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2021
Schwarm, Christian, Gola, Damian, Holtsche, Maike M., Dieterich, Anabelle, Bhandari, Anita, Freitag, Miriam, Nuernberg, Peter, Toliat, Mohammad, Lieb, Wolfgang, Wittig, Michael, Franke, Andre 
ORCID: 0000-0003-1530-5811, Worm, Margitta, Sticherling, Michael, Ehrchen, Jan, Guenther, Claudia, Glaeser, Regine, Peitsch, Wiebke K., Sardy, Miklos, Eming, Ruediger, Hertl, Michael, Benoit, Sandrine, Goebeler, Matthias, Pfoehler, Claudia, Kunz, Manfred, Kreuter, Alexander ORCID: 0000-0003-2275-499X, van Beek, Nina, Erdmann, Jeanette ORCID: 0000-0002-4486-6231, Busch, Hauke, Zillikens, Detlef, Sadik, Christian D., Hirose, Misa, Koenig, Inke R., Schmidt, Enno and Ibrahim, Saleh M.
(2021).
Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and-DRB1*07:01, in Germans.
Orphanet J. Rare Dis., 16 (1).
LONDON:
BMC.
ISSN 1750-1172
2019
Bustos, Bernabe I., Perez-Palma, Eduardo ORCID: 0000-0003-0546-5141, Buch, Stephan, Azocar, Lorena, Riveras, Eleodoro, Ugarte, Giorgia D., Toliat, Mohammad, Nuernberg, Peter, Lieb, Wolfgang, Franke, Andre, Hinz, Sebastian, Burmeister, Greta, von Schoenfels, Witigo, Schafmayer, Clemens, Voelzke, Henry, Voelker, Uwe, Homuth, Georg, Lerch, Markus M. ORCID: 0000-0002-9643-8263, Luis Santos, Jose, Puschel, Klaus, Bambs, Claudia, Carlos Roa, Juan, Gutierrez, Rodrigo A., Hampe, Jochen ORCID: 0000-0002-2421-6127, De Ferrari, Giancarlo V. and Francisco Miquel, Juan
(2019).
Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry.
Sci Rep, 9.
LONDON:
NATURE PUBLISHING GROUP.
ISSN 2045-2322
Perrech, Moritz, Dreher, Lena, Roehn, Gabriele, Stavrinou, Pantelis, Krischek, Boris, Toliat, Mohammad, Goldbrunner, Roland and Timmer, Marco (2019). Qualitative and Quantitative Analysis of IDH1 Mutation in Progressive Gliomas by Allele-Specific qPCR and Western Blot Analysis. Technol. Cancer Res. Treat., 18. THOUSAND OAKS: SAGE PUBLICATIONS INC. ISSN 1533-0338
2018
Eisenberger, Tobias, Di Donato, Nataliya ORCID: 0000-0001-9439-4677, Decker, Christian, Delle Vedove, Andrea, Neuhaus, Christine, Nuernberg, Gudrun, Toliat, Mohammad, Nuernberg, Peter, Muerbe, Dirk and Bolz, Hanno Joern
(2018).
A C-terminal nonsense mutation links PTPRQ with autosomal-dominant hearing loss, DFNA73.
Genet. Med., 20 (6).
S. 614 - 622.
NEW YORK:
NATURE PUBLISHING GROUP.
ISSN 1530-0366