron 100 (4), 846-859. e7, 2018	99	2018
Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway G Tian, XH Jaglin, DA Keays, F Francis, J Chelly, NJ Cowan Human molecular genetics 19 (18), 3599-3613, 2010	77	2010
The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons L Davidovic, E Bechara, M Gravel, XH Jaglin, S Tremblay, A Sik, ... Human molecular genetics 15 (9), 1525-1538, 2006	77	2006
Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration R Belvindrah, K Natarajan, P Shabajee, E Bruel-Jungerman, J Bernard, ... Journal of Cell Biology 216 (8), 2443-2461, 2017	74	2017
Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype M Lecourtois, K Poirier, G Friocourt, X Jaglin, A Goldenberg, ... Acta neuropathologica 119, 779-789, 2010	65	2010
A pachygyria-causing α-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB G Tian, XP Kong, XH Jaglin, J Chelly, D Keays, NJ Cowan Molecular Biology of the Cell 19 (3), 1152-1161, 2008	58	2008
The origin of neocortical nitric oxide synthase-expressing inhibitory neurons XH Jaglin, J Hjerling-Leffler, G Fishell, R Batista-Brito Cortical NO interneurons from embryogenesis to functions, 49, 2012	42	2012
Nova proteins direct synaptic integration of somatostatin interneurons through activity-dependent alternative splicing LA Ibrahim, B Wamsley, N Alghamdi, N Yusuf, E Sevier, A Hairston, ... Elife 12, e86842, 2023	7	2023
Nova proteins direct synaptic integration of somatostatin interneurons through activity-dependent alternative splicing B Wamsley, LA Ibrahim, N Yusuf, E Fisher, XH Jaglin, Q Xu, L Guo, ... BioRxiv, 2019	2	2019
A foot in the door: how the chromatin modifier Brg1 and Pax6 jointly potentiate adult neurogenesis XH Jaglin, G Fishell Cell Stem Cell 13 (4), 373-374, 2013	2	2013
Tubulin-related malformations of cortical development XH Jaglin, J Chelly, N Bahi-Buisson Cytoskeleton and Human Disease, 315-341, 2012	1	2012

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