Susen Winkler

1.3k total citations
19 papers, 750 citations indexed

About

Susen Winkler is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Susen Winkler has authored 19 papers receiving a total of 750 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Cellular and Molecular Neuroscience, 10 papers in Neurology and 9 papers in Molecular Biology. Recurrent topics in Susen Winkler's work include Parkinson's Disease Mechanisms and Treatments (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Nuclear Receptors and Signaling (5 papers). Susen Winkler is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Nuclear Receptors and Signaling (5 papers). Susen Winkler collaborates with scholars based in Germany, Italy and Serbia. Susen Winkler's co-authors include Christine Klein, Katja Lohmann, Vladimir Kostić, K. Lohmann-Hedrich, Thora Lohnau, Johann Hagenah, Ana Djarmati, Robert A. Wilcox, Norbert Brüggemann and Peter P. Pramstaller and has published in prestigious journals such as Neurology, The Lancet Neurology and Movement Disorders.

In The Last Decade

Susen Winkler

19 papers receiving 733 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Susen Winkler Germany 15 559 342 204 124 90 19 750
Mark P. DeAndrade United States 13 454 0.8× 225 0.7× 98 0.5× 71 0.6× 132 1.5× 18 595
Michele L. Rajput Canada 13 716 1.3× 238 0.7× 72 0.4× 124 1.0× 126 1.4× 15 793
Anne Bertrand France 11 507 0.9× 433 1.3× 122 0.6× 70 0.6× 66 0.7× 18 749
Nathaniel R. Whaley United States 11 545 1.0× 342 1.0× 103 0.5× 75 0.6× 64 0.7× 12 670
Mónica Díez-Fairén Spain 11 242 0.4× 112 0.3× 104 0.5× 74 0.6× 35 0.4× 19 385
Rou-Shayn Chen Taiwan 14 425 0.8× 184 0.5× 171 0.8× 184 1.5× 61 0.7× 18 601
Nathan Levine United States 10 432 0.8× 292 0.9× 182 0.9× 94 0.8× 36 0.4× 15 700
Jaione Irigoyen Spain 10 436 0.8× 178 0.5× 120 0.6× 142 1.1× 90 1.0× 11 597
Ignacio Rubio‐Agusti United Kingdom 11 347 0.6× 197 0.6× 110 0.5× 97 0.8× 24 0.3× 13 591
Francesco Giribaldi Italy 7 262 0.5× 217 0.6× 146 0.7× 48 0.4× 56 0.6× 7 484

Countries citing papers authored by Susen Winkler

Since Specialization
Citations

This map shows the geographic impact of Susen Winkler's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Susen Winkler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Susen Winkler more than expected).

Fields of papers citing papers by Susen Winkler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susen Winkler. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Susen Winkler. The network helps show where Susen Winkler may publish in the future.

Co-authorship network of co-authors of Susen Winkler

This figure shows the co-authorship network connecting the top 25 collaborators of Susen Winkler. A scholar is included among the top collaborators of Susen Winkler based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Susen Winkler. Susen Winkler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Wilcox, Robert A., Ingrid Brænne, Norbert Brüggemann, et al.. (2014). Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only. Journal of Neurology. 262(1). 187–193. 6 indexed citations
2.
Doss, Sarah, Katja Lohmann, Philip Seibler, et al.. (2013). Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation. Journal of Neurology. 261(1). 207–212. 31 indexed citations
3.
Kumar, Kishore R., Philip Seibler, Franca Vulinović, et al.. (2013). A Novel OPA3 Mutation Revealed by Exome Sequencing. JAMA Neurology. 70(6). 783–783. 23 indexed citations
4.
Brüggemann, Norbert, J. Hagenah, Peter Bauer, et al.. (2011). Autosomal dominant Parkinson’s disease in a large German pedigree. Acta Neurologica Scandinavica. 126(2). 129–137. 2 indexed citations
5.
Wilcox, Robert A., Susen Winkler, Katja Lohmann, & Christine Klein. (2011). Whispering dysphonia in an Australian family (DYT4): A clinical and genetic reappraisal. Movement Disorders. 26(13). 2404–2408. 43 indexed citations
6.
Schneider, Susanne A., Alfredo Ramı́rez, Kaveh Shafiee, et al.. (2011). Homozygous THAP1 mutations as cause of early‐onset generalized dystonia. Movement Disorders. 26(5). 858–861. 28 indexed citations
7.
Zittel, Simone, Christian K.E. Moll, Norbert Brüggemann, et al.. (2010). Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families. Movement Disorders. 25(14). 2405–2412. 31 indexed citations
8.
Winkler, Susen, et al.. (2010). Neurological disorders in rural Africa - a systematic approach. 27(2). 9 indexed citations
9.
Brüggemann, Norbert, Manfred Mitterer, Ana Djarmati, et al.. (2009). Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers. Parkinsonism & Related Disorders. 15(6). 425–429. 35 indexed citations
10.
Djarmati, Ana, Johann Hagenah, Kathrin Reetz, et al.. (2009). ATP13A2 variants in early‐onset Parkinson's disease patients and controls. Movement Disorders. 24(14). 2104–2111. 55 indexed citations
11.
Djarmati, Ana, Susanne A. Schneider, Katja Lohmann, et al.. (2009). Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study. The Lancet Neurology. 8(5). 447–452. 94 indexed citations
12.
Moro, Elena, Jens Volkmann, Inke R. König, et al.. (2008). Bilateral subthalamic stimulation in Parkin and PINK1 parkinsonism. Neurology. 70(14). 1186–1191. 50 indexed citations
13.
Portnoï, Marie‐France, K. Lohmann-Hedrich, Boris Keren, et al.. (2008). Myoclonus-Dystonia Due to Maternal Uniparental Disomy. Archives of Neurology. 65(10). 1380–5. 30 indexed citations
14.
Muhle, Hiltrud, Anja Neumann, K. Lohmann-Hedrich, et al.. (2008). Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families. Movement Disorders. 23(8). 1113–1121. 52 indexed citations
15.
Winkler, Susen, Jannis Hagenah, S. Lincoln, et al.. (2007). α-Synuclein and Parkinson disease susceptibility. Neurology. 69(18). 1745–1750. 112 indexed citations
16.
Hedrich, Katja, Susen Winkler, Johann Hagenah, et al.. (2006). Recurrent LRRK2 (Park8) mutations in early‐onset Parkinson's disease. Movement Disorders. 21(9). 1506–1510. 39 indexed citations
17.
Klein, Christine, Ana Djarmati, Katja Hedrich, et al.. (2005). PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism. European Journal of Human Genetics. 13(9). 1086–1093. 92 indexed citations
18.
White, Beverly J., et al.. (1999). A 6-Year Experience Demonstrates the Utility of Screening for Both Cytogenetic and FMR-1 Abnormalities in Patients with Mental Retardation. Genetic Testing. 3(3). 291–296. 14 indexed citations
19.
Darke, C., Susen Winkler, M.G. Guttridge, et al.. (1999). Molecular, Serological and Population Studies of the Alleles and Products of HLA-B*41. PubMed. 16(3). 139–149. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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