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PreviewIssue DateTitleAuthor(s)
2004Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardationFreude, K.; Hoffmann, K.; Jensen, L.; Delatycki, M.; des Portes, V.; Moser, B.; Hamel, B.; van Bokhoven, H.; Moraine, C.; Fryns, J.; Chelly, J.; Gecz, J.; Lenzner, S.; Kalscheuer, V.; Ropers, H.
2014Nonsense-mediated mRNA decay: Inter-individual variability and human diseaseNguyen, L.; Wilkinson, M.; Gecz, J.
2007Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humansWu, Y.; Arai, A.; Rumbaugh, G.; Srivastava, A.; Turner, G.; Hayashi, T.; Suzuki, E.; Jiang, Y.; Zhang, L.; Rodriguez, J.; Boyle, J.; Tarpey, P.; Raymond, F.; Nevelsteen, J.; Froyen, G.; Stratton, M.; Futreal, P.; Gecz, J.; Stevenson, R.; Schwartz, C.; et al.
2005Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardationJensen, L.; Amende, M.; Gurok, U.; Moser, B.; Gimmel, V.; Tzschach, A.; Janecke, A.; Tariverdian, G.; Chelly, J.; Fryns, J.; Van Esch, H.; Kleefstra, T.; Hamel, B.; Moraine, C.; Gecz, J.; Turner, G.; Reinhardt, R.; Kalscheuer, V.; Ropers, H.; Lenzer, S.
2007Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic regionFroyen, G.; Bauters, M.; Boyle, J.; Van Esch, H.; van Bokhoven, H.; Ropers, H.; Moraine, C.; Chelly, J.; Fryns, J.; Marynen, P.; Gecz, J.; Turner, G.
2011Identification of a microRNA that activates gene expression by repressing nonsense-mediated RNA decayBruno, I.; Karam, R.; Huang, L.; Bhardwaj, A.; Lou, C.; Shum, E.; Song, H.; Corbett, M.; Gifford, W.; Gecz, J.; Pfaff, S.; Wilkinson, M.
2012A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disabilityHuang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
2009The genetic landscape of intellectual disability arising from chromosome XGecz, J.; Shoubridge, C.; Corbett, M.
2014Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformationsScheffer, I.; Heron, S.; Regan, B.; Mandelstam, S.; Crompton, D.; Hodgson, B.; Licchetta, L.; Provini, F.; Bisulli, F.; Vadlamudi, L.; Gecz, J.; Connelly, A.; Tinuper, P.; Ricos, M.; Berkovic, S.; Dibbens, L.
2015Cerebral palsy: causes, pathways, and the role of genetic variantsMacLennan, A.; Thompson, S.; Gecz, J.