Health professionals facing the coronavirus disease 2019 (COVID-19) pandemic: What are the mental health risks?
El-Hage, W, Hingray, C, Lemogne, C, Yrondi, A, Brunault, P, Bienvenu, T, Etain, B, Paquet, C, Gohier, B, Bennabi, D, Birmes, P, Sauvaget, A, Fakra, E, Prieto, N, Bulteau, S, Vidailhet, P, Camus, V, Leboyer, M, Krebs, M-O, Aouizerate, B
Published in Encéphale (01.06.2020)
Published in Encéphale (01.06.2020)
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Gene expression of protein synthesis, immunity and brain pathways specifically altered in Anorexia Nervosa
Ramoz, N, Verebi, C, Lebrun, N, Duriez, P, Gorwood, P, Bienvenu, T
Published in European psychiatry (01.08.2024)
Published in European psychiatry (01.08.2024)
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Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders
El Khouri, E., Ghoumid, J., Haye, D., Giuliano, F., Drevillon, L., Briand-Suleau, A., De La Grange, P., Nau, V., Gaillon, T., Bienvenu, T., Jacquemin-Sablon, H., Goossens, M., Amselem, S., Giurgea, I.
Published in Molecular psychiatry (01.07.2021)
Published in Molecular psychiatry (01.07.2021)
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Functional characterization and phenotypic spectrum of three recurrent disease-causing deep intronic variants of the CFTR gene
Bergougnoux, A., Délétang, K., Pommier, A., Varilh, J., Houriez, F., Altieri, J.P., Koenig, M., Férec, C., Claustres, M., Lalau, G., Bienvenu, T., Audrézet, M.P., Pagin, A., Girodon, E., Raynal, C., Taulan-Cadars, M.
Published in Journal of cystic fibrosis (01.07.2019)
Published in Journal of cystic fibrosis (01.07.2019)
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CFTR gene variants: a predisposition factor to aquagenic palmoplantar keratoderma
Raynal, C., Girodon, E., Audrezet, M.P., Cabet, F., Pagin, A., Reboul, M.P., Dufernez, F., Fergelot, P., Bergougnoux, A., Fanen, P., Ferec, C., Bienvenu, T.
Published in British journal of dermatology (1951) (01.11.2019)
Published in British journal of dermatology (1951) (01.11.2019)
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Wiedemann‐Steiner syndrome as a major cause of syndromic intellectual disability: A study of 33 French cases
Baer, S., Afenjar, A., Smol, T., Piton, A., Gérard, B., Alembik, Y., Bienvenu, T., Boursier, G., Boute, O., Colson, C., Cordier, M.‐P., Cormier‐Daire, V., Delobel, B., Doco‐Fenzy, M., Duban‐Bedu, B., Fradin, M., Geneviève, D., Goldenberg, A., Grelet, M., Haye, D., Heron, D., Isidor, B., Keren, B., Lacombe, D., Lèbre, A.‐S., Lesca, G., Masurel, A., Mathieu‐Dramard, M., Nava, C., Pasquier, L., Petit, A., Philip, N., Piard, J., Rondeau, S., Saugier‐Veber, P., Sukno, S., Thevenon, J., Van‐Gils, J., Vincent‐Delorme, C., Willems, M., Schaefer, E., Morin, G.
Published in Clinical genetics (01.07.2018)
Published in Clinical genetics (01.07.2018)
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Autism spectrum disorder recurrence, resulting of germline mosaicism for a CHD2 gene missense variant
Lebrun, N., Parent, P., Gendras, J., Billuart, P., Poirier, K., Bienvenu, T.
Published in Clinical genetics (01.12.2017)
Published in Clinical genetics (01.12.2017)
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Identification of intellectual disability genes showing circadian clock-dependent expression in the mouse hippocampus
Renaud, J, Dumont, F, Khelfaoui, M, Foisset, S.R, Letourneur, F, Bienvenu, T, Khwaja, O, Dorseuil, O, Billuart, P
Published in Neuroscience (12.11.2015)
Published in Neuroscience (12.11.2015)
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Penetrance is a critical parameter for assessing the disease liability of CFTR variants
Boussaroque, A., Audrézet, M.-P., Raynal, C., Sermet-Gaudelus, I., Bienvenu, T., Férec, C., Bergougnoux, A., Lopez, M., Scotet, V., Munck, A., Girodon, E.
Published in Journal of cystic fibrosis (01.11.2020)
Published in Journal of cystic fibrosis (01.11.2020)
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Absence of annulus in human asthenozoospermia: Case Report
Lhuillier, P., Rode, B., Escalier, D., Lorès, P., Dirami, T., Bienvenu, T., Gacon, G., Dulioust, E., Touré, A.
Published in Human reproduction (Oxford) (01.06.2009)
Published in Human reproduction (Oxford) (01.06.2009)
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De novo SCN1A mutations in migrating partial seizures of infancy
Carranza Rojo, D, Hamiwka, L, McMahon, J M, Dibbens, L M, Arsov, T, Suls, A, Stödberg, T, Kelley, K, Wirrell, E, Appleton, B, Mackay, M, Freeman, J L, Yendle, S C, Berkovic, S F, Bienvenu, T, De Jonghe, P, Thorburn, D R, Mulley, J C, Mefford, H C, Scheffer, I E
Published in Neurology (26.07.2011)
Published in Neurology (26.07.2011)
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The multi-faceted nature of 15 CFTR exonic variations: Impact on their functional classification and perspectives for therapy
Bergougnoux, A., Billet, A., Ka, C., Heller, M., Degrugillier, F., Vuillaume, M.-L., Thoreau, V., Sasorith, S., Bareil, C., Thèze, C., Ferec, C., Gac, G. Le, Bienvenu, T., Bieth, E., Gaston, V., Lalau, G., Pagin, A., Malinge, M.-C., Dufernez, F., Lemonnier, L., Koenig, M., Fergelot, P., Claustres, M., Taulan-Cadars, M., Kitzis, A., Reboul, M.-P., Becq, F., Fanen, P., Mekki, C., Audrezet, M.-P., Girodon, E., Raynal, C.
Published in Journal of cystic fibrosis (01.05.2023)
Published in Journal of cystic fibrosis (01.05.2023)
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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
Bienvenu, Thierry, Poirier, Karine, Friocourt, Gaelle, Bahi, Nadia, Beaumont, Delphine, Fauchereau, Fabien, Ben Jeema, Lamia, Zemni, Ramzi, Vinet, Marie-Claude, Francis, Fiona, Couvert, Philippe, Gomot, Marie, Moraine, Claude, van Bokhoven, Hans, Kalscheuer, Vera, Frints, Suzanne, Gecz, Josef, Ohzaki, Kanae, Chaabouni, Habiba, Fryns, Jean-Pierre, Desportes, Vincent, Beldjord, Cherif, Chelly, Jamel
Published in Human molecular genetics (15.04.2002)
Published in Human molecular genetics (15.04.2002)
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The association of severe encephalopathy and question mark ear is highly suggestive of loss of MEF2C function
Gordon, C.T., Tessier, A., Demir, Z., Goldenberg, A., Oufadem, M., Voisin, N., Pingault, V., Bienvenu, T., Lyonnet, S., de Pontual, L., Amiel, J.
Published in Clinical genetics (01.02.2018)
Published in Clinical genetics (01.02.2018)
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The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening
Thauvin-Robinet, C, Munck, A, Huet, F, Génin, E, Bellis, G, Gautier, E, Audrézet, M-P, Férec, C, Lalau, G, Georges, M Des, Claustres, M, Bienvenu, T, Gérard, B, Boisseau, P, Cabet-Bey, F, Feldmann, D, Clavel, C, Bieth, E, Iron, A, Simon-Bouy, B, Costa, C, Medina, R, Leclerc, J, Hubert, D, Nové-Josserand, R, Sermet-Gaudelus, I, Rault, G, Flori, J, Leroy, S, Wizla, N, Bellon, G, Haloun, A, Perez-Martin, S, d’Acremont, G, Corvol, H, Clément, A, Houssin, E, Binquet, C, Bonithon-Kopp, C, Alberti-Boulmé, C, Morris, M A, Faivre, L, Goossens, M, Roussey, M
Published in Journal of medical genetics (01.11.2009)
Published in Journal of medical genetics (01.11.2009)
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Novel FOXG1 mutations associated with the congenital variant of Rett syndrome
Mencarelli, M A, Spanhol-Rosseto, A, Artuso, R, Rondinella, D, De Filippis, R, Bahi-Buisson, N, Nectoux, J, Rubinsztajn, R, Bienvenu, T, Moncla, A, Chabrol, B, Villard, L, Krumina, Z, Armstrong, J, Roche, A, Pineda, M, Gak, E, Mari, F, Ariani, F, Renieri, A
Published in Journal of medical genetics (01.01.2010)
Published in Journal of medical genetics (01.01.2010)
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