Susen Winkler

Most-cited papers

1. Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

   A. Djarmati, S. Schneider, K. Lohmann, Susen Winkler +15 more

   2009Lancet Neurology188 citations

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2. Whispering Dysphonia (DYT4 Dystonia) Is Caused by a Mutation in the TUBB4 Gene

   K. Lohmann, Robert A. Wilcox, Susen Winkler, A. Ramírez +25 more

   2013Annals of Neurology158 citations Open access

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3. PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism

   C. Klein, A. Djarmati, K. Hedrich, Nora Schäfer +14 more

   2005European Journal of Human Genetics154 citations

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4. α-Synuclein and Parkinson disease susceptibility

   Susen Winkler, J. Hagenah, Sarah J. Lincoln, M. Heckman +5 more

   2007Neurology136 citations

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5. Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism

   E. Moro, J. Volkmann, I. König, Susen Winkler +14 more

   2008Neurology82 citations

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6. ATP13A2 variants in early‐onset Parkinson's disease patients and controls

   A. Djarmati, J. Hagenah, K. Reetz, Susen Winkler +15 more

   2009Movement Disorders76 citations Open access

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7. Whispering dysphonia in an Australian family (DYT4): A clinical and genetic reappraisal

   R. Wilcox, Susen Winkler, K. Lohmann, C. Klein

   2011Movement Disorders65 citations

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8. Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families

   H. Muhle, A. Neumann, K. Lohmann-Hedrich, T. Lohnau +7 more

   2008Movement Disorders65 citations

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9. Myoclonus-dystonia due to maternal uniparental disomy.

   E. Guettard, M. Portnoi, K. Lohmann-Hedrich, B. Keren +8 more

   2008Archives of Neurology59 citations Open access

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10. Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus?

    K. Lohmann, A. Schmidt, A. Schillert, Susen Winkler +36 more

    2014Movement Disorders56 citations Open access

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11. Recurrent LRRK2 (Park8) mutations in early‐onset Parkinson's disease

    K. Hedrich, Susen Winkler, J. Hagenah, K. Kabakci +7 more

    2006Movement Disorders56 citations

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12. Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families

    S. Zittel, C. Moll, N. Bruggemann, V. Tadić +11 more

    2010Movement Disorders48 citations

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13. Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.

    N. Bruggemann, M. Mitterer, Andrea J. Lanthaler, A. Djarmati +8 more

    2009Parkinsonism & Related Disorders45 citations

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14. Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation

    S. Doss, K. Lohmann, P. Seibler, B. Arns +15 more

    2013Journal of Neurology43 citations

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15. Homozygous THAP1 mutations as cause of early‐onset generalized dystonia

    S. Schneider, A. Ramírez, K. Shafiee, Frank J. Kaiser +10 more

    2011Movement Disorders42 citations

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16. A novel OPA3 mutation revealed by exome sequencing: an example of reverse phenotyping.

    Beenish Arif, K. Kumar, P. Seibler, F. Vulinovic +11 more

    2013JAMA Neurology30 citations Open access

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17. Association of Parkinson disease to PARK16 in a Chilean sample.

    A. Ramirez, A. Ziegler, Susen Winkler, J. Kottwitz +10 more

    2011Parkinsonism & Related Disorders23 citations

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18. Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only

    R. Wilcox, Ingrid Brænne, N. Bruggemann, Susen Winkler +4 more

    2014Journal of Neurology8 citations Open access

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19. Genetic risk factors in Parkinson disease: Single gene effects and interactions of genotypes

    Anna Göbel, E. Macklin, Susen Winkler, R. Betensky +3 more

    2012Journal of Neurology8 citations Open access

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20. Recurrent LRRK 2 ( Park 8 ) Mutations in Early-Onset Parkinson ’ s Disease

    K. Hedrich, Susen Winkler, J. Hagenah, K. Kabakci +7 more

    20068 citations

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21. The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease

    Susen Winkler, Eva-Juliane Vollstedt, M. Kasten, Daniel Alvarez-Fischer +2 more

    2014Journal of Neurology4 citations

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22. Autosomal dominant Parkinson’s disease in a large German pedigree

    N. Bruggemann, W. Külper, J. Hagenah, Peter Bauer +13 more

    2012Acta Neurologica Scandinavica2 citations Open access

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23. Identification of the genetic cause in the Australian family with spasmodic dysphonia (DYT4)

    Susen Winkler, A. Ramírez, J. Nahrstaedt, C. Hemmelmann +7 more

    20120 citations

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24. Identification of a genetic risk factor for musician's dystonia

    K. Lohmann, A. Schmidt, C. Hemmelmann, Susen Winkler +14 more

    20120 citations

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25. P151 A homozygous THAP1 mutation as cause of early-onset generalized dystonia

    K. Lohmann, A. Ramírez, F. Kaiser, K. Shafiee +10 more

    20110 citations

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26. THAP1 (DYT6) mutations are a frequent cause of generalized dystonia with prominent spasmodic dysphonia

    K. Lohmann, S. Schneider, A. Djarmati, Susen Winkler +15 more

    20090 citations

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27. P1.070 Mutations in the THAP1 (DYT6) gene - a cause of generalized dystonia with prominent spasmodic dysphonia

    S. Schneider, A. Djarmati, K. Lohmann, Susen Winkler +14 more

    20090 citations

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