Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project
Perroud, N, Uher, R, Ng, M Y M, Guipponi, M, Hauser, J, Henigsberg, N, Maier, W, Mors, O, Gennarelli, M, Rietschel, M, Souery, D, Dernovsek, M Z, Stamp, A S, Lathrop, M, Farmer, A, Breen, G, Aitchison, K J, Lewis, C M, Craig, I W, McGuffin, P
Published in The pharmacogenomics journal (01.02.2012)
Published in The pharmacogenomics journal (01.02.2012)
Get full text
Journal Article
Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative Disorder
Varvagiannis, K, Hanquinet, S, Billieux, M H, De Luca, R, Rimensberger, P, Lidgren, M, Guipponi, M, Makrythanasis, P, Blouin, J L, Antonarakis, S E, Steinfeld, R, Kern, I, Poretti, A, Fluss, J, Fokstuen, S
Published in Neuropediatrics (01.04.2018)
Published in Neuropediatrics (01.04.2018)
Get more information
Journal Article
New insights into the pharmacogenomics of antidepressant response from the GENDEP and STARD studies: rare variant analysis and high-density imputation
Fabbri, C, Tansey, K E, Perlis, R H, Hauser, J, Henigsberg, N, Maier, W, Mors, O, Placentino, A, Rietschel, M, Souery, D, Breen, G, Curtis, C, Sang-Hyuk, L, Newhouse, S, Patel, H, Guipponi, M, Perroud, N, Bondolfi, G, O'Donovan, M, Lewis, G, Biernacka, J M, Weinshilboum, R M, Farmer, A, Aitchison, K J, Craig, I, McGuffin, P, Uher, R, Lewis, C M
Published in The pharmacogenomics journal (22.05.2018)
Published in The pharmacogenomics journal (22.05.2018)
Get full text
Journal Article
Wes of a Consanguineous Family with Schizophrenia and Mental Retardation in North Algeria
Dahdouh Guermouche, A, Guipponi, M, Prados, J, Antonarakis, S
Published in European psychiatry (28.03.2015)
Published in European psychiatry (28.03.2015)
Get full text
Journal Article
The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro
Guipponi, Michel, Vuagniaux, Grégoire, Wattenhofer, Marie, Shibuya, Kazunori, Vazquez, Maria, Dougherty, Loretta, Scamuffa, Nathalie, Guida, Elizabeth, Okui, Michiyo, Rossier, Colette, Hancock, Manuela, Buchet, Karine, Reymond, Alexandre, Hummler, Edith, Marzella, Phillip L., Kudoh, Jun, Shimizu, Nobuyoshi, Scott, Hamish S., Antonarakis, Stylianos E., Rossier, Bernard C.
Published in Human molecular genetics (01.11.2002)
Published in Human molecular genetics (01.11.2002)
Get full text
Journal Article
Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders
Fokstuen, S, Makrythanasis, P, Hammar, E, Guipponi, M, Ranza, E, Varvagiannis, K, Santoni, F A, Albarca-Aguilera, M, Poleggi, M E, Couchepin, F, Brockmann, C, Mauron, A, Hurst, S A, Moret, C, Gehrig, C, Vannier, A, Bevillard, J, Araud, T, Gimelli, S, Stathaki, E, Paoloni-Giacobino, A, Bottani, A, Sloan-Béna, F, Sizonenko, L D'Amato, Mostafavi, M, Hamamy, H, Nouspikel, T, Blouin, J L, Antonarakis, S E
Published in Human genomics (28.06.2016)
Published in Human genomics (28.06.2016)
Get full text
Journal Article
Consangunity and psychosis in Algeria. A family study
Dahdouh Guermouche, A, Prados, J, Guipponi, M, Bena, F, Stenz, L, Semaoune, B, Antonarakis, S, Hamamy, H
Published in European psychiatry (01.11.2015)
Published in European psychiatry (01.11.2015)
Get full text
Journal Article
No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients
Guipponi, M, Santoni, F, Schneider, M, Gehrig, C, Bustillo, X B, Kates, W R, Morrow, B, Armando, M, Vicari, S, Sloan-Béna, F, Gagnebin, M, Shashi, V, Hooper, S R, Eliez, S, Antonarakis, S E
Published in Translational psychiatry (21.02.2017)
Published in Translational psychiatry (21.02.2017)
Get full text
Journal Article
Copy number variants and therapeutic response to antidepressant medication in major depressive disorder
Tansey, K E, Rucker, J J H, Kavanagh, D H, Guipponi, M, Perroud, N, Bondolfi, G, Domenici, E, Evans, D M, Hauser, J, Henigsberg, N, Jerman, B, Maier, W, Mors, O, O'Donovan, M, Peters, T J, Placentino, A, Rietschel, M, Souery, D, Aitchison, K J, Craig, I, Farmer, A, Wendland, J R, Malafosse, A, Lewis, G, Kapur, S, McGuffin, P, Uher, R
Published in The pharmacogenomics journal (01.08.2014)
Published in The pharmacogenomics journal (01.08.2014)
Get full text
Journal Article
Association of the connexin36 gene with juvenile myoclonic epilepsy
Mas, C, Taske, N, Deutsch, S, Guipponi, M, Thomas, P, Covanis, A, Friis, M, Kjeldsen, M J, Pizzolato, G P, Villemure, J-G, Buresi, C, Rees, M, Malafosse, A, Gardiner, M, Antonarakis, S E, Meda, P
Published in Journal of medical genetics (01.07.2004)
Published in Journal of medical genetics (01.07.2004)
Get full text
Journal Article
412 Combination of Genomic Technologies and Consanguinity in Order to Identify Pathogenic Variants in Recessive Disorders
Makrythanasis, P, Nelis, M, Santoni, FA, Guipponi, M, Béna, F, Vanier, A, Duriaux-Sail, G, Gimelli, S, Stathaki, E, Falconnet, E, Temtamy, S, Megarbane, A, Aglan, M, Zaki, M, Fokstuen, S, Bottani, A, Masri, A, Psoni, S, Kitsiou, S, Frissyra, H, Kanavakis, E, All-Allawi, N, Sefiani, A, Al-Hait, S, Elalaoui, S, Jalkh, N, Al-Gazali, L, Al-Jasmi, F, Bouhamed, H Chaabouni, Hamamy, H, Antonarakis, SE
Published in Archives of disease in childhood (01.10.2012)
Published in Archives of disease in childhood (01.10.2012)
Get full text
Journal Article
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q
GUIPPONI, M, RIVIER, F, VIGEVANO, F, BECK, C, CRESPEL, A, ECHENNE, B, LUCCHINI, P, SEBASTIANELLI, R, BALDY-MOULINIER, M, MALAFOSSE, A
Published in Human molecular genetics (01.03.1997)
Published in Human molecular genetics (01.03.1997)
Get full text
Journal Article
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)
Giorgio, Elisa, Robyr, Daniel, Spielmann, Malte, Ferrero, Enza, Di Gregorio, Eleonora, Imperiale, Daniele, Vaula, Giovanna, Stamoulis, Georgios, Santoni, Federico, Atzori, Cristiana, Gasparini, Laura, Ferrera, Denise, Canale, Claudio, Guipponi, Michel, Pennacchio, Len A, Antonarakis, Stylianos E, Brussino, Alessandro, Brusco, Alfredo
Published in Human molecular genetics (01.06.2015)
Published in Human molecular genetics (01.06.2015)
Get full text
Journal Article
A nonsense mutation in the α4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI)
Beck, C., Moulard, B., Steinlein, O., Guipponi, M., Vallee, L., Montpied, P., Baldy-Moulnier, M., Malafosse, A.
Published in Neurobiology of disease (01.11.1994)
Published in Neurobiology of disease (01.11.1994)
Get full text
Journal Article
SHANK3 mutation in consanguineous schizophrenia family in northwest Algeria
Dahdouh, A., Prados, J., Guipponi, M., Bena, F., Adouan, W., Antonarakis, S.
Published in European psychiatry (01.04.2017)
Published in European psychiatry (01.04.2017)
Get full text
Journal Article
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
Masmoudi, S., Antonarakis, S.E., Schwede, T., Ghorbel, A.M., Grati, M., Pappasavas, M.-P., Drira, M., Elgaied-Boulila, A., Wattenhofer, M., Rossier, C., Scott, H.S., Ayadi, H., Guipponi, M.
Published in Human mutation (01.02.2002)
Published in Human mutation (01.02.2002)
Get full text
Journal Article
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
Béna, Frédérique, Bruno, Damien L., Eriksson, Mats, van Ravenswaaij-Arts, Conny, Stark, Zornitza, Dijkhuizen, Trijnie, Gerkes, Erica, Gimelli, Stefania, Ganesamoorthy, Devika, Thuresson, Ann Charlotte, Labalme, Audrey, Till, Marianne, Bilan, Frédéric, Pasquier, Laurent, Kitzis, Alain, Dubourgm, Christele, Rossi, Massimiliano, Bottani, Armand, Gagnebin, Maryline, Sanlaville, Damien, Gilbert-Dussardier, Brigitte, Guipponi, Michel, van Haeringen, Arie, Kriek, Marjolein, Ruivenkamp, Claudia, Antonarakis, Stylianos E., Anderlid, Britt Marie, Slater, Howard R., Schoumans, Jacqueline
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2013)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.06.2013)
Get full text
Journal Article
Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis
Tansey, Katherine E, Guipponi, Michel, Perroud, Nader, Bondolfi, Guido, Domenici, Enrico, Evans, David, Hall, Stephanie K, Hauser, Joanna, Henigsberg, Neven, Hu, Xiaolan, Jerman, Borut, Maier, Wolfgang, Mors, Ole, O'Donovan, Michael, Peters, Tim J, Placentino, Anna, Rietschel, Marcella, Souery, Daniel, Aitchison, Katherine J, Craig, Ian, Farmer, Anne, Wendland, Jens R, Malafosse, Alain, Holmans, Peter, Lewis, Glyn, Lewis, Cathryn M, Stensbøl, Tine Bryan, Kapur, Shitij, McGuffin, Peter, Uher, Rudolf
Published in PLoS medicine (01.10.2012)
Published in PLoS medicine (01.10.2012)
Get full text
Journal Article