Thora Lohnau

1.3k total citations
16 papers, 709 citations indexed

About

Thora Lohnau is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Thora Lohnau has authored 16 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Molecular Biology. Recurrent topics in Thora Lohnau's work include Parkinson's Disease Mechanisms and Treatments (9 papers), Neurological disorders and treatments (5 papers) and Nuclear Receptors and Signaling (4 papers). Thora Lohnau is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (9 papers), Neurological disorders and treatments (5 papers) and Nuclear Receptors and Signaling (4 papers). Thora Lohnau collaborates with scholars based in Germany, Italy and United States. Thora Lohnau's co-authors include Christine Klein, Ana Djarmati, Katja Hedrich, Peter P. Pramstaller, Susen Winkler, Katja Lohmann, Johann Hagenah, Karin Wiegers, Norman Kock and Anja Hiller and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Cell Biology and Neurology.

In The Last Decade

Thora Lohnau

16 papers receiving 700 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thora Lohnau Germany	15	497	295	219	174	98	16	709
Szu‐Chia Lai Taiwan	16	381 0.8×	177 0.6×	179 0.8×	118 0.7×	81 0.8×	30	643
Michel Borg France	11	530 1.1×	342 1.2×	290 1.3×	36 0.2×	48 0.5×	12	862
David Crosiers Belgium	14	391 0.8×	104 0.4×	96 0.4×	77 0.4×	75 0.8×	32	523
K. Lohmann-Hedrich Germany	9	458 0.9×	229 0.8×	134 0.6×	112 0.6×	114 1.2×	9	576
Mark P. DeAndrade United States	13	454 0.9×	225 0.8×	98 0.4×	186 1.1×	132 1.3×	18	595
Nathan Levine United States	10	432 0.9×	292 1.0×	182 0.8×	42 0.2×	36 0.4×	15	700
Erin Furr Stimming United States	11	207 0.4×	289 1.0×	290 1.3×	181 1.0×	38 0.4×	30	619
Arlene R. Ng Philippines	12	406 0.8×	214 0.7×	174 0.8×	38 0.2×	63 0.6×	24	593
Sara Carrideo Italy	14	317 0.6×	293 1.0×	201 0.9×	17 0.1×	102 1.0×	16	640
Tomoko Nihira Japan	10	252 0.5×	193 0.7×	174 0.8×	42 0.2×	31 0.3×	13	448

Countries citing papers authored by Thora Lohnau

Since Specialization

Citations

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

Fields of papers citing papers by Thora Lohnau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thora Lohnau

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

All Works

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16 of 16 papers shown

Vos, Melissa, et al.. (2021). Ceramide accumulation induces mitophagy and impairs β-oxidation in PINK1 deficiency. Proceedings of the National Academy of Sciences. 118(43). 54 indexed citations

Vos, Melissa, Jef Swerts, Matteo Rossi, et al.. (2017). Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency. The Journal of Cell Biology. 216(3). 695–708. 56 indexed citations

Seibler, Philip, Diana Braunholz, Reinhard Depping, et al.. (2014). THAP1, the gene mutated in DYT6 dystonia, autoregulates its own expression. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1839(11). 1196–1204. 18 indexed citations

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

Weißbach, Anne, Norbert Brüggemann, Alexander Schmidt, et al.. (2012). Exome sequencing in a family with restless legs syndrome. Movement Disorders. 27(13). 1686–1689. 17 indexed citations

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

Kaiser, Frank J., Aleksandar Raković, Diana Braunholz, et al.. (2010). The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6). Annals of Neurology. 68(4). 554–559. 64 indexed citations

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

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.

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

11.

Lohmann-Hedrich, K., Anja Neumann, André Kleensang, et al.. (2007). Evidence for linkage of restless legs syndrome to chromosome 9p. Neurology. 70(9). 686–694. 26 indexed citations

12.

Djarmati, Ana, Katja Hedrich, Marina Svetel, et al.. (2006). Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?. Movement Disorders. 21(9). 1526–1530. 36 indexed citations

13.

Hedrich, Katja, Johann Hagenah, Ana Djarmati, et al.. (2006). Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease. Archives of Neurology. 63(6). 833–833. 104 indexed citations

14.

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

15.

Djarmati, Ana, Kemal Kabakci, Irene Pichler, et al.. (2005). Co‐occurrence of restless legs syndrome and Parkin mutations in two families. Movement Disorders. 21(2). 258–263. 26 indexed citations

16.

Hagenah, J., Rachel Saunders‐Pullman, Katja Hedrich, et al.. (2005). High mutation rate in dopa-responsive dystonia: Detection with comprehensive GCHI screening. Neurology. 64(5). 908–911. 65 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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