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Issue DateTitleAuthor(s)
23-Mar-2022DNA methylation in Friedreich ataxia silences expression of frataxin isoform ERodden, LN; Gilliam, KM; Lam, C; Rojsajjakul, T; Mesaros, C; Dionisi, C; Pook, M; Pandolfo, M; Lynch, DR; Blair, IA; Bidichandani, SI
20-Dec-2022Language impairment in the genetic forms of behavioural variant frontotemporal dementiaSamra, K; MacDougall, AM; Bouzigues, A; Bocchetta, M; Cash, DM; Greaves, CV; Convery, RS; van Swieten, JC; Seelaar, H; Jiskoot, L; Moreno, F; Lombardi, J; Anderl-Straub, S; Rollin, A; Kuchcinski, G; Tábuas-Pereira, M; Masellis, M; Afonso, S; Tartaglia, MC; Rowe, JB; Borroni, B; Gasparotti, R; Finger, E; Arighi, A; Synofzik, M; Rossi, G; Galimberti, D; Vandenberghe, R; de Mendonça, A; Butler, CR; Gerhard, A; Ducharme, S; Archetti, S; Le Ber, I; Tiraboschi, P; Fenoglio, C; Santana, I; Pasquier, F; Giaccone, G; Levin, J; Otto, M; Sorbi, S; Rohrer, JD; Gazzina, S; Russell, LL; Nelson, A; Thomas, DL; Scarpini, E; Todd, E; Benotmane, H; Nicholas, J; Di Fede, G; Shafei, R; Timberlake, C; Cantoni, V; Cope, T; Rittman, T; Benussi, A; Premi, E; Fumagalli, G; Caroppo, P; Borracci, V; Tiraboschi, P; Prioni, S; Redaelli, V; Tang-Wai, D; Olives, J; Rogaeva, E; Verdelho, A; Castelo-Branco, M; Gabilondo, A; Freedman, M; Keren, R; Black, S; Mitchell, S; Shoesmith, C; Bartha, R; Balasa, M; Rademakers, R; Poos, J; Maruta, C; Papma, JM; Giannini, L; Gorostidi, A; van Minkelen, R; Pijnenburg, Y; Nacmias, B; Ferrari, C; Bargalló, N; Polito, C; Lombardi, G; Bessi, V; Ferreira, CB; Veldsman, M; Andersson, C; Thonberg, H; Villanua, J; Öijerstedt, L; Jelic, V; Borrego-Ecija, S; Thompson, P; Langheinrich, T; Lladó, A; Antonell, A; Miltenberger, G; Cañada, M; do Couto, FS; Tainta, M; Zulaica, M; Barandiaran, M; Alves, P; Bertoux, M; Bender, B; Duro, D; Wilke, C; Sanchez-Valle, R; Graf, L; Vogels, A; Vandenbulcke, M; Van Damme, P; Bruffaerts, R; Poesen, K; Lebouvier, T; Rosa-Neto, P; Gauthier, S; Leitão, MJ; Camuzat, A; Brice, A; Laforce, R; Bertrand, A; Funkiewiez, A; Rinaldi, D; Saracino, D; Deramecourt, V; Colliot, O; Sayah, S; Prix, C; Almeida, MR; Wlasich, E; Wagemann, O; Loosli, S; Graff, C; Schönecker, S; Hoegen, T; Santiago, B
22-Dec-20223D genome organizationSilahtaroglu, A; Bridger, JM; Lei, EP
17-Nov-2022Motor symptoms in genetic frontotemporal dementia: developing a new module for clinical rating scalesSamra, K; MacDougall, AM; Peakman, G; Bouzigues, A; Bocchetta, M; Cash, DM; Greaves, CV; Convery, RS; van Swieten, JC; Jiskoot, L; Seelaar, H; Butler, CR; Fenoglio, C; Rohrer, JD; Gerhard, A; Ducharme, S; Le Ber, I; Tiraboschi, P; Santana, I; Pasquier, F; Levin, J; Shoesmith, C; Otto, M; Russell, LL; Nelson, A; Bocchetta, M; Cash, D; Thomas, DL; Todd, E; Ferrari, C; Benotmane, H; Timberlake, C; Gabilondo, A; Cope, T; Rittman, T; Benussi, A; Premi, E; Gasparotti, R; Thompson, P; Archetti, S; Fumagalli, G; do Couto, FS; Borracci, V; Polito, C; Rossi, G; Giaccone, G; Di Fede, G; Caroppo, P; Ferreira, CB; Tiraboschi, P; Prioni, S; Langheinrich, T; Redaelli, V; Lladó, A; Bartha, R; Tang-Wai, D; Rogaeva, E; Castelo-Branco, M; Freedman, M; Keren, R; Black, S; Mitchell, S; Miltenberger, G; Rademakers, R; Poos, J; Papma, JM; Giannini, L; van Minkelen, R; Pijnenburg, Y; Gauthier, S; Nacmias, B; Lombardi, G; Bessi, V; Veldsman, M; Andersson, C; Thonberg, H; Öijerstedt, L; Prix, C; Jelic, V; Antonell, A; Graff, C; Olives, J; Balasa, M; Bargalló, N; Borrego-Ecija, S; Verdelho, A; Kuchcinski, G; Maruta, C; Gorostidi, A; Laforce, R; Villanua, J; Wlasich, E; Cañada, M; Tainta, M; Zulaica, M; Barandiaran, M; Moreno, F; Alves, P; Bender, B; Bertoux, M; Wilke, C; Lebouvier, T; Camuzat, A; Graf, L; Vogels, A; Vandenbulcke, M; Van Damme, P; Bruffaerts, R; Poesen, K; Rosa-Neto, P; Sanchez-Valle, R; Brice, A; Bertrand, A; Funkiewiez, A; Rinaldi, D; Saracino, D; Colliot, O; Sorbi, S; Sayah, S; Wagemann, O; Loosli, S; Schönecker, S; Hoegen, T; Lombardi, J; Anderl-Straub, S; Nicholas, J; Rollin, A; Deramecourt, V; Arighi, A; Santiago, B; Duro, D; Leitão, MJ; Almeida, MR; Tábuas-Pereira, M; Gazzina, S; Afonso, S; Masellis, M; Samra, K; Tartaglia, C; Shafei, R; Rowe, JB; Borroni, B; Finger, E; Synofzik, M; Galimberti, D; Vandenberghe, R; de Mendonça, A; Cantoni, V
29-Dec-2022Associations of genetically predicted fatty acid levels across the phenome: A mendelian randomisation studyZagkos, L; Dib, MJ; Pinto, R; Gill, D; Koskeridis, F; Drenos, F; Markozannes, G; Elliott, P; Zuber, V; Tsilidis, K; Dehghan, A; Tzoulaki, I
5-May-2022HIV- 1 lentivirus tethering to the genome is associated with transcription factor binding sites found in genes that favour virus survivalSuleman, S; Payne, A; Bowden, J; Al Haque, S; Zahn, M; Fawaz, S; Khalifa, M; Jobling, S; Hay, D; Franco, M; Fronza, R; Wang, W; Strobel-Freidekind, O; Deichmann, A; Takeuchi, Y; Waddington, SN; Gil-Farina, I; Schmidt, M; Themis, M
4-Jan-2022Latent subtypes of manic and/or irritable episode symptoms in two population-based cohortsArathimos, R; Fabbri, C; Vassos, E; Davis, KAS; Pain, O; Gillett, A; Coleman, JRI; Hanscombe, K; Hagenaars, S; Jermy, B; Corbett, A; Ballard, C; Aarsland, D; Creese, B; Lewis, CM