Publikationen von Juliane Winkelmann

Tilch, E.; Schormair, B.; Zhao, C.; Hoegl, B.; Stefani, A.; Berger, K.; Trenkwalder, C.; Bachmann, C. G.; Hornyak, M.; Fietze, I. et al.; Mueller-Nurasyid, M.; Peters, A.; Herms, S.; Noethen, M. M.; Mueller-Myhsok, B.; Oexle, K.; Winkelmann, J.: ExomeChip-based rare variant association study in restless legs syndrome. SLEEP MEDICINE 94, S. 26 - 30 (2022)

Oexle, K.; Schormair, B.; Ried, J. S.; Czamara, D.; Heim, K.; Frauscher, B.; Hoegl, B.; Trenkwalder, C.; Fiedler, G. M.; Thiery, J. et al.; Lichtner, P.; Prokisch, H.; Specht, M.; Mueller-Myhsok, B.; Doering, A.; Gieger, C.; Peters, A.; Wichmann, H.-E.; Meitinger, T.; Winkelmann, J.: Dilution of candidates: the case of iron-related genes in restless legs syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS 21 (4), S. 410 - 414 (2013)

Schormair, B.; Plag, J.; Kaffe, M.; Gross, N.; Czamara, D.; Samtleben, W.; Lichtner, P.; Ströhle, A.; Stefanidis, I.; Vainas, A. et al.; Dardiotis, E.; Sakkas, G. K.; Gieger, C.; Müller-Myhsok, B.; Meitinger, T.; Heemann, U.; Hadjigeorgiou, G. M.; Oexle, K.; Winkelmann, J.: MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease. Journal of Medical Genetics 48 (7), S. 462 - 466 (2011)

Winkelmann, J.; Czamara, D.; Schormair, B.; Knauf, F.; Schulte, E. C.; Trenkwalder, C.; Dauvilliers, Y.; Polo, O.; Högl, B.; Berger, K. et al.; Fuhs, A.; Gross, N.; Stiasny-Kolster, K.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Xiong, L.; Montplaisir, J.; Rouleau, G. A.; Fietze, I.; Vavrova, J.; Kemlink, D.; Sonka, K.; Nevsimalova, S.; Lin, S. C.; Wszolek, Z.; Vilarino-Guell, C.; Farrer, M. J.; Gschliesser, V.; Frauscher, B.; Falkenstetter, T.; Poewe, W.; Allen, R. P.; Earley, C. J.; Ondo, W. G.; Le, W. D.; Spieler, D.; Kaffe, M.; Zimprich, A.; Kettunen, J.; Perola, M.; Silander, K.; Cournu-Rebeix, I.; Francavilla, M.; Fontenille, C.; Fontaine, B.; Vodicka, P.; Prokisch, H.; Lichtner, P.; Peppard, P.; Faraco, J.; Mignot, E.; Gieger, C.; Illig, T.; Wichmann, H. E.; Müller-Myhsok, B.; Meitinger, T.: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1. PLoS Genetics 7 (7), e1002171 (2011)

Oexle, K.; Ried, J. S.; Hicks, A. A.; Tanaka, T.; Hayward, C.; Bruegel, M.; Gögele, M.; Lichtner, P.; Müller-Myhsok, B.; Döring, A. et al.; Illig, T.; Schwienbacher, C.; Minelli, C.; Pichler, I.; Fiedler, G. M.; Thiery, J.; Rudan, I.; Wright, A. F.; Campbell, H.; Ferrucci, L.; Bandinelli, S.; Pramstaller, P. P.; Wichmann, H. E.; Gieger, C.; Winkelmann, J.; Meitinger, T.: Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Human Molecular Genetics 20 (5), S. 1042 - 1047 (2011)

Fulda, S.; Beitinger, M. E.; Reppermund, S.; Winkelmann, J.; Wetter, T. C.: Short-Term Attention and Verbal Fluency is Decreased in Restless Legs Syndrome Patients. Movement Disorders 25 (15), S. 2641 - 2648 (2010)

Kemlink, D.; Polo, O.; Frauscher, B.; Gschliesser, V.; Hogl, B.; Poewe, W.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S. et al.; Schormair, B.; Lichtner, P.; Silander, K.; Peltonen, L.; Gieger, C.; Wichmann, H. E.; Zimprich, A.; Roeske, D.; Müller-Myhsok, B.; Meitinger, T.; Winkelmann, J.: Replication of restless legs syndrome loci in three European populations. Journal of Medical Genetics 46 (5), S. 315 - 318 (2009)

Kemlink, D.; Vavrova, J.; Högl, B.; Frauscher, B.; Polo, O.; Silander, K.; Müller-Myhsok, B.; Winkelmann, J.: Independent replication of association of restless legs syndrome to MEIS1, BTBD9 and MAP2K5/LBXCOR1 in the European population. Journal of Sleep Research 17 (Suppl. 1), S. 26 - 26 (2008)

Ambrosius, U.; Lietzenmaier, S.; Wehrle, R.; Wichniak, A.; Kalus, S.; Winkelmann, J.; Bettecken, T.; Holsboer, F.; Yassouridis, A.; Friess, E.: Heritability of sleep electroencephalogram. Biological Psychiatry 64 (4), S. 344 - 348 (2008)

Schormair, B.; Kemlink, D.; Roeske, D.; Eckstein, G.; Xiong, L.; Lichtner, P.; Ripke, S.; Trenkwalder, C.; Zimprich, A.; Stiasny-Kolster, K. et al.; Oertel, W.; Bachmann, C. G.; Paulus, W.; Högl, B.; Frauscher, B.; Gschliesser, V.; Poewe, W.; Peglau, I.; Vodicka, P.; Vavrova, J.; Sonka, K.; Nevsimalova, S.; Montplaisir, J.; Turecki, G.; Rouleau, G.; Gieger, C.; Illig, T.; Wichmann, H. E.; Holsboer, F.; Mueller-Myhsok, B.; Meitinger, T.; Winkelmann, J.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nature Genetics 40 (8), S. 946 - 948 (2008)

Ambrosius, U.; Lietzenmaier, S.; Wehrle, R.; Wichniak, A.; Kalus, S.; Bettecken, T.; Winkelmann, J.; Yassouridis, A.; Holsboer, F.; Friess, E.: Heritability of sleep EEG. International Journal of Neuropsychopharmacology 11 (Suppl. 1), S. 229 - 230 (2008)

Kemlink, D.; Plazzi, G.; Vetrugno, R.; Provini, F.; Polo, O.; Stiasny-Kolster, K.; Oertel, W.; Nevsimalova, S.; Sonka, K.; Högl, B. et al.; 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. Neurogenetics 9 (2), S. 75 - 82 (2008)

Winkelmann, J.; Müller-Myhsok, B.: Genetics of restless legs syndrome - A burning urge to move. Neurology 70 (9), S. 664 - 665 (2008)

Winkelmann, J.; Lichtner, P.; Schormair, B.; Uhr, M.; Hauk, S.; Stiasny-Kolster, K.; Trenkwalder, C.; Paulus, W.; Peclau, I.; Eisensehr, I. et al.; 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. Movement Disorders 23 (3), S. 350 - 358 (2008)

Garcia-Borreguero, D.; Allen, R. P.; Kohnen, R.; Högl, B.; Trenkwalder, C.; Oertel, W.; Hening, W. A.; Paulus, W.; Rye, D.; Walters, A. et al.; Winkelmann, J.; Earley, C. J.: "Diagnostic standards for dopaminergic augmentation of restless legs syndrome: Report from a world association of sleep medicine - International restless legs syndrome study group consensus conference at the Max Planck Institute" [vol 8, pg 520, 2007]. Sleep Medicine 8 (7-8), S. 788 - 788 (2007)

Garcia-Borreguero, D.; Allen, R. P.; Kohnen, R.; Högl, B.; Trenkwalder, C.; Oertel, W.; Hening, W. A.; Paulus, W.; Rye, D.; Walters, A. et al.; Winkelmann, J.: Diagnostic standards for dopaminergic augmentation of restless legs syndrome: Report from a World Association of Sleep Medicine - International Restless Legs Syndrome Study Group consensus conference at the Max Planck Institute. Sleep Medicine 8 (5), S. 520 - 530 (2007)

Kemlink, D.; Montagna, P.; Winkelmann, J.: Suggestive evidence for a new Restless Legs Syndrome (RLS) locus on chromosome 19. European Journal of Neurology 14 (Suppl. 1), S. 14 - 14 (2007)

Winkelmann, J.: Dopamine agonists in the management of restless legs syndrome - Addressing an underrecognized socioeconomic burden. European Journal of Neurology 14 (Suppl. 1), S. 325 - 325 (2007)

Winkelmann, J.; Schormair, B.; Lichtner, P.; Ripke, S.; Xiong, L.; Jalilzadeh, S.; Fulda, S.; Pütz, B.; Eckstein, G.; Hauk, S. et al.; Trenkwalder, C.; Zimprich, A.; 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, E.; Holsboer, F.; Müller-Myhsok, B.; Meitinger, T.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nature Genetics 39 (8), S. 1000 - 1006 (2007)

Kemlink, D.; Polo, O.; Montagna, P.; Provini, F.; Stiasny-Kolster, K.; Oertel, W.; de Weerd, A.; Nevsimalova, S.; Sonka, K.; Högl, B. et al.; 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 loci 2 and 3 in a European restless legs syndrome population. Movement Disorders 22 (2), S. 207 - 212 (2007)