Publications of Hans Hilger Ropers

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), pp. 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), pp. 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), pp. 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", Welt (2020-09-12 Ed.), p. 20 (2020)