 | Up a level |
2015
Thoenes, Michaela, Zimmermann, Ulrike, Ebermann, Inga, Ptok, Martin, Lewis, Morag A., Thiele, Holger, Morlot, Susanne, Hess, Markus M., Gal, Andreas, Eisenberger, Tobias, Bergmann, Carsten, Nuernberg, Gudrun, Nuernberg, Peter, Steel, Karen P., Knipper, Marlies and Bolz, Hanno Joern (2015). OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet J. Rare Dis., 10. LONDON: BMC. ISSN 1750-1172
Thoenes, Michaela, Zimmermann, Ulrike, Ebermann, Inga, Ptok, Martin, Lewis, Morag A., Thiele, Holger, Morlot, Susanne, Hess, Markus M., Gal, Andreas, Eisenberger, Tobias, Bergmann, Carsten, Nuernberg, Gudrun, Nuernberg, Peter, Steel, Karen P., Knipper, Marlies and Bolz, Hanno Joern (2015). OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet J. Rare Dis., 10. LONDON: BMC. ISSN 1750-1172
2014
Linder, Bastian 
ORCID: 0000-0003-1203-3136, Hirmer, Anja, Gal, Andreas, Ruether, Klaus, Bolz, Hanno Joern, Winkler, Christoph ORCID: 0000-0003-4688-6241, Laggerbauer, Bernhard and Fischer, Utz ORCID: 0000-0002-1465-6591
(2014).
Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa.
PLoS One, 9 (11).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203
2013
Eisenberger, Tobias, Neuhaus, Christine, Khan, Arif O., Decker, Christian, Preising, Markus N., Friedburg, Christoph, Bieg, Anika, Gliem, Martin, Issa, Peter Charbel ORCID: 0000-0002-0351-6673, Holz, Frank G., Baig, Shahid M., Hellenbroich, Yorck, Galvez, Alberto, Platzer, Konrad ORCID: 0000-0001-6127-6308, Wollnik, Bernd, Laddach, Nadja, Ghaffari, Saeed Reza, Rafati, Maryam, Botzenhart, Elke, Tinschert, Sigrid, Boerger, Doris, Bohring, Axel, Schreml, Julia, Koertge-Jung, Stefani, Schell-Apacik, Chayim, Bakur, Khadijah ORCID: 0000-0002-0668-1762, Al-Aama, Jumana Y., Neuhann, Teresa, Herkenrath, Peter, Nuernberg, Gudrun, Nuernburg, Peter, Davis, John S., Gal, Andreas, Bergmann, Carsten, Lorenz, Birgit and Bolz, Hanno J.
(2013).
Increasing the Yield in Targeted Next-Generation Sequencing by Implicating CNV Analysis, Non-Coding Exons and the Overall Variant Load: The Example of Retinal Dystrophies.
PLoS One, 8 (11).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203
2010
Winterer, Georg, Mittelstrass, Kirstin, Giegling, Ina, Lamina, Claudia ORCID: 0000-0002-5398-5806, Fehr, Christoph, Brenner, Hermann ORCID: 0000-0002-6129-1572, Breitling, Lutz P., Nitz, Barbara ORCID: 0000-0001-6289-7237, Raum, Elke, Mueller, Heiko, Gallinat, Juergen, Gal, Andreas, Heim, Katharina, Prokisch, Holger ORCID: 0000-0003-2379-6286, Meitinger, Thomas ORCID: 0000-0002-8838-8403, Hartmann, Annette M., Moeller, Hans-Juergen, Gieger, Christian ORCID: 0000-0001-6986-9554, Wichmann, H-Erich, Illig, Thomas, Dahmen, Norbert and Rujescu, Dan
(2010).
Risk Gene Variants for Nicotine Dependence in the CHRNA5-CHRNA3-CHRNB4 Cluster Are Associated With Cognitive Performance.
Am. J. Med. Genet. B, 153B (8).
S. 1448 - 1459.
HOBOKEN:
WILEY.
ISSN 1552-485X