Fils d'Ariane

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Srivastava, S., Niranjan, T., May, M.M., Tarpey, P., Allen, W., Hackett, A., Jouk, P.-S., Raymond, L., Briault, S., Skinner, C., Toutain, A., Gecz, J., Heath, W., Stevenson, R.E., Schwartz, C.E. & Wang, T. (2019) Dysregulations of sonic hedgehog signaling in MED12-related X-linked intellectual disability disorders. Mol Genet Genomic Med 7, e00569.

Felgerolle, C., Hébert, B., Ardourel, M., Meyer-Dilhet, G., Menuet, A., Pinto-Morais, K., Bizot, J.-C., Pichon, J., Briault, S. & Perche, O. (2019) Visual Behavior Impairments as an Aberrant Sensory Processing in the Mouse Model of Fragile X Syndrome. Front Behav Neurosci 13.

Thulliez, M., Laudier, B., Vignal-Clermont, C., Hardy, G. & Bonicel, P. (2018) [New mitochondrial DNA mutation in Leber’s hereditary optic neuropathy: A case report]. J Fr Ophtalmol 41, e293–e299.

Santos-Durán, G.N., Ferreiro-Galve, S., Menuet, A., Mazan, S., Rodríguez-Moldes, I. & Candal, E. (2018) The Shark Basal Hypothalamus: Molecular Prosomeric Subdivisions and Evolutionary Trends. Front Neuroanat 12, 17.

Perche, O., Felgerolle, C., Ardourel, M., Bazinet, A., Pâris, A., Rossignol, R., Meyer-Dilhet, G., Mausset-Bonnefont, A.-L., Hébert, B., Laurenceau, D., Montécot-Dubourg, C., Menuet, A., Bizot, J.-C., Pichon, J., Ranchon-Cole, I. & Briault, S. (2018) Early Retinal Defects in Fmr1-/y Mice: Toward a Critical Role of Visual Dys-Sensitivity in the Fragile X Syndrome Phenotype? Front Cell Neurosci 12, 96.

Laugeray, A., Oummadi, A., Jourdain, C., Feat, J., Meyer-Dilhet, G., Menuet, A., Plé, K., Gay, M., Routier, S., Mortaud, S. & Guillemin, G.J. (2018) Perinatal Exposure to the Cyanotoxin β-N-Méthylamino-L-Alanine (BMAA) Results in Long-Lasting Behavioral Changes in Offspring-Potential Involvement of DNA Damage and Oxidative Stress. Neurotox Res 33, 87–112.

Lagadec, R., Lanoizelet, M., Sánchez-Farías, N., Hérard, F., Menuet, A., Mayeur, H., Billoud, B., Rodriguez-Moldes, I., Candal, E. & Mazan, S. (2018) Neurogenetic asymmetries in the catshark developing habenulae: mechanistic and evolutionary implications. Sci Rep 8, 4616.

Feat-Vetel, J., Larrigaldie, V., Meyer-Dilhet, G., Herzine, A., Mougin, C., Laugeray, A., Gefflaut, T., Richard, O., Quesniaux, V., Montécot-Dubourg, C. & Mortaud, S. (2018) Multiple effects of the herbicide glufosinate-ammonium and its main metabolite on neural stem cells from the subventricular zone of newborn mice. Neurotoxicology 69, 152–163.

Benmerzoug, S., Rose, S., Bounab, B., Gosset, D., Duneau, L., Chenuet, P., Mollet, L., Le Bert, M., Lambers, C., Geleff, S., Roth, M., Fauconnier, L., Sedda, D., Carvalho, C., Perche, O., Laurenceau, D., Ryffel, B., Apetoh, L., Kiziltunc, A., Uslu, H., Albez, F.S., Akgun, M., Togbe, D. & Quesniaux, V.F.J. (2018) STING-dependent sensing of self-DNA drives silica-induced lung inflammation. Nat Commun 9, 5226.

Reverchon, F., Mortaud, S., Sivoyon, M., Maillet, I., Laugeray, A., Palomo, J., Montécot, C., Herzine, A., Meme, S., Meme, W., Erard, F., Ryffel, B., Menuet, A. & Quesniaux, V.F.J. (2017) IL-33 receptor ST2 regulates the cognitive impairments associated with experimental cerebral malaria. PLoS Pathog 13, e1006322.

Laugeray, A., Herzine, A., Perche, O., Richard, O., Montecot-Dubourg, C., Menuet, A., Mazaud-Guittot, S., Lesné, L., Jegou, B. & Mortaud, S. (2017) In utero and lactational exposure to low-doses of the pyrethroid insecticide cypermethrin leads to neurodevelopmental defects in male mice-An ethological and transcriptomic study. PLoS ONE 12, e0184475.

Aksoy, I., Utami, K.H., Winata, C.L., Hillmer, A.M., Rouam, S.L., Briault, S., Davila, S., Stanton, L.W. & Cacheux, V. (2017) Personalized genome sequencing coupled with iPSC technology identifies GTDC1 as a gene involved in neurodevelopmental disorders. Hum Mol Genet 26, 367–382.

Zarpelon, A.C., Rodrigues, F.C., Lopes, A.H., Souza, G.R., Carvalho, T.T., Pinto, L.G., Xu, D., Ferreira, S.H., Alves-Filho, J.C., McInnes, I.B., Ryffel, B., Quesniaux, V.F.J., Reverchon, F., Mortaud, S., Menuet, A., Liew, F.Y., Cunha, F.Q., Cunha, T.M. & Verri, W.A. (2016) Spinal cord oligodendrocyte-derived alarmin IL-33 mediates neuropathic pain. FASEB J 30, 54–65.

Féron, F., Gepner, B., Lacassagne, E., Stephan, D., Mesnage, B., Blanchard MP, Boulanger N, Tardif C., Devèze, A., Rousseau, S., Suzuki, K., Izpisua Belmonte, J.C., Khrestchatisky, M., Nivet, E. and Erard-Garcia, M. (2016) Olfactory stem cells reveal MOCOS as a new player in autism spectrum disorders. Mol Psychiatry 9:1215-1224.

Santos-Durán, G.N., Ferreiro-Galve, S., Menuet, A., Quintana-Urzainqui, I., Mazan, S., Rodríguez-Moldes, I. & Candal, E. (2016) The Shark Alar Hypothalamus: Molecular Characterization of Prosomeric Subdivisions and Evolutionary Trends. Front Neuroanat 10, 113.

Maillet, I., Perche, O., Pâris, A., Richard, O., Gombault, A., Herzine, A., Pichon, J., Huaux, F., Mortaud, S., Ryffel, B., Quesniaux, V.F.J. & Montécot-Dubourg, C. (2016) Glufosinate aerogenic exposure induces glutamate and IL-1 receptor dependent lung inflammation. Clin Sci 130, 1939–1954.

Laudier, B., Epiais, T., Pâris, A., Menuet, A., Briault, S., Ozsancak, C. & Perche, O. (2016) Molecular and clinical analyses with neuropsychological assessment of a case of del(10)(q26.2qter) without intellectual disability: Genomic and transcriptomic combined approach and review of the literature. Am J Med Genet A 170, 1806–1812.

Herzine, A., Laugeray, A., Feat, J., Menuet, A., Quesniaux, V., Richard, O., Pichon, J., Montécot-Dubourg, C., Perche, O. & Mortaud, S. (2016) Perinatal Exposure to Glufosinate Ammonium Herbicide Impairs Neurogenesis and Neuroblast Migration through Cytoskeleton Destabilization. Front Cell Neurosci 10, 191.

Guimarães-Souza, E.M., Perche, O., Morgans, C.W., Duvoisin, R.M. & Calaza, K.C. (2016) Fragile X Mental Retardation Protein expression in the retina is regulated by light. Exp Eye Res 146, 72–82.

Calas, A.-G., Perche, O., Richard, O., Perche, A., Pâris, A., Lauga, F., Herzine, A., Palomo, J., Ardourel, M.-Y., Menuet, A., Mortaud, S., Pichon, J. & Montécot-Dubourg, C. (2016) Characterization of seizures induced by acute exposure to an organophosphate herbicide, glufosinate-ammonium. Neuroreport 27, 532–541.

Santos-Durán, G.N., Menuet, A., Lagadec, R., Mayeur, H., Ferreiro-Galve, S., Mazan, S., Rodríguez-Moldes, I. & Candal, E. (2015) Prosomeric organization of the hypothalamus in an elasmobranch, the catshark Scyliorhinus canicula. Front Neuroanat 9, 37.

Nadal, M., Laudier, B., Malinge, M.C., Binois, R. & Estève, E. (2015) [Aquagenic palmar keratoderma in a patient heterozygous for the mutation c.3197G>C in the CFTR gene]. Ann Dermatol Venereol 142, 201–205.

Lagadec, R., Laguerre, L., Menuet, A., Amara, A., Rocancourt, C., Péricard, P., Godard, B.G., Celina Rodicio, M., Rodriguez-Moldes, I., Mayeur, H., Rougemont, Q., Mazan, S. & Boutet, A. (2015) The ancestral role of nodal signalling in breaking L/R symmetry in the vertebrate forebrain. Nat Commun 6, 6686.

Vanmarsenille, L., Giannandrea, M., Fieremans, N., Verbeeck, J., Belet, S., Raynaud, M., Vogels, A., Männik, K., Õunap, K., Jacqueline, V., Briault, S., Van Esch, H., D’Adamo, P. & Froyen, G. (2014) Increased dosage of RAB39B affects neuronal development and could explain the cognitive impairment in male patients with distal Xq28 copy number gains. Hum Mutat 35, 377–383.

Utami, K.H., Hillmer, A.M., Aksoy, I., Chew, E.G.Y., Teo, A.S.M., Zhang, Z., Lee, C.W.H., Chen, P.J., Seng, C.C., Ariyaratne, P.N., Rouam, S.L., Soo, L.S., Yousoof, S., Prokudin, I., Peters, G., Collins, F., Wilson, M., Kakakios, A., Haddad, G., Menuet, A., Perche, O., Tay, S.K.H., Sung, K.W.K., Ruan, X., Ruan, Y., Liu, E.T., Briault, S., Jamieson, R.V., Davila, S. & Cacheux, V. (2014) Detection of chromosomal breakpoints in patients with developmental delay and speech disorders. PLoS ONE 9, e90852.

Rossignol, R., Ranchon-Cole, I., Pâris, A., Herzine, A., Perche, A., Laurenceau, D., Bertrand, P., Cercy, C., Pichon, J., Mortaud, S., Briault, S., Menuet, A. & Perche, O. (2014) Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome. PLoS ONE 9, e105996.

Perche, O., Vergnaud-Gauduchon, J., Morand, C., Dubray, C., Mazur, A. & Vasson, M.-P. (2014) Orange juice and its major polyphenol hesperidin consumption do not induce immunomodulation in healthy well-nourished humans. Clin Nutr 33, 130–135.

Laugeray, A., Herzine, A., Perche, O., Hébert, B., Aguillon-Naury, M., Richard, O., Menuet, A., Mazaud-Guittot, S., Lesné, L., Briault, S., Jegou, B., Pichon, J., Montécot-Dubourg, C. & Mortaud, S. (2014) Pre- and postnatal exposure to low dose glufosinate ammonium induces autism-like phenotypes in mice. Front Behav Neurosci 8, 390.

Hébert, B., Pietropaolo, S., Même, S., Laudier, B., Laugeray, A., Doisne, N., Quartier, A., Lefeuvre, S., Got, L., Cahard, D., Laumonnier, F., Crusio, W.E., Pichon, J., Menuet, A., Perche, O. & Briault, S. (2014) Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by a BKCa channel opener molecule. Orphanet J Rare Dis 9, 124.

Clot, F., Rovelet-Lecrux, A., Lamari, F., Noël, S., Keren, B., Camuzat, A., Michon, A., Jornea, L., Laudier, B., de Septenville, A., Caroppo, P., Campion, D., Cazeneuve, C., Brice, A., LeGuern, E., Le Ber, I. & French clinical and genetic research network on FTLD/FTLD-ALS. (2014) Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics 15, 95–100.

Briault, S. & Hébert, B. (2014) L’apport de la génétique à la compréhension des origines de l’autisme. Dunod.

Perche, O., Menuet, A., Marcos, M., Liu, L., Pâris, A., Utami, K.H., Kervran, D., Cacheux, V., Laudier, B. & Briault, S. (2013) Combined deletion of two Condensin II system genes (NCAPG2 and MCPH1) in a case of severe microcephaly and mental deficiency. Eur J Med Genet 56, 635–641.

Perche, O., Haddad, G., Menuet, A., Callier, P., Marcos, M., Briault, S. & Laudier, B. (2013) Dysregulation of FOXG1 pathway in a 14q12 microdeletion case. Am J Med Genet A 161A, 3072–3077.

Leroy, C., Landais, E., Briault, S., David, A., Tassy, O., Gruchy, N., Delobel, B., Grégoire, M.-J., Leheup, B., Taine, L., Lacombe, D., Delrue, M.-A., Toutain, A., Paubel, A., Mugneret, F., Thauvin-Robinet, C., Arpin, S., Le Caignec, C., Jonveaux, P., Beri, M., Leporrier, N., Motte, J., Fiquet, C., Brichet, O., Mozelle-Nivoix, M., Sabouraud, P., Golovkine, N., Bednarek, N., Gaillard, D. & Doco-Fenzy, M. (2013) The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients. Eur J Hum Genet 21, 602–612.

Vu, P.Y., Toutain, J., Cappellen, D., Delrue, M.-A., Daoud, H., El Moneim, A.A., Barat, P., Montaubin, O., Bonnet, F., Dai, Z.Q., Philippe, C., Tran, C.T., Rooryck, C., Arveiler, B., Saura, R., Briault, S., Lacombe, D. & Taine, L. (2012) A homozygous balanced reciprocal translocation suggests LINC00237 as a candidate gene for MOMO (macrosomia, obesity, macrocephaly, and ocular abnormalities) syndrome. Am J Med Genet A 158A, 2849–2856.

Trojan, J., Pan, Y.X., Wei, M.X., Ly, A., Shevelev, A., Bierwagen, M., Ardourel, M.-Y., Trojan, L.A., Alvarez, A., Andres, C., Noguera, M.C., Briceno, I., Aristizabal, B.H., Kasprzak, H., Duc, H.T. & Anthony, D.D. (2012) Methodology for Anti-Gene Anti-IGF-I Therapy of Malignant Tumours. Chemother Res Pract 2012, 721873.

Perche, O., Laudier, B., Menuet, A., Odent, S., Laumonnier, F. & Briault, S. (2012) FG syndrome: the FGS2 locus revisited. Am J Med Genet A 158A, 1489–1492.

Godin, F., Villette, S., Vallée, B., Doudeau, M., Morisset-Lopez, S., Ardourel, M., Hevor, T., Pichon, C. & Bénédetti, H. (2012) A fraction of neurofibromin interacts with PML bodies in the nucleus of the CCF astrocytoma cell line. Biochem Biophys Res Commun 418, 689–694.

Villar-Cerviño, V., Rocancourt, C., Menuet, A., Da Silva, C., Wincker, P., Anadón, R., Mazan, S. & Rodicio, M.C. (2010) A vesicular glutamate transporter in lampreys: cDNA cloning and early expression in the nervous system. J Chem Neuroanat 40, 71–81.

Trojan, J., Ly, A., Wei, M.X., Bierwagen, M., Kopinski, P., Pan, Y., Ardourel, M.-Y., Dufour, T., Shevelev, A., Trojan, L.A., François, J.-C., Andres, C., Popiela, T., Chatel, M., Kasprzak, H., Anthony, D.D. & Duc, H.T. (2010) Antisense anti IGF-I cellular therapy of malignant tumours: immune response in cancer patients. Biomed Pharmacother 64, 576–578.

Perche, O., Laumonnier, F., Baala, L., Ardourel, M.-Y., Menuet, A., Robin, V., Mortaud, S., Montécot-Dubourg, C., Richard, O., Pichon, J. & Briault, S. (2010) [Autism, genetics and synaptic function alterations]. Pathol Biol 58, 381–386.

Laumonnier, F., Shoubridge, C., Antar, C., Nguyen, L.S., Van Esch, H., Kleefstra, T., Briault, S., Fryns, J.P., Hamel, B., Chelly, J., Ropers, H.H., Ronce, N., Blesson, S., Moraine, C., Gécz, J. & Raynaud, M. (2010) Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism. Mol Psychiatry 15, 767–776.

Abellan, A., Menuet, A., Dehay, C., Medina, L. & Rétaux, S. (2010) Differential expression of LIM-homeodomain factors in Cajal-Retzius cells of primates, rodents, and birds. Cereb Cortex 20, 1788–1798.