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Müller, T.D. ; Reichwald, K. ; Bröner, G. ; Kirschner, J. ; Nguyen, T.T. ; Scherag, A. ; Herzog, W. ; Herpertz-Dahlmann, B. ; Lichtner, P. ; Meitinger, T. ; Platzer, M. ; Schäer, H. ; Hebebrand, J. ; Hinney, A.
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa.Fatar, M. ; Stroick, M. ; Steffens, M. ; Senn, E. ; Reuter, B. ; Bukow, S. ; Griebe, M. ; Alonso, A. ; Lichtner, P. ; Bugert, P. ; Meitinger, T. ; Wienker, T.F. ; Hennerici, MG.
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes.Kemlink, D. ; Plazzi, G. ; Vetrugno, R. ; Provini, F. ; Polo, O. ; Stiasny-Kolster, K. ; Oertel, W. ; Nevsimalova, S. ; Sonka, K. ; Högl, B. ; Frauscher, B. ; Hadjigeorgiou, G.M. ; Pramstaller, P.P. ; Lichtner, P. ; Meitinger, T. ; Müller-Myhsok, B. ; Winkelmann, J. ; Montagna, P.
Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13.Ramser, J. ; Ahearn, M.E. ; Lenski, C. ; Yariz, K.O. ; Hellebrand, H. ; von, Rhein, M. ; Clark, R.D. ; Schmutzler, R.K. ; Lichtner, P. ; Hoffman, E.P. ; Meindl, A. ; Baumbach-Reardon, L.
Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy.Bouatia-Naji, N. ; De, Graeve, F. ; Brönner, G. ; Lecoeur, C. ; Vatin, V. ; Durand, E. ; Lichtner, P. ; Nguyen, T.T. ; Heude, B. ; Weill, J. ; Lévy-Marchal, C. ; Hebebrand, J. ; Froguel, P. ; Meyre, D.
INS VNTR is not associated with childhood obesity in 1,023 families: A family-based study.Wermter, A.K. ; Scherag, A. ; Meyre, D. ; Reichwald, K. ; Durand, E. ; Nguyen, T.T. ; Koberwitz, K. ; Lichtner, P. ; Meitinger, T. ; Schäfer, H. ; Hinney, A. ; Froguel, P. ; Hebebrand, J. ; Brönner, G.
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: First evidence of polar overdominance in humans.Schormair, B. ; Kemlink, D. ; Roeske, D. ; Eckstein, G.N. ; Xiong, L. ; Lichtner, P. ; Ripke, S. ; Trenkwalder, C. ; ; Stiasny-Kolster, K. ; Oertel, W. ; Bachmann, C.G. ; Paulus, W. ; Högl, B. ; Frauscher, B. ; Gschliesser, V. ; Poewe, W. ; Peglau, I. ; Vodicka, P. ; Vávrová, J. ; Sonka, K. ; Nevsimalova, S. ; Montplaisir, J. ; Turecki, G. ; Rouleau, G. ; Gieger, C. ; Illig, T. ; Wichmann, H.-E. ; Holsboer, F. ; Müller-Myhsok, B. ; Meitinger, T. ; Winkelmann, J.
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.Gschwendtner, A. ; Ripke, S. ; Freilinger, T. ; Lichtner, P. ; Müller-Myhsok, B. ; Wichmann, H.-E. ; Meitinger, T. ; Dichgans, M.
Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans.Lücking, C.B. ; Lichtner, P. ; Dichgans, M. ; Illig, T. ; Gieger, C. ; Berg, D. ; Gasser, T.
Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease.Winkelmann, J. ; Lichtner, P. ; Schormair, B. ; Uhr, M. ; Hauk, S. ; Stiasny-Kolster, K. ; Trenkwalder, C. ; Paulus, W. ; Peglau, I. ; Eisensehr, I. ; Illig, T. ; Wichmann, H.-E. ; Pfister, H. ; Golic, J. ; Bettecken, T. ; Pütz, B. ; Holsboer, F. ; Meitinger, T. ; Müller-Myhsok, B.
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.