Hagens, O.: Search for genes involved in human cognition : molecular characterisation of two novel genes, FBXO25 and KIAA1202, disrupted by a translocation in a mentally retarded patient. Doktorarbeit, Freie Universität, Berlin (2006).
Dadgar, S., O. Hagens, S. R. Dadgar, E. N. Haghighi, S. Schimpf, B. Wissinger and M. Garshasbi: Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy. In: Experimental Eye Research 83, 3, 702-706 (2006).
doi: 10.1016/j.exer.2006.03.004
Hagens, O., A. Ballabio, V. M. Kalscheuer, J.-P. Kraehenbuhl, M. V. Schiaffino, P. Smith, O. Staub, J. Hildebrand and J. B. Wallingford: A new standard nomenclature for proteins related to Apx and Shroom. In: BMC Cell Biology 7, 18-19 (2006).
doi: 10.1186/1471-2121-7-18
Cossée, M., B. Demeer, P. Blanchet, B. Echenne, D. Singh, O. Hagens, M. Antin, S. Finck, L. Vallee, H. Dollfus, S. Hegde, K. Springell, B. K. Thelma, G. Woods, V. M. Kalscheuer and J.-L. Mandel: Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect. In: European Journal of Human Genetics : the Official Journal of the European Society of Human Genetics 14, 4, 418-425 (2006).
doi: 10.1038/sj.ejhg.5201593
Hagens, O., A. Dubos, F. Abidi, G. Barbi, L. Van Zutven, M. Hoeltzenbein, N. Tommerup, C. Moraine, J.-P. Fryns, J. Chelly, H. van Bokhoven, J. Gécz, H. Dollfus, H.-H. Ropers, C. E. Schwartz, R. de Cassia Stocco dos Santos, V. M. Kalscheuer and A. Hanauer: Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation. In: Human Genetics 118, 5, 578-590 (2006).
doi: 10.1007/s00439-005-0072-2
Hagens, O., E. Minina, S. Schweiger, H.-H. Ropers and V. M. Kalscheuer: Characterization of FBX25, encoding a novel brain-expressed F-box protein. In: Biochimica et Biophysica Acta (BBA) - General Subjects 1760, 1, 110-118 (2006).
doi: 10.1016/j.bbagen.2005.09.018
Shoichet, S. A., L. Duprez, O. Hagens, V. Waetzig, C. Menzel, T. Herdegen, S. Schweiger, B. Dan, E. Vamos, H.-H. Ropers and V. M. Kalscheuer: Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy. In: Human Genetics 118, 5, 559-567 (2006).
doi: 10.1007/s00439-005-0084-y
Kalscheuer, V. M., K. Freude, L. Musante, L. R. Jensen, H. G. Yntema, J. Gecz, A. Sefiani, K. Hoffmann, B. Moser, S. Haas, U. Gurok, S. Haesler, B. Aranda, A. Nshedjan, A. Tzschach, N. Hartmann, T.-C. Roloff, S. Shoichet, O. Hagens, J. Tao, H. van Bokhoven, G. Turner, J. Chelly, C. Moraine, J.-P. Fryns, U. Nuber, M. Hoeltzenbein, C. Scharff, H. Scherthan, S. Lenzner, B. C. J. Hamel, S. Schweiger and H.-H. Ropers: Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation. In: Nature Genetics 35, 4, 313-315 (2003).
doi: 10.1038/ng1264
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