Publikationen von 0000-0002-9323-7140
(ORCID: 0000-0002-9323-7140)

Friedrich, U., Myers, C. A., Fritsche, L. G. , Milenkovic, Andrea, Wolf, A., Corbo, J. C. und Weber, Bernhard H. F. (2011) Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency. Human Molecular Genetics 20, S. 1387-1399. Volltext nicht vorhanden.

Corbo, Joseph C. , Lawrence, Karen A. , Karlstetter, Marcus, Myers, Connie A., Abdelaziz, Musa, Dirkes, William, Weigelt, Karin, Seifert, Martin, Benes, Vladimir , Fritsche, Lars G. , Weber, Bernhard H. F. und Langmann, Thomas (2010) CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors. Genome research 20 (11), S. 1512-25. Volltext nicht vorhanden.

Langmann, Thomas, Di Gioia, S. A., Rau, I., Stöhr, Heidi, Maksimovic, N. S., Corbo, J. C. , Renner, Agnes B., Zrenner, Eberhart, Kumaramanickavel, G., Karlstetter, Marcus, Arsenijevic, Y., Weber, Bernhard H. F. , make_name_string expected hash reference und make_name_string expected hash reference (2010) Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa. American Journal of Human Genetics 87, S. 376-381. Volltext nicht vorhanden.