Susen Winkler - Concepedia

Concepedia

Author

Susen Winkler

University of Lübeck

Also Known As

S Winkler, S. Winkler, Shelly Winkler, Susen Winkler

28

Publications

1.3K

Citations

18

H-Index

17

Concepts

All Affiliations

University of Lübeck University Medical Center Hamburg-Eppendorf Christian-Albrechts-Universität zu Kiel Universität Hamburg University of Belgrade

SW

About

Susen Winkler is an author at University of Lübeck specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	226
2	Molecular Genetics	2	2	94
3	Natural Sciences	1	1	54
4	Molecular Biology	1	1	54
5	Neurology	1	1	132

Susen Winkler

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17

Publications

1.3K

Citations

17

H-Index

	Year	Citations
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study Ana Djarmati, Susanne A. Schneider, Katja Lohmann, The Lancet Neurology PhoniatricsGeneticsPediatric DysphoniaGenetic Screening StudyProminent Spasmodic Dysphonia	2009	145
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the <i>TUBB4</i> gene Katja Lohmann, Robert A. Wilcox, Susen Winkler, Annals of Neurology	2012	142
α-Synuclein and Parkinson disease susceptibility Susen Winkler, Jannis Hagenah, S. Lincoln, Neurology	2007	139
PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism Christine Klein, Ana Djarmati, Katja Hedrich, European Journal of Human Genetics Early-onset ParkinsonismDj-1 MutationsMendelian DisorderNeurological DisorderParkinson Disease	2005	132
Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families Hiltrud Muhle, Anja Neumann, K. Lohmann-Hedrich, Movement Disorders	2008	75
Bilateral subthalamic stimulation in <i>Parkin</i> and <i>PINK1</i> parkinsonism Elena Moro, Jens Volkmann, Inke R. König, Neurology	2008	73
<i>ATP13A2</i> variants in early‐onset Parkinson's disease patients and controls Ana Djarmati, Johann Hagenah, Kathrin Reetz, Movement Disorders	2009	73
Whispering dysphonia in an Australian family (DYT4): A clinical and genetic reappraisal Robert A. Wilcox, Susen Winkler, Katja Lohmann, Movement Disorders	2011	66
Genome‐wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus? Katja Lohmann, Alexander Schmidt, Arne Schillert, Movement Disorders	2013	57
Myoclonus-Dystonia Due to Maternal Uniparental Disomy E. Guettard, Marie‐France Portnoï, K. Lohmann-Hedrich, Archives of Neurology	2008	55

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