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2011 1
2013 1
2019 1
2020 0
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[Leber's Hereditary Optic Neuropathy].
Priglinger C, Klopstock T, Rudolph G, Priglinger SG. Priglinger C, et al. Among authors: rudolph g. Klin Monbl Augenheilkd. 2019 Nov;236(11):1271-1282. doi: 10.1055/a-0972-1552. Epub 2019 Oct 22. Klin Monbl Augenheilkd. 2019. PMID: 31639883 German.
Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response.
Wissinger B, Schaich S, Baumann B, Bonin M, Jägle H, Friedburg C, Varsányi B, Hoyng CB, Dollfus H, Heckenlively JR, Rosenberg T, Rudolph G, Kellner U, Salati R, Plomp A, De Baere E, Andrassi-Darida M, Sauer A, Wolf C, Zobor D, Bernd A, Leroy BP, Enyedi P, Cremers FP, Lorenz B, Zrenner E, Kohl S. Wissinger B, et al. Among authors: rudolph g. Hum Mutat. 2011 Dec;32(12):1398-406. doi: 10.1002/humu.21580. Epub 2011 Sep 12. Hum Mutat. 2011. PMID: 21882291 Free article.
Convergence of evolutionary algorithms on the n-dimensional continuous space.
Agapie A, Agapie M, Rudolph G, Zbaganu G. Agapie A, et al. Among authors: rudolph g. IEEE Trans Cybern. 2013 Oct;43(5):1462-72. doi: 10.1109/TCYB.2013.2257748. Epub 2013 May 3. IEEE Trans Cybern. 2013. PMID: 23757563