Karin Wiegers

730 total citations
11 papers, 428 citations indexed

About

Karin Wiegers is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Karin Wiegers has authored 11 papers receiving a total of 428 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Neurology, 8 papers in Cellular and Molecular Neuroscience and 3 papers in Molecular Biology. Recurrent topics in Karin Wiegers's work include Neurological disorders and treatments (7 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Karin Wiegers is often cited by papers focused on Neurological disorders and treatments (7 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Karin Wiegers collaborates with scholars based in Germany, United States and Italy. Karin Wiegers's co-authors include Christine Klein, Katja Hedrich, Peter P. Pramstaller, Thora Lohnau, P. Vieregge, E. Schwinger, Jennifer Garrels, Susen Winkler, Laurie J. Ozelius and Martin Kann and has published in prestigious journals such as Neurology, Annals of Neurology and Movement Disorders.

In The Last Decade

Karin Wiegers

11 papers receiving 424 citations

Peers

Countries citing papers authored by Karin Wiegers

Since Specialization

Citations

This map shows the geographic impact of Karin Wiegers'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 Karin Wiegers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Wiegers more than expected).

Fields of papers citing papers by Karin Wiegers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Karin Wiegers. 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 Karin Wiegers. The network helps show where Karin Wiegers may publish in the future.

Co-authorship network of co-authors of Karin Wiegers

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Wiegers. A scholar is included among the top collaborators of Karin Wiegers 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 Karin Wiegers. Karin Wiegers is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia 2017 ·JAMA Neurology ·Katja Lohmann, Claire Redin, Holger Tönnies, Susan Bressman, (unknown), Karin Wiegers, (unknown), Yorck Hellenbroich, Aleksandar Raković, Deborah Raymond, Laurie J. Ozelius, E. Schwinger, Reiner Siebert, Michael E. Talkowski, Rachel Saunders‐Pullman, Christine Klein	5
2	Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only 2014 ·Journal of Neurology ·Robert A. Wilcox, Ingrid Brænne, Norbert Brüggemann, Susen Winkler, Karin Wiegers, Lars Bertram, Tim Anderson, Katja Lohmann	6
3	Unraveling Cellular Phenotypes of NovelTorsinA/TOR1AMutations 2014 ·Human Mutation ·Franca Vulinović, Katja Lohmann, Aleksandar Raković, Philipp Capetian, Daniel Alvarez‐Fischer, Alexander Schmidt, Anne Weißbach, (unknown), Frank J. Kaiser, Karin Wiegers, A. Ferbert, Arndt Rolfs, Christine Klein, Philip Seibler	25
4	Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation 2013 ·Journal of Neurology ·Sarah Doss, Katja Lohmann, Philip Seibler, (unknown), Thomas Klopstock, Christine Zühlke, (unknown), Susen Winkler, Thora Lohnau, Mario Drungowski, Peter Nürnberg, Karin Wiegers, Ebba Lohmann, Sadaf Naz, Meike Kasten, Georg Böhner, Alfredo Ramı́rez, Matthias Endres, Christine Klein	31
5	Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers 2009 ·Parkinsonism & Related Disorders ·Norbert Brüggemann, Manfred Mitterer, (unknown), Ana Djarmati, Johann Hagenah, Karin Wiegers, Susen Winkler, Heike Pawlack, Thora Lohnau, Peter P. Pramstaller, Christine Klein, Katja Lohmann	35
6	PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism 2005 ·European Journal of Human Genetics ·Christine Klein, Ana Djarmati, Katja Hedrich, (unknown), Cesa Scaglione, Roberta Marchese, Norman Kock, Birgitt Schüle, Anja Hiller, Thora Lohnau, Susen Winkler, Karin Wiegers, Robert Hering, Peter Bauer, Olaf Rieß, Giovanni Abbruzzese, Paolo Martinelli, Peter P. Pramstaller	92
7	High mutation rate in dopa-responsive dystonia: Detection with comprehensive GCHI screening 2005 ·Neurology ·J. Hagenah, Rachel Saunders‐Pullman, Katja Hedrich, Kemal Kabakci, (unknown), Karin Wiegers, (unknown), Thora Lohnau, Deborah Raymond, P. Vieregge, (unknown), L. J. Ozelius, S. B. Bressman, Christine Klein	65
8	Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutations 2004 ·Neurology ·Katja Hedrich, Éric Meyer, Birgitt Schüle, Norman Kock, Patrícia de Carvalho Aguiar, Karin Wiegers, J.H.T.M. Koelman, Jennifer Garrels, Roland Dürr, (unknown), E. Schwinger, Laurie J. Ozelius, G. Bernhard Landwehrmeyer, A. Jon Stoessl, Marina A.J. Tijssen, Christine Klein	26
9	Clinical and genetic features of myoclonus–dystonia in 3 cases: A video presentation 2003 ·Movement Disorders ·Norman Kock, Meike Kasten, Birgitt Schüle, Katja Hedrich, Karin Wiegers, Kemal Kabakci, Johann Hagenah, Peter P. Pramstaller, Matthias Nitschke, Alexander Münchau, Jürgen Sperner, Christine Klein	11
10	Role of parkin mutations in 111 community‐based patients with early‐onset parkinsonism 2002 ·Annals of Neurology ·Martin Kann, Helfried Jacobs, (unknown), (unknown), Katja Hedrich, Jennifer Garrels, Karin Wiegers, E. Schwinger, Peter P. Pramstaller, Xandra O. Breakefield, Laurie J. Ozelius, P. Vieregge, Christine Klein	110
11	Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia 2002 ·Neurology ·Christine Klein, Katja Hedrich, Kemal Kabakci, (unknown), Karin Wiegers, Olfert Landt, J. Hagenah, E. Schwinger, Peter P. Pramstaller, L. J. Ozelius, Kıvılcım Gücüyener, Sabiha Aysun, Eşref Demir	22

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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