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Wang, H.J. ; Wermter, AK. ; Nguyen, T.T. ; Scherag, A. ; Reichwald, K. ; Waldenmaier, B. ; Lichtner, P. ; Bettecken, T. ; Hebebrand, J. ; Hinney, A.
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans.Müller, T.D. ; Reichwald, K. ; Wermter, A.K. ; Brönner, G. ; Nguyen, T.T. ; Friedel, S. ; Koberwitz, K. ; Engeli, S. ; Lichtner, P. ; Meitinger, T. ; Schäfer, H. ; Hebebrand, J. ; Hinney, A.
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.Kemlink, D. ; Polo, O. ; Montagna, P. ; Provini, F. ; Stiasny-Kolster, K. ; Oertel, W. ; de Weerd, A. ; Nevsimalova, S. ; Sonka, K. ; Högl, B. ; Frauscher, B. ; Poewe, W. ; Trenkwalder, C. ; Pramstaller, P.P. ; Ferini-Strambi, L. ; Zucconi, M. ; Konofal, E. ; Arnulf, I. ; Hadjigeorgiou, G.M. ; Happe, S. ; Klein, C. ; Hiller, A. ; Lichtner, P. ; Meitinger, T. ; Müller-Myhsok, B. ; Winkelmann, J.
Family-based association study of the restless legs syndrome loci 2 and 3 in a European population.Winkelmann, J. ; Schormair, B. ; Lichtner, P. ; Ripke, S. ; Xiong, L. ; Jalilzadeh, S ; Fulda, S. ; Pütz, B. ; Eckstein, G. ; Hauk, S. ; Trenkwalder, C. ; ; Stiasny-Kolster, K. ; Oertel, W. ; Bachmann, C.G. ; Paulus, W. ; Peglau, I. ; Eisensehr, I. ; Montplaisir, J. ; Turecki, G. ; Rouleau, G. ; Gieger, C. ; Illig, T. ; Wichmann, H.-E. ; Holsboer, F. ; Müller-Myhsok, B. ; Meitinger, T.
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.Haubenberger, D. ; Bonelli, S. ; Hotzy, C. ; Leitner, P. ; Lichtner, P. ; Samal, D. ; Katzenschlager, R. ; Djamshidian, A. ; Brücke, T. ; Steffelbauer, M. ; Bancher, C. ; Grossmann, J. ; Ransmayr, G. ; Strom, T.M. ; Meitinger, T. ; Gasser, T. ; Auff, E. ;
A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease.Collin, R.W. ; Kalay, E. ; Oostrik, J. ; Caylan, R. ; Wollnik, B. ; Arslan, S. ; den Hollander, A.I. ; Birinci, Y. ; Lichtner, P. ; Strom, T.M. ; Toraman, B. ; Hoefsloot, L.H. ; Cremers, C.W. ; Brunner, H.G. ; Cremers, F.P. ; Karaguzel, A. ; Kremer, H.
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.Fisher, S.A. ; Rivera, A. ; Fritsche, L.G. ; Keilhauer, C.N. ; Lichtner, P. ; Meitinger, T. ; Rudolph, G. ; Weber, B.H.F.
Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD).