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Jean-Christophe Roux, Ph.D - Publications

Affiliations: 
Marseille Medical Genetics INSERM/Aix-Marseille University 
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46 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Panayotis N, Ehinger Y, Felix MS, Roux JC. State-of-the-art therapies for Rett syndrome. Developmental Medicine and Child Neurology. PMID 36056801 DOI: 10.1111/dmcn.15383  0.794
2021 Felix MS, Borloz E, Metwally K, Dauba A, Larrat B, Matagne V, Ehinger Y, Villard L, Novell A, Mensah S, Roux JC. Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in Mice. Pharmaceutics. 13. PMID 34452206 DOI: 10.3390/pharmaceutics13081245  0.768
2021 Borloz E, Villard L, Roux JC. Rett syndrome: think outside the (skull) box. Faculty Reviews. 10: 59. PMID 34308425 DOI: 10.12703/r/10-59  0.79
2021 Ehinger Y, Matagne V, Cunin V, Borloz E, Seve M, Bourgoin-Voillard S, Borges-Correia A, Villard L, Roux JC. Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome. International Journal of Molecular Sciences. 22. PMID 33919253 DOI: 10.3390/ijms22094316  0.791
2020 Matagne V, Borloz E, Ehinger Y, Saidi L, Villard L, Roux JC. Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome. Neurobiology of Disease. 149: 105235. PMID 33383186 DOI: 10.1016/j.nbd.2020.105235  0.78
2020 Milh M, Roubertoux P, Biba N, Chavany J, Spiga Ghata A, Fulachier C, Collins SC, Wagner C, Roux JC, Yalcin B, Félix MS, Molinari F, Lenck-Santini PP, Villard L. A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment. Epilepsia. PMID 32239694 DOI: 10.1111/Epi.16494  0.532
2020 Ehinger Y, Bruyère J, Panayotis N, Abada YS, Borloz E, Matagne V, Scaramuzzino C, Vitet H, Delatour B, Saidi L, Villard L, Saudou F, Roux JC. Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice. Embo Molecular Medicine. e10889. PMID 31913581 DOI: 10.15252/Emmm.201910889  0.766
2018 Ehinger Y, Matagne V, Villard L, Roux JC. Rett syndrome from bench to bedside: recent advances. F1000research. 7: 398. PMID 29636907 DOI: 10.12688/F1000Research.14056.1  0.804
2018 Mancini J, Dubus JC, Jouve E, Roux JC, Franco P, Lagrue E, Castelnau P, Cances C, Chaix Y, Rougeot-Jung C, Cornu C, Desportes V, Vallée L, Bahi-Buisson N, Truillet R, et al. Effect of desipramine on patients with breathing disorders in RETT syndrome. Annals of Clinical and Translational Neurology. 5: 118-127. PMID 29468173 DOI: 10.1002/Acn3.468  0.59
2016 Matagne V, Ehinger Y, Saidi L, Borges-Correia A, Barkats M, Bartoli M, Villard L, Roux JC. A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome. Neurobiology of Disease. 99: 1-11. PMID 27974239 DOI: 10.1016/J.Nbd.2016.12.009  0.836
2015 Roux JC, Villard L. Neurobehavioral testing of mouse models of Rett syndrome Neuromethods. 100: 399-430. DOI: 10.1007/978-1-4939-2250-5_16  0.492
2014 El-Khoury R, Panayotis N, Matagne V, Ghata A, Villard L, Roux JC. GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice. Plos One. 9: e92169. PMID 24667344 DOI: 10.1371/Journal.Pone.0092169  0.785
2013 Kaddoum L, Panayotis N, Mazarguil H, Giglia-Mari G, Roux JC, Joly E. Isoform-specific anti-MeCP2 antibodies confirm that expression of the e1 isoform strongly predominates in the brain. F1000research. 2: 204. PMID 24555100 DOI: 10.12688/F1000Research.2-204.V1  0.751
2013 Sanchez-Mut JV, Aso E, Panayotis N, Lott I, Dierssen M, Rabano A, Urdinguio RG, Fernandez AF, Astudillo A, Martin-Subero JI, Balint B, Fraga MF, Gomez A, Gurnot C, Roux JC, et al. DNA methylation map of mouse and human brain identifies target genes in Alzheimer's disease. Brain : a Journal of Neurology. 136: 3018-27. PMID 24030951 DOI: 10.1093/Brain/Awt237  0.747
2013 Cacciagli P, Sutera-Sardo J, Borges-Correia A, Roux JC, Dorboz I, Desvignes JP, Badens C, Delepine M, Lathrop M, Cau P, Lévy N, Girard N, Sarda P, Boespflug-Tanguy O, Villard L. Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus. American Journal of Human Genetics. 93: 579-86. PMID 24011989 DOI: 10.1016/J.Ajhg.2013.07.023  0.591
2012 Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L. [Unexpected link between Huntington disease and Rett syndrome]. Mã©Decine Sciences : M/S. 28: 44-6. PMID 22289830 DOI: 10.1051/Medsci/2012281016  0.773
2012 Roux JC, Zala D, Panayotis N, Borges-Correia A, Saudou F, Villard L. Modification of Mecp2 dosage alters axonal transport through the Huntingtin/Hap1 pathway. Neurobiology of Disease. 45: 786-95. PMID 22127389 DOI: 10.1016/J.Nbd.2011.11.002  0.804
2011 Panayotis N, Ghata A, Villard L, Roux JC. Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain. Bmc Neuroscience. 12: 47. PMID 21609470 DOI: 10.1186/1471-2202-12-47  0.831
2011 Panayotis N, Pratte M, Borges-Correia A, Ghata A, Villard L, Roux JC. Morphological and functional alterations in the substantia nigra pars compacta of the Mecp2-null mouse. Neurobiology of Disease. 41: 385-97. PMID 20951208 DOI: 10.1016/J.Nbd.2010.10.006  0.808
2011 Pratte M, Panayotis N, Ghata A, Villard L, Roux JC. Progressive motor and respiratory metabolism deficits in post-weaning Mecp2-null male mice. Behavioural Brain Research. 216: 313-20. PMID 20713094 DOI: 10.1016/J.Bbr.2010.08.011  0.826
2010 Roux JC, Panayotis N, Dura E, Villard L. Progressive noradrenergic deficits in the locus coeruleus of Mecp2 deficient mice. Journal of Neuroscience Research. 88: 1500-9. PMID 19998492 DOI: 10.1002/Jnr.22312  0.806
2010 Roux JC, Villard L. Biogenic amines in Rett syndrome: the usual suspects. Behavior Genetics. 40: 59-75. PMID 19851857 DOI: 10.1007/S10519-009-9303-Y  0.622
2009 Cantagrel V, Haddad MR, Ciofi P, Andrieu D, Lossi AM, Maldergem Lv, Roux JC, Villard L. Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation. Gene Expression Patterns : Gep. 9: 423-9. PMID 19524067 DOI: 10.1016/J.Gep.2009.06.001  0.584
2008 Roux JC, Dura E, Villard L. Tyrosine hydroxylase deficit in the chemoafferent and the sympathoadrenergic pathways of the Mecp2 deficient mouse. Neuroscience Letters. 447: 82-6. PMID 18834926 DOI: 10.1016/J.Neulet.2008.09.045  0.798
2008 Dura E, Villard L, Roux JC. Expression of methyl CpG binding protein 2 (Mecp2) during the postnatal development of the mouse brainstem. Brain Research. 1236: 176-84. PMID 18761004 DOI: 10.1016/J.Brainres.2008.08.021  0.773
2007 Peyronnet J, Roux JC, Mamet J, Perrin D, Lachuer J, Pequignot JM, Dalmaz Y. Developmental plasticity of the carotid chemoafferent pathway in rats that are hypoxic during the prenatal period. The European Journal of Neuroscience. 26: 2865-72. PMID 18001283 DOI: 10.1111/J.1460-9568.2007.05884.X  0.584
2007 Roux JC, Villard L. [Pharmacological treatment of Rett syndrome improves breathing and survival in a mouse model]. Mã©Decine Sciences : M/S. 23: 805-7. PMID 17937887 DOI: 10.1051/Medsci/20072310805  0.556
2007 Roux JC, Dura E, Moncla A, Mancini J, Villard L. Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome. The European Journal of Neuroscience. 25: 1915-22. PMID 17439480 DOI: 10.1111/J.1460-9568.2007.05466.X  0.791
2006 Villard L, Roux JC. [Noradrenaline deficiency as the origin of respiratory disorders in Rett syndrome an animal model]. Mã©Decine Sciences : M/S. 22: 81-3. PMID 16386227 DOI: 10.1051/Medsci/200622181  0.566
2005 Viemari JC, Roux JC, Tryba AK, Saywell V, Burnet H, Peña F, Zanella S, Bévengut M, Barthelemy-Requin M, Herzing LB, Moncla A, Mancini J, Ramirez JM, Villard L, Hilaire G. Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 11521-30. PMID 16354910 DOI: 10.1523/Jneurosci.4373-05.2005  0.643
2005 Roux JC, Brismar H, Aperia A, Lagercrantz H. Developmental changes in HIF transcription factor in carotid body: relevance for O2 sensing by chemoreceptors. Pediatric Research. 58: 53-7. PMID 15879294 DOI: 10.1203/01.Pdr.0000163390.78239.Ea  0.46
2005 Cohen G, Roux JC, Grailhe R, Malcolm G, Changeux JP, Lagercrantz H. Perinatal exposure to nicotine causes deficits associated with a loss of nicotinic receptor function. Proceedings of the National Academy of Sciences of the United States of America. 102: 3817-21. PMID 15738419 DOI: 10.1073/Pnas.0409782102  0.452
2004 Soulage C, Pascual O, Roux JC, Denavit-Saubié M, Pequignot JM. Chemosensory inputs and neural remodeling in carotid body and brainstem catecholaminergic cells. Advances in Experimental Medicine and Biology. 551: 53-8. PMID 15602943 DOI: 10.1007/0-387-27023-X_9  0.572
2004 Pascual O, Roux JC, Soulage C, Morin-Surun MP, Denavit-Saubié M, Pequignot JM. Carotid chemodenervation approach to study oxygen sensing in brain stem catecholaminergic cells. Methods in Enzymology. 381: 422-49. PMID 15063691 DOI: 10.1016/S0076-6879(04)81029-2  0.564
2004 Nsegbe E, Wallén-Mackenzie A, Dauger S, Roux JC, Shvarev Y, Lagercrantz H, Perlmann T, Herlenius E. Congenital hypoventilation and impaired hypoxic response in Nurr1 mutant mice. The Journal of Physiology. 556: 43-59. PMID 14742729 DOI: 10.1113/Jphysiol.2003.058560  0.589
2003 Peyronnet J, Roux JC, Perrin D, Pequignot JM, Lagercrantz H, Dalmaz Y. Prenatal hypoxia and early postnatal maturation of the chemoafferent pathway. Advances in Experimental Medicine and Biology. 536: 525-33. PMID 14635708 DOI: 10.1007/978-1-4419-9280-2_66  0.615
2003 Roux JC, Mamet J, Perrin D, Peyronnet J, Royer C, Cottet-Emard JM, Pequignot JM, Dalmaz Y. Neurochemical development of the brainstem catecholaminergic cell groups in rat. Journal of Neural Transmission (Vienna, Austria : 1996). 110: 51-65. PMID 12541012 DOI: 10.1007/s00702-002-0767-7  0.485
2002 Peyronnet J, Dalmaz Y, Ehrström M, Mamet J, Roux JC, Pequignot JM, Thorén HP, Lagercrantz H. Long-lasting adverse effects of prenatal hypoxia on developing autonomic nervous system and cardiovascular parameters in rats. Pflã¼Gers Archiv : European Journal of Physiology. 443: 858-65. PMID 11889586 DOI: 10.1007/S00424-001-0766-9  0.635
2002 Mamet J, Peyronnet J, Roux JC, Perrin D, Cottet-Emard JM, Pequignot JM, Lagercrantz H, Dalmaz Y. Long-term prenatal hypoxia alters maturation of adrenal medulla in rat. Pediatric Research. 51: 207-14. PMID 11809916 DOI: 10.1203/00006450-200202000-00014  0.629
2001 Roux J, Peyronnet J, Mamet J, Perrin D, Lagercrantz H, Dalmaz Y, Pequignot J. Respiratory Research. 2: P20. DOI: 10.1186/Rr137  0.664
2001 Malhière S, Dalmaz Y, Perrin D, Roux J, Lagercrantz H, Pequignot J, Peyronnet J. Respiratory Research. 2: P16. DOI: 10.1186/Rr132  0.641
2000 Roux JC, Pequignot JM, Dumas S, Pascual O, Ghilini G, Pequignot J, Mallet J, Denavit-Saubié M. O2-sensing after carotid chemodenervation: hypoxic ventilatory responsiveness and upregulation of tyrosine hydroxylase mRNA in brainstem catecholaminergic cells. The European Journal of Neuroscience. 12: 3181-90. PMID 10998102 DOI: 10.1046/J.1460-9568.2000.00208.X  0.558
2000 Roux JC, Peyronnet J, Pascual O, Dalmaz Y, Pequignot JM. Neurochemical reorganization of O2 chemoreflex pathway after carotid body denervation in rats. Advances in Experimental Medicine and Biology. 475: 823-8. PMID 10849725  0.448
2000 Peyronnet J, Roux JC, Geloën A, Tang LQ, Pequignot JM, Lagercrantz H, Dalmaz Y. Prenatal hypoxia impairs the postnatal development of neural and functional chemoafferent pathway in rat. The Journal of Physiology. 524: 525-37. PMID 10766931 DOI: 10.1111/J.1469-7793.2000.00525.X  0.606
2000 Roux JC, Peyronnet J, Pascual O, Dalmaz Y, Pequignot JM. Ventilatory and central neurochemical reorganisation of O2 chemoreflex after carotid sinus nerve transection in rat. The Journal of Physiology. 522: 493-501. PMID 10713972  0.482
2000 Royer C, Lachuer J, Crouzoulon G, Roux JC, Peyronnet J, Mamet J, Pequignot JM, Dalmaz Y. Effects of gestational hypoxia on mRNA levels of Glut3 and Glut4 transporters, hypoxia inducible factor-1 and thyroid hormone receptors in developing rat brain Brain Research. 856: 119-128. PMID 10677618 DOI: 10.1016/S0006-8993(99)02365-3  0.586
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