Publikationen von Hans Hilger Ropers

Borg, I.; Squire, M.; Menzel, C.; Stout, K.; Morgan, D.; Willatt, L.; O’Brien, P. C. M.; Ferguson-Smith, M. A.; Ropers, H. H.; Tommerup, N. et al.; Kalscheuer, V. M.; Sargan, D. R.: A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation. Journal of Medical Genetics 39 (6), S. 391 - 399 (2002)

Tümer, Z.; Croucher, P. J. P.; Jensen, L. R.; Hampe, J.; Hansen, C.; Kalscheuer, V.; Ropers, H. H.; Tommerup, N.; Schreiber, S.: Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13–14 (IBD2). Gene 288 (1-2), S. 179 - 185 (2002)

Meloni, I.; Muscettola, M.; Raynaud, M.; Longo, I.; Bruttini, M.; Moizard, M.-P.; Gomot, M.; Chelly, J.; des Portes, V.; Fryns, J.-P. et al.; Ropers, H. H.; Magi, B.; Bellan, C.; Volpi, N.; Yntema, H. G.; Lewis, S. E.; Schaffer, J. E.; Renieri, A.: FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. Nature Genetics 30 (4), S. 436 - 440 (2002)

Raderschall, E.; Bazarov, A.; Cao, J.; Lurz, R.; Smith, A.; Mann, W.; Ropers, H. H.; Sedivy, J. M.; Golub, E. I.; Fritz, E. et al.; Haaf, T.: Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science 115 (1), S. 153 - 164 (2002)

Raderschall, E.; Bazarov, A.; Cao, J.; Lurz, R.; Smith, A.; Mann, W.; Ropers, H. H.; Sedivy, J. M.; Golub, E. I.; Fritz, E. et al.; Haaf, T.: Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis. Journal of Cell Science 115 (1), S. 153 - 164 (2002)

Zanni, G.; van Esch, H.; Bensalem, A.; Saillour, Y.; Poirier, K.; Castelnau, L.; Ropers, H.-H.; . de Brouwer, A. P. M.; Laumonnier, F.; Fryns, J.-P. et al.; Chelly, J.: A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation.

Erdogan, F.: Typisierung biallelischer Marker (SNPs) mit DNS-Mikrorastern. Dissertation, Freie Universtität Berlin, Berlin (2003)

Genetics of early onset cognitive impairment. Annual Reviews, Palo Alto, CA

Ropers, H.-H.: "Man sollte sich von dem Gedanken lösen, dass unser Genom uns allein gehört". (2020)