Juliane Winkelmann

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Juliane Winkelmann

Dr.med.

1997 …2025

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  • 2013

    ImmunoChip Study Implicates Antigen Presentation to T Cells in Narcolepsy

    Faraco, J., Lin, L., Kornum, B. R., Kenny, E. E., Trynka, G., Einen, M., Rico, T. J., Lichtner, P., Dauvilliers, Y., Arnulf, I., Lecendreux, M., Javidi, S., Geisler, P., Mayer, G., Pizza, F., Poli, F., Plazzi, G., Overeem, S., Lammers, G. J. & Kemlink, D. & 28 others, Sonka, K., Nevsimalova, S., Rouleau, G., Desautels, A., Montplaisir, J., Frauscher, B., Ehrmann, L., Högl, B., Jennum, P., Bourgin, P., Peraita-Adrados, R., Iranzo, A., Bassetti, C., Chen, W. M., Concannon, P., Thompson, S. D., Damotte, V., Fontaine, B., Breban, M., Gieger, C., Klopp, N., Deloukas, P., Wijmenga, C., Hallmayer, J., Onengut-Gumuscu, S., Rich, S. S., Winkelmann, J. & Mignot, E., Feb 2013, In: PLoS Genetics. 9, 2, e1003270.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    183 Scopus citations

  • Mitochondrial membrane protein associated neurodegenration: A novel variant of neurodegeneration with brain iron accumulation

    Schulte, E. C., Claussen, M. C., Jochim, A., Haack, T., Hartig, M., Hempel, M., Prokisch, H., Haun-Jünger, U., Winkelmann, J., Hemmer, B., Förschler, A. & Ilg, R., Feb 2013, In: Movement Disorders. 28, 2, p. 224-227 4 p.

    Research output: Contribution to journal › Article › peer-review

    40 Scopus citations

  • Niemann-pick C disease gene mutations and age-related neurodegenerative disorders

    Zech, M., Nübling, G., Castrop, F., Jochim, A., Schulte, E. C., Mollenhauer, B., Lichtner, P., Peters, A., Gieger, C., Marquardt, T., Vanier, M. T., Latour, P., Klünemann, H., Trenkwalder, C., Diehl-Schmid, J., Perneczky, R., Meitinger, T., Oexle, K., Haslinger, B. & Lorenzl, S. & 1 others, Winkelmann, J., 30 Dec 2013, In: PLoS ONE. 8, 12, e82879.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    48 Scopus citations

  • Prolonged release oxycodone-naloxone for treatment of severe restless legs syndrome after failure of previous treatment: A double-blind, randomised, placebo-controlled trial with an open-label extension

    Trenkwalder, C., Beneš, H., Grote, L., García-Borreguero, D., Högl, B., Hopp, M., Bosse, B., Oksche, A., Reimer, K., Winkelmann, J., Allen, R. P. & Kohnen, R., Dec 2013, In: The Lancet Neurology. 12, 12, p. 1141-1150 10 p.

    Research output: Contribution to journal › Article › peer-review

    177 Scopus citations

  • Rare variants in PLXNA4 and Parkinson's disease

    Schulte, E. C., Stahl, I., Czamara, D., Ellwanger, D. C., Eck, S., Graf, E., Mollenhauer, B., Zimprich, A., Lichtner, P., Haubenberger, D., Pirker, W., Brücke, T., Bereznai, B., Molnar, M. J., Peters, A., Gieger, C., Müller-Myhsok, B., Trenkwalder, C. & Winkelmann, J., 11 Nov 2013, In: PLoS ONE. 8, 11, e79145.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    15 Scopus citations

  • Suicidal ideation in a European Huntington's disease population

    The REGISTRY investigators of the European Huntington's Disease Network, 1 Oct 2013, In: Journal of Affective Disorders. 151, 1, p. 248-258 11 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    64 Scopus citations

  • The role of SCARB2 as susceptibility factor in Parkinson's disease

    Hopfner, F., Schulte, E. C., Mollenhauer, B., Bereznai, B., Knauf, F., Lichtner, P., Zimprich, A., Haubenberger, D., Pirker, W., Brücke, T., Peters, A., Gieger, C., Kuhlenbäumer, G., Trenkwalder, C. & Winkelmann, J., Apr 2013, In: Movement Disorders. 28, 4, p. 538-540 3 p.

    Research output: Contribution to journal › Article › peer-review

    42 Scopus citations

  • When restless legs syndrome turns malignant.

    Schulte, E. C., Gross, N., Slawik, H. & Winkelmann, J., Jun 2013, In: Sleep Medicine. 14, 6, p. 575-577 3 p.

    Research output: Contribution to journal › Article › peer-review

    8 Scopus citations

  • β-defensin genomic copy number does not influence the age of onset in huntington’s disease

    REGISTRY investigators of the European Huntington’s Disease Network, 1 Jan 2013, In: Journal of Huntington's Disease. 2, 1, p. 107-124 18 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    1 Scopus citations
  • 2012

    Crowned-Dens-Syndrom: Eine seltene Differenzialdiagnose akut aufgetretener Nackenschmerzen

    Translated title of the contribution: Crowned dens syndrome: A rare differential diagnosis of acute neck painKnier, B., Boeckh-Behrens, T., Murgan, I., Wörtler, K., Hemmer, B. & Winkelmann, J., Oct 2012, In: Nervenarzt. 83, 10, p. 1308-1311 4 p.

    Research output: Contribution to journal › Article › peer-review

  • Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease

    Jostins, L., Ripke, S., Weersma, R. K., Duerr, R. H., McGovern, D. P., Hui, K. Y., Lee, J. C., Schumm, L. P., Sharma, Y., Anderson, C. A., Essers, J., Mitrovic, M., Ning, K., Cleynen, I., Theatre, E., Spain, S. L., Raychaudhuri, S., Goyette, P., Wei, Z. & Abraham, C. & 86 others, Achkar, J. P., Ahmad, T., Amininejad, L., Ananthakrishnan, A. N., Andersen, V., Andrews, J. M., Baidoo, L., Balschun, T., Bampton, P. A., Bitton, A., Boucher, G., Brand, S., Büning, C., Cohain, A., Cichon, S., D’amato, M., Jong, D. D., Devaney, K. L., Dubinsky, M., Edwards, C., Ellinghaus, D., Ferguson, L. R., Franchimont, D., Fransen, K., Gearry, R., Georges, M., Gieger, C., Glas, J., Haritunians, T., Hart, A., Hawkey, C., Hedl, M., Hu, X., Karlsen, T. H., Kupcinskas, L., Kugathasan, S., Latiano, A., Laukens, D., Lawrance, I. C., Lees, C. W., Louis, E., Mahy, G., Mansfield, J., Morgan, A. R., Mowat, C., Newman, W., Palmieri, O., Ponsioen, C. Y., Potocnik, U., Prescott, N. J., Regueiro, M., Rotter, J. I., Russell, R. K., Sanderson, J. D., Sans, M., Satsangi, J., Schreiber, S., Simms, L. A., Sventoraityte, J., Targan, S. R., Taylor, K. D., Tremelling, M., Verspaget, H. W., Vos, M. D., Wijmenga, C., Wilson, D. C., Winkelmann, J., Xavier, R. J., Zeissig, S., Zhang, B., Zhang, C. K., Zhao, H., Silverberg, M. S., Annese, V., Hakonarson, H., Brant, S. R., Radford-Smith, G., Mathew, C. G., Rioux, J. D., Schadt, E. E., Daly, M. J., Franke, A., Parkes, M., Vermeire, S., Barrett, J. C. & Cho, J. H., 1 Nov 2012, In: Nature. 491, 7422, p. 119-124 6 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    3729 Scopus citations

  • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

    Tsoi, L. C., Spain, S. L., Knight, J., Ellinghaus, E., Stuart, P. E., Capon, F., Ding, J., Li, Y., Tejasvi, T., Gudjonsson, J. E., Kang, H. M., Allen, M. H., McManus, R., Novelli, G., Samuelsson, L., Schalkwijk, J., Ståhle, M., Burden, A. D., Smith, C. H. & Cork, M. J. & 180 others, Estivill, X., Bowcock, A. M., Krueger, G. G., Weger, W., Worthington, J., Tazi-Ahnini, R., Nestle, F. O., Hayday, A., Hoffmann, P., Winkelmann, J., Wijmenga, C., Langford, C., Edkins, S., Andrews, R., Blackburn, H., Strange, A., Band, G., Pearson, R. D., Vukcevic, D., Spencer, C. C. A., Deloukas, P., Mrowietz, U., Schreiber, S., Weidinger, S., Koks, S., Kingo, K., Esko, T., Metspalu, A., Lim, H. W., Voorhees, J. J., Weichenthal, M., Wichmann, H. E., Chandran, V., Rosen, C. F., Rahman, P., Gladman, D. D., Griffiths, C. E. M., Reis, A., Kere, J., Nnair, R. P., Franke, A., Barker, J. N., Abecasis, G. R., Eelder, J. T., Ttrembath, R., Duffin, K. C., Helms, C., Goldgar, D., Paschall, J., Malloy, M. J., Pullinger, C. R., Kane, J. P., Gardner, J., Perlmutter, A., Miner, A., Feng, B. J., Hiremagalore, R., Ike, R. W., Christophers, E., Henseler, T., Ruether, A., Schrodi, S. J., Prahalad, S., Guthery, S. L., Fischer, J., Liao, W., Kwok, P., Menter, A., Lathrop, G. M., Wise, C., Begovich, A. B., Onoufriadis, A., Weale, M. E., Hofer, A., Salmhofer, W., Wolf, P., Kainu, K., Saarialho-Kere, U., Suomela, S., Badorf, P., Hüffmeier, U., Kurrat, W., Küster, W., Lascorz, J., Mössner, R., Schürmeier-Horst, F., Ständer, M., Traupe, H., Bergboer, J. G. M., Heijer, M. D., Van De Kerkhof, P. C., Zeeuwen, P. L. J. M., Barnes, L., Campbell, L. E., Cusack, C., Coleman, C., Conroy, J., Ennis, S., Fitzgerald, O., Gallagher, P., Irvine, A. D., Kirby, B., Markham, T., McLean, W. H. I., McPartlin, J., Rogers, S. F., Ryan, A. W., Zawirska, A., Giardina, E., Lepre, T., Perricone, C., Martín-Ezquerra, G., Pujol, R. M., Riveira-Munoz, E., Inerot, A., Naluai, Å. T., Mallbris, L., Wolk, K., Leman, J., Barton, A., Warren, R. B., Young, H. S., Ricano-Ponce, I., Trynka, G., Pellett, F. J., Henschel, A., Aurand, M., Bebo, B., Gieger, C., Illig, T., Moebus, S., Jöckel, K. H., Erbel, R., Donnelly, P., Peltonen, L., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Craddock, N., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., McCarthy, M. I., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Samani, N., Viswanathan, A. C., Wood, N. W., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Su, Z., Hunt, S. E., Gwilliam, R., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O. T., Liddle, J., Perez, M. L., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Neir, R. P., Elder, J. T. & Trembath, R. C., 1 Dec 2012, In: Nature Genetics. 44, 12, p. 1341-1348 8 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    807 Scopus citations

  • Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy

    Winkelmann, J., Lin, L., Schormair, B., Kornum, B. R., Faraco, J., Plazzi, G., Melberg, A., Cornelio, F., Urban, A. E., Pizza, F., Poli, F., Grubert, F., Wieland, T., Graf, E., Hallmayer, J., Strom, T. M. & Mignot, E., May 2012, In: Human Molecular Genetics. 21, 10, p. 2205-2210 6 p., dds035.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    206 Scopus citations

  • Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases

    Arnold, M., Hartsperger, M. L., Baurecht, H., Rodríguez, E., Wachinger, B., Franke, A., Kabesch, M., Winkelmann, J., Pfeufer, A., Romanos, M., Illig, T., Mewes, H. W., Stümpflen, V. & Weidinger, S., 18 Sep 2012, In: BMC Genomics. 13, 1, 490.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    2 Scopus citations

  • PSEA: Phenotype Set Enrichment Analysis--a new method for analysis of multiple phenotypes.

    Ried, J. S., Döring, A., Oexle, K., Meisinger, C., Winkelmann, J., Klopp, N., Meitinger, T., Peters, A., Suhre, K., Wichmann, H. E. & Gieger, C., Apr 2012, In: Genetic epidemiology. 36, 3, p. 244-252 9 p.

    Research output: Contribution to journal › Article › peer-review

    17 Scopus citations

  • Restless legs syndrome in Czech patients with multiple sclerosis: An epidemiological and genetic study

    Vávrová, J., Kemlink, D., Šonka, K., Havrdová, E., Horáková, D., Pardini, B., Müller-Myhsok, B. & Winkelmann, J., Aug 2012, In: Sleep Medicine. 13, 7, p. 848-851 4 p.

    Research output: Contribution to journal › Article › peer-review

    36 Scopus citations

  • Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease

    Schulte, E. C., Mollenhauer, B., Zimprich, A., Bereznai, B., Lichtner, P., Haubenberger, D., Pirker, W., Brücke, T., Molnar, M. J., Peters, A., Gieger, C., Trenkwalder, C. & Winkelmann, J., Aug 2012, In: Neurogenetics. 13, 3, p. 281-285 5 p.

    Research output: Contribution to journal › Article › peer-review

    26 Scopus citations

  • Variation within the Huntington's disease gene influences normal brain structure

    Mühlau, M., Winkelmann, J., Rujescu, D., Giegling, I., Koutsouleris, N., Gaser, C., Arsic, M., Weindl, A., Reiser, M. & Meisenzahl, E. M., 3 Jan 2012, In: PLoS ONE. 7, 1, e29809.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    31 Scopus citations
  • 2011

    Absence of an orphan mitochondrial protein, C19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation

    Hartig, M. B., Iuso, A., Haack, T., Kmiec, T., Jurkiewicz, E., Heim, K., Roeber, S., Tarabin, V., Dusi, S., Krajewska-Walasek, M., Jozwiak, S., Hempel, M., Winkelmann, J., Elstner, M., Oexle, K., Klopstock, T., Mueller-Felber, W., Gasser, T., Trenkwalder, C. & Tiranti, V. & 5 others, Kretzschmar, H., Schmitz, G., Strom, T. M., Meitinger, T. & Prokisch, H., 7 Oct 2011, In: American Journal of Human Genetics. 89, 4, p. 543-550 8 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    222 Scopus citations

  • A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset parkinson disease

    Zimprich, A., Benet-Pagès, A., Struhal, W., Graf, E., Eck, S. H., Offman, M. N., Haubenberger, D., Spielberger, S., Schulte, E. C., Lichtner, P., Rossle, S. C., Klopp, N., Wolf, E., Seppi, K., Pirker, W., Presslauer, S., Mollenhauer, B., Katzenschlager, R., Foki, T. & Hotzy, C. & 14 others, Reinthaler, E., Harutyunyan, A., Kralovics, R., Peters, A., Zimprich, F., Brücke, T., Poewe, W., Auff, E., Trenkwalder, C., Rost, B., Ransmayr, G., Winkelmann, J., Meitinger, T. & Strom, T. M., 15 Jul 2011, In: American Journal of Human Genetics. 89, 1, p. 168-175 8 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    704 Scopus citations

  • Common variants in P2RY11 are associated with narcolepsy

    Kornum, B. R., Kawashima, M., Faraco, J., Lin, L., Rico, T. J., Hesselson, S., Axtell, R. C., Kuipers, H., Weiner, K., Hamacher, A., Kassack, M. U., Han, F., Knudsen, S., Li, J., Dong, X., Winkelmann, J., Plazzi, G., Nevsimalova, S., Hong, S. C. & Honda, Y. & 40 others, Honda, M., Högl, B., Ton, T. G. N., Montplaisir, J., Bourgin, P., Kemlink, D., Huang, Y. S., Warby, S., Einen, M., Eshragh, J. L., Miyagawa, T., Desautels, A., Ruppert, E., Hesla, P. E., Poli, F., Pizza, F., Frauscher, B., Jeong, J. H., Lee, S. P., Strohl, K. P., Longstreth, W. T., Kvale, M., Dobrovolna, M., Ohayon, M. M., Nepom, G. T., Wichmann, H. E., Rouleau, G. A., Gieger, C., Levinson, D. F., Gejman, P. V., Meitinger, T., Peppard, P., Young, T., Jennum, P., Steinman, L., Tokunaga, K., Kwok, P. Y., Risch, N., Hallmayer, J. & Mignot, E., Jan 2011, In: Nature Genetics. 43, 1, p. 66-71 6 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    188 Scopus citations

  • Genetics of sleep disorders

    Winkelmann, J. & Kimura, M., 2011, In: Handbook of Clinical Neurology. 99, C, p. 681-693 13 p.

    Research output: Contribution to journal › Article › peer-review

    8 Scopus citations

  • Genome-Wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

    Winkelmann, J., Czamara, D., Schormair, B., Knauf, F., Schulte, E. C., Trenkwalder, C., Dauvilliers, Y., Polo, O., Högl, B., Berger, K., Fuhs, A., Gross, N., Stiasny-Kolster, K., Oertel, W., Bachmann, C. G., Paulus, W., Xiong, L., Montplaisir, J., Rouleau, G. A. & Fietze, I. & 37 others, Vávrová, J., Kemlink, D., Sonka, K., Nevsimalova, S., Lin, S. C., Wszolek, Z., Vilariño-Güell, 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., Jul 2011, In: PLoS Genetics. 7, 7, e1002171.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    153 Scopus citations

  • MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease

    Schormair, B., Plag, J., Kaffe, M., Groß, N., Czamara, D., Samtleben, W., Lichtner, P., Ströhle, A., Stefanidis, I., Vainas, A., Dardiotis, E., Sakkas, G. K., Gieger, C., Müller-Myhsok, B., Meitinger, T., Heemann, U., Hadjigeorgiou, G. M., Oexle, K. & Winkelmann, J., Jul 2011, In: Journal of Medical Genetics. 48, 7, p. 462-466 5 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    54 Scopus citations

  • Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels

    Oexle, K., Ried, J. S., Hicks, A. A., Tanaka, T., Hayward, C., Bruegel, M., Gögele, M., Lichtner, P., Müller-Myhsok, B., Döring, A., Illig, T., Schwienbacher, C., Minelli, C., Pichler, I., Fiedler, G. M., Thiery, J., Rudan, I., Wright, A. F., Campbell, H. & Ferrucci, L. & 6 others, Bandinelli, S., Pramstaller, P. P., Wichmann, H. E., Gieger, C., Winkelmann, J. & Meitinger, T., Mar 2011, In: Human Molecular Genetics. 20, 5, p. 1042-1047 6 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    60 Scopus citations

  • Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features

    Hopfner, F., Schormair, B., Knauf, F., Berthele, A., Tölle, T. R., Baron, R., Maier, C., Treede, R. D., Binder, A., Sommer, C., Maihöfner, C., Kunz, W., Zimprich, F., Heemann, U., Pfeufer, A., Näbauer, M., Kääb, S., Nowak, B., Gieger, C. & Lichtner, P. & 3 others, Trenkwalder, C., Oexle, K. & Winkelmann, J., 27 Oct 2011, In: BMC Neurology. 11, 134.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    24 Scopus citations

  • Parkinson's disease risk score: Moving to a premotor diagnosis

    Winkler, J., Ehret, R., Büttner, T., Dillmann, U., Fogel, W., Sabolek, M., Winkelmann, J. & Kassubek, J., May 2011, In: Journal of Neurology. 258, SUPPL. 2, p. S311-S315

    Research output: Contribution to journal › Article › peer-review

    38 Scopus citations

  • Restless-legs-Syndrom und kardiovaskuläres Risiko

    Translated title of the contribution: Restless legs syndrome and cardiovascular riskSchulte, E. C., Spieler, D. & Winkelmann, J., Aug 2011, In: Nervenarzt. 82, 8, p. 1006-1011 6 p.

    Research output: Contribution to journal › Article › peer-review

    3 Scopus citations

  • The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: A multicenter case-control study

    Leppä, V., Surakka, I., Tienari, P. J., Elovaara, I., Compston, A., Sawcer, S., Robertson, N., de Jager, P. L., Aubin, C., Hafler, D. A., Oturai, A. B., Søndergaard, H. B., Sellebjerg, F., Sørensen, P. S., Hemmer, B., Cepok, S., Winkelmann, J., Wichmann, H. E., Comabella, M. & Bustamante, M. F. & 24 others, Montalban, X., Olsson, T., Kockum, I., Hillert, J., Alfredsson, L., Goris, A., Dubois, B., Mero, I. L., Smestad, C., Celius, E. G., Harbo, H. F., D'Alfonso, S., Bergamaschi, L., Leone, M., Ristori, G., Kappos, L., Hauser, S. L., Cournu-Rebeix, I., Fontaine, B., Boonen, S., Polman, C., Palotie, A., Peltonen, L. & Saarela, J., 2011, In: PLoS ONE. 6, 4, e18813.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    63 Scopus citations

  • Variant screening of the coding regions of MEIS1 in patients with restless legs syndrome

    Schulte, E. C., Knauf, F., Kemlink, D., Schormair, B., Lichtner, P., Gieger, C., Meitinger, T. & Winkelmann, J., 22 Mar 2011, In: Neurology. 76, 12, p. 1106-1108 3 p.

    Research output: Contribution to journal › Article › peer-review

    13 Scopus citations

  • When Parkinson's disease patients go to sleep: Specific sleep disturbances related to Parkinson's disease

    Schulte, E. C. & Winkelmann, J., May 2011, In: Journal of Neurology. 258, SUPPL. 2, p. S328-S335

    Research output: Contribution to journal › Article › peer-review

    39 Scopus citations
  • 2010

    Common variants at 10 genomic loci influence hemoglobin A1C levels via glycemic and nonglycemic pathways

    Soranzo, N., Sanna, S., Wheeler, E., Gieger, C., Radke, D., Dupuis, J., Bouatia-Naji, N., Langenberg, C., Prokopenko, I., Stolerman, E., Sandhu, M. S., Heeney, M. M., Devaney, J. M., Reilly, M. P., Ricketts, S. L., Stewart, A. F. R., Voight, B. F., Willenborg, C., Wright, B. & Altshuler, D. & 157 others, Arking, D., Balkau, B., Barnes, D., Boerwinkle, E., Böhm, B., Bonnefond, A., Bonnycastle, L. L., Boomsma, D. I., Bornstein, S. R., Böttcher, Y., Bumpstead, S., Burnett-Miller, M. S., Campbell, H., Cao, A., Chambers, J., Clark, R., Collins, F. S., Coresh, J., De Geus, E. J. C., Dei, M., Deloukas, P., Döring, A., Egan, J. M., Elosua, R., Ferrucci, L., Forouhi, N., Fox, C. S., Franklin, C., Franzosi, M. G., Gallina, S., Goel, A., Graessler, J., Grallert, H., Greinacher, A., Hadley, D., Hall, A., Hamsten, A., Hayward, C., Heath, S., Herder, C., Homuth, G., Hottenga, J. J., Hunter-Merrill, R., Illig, T., Jackson, A. U., Jula, A., Kleber, M., Knouff, C. W., Kong, A., Kooner, J., Köttgen, A., Kovacs, P., Krohn, K., Kühnel, B., Kuusisto, J., Laakso, M., Lathrop, M., Lecoeur, C., Li, M., Li, M., Loos, R. J. F., Luan, J., Lyssenko, V., Mägi, R., Magnusson, P. K. E., Mälarstig, A., Mangino, M., Martínez-Larrad, M. T., März, W., McArdle, W. L., McPherson, R., Meisinger, C., Meitinger, T., Melander, O., Mohlke, K. L., Mooser, V. E., Morken, M. A., Narisu, N., Nathan, D. M., Nauck, M., O'Donnell, C., Oexle, K., Olla, N., Pankow, J. S., Payne, F., Peden, J. F., Pedersen, N. L., Peltonen, L., Perola, M., Polasek, O., Porcu, E., Rader, D. J., Rathmann, W., Ripatti, S., Rocheleau, G., Roden, M., Rudan, I., Salomaa, V., Saxena, R., Schlessinger, D., Schunkert, H., Schwarz, P., Seedorf, U., Selvin, E., Serrano-Ríos, M., Shrader, P., Silveira, A., Siscovick, D., Song, K., Spector, T. D., Stefansson, K., Steinthorsdottir, V., Strachan, D. P., Strawbridge, R., Stumvoll, M., Surakka, I., Swift, A. J., Tanaka, T., Teumer, A., Thorleifsson, G., Thorsteinsdottir, U., Tönjes, A., Usala, G., Vitart, V., Völzke, H., Wallaschofski, H., Waterworth, D. M., Watkins, H., Wichmann, H. E., Wild, S. H., Willemsen, G., Williams, G. H., Wilson, J. F., Winkelmann, J., Wright, A. F., Zabena, C., Zhao, J. H., Epstein, S. E., Erdmann, J., Hakonarson, H. H., Kathiresan, S., Khaw, K. T., Roberts, R., Samani, N. J., Fleming, M. D., Sladek, R., Abecasis, G., Boehnke, M., Froguel, P., Groop, L., McCarthy, M. I., Kao, W. H. L., Florez, J. C., Uda, M., Wareham, N. J., Barroso, I. & Meigs, J. B., Dec 2010, In: Diabetes. 59, 12, p. 3229-3239 11 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    349 Scopus citations

  • IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci

    Esposito, F., Patsopoulos, N. A., Cepok, S., Kockum, I., Leppä, V., Booth, D. R., Heard, R. N., Stewart, G. J., Cox, M., Scott, R. J., Lechner-Scott, J., Goris, A., Dobosi, R., Dubois, B., Rioux, J. D., Oturai, A. B., Søndergaard, H. B., Sellebjerg, F., Sørensen, P. S. & Reunanen, M. & 49 others, Koivisto, K., Cournu-Rebeix, I., Fontaine, B., Winkelmann, J., Gieger, C., Infante-Duarte, C., Zipp, F., Bergamaschi, L., Leone, M., Bergamaschi, R., Cavalla, P., Lorentzen, A. R., Mero, I. L., Celius, E. G., Harbo, H. F., Spurkland, A., Comabella, M., Bryneda, B., Alfredsson, L., Bernardinelli, L., Robertson, N. P., Hawkins, C. P., Barcellos, L. F., Beecham, G., Bush, W., Cree, B. A. C., Daly, M. J., Ivinson, A. J., Aubin, C., Compston, A., D'Alfonso, S., Haines, J. L., Hauser, S. L., Hemmer, B., Hillert, J., McCauley, J. L., Oksenberg, J., Olsson, T., Palotie, A., Peltonen, L., Pericak-Vance, M. A., Saarela, J., Sawcer, S. J., Stranger, B., Boneschi, F. M., Comi, G., Hafler, D. A., De Bakker, P. I. W. & De Jager, P. L., Jul 2010, In: Genes and Immunity. 11, 5, p. 397-405 9 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    64 Scopus citations

  • Short-term attention and verbal fluency is decreased in restless legs syndrome patients

    Fulda, S., Beitinger, M. E., Reppermund, S., Winkelmann, J. & Wetter, T. C., Nov 2010, In: Movement Disorders. 25, 15, p. 2641-2648 8 p.

    Research output: Contribution to journal › Article › peer-review

    61 Scopus citations
  • 2009

    Narcolepsy is strongly associated with the T-cell receptor alpha locus

    Hallmayer, J., Faraco, J., Lin, L., Hesselson, S., Winkelmann, J., Kawashima, M., Mayer, G., Plazzi, G., Nevsimalova, S., Bourgin, P., Hong, S. S. C., Honda, Y., Honda, M., Högl, B., Longstreth, W. T., Montplaisir, J., Kemlink, D., Einen, M., Chen, J. & Musone, S. L. & 28 others, Akana, M., Miyagawa, T., Duan, J., Desautels, A., Erhardt, C., Hesla, P. E., Poli, F., Frauscher, B., Jeong, J. H., Lee, S. P., Ton, T. G. N., Kvale, M., Kolesar, L., Dobrovolná, M., Nepom, G. T., Salomon, D., Wichmann, H. E., Rouleau, G. A., Gieger, C., Levinson, D. F., Gejman, P. V., Meitinger, T., Young, T., Peppard, P., Tokunaga, K., Kwok, P. Y., Risch, N. & Mignot, E., Jun 2009, In: Nature Genetics. 41, 6, p. 708-711 4 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    405 Scopus citations

  • Replication of restless legs syndrome loci in three european populations

    Kemlink, D., Polo, O., Frauscher, B., Gschliesser, V., Högl, B., Poewe, W., Vodicka, P., Vavrova, J., Sonka, K., Nevsimalova, S., Schormair, B., Lichtner, P., Silander, K., Peltonen, L., Gieger, C., Wichmann, H. E., Zimprich, A., Roeske, D., BMUller-Myhsok & Meitinger, T. & 1 others, Winkelmann, J., May 2009, In: Journal of Medical Genetics. 46, 5, p. 315-318 4 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    71 Scopus citations
  • 2008

    Heritability of Sleep Electroencephalogram

    Ambrosius, U., Lietzenmaier, S., Wehrle, R., Wichniak, A., Kalus, S., Winkelmann, J., Bettecken, T., Holsboer, F., Yassouridis, A. & Friess, E., 15 Aug 2008, In: Biological Psychiatry. 64, 4, p. 344-348 5 p.

    Research output: Contribution to journal › Article › peer-review

    134 Scopus citations

  • PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

    Schormair, B., Kemlink, D., Roeske, D., Eckstein, G., Xiong, L., Lichtner, P., Ripke, S., Trenkwalder, C., Zimprich, A., Stiasny-Kolster, K., Oertel, W., Bachmann, C. G., Paulus, W., Högl, B., Frauscher, B., Gschliesser, V., Poewe, W., Peglau, I., Vodicka, P. & Vávrová, J. & 12 others, 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., Aug 2008, In: Nature Genetics. 40, 8, p. 946-948 3 p.

    Research output: Contribution to journal › Article › peer-review

    238 Scopus citations

  • Suggestive evidence for linkage for restless legs syndrome on chromosome 19p13

    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-Myshok, B., Winkelmann, J. & Montagna, P., May 2008, In: Neurogenetics. 9, 2, p. 75-82 8 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    59 Scopus citations

  • Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome

    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., 15 Feb 2008, In: Movement Disorders. 23, 3, p. 350-358 9 p.

    Research output: Contribution to journal › Article › peer-review

    104 Scopus citations
  • 2007

    Animal studies in restless legs syndrome

    Baier, P. C., Ondo, W. G. & Winkelmann, J., 2007, In: Movement Disorders. 22, SUPPL. 18, p. S459-S465

    Research output: Contribution to journal › Article › peer-review

    14 Scopus citations

  • Augmentation as a treatment complication of restless legs syndrome: Concept and management

    García-Borreguero, D., Allen, R. P., Benes, H., Earley, C., Happe, S., Högl, B., Kohnen, R., Paulus, W., Rye, D. & Winkelmann, J., 2007, In: Movement Disorders. 22, SUPPL. 18, p. S476-S484

    Research output: Contribution to journal › Article › peer-review

    83 Scopus citations

  • Clinical trials in restless legs syndrome - Recommendations of the European RLS Study Group (EURLSSG)

    Trenkwalder, C., Kohnen, R., Allen, R. P., Beneš, H., Ferini-Strambi, L., Garcia-Borreguero, D., Hadjigeorgiou, G. M., Happe, S., Högl, B., Hornyak, M., Klein, C., Nass, A., Montagna, P., Oertel, W. H., O'Keeffe, S., Paulus, W., Poewe, W., Provini, F., Pramstaller, P. P. & Sieminski, M. & 6 others, Sonka, K., Stiasny-Kolster, K., De Weerd, A., Wetter, T. C., Winkelmann, J. & Zucconi, M., 2007, In: Movement Disorders. 22, SUPPL. 18, p. S495-S504

    Research output: Contribution to journal › Article › peer-review

    25 Scopus citations

  • 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

    García-Borreguero, D., Allen, R. P., Kohnen, R., Högl, B., Trenkwalder, C., Oertel, W., Hening, W. A., Paulus, W., Rye, D., Walters, A. & Winkelmann, J., Aug 2007, In: Sleep Medicine. 8, 5, p. 520-530 11 p.

    Research output: Contribution to journal › Article › peer-review

    252 Scopus citations

  • Family-based association study of the restless legs syndrome loci 2 and 3 in a European population

    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. & 6 others, Klein, C., Hiller, A., Lichtner, P., Meitinger, T., Müller-Myshok, B. & Winkelmann, J., 15 Jan 2007, In: Movement Disorders. 22, 2, p. 207-212 6 p.

    Research output: Contribution to journal › Article › peer-review

    29 Scopus citations

  • Genetics of restless legs syndrome (RLS): State-of-the-art and future directions

    Winkelmann, J., Polo, O., Provini, F., Nevsimalova, S., Kemlink, D., Sonka, K., Högl, B., Poewe, W., Stiasny-Kolster, K., Oertel, W., De Weerd, A., Strambi, L. F., Zucconi, M., Pramstaller, P. P., Arnulf, I., Trenkwalder, C., Klein, C., Hadjigeorgiou, G. M., Happe, S. & Rye, D. & 1 others, Montagna, P., 2007, In: Movement Disorders. 22, SUPPL. 18, p. S449-S458

    Research output: Contribution to journal › Article › peer-review

    72 Scopus citations

  • Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

    Winkelmann, J., Schormair, B., Lichtner, P., Ripke, S., Xiong, L., Jalilzadeh, S., Fulda, S., Pütz, B., Eckstein, G., Hauk, S., Trenkwalder, C., Zimprich, A., Stiasny-Kolster, K., Oertel, W., Bachmann, C. G., Paulus, W., Peglau, I., Eisensehr, I., Montplaisir, J. & Turecki, G. & 7 others, Rouleau, G., Gieger, C., Illig, T., Wichmann, H. E., Holsboer, F., Müller-Myhsok, B. & Meitinger, T., Aug 2007, In: Nature Genetics. 39, 8, p. 1000-1006 7 p.

    Research output: Contribution to journal › Article › peer-review

    577 Scopus citations
  • 2006

    Begutachtung des restless legs syndroms - Zusammenfassung der konsensusempfehlung

    Translated title of the contribution: Surveys on restless legs syndrome: Summary of consensus recommendationsHappe, S., Beneš, H., Hornyak, M., Kotterba, S., Mayer, G., Stiasny-Kolster, K., Clarenbach, P., Eisensehr, I., Fulda, S., Haan, J., Högl, B., Lüdemann, P., Meier, A., Nass, A., Salaschek, M., Trenkwalder, C., Walther, B., Wetter, T. C., Winkelmann, J. & Young, P., Nov 2006, In: Somnologie. 10, 4, p. 206-209 4 p.

    Research output: Contribution to journal › Article › peer-review

    2 Scopus citations

  • Evidence for further genetic heterogeneity and confirmation of RLS-1 in restless legs syndrome

    Winkelmann, J., Lichtner, P., Pütz, B., Trenkwalder, C., Hauk, S., Meitinger, T., Strom, T. & Muller-Myhsok, B., Jan 2006, In: Movement Disorders. 21, 1, p. 28-33 6 p.

    Research output: Contribution to journal › Article › peer-review

    73 Scopus citations

  • Paroxetine treatment improves motor symptoms in patients with multiple system atrophy

    Friess, E., Kuempfel, T., Modell, S., Winkelmann, J., Holsboer, F., Ising, M. & Trenkwalder, C., Oct 2006, In: Parkinsonism and Related Disorders. 12, 7, p. 432-437 6 p.

    Research output: Contribution to journal › Article › peer-review

    41 Scopus citations