Birgit Liss

8.3k total citations · 2 hit papers
73 papers, 6.2k citations indexed

About

Birgit Liss is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Birgit Liss has authored 73 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Molecular Biology, 45 papers in Cellular and Molecular Neuroscience and 17 papers in Neurology. Recurrent topics in Birgit Liss's work include Neuroscience and Neuropharmacology Research (29 papers), Ion channel regulation and function (19 papers) and Parkinson's Disease Mechanisms and Treatments (15 papers). Birgit Liss is often cited by papers focused on Neuroscience and Neuropharmacology Research (29 papers), Ion channel regulation and function (19 papers) and Parkinson's Disease Mechanisms and Treatments (15 papers). Birgit Liss collaborates with scholars based in Germany, United Kingdom and United States. Birgit Liss's co-authors include Jochen Roeper, Axel Neu, Andrea Hetzel, Stephan Lammel, Falk Schlaudraff, Jan Gründemann, Susumu Seino, Frances M. Ashcroft, Takashi Miki and Johanna Duda and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Neuron.

In The Last Decade

Birgit Liss

73 papers receiving 6.1k citations

Hit Papers

Hereditary parkinsonism with dementia is caused by mutati... 2006 2026 2012 2019 2006 2008 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Birgit Liss Germany 39 3.2k 2.8k 1.7k 1.0k 925 73 6.2k
Jochen Roeper Germany 40 4.4k 1.4× 3.5k 1.2× 1.6k 0.9× 1.5k 1.5× 810 0.9× 84 7.3k
Jeffrey H. Kordower United States 46 4.6k 1.4× 2.8k 1.0× 1.8k 1.1× 811 0.8× 1.1k 1.2× 109 7.5k
José L. Lanciego Spain 49 3.5k 1.1× 1.9k 0.7× 2.2k 1.3× 1.3k 1.2× 573 0.6× 143 7.1k
Matthias Klugmann Australia 43 3.3k 1.0× 3.6k 1.3× 465 0.3× 747 0.7× 878 0.9× 99 7.4k
Farrukh A. Chaudhry Norway 38 4.9k 1.5× 3.1k 1.1× 1.2k 0.7× 948 0.9× 1.0k 1.1× 73 7.4k
William A. Staines Canada 46 4.3k 1.4× 3.5k 1.3× 696 0.4× 865 0.8× 1.1k 1.2× 118 7.8k
Christian Kubisch Germany 37 2.2k 0.7× 4.6k 1.6× 1.1k 0.6× 336 0.3× 739 0.8× 144 7.3k
Henry J. Waldvogel New Zealand 54 4.1k 1.3× 3.5k 1.2× 2.1k 1.2× 634 0.6× 1.8k 1.9× 157 8.0k
Luis B. Tovar‐y‐Romo Sweden 42 5.3k 1.7× 2.3k 0.8× 1.3k 0.7× 781 0.8× 823 0.9× 111 8.0k

Countries citing papers authored by Birgit Liss

Since Specialization
Citations

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

Fields of papers citing papers by Birgit Liss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Liss

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

All Works

20 of 20 papers shown
1.
Nie, Yu, Patrick F. Chinnery, Heike Endepols, et al.. (2024). Preserved striatal innervation maintains motor function despite severe loss of nigral dopaminergic neurons. Brain. 147(9). 3189–3203. 7 indexed citations
2.
Ramírez‐Franco, Jorge, Michael Fauler, Johanna Duda, et al.. (2023). Deep learning-based image analysis identifies a DAT-negative subpopulation of dopaminergic neurons in the lateral Substantia nigra. Communications Biology. 6(1). 1146–1146. 5 indexed citations
3.
Veen, Bastiaan van der, Thomas Akam, Birgit Liss, et al.. (2023). Control of sustained attention and impulsivity by Gq-protein signalling in parvalbumin interneurons of the anterior cingulate cortex. Translational Psychiatry. 13(1). 243–243. 8 indexed citations
4.
Heß, Simon, Johanna Duda, Toni Schneider, et al.. (2022). β2-subunit alternative splicing stabilizes Cav2.3 Ca2+ channel activity during continuous midbrain dopamine neuron-like activity. eLife. 11. 11 indexed citations
5.
Duda, Johanna, Michael Fauler, Jan Gründemann, & Birgit Liss. (2018). Cell-Specific RNA Quantification in Human SN DA Neurons from Heterogeneous Post-mortem Midbrain Samples by UV-Laser Microdissection and RT-qPCR. Methods in molecular biology. 1723. 335–360. 9 indexed citations
6.
Ortner, Nadine J., Antonios Dougalis, Maria Kharitonova, et al.. (2017). Lower Affinity of Isradipine for L-Type Ca 2+ Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's Disease. Journal of Neuroscience. 37(28). 6761–6777. 62 indexed citations
7.
Dougalis, Antonios, Gillian A. Matthews, Birgit Liss, & Mark A. Ungless. (2017). Ionic currents influencing spontaneous firing and pacemaker frequency in dopamine neurons of the ventrolateral periaqueductal gray and dorsal raphe nucleus (vlPAG/DRN): A voltage-clamp and computational modelling study. Journal of Computational Neuroscience. 42(3). 275–305. 12 indexed citations
8.
Liss, Birgit. (2016). Calcium modulation of somatodendritic dopamine D2 autoreceptor responses. 4(Suppl. 2). A6.2–A6.2. 1 indexed citations
9.
Krabbe, Sabine, Johanna Duda, Julia Schiemann, et al.. (2015). Increased dopamine D2 receptor activity in the striatum alters the firing pattern of dopamine neurons in the ventral tegmental area. Proceedings of the National Academy of Sciences. 112(12). E1498–506. 50 indexed citations
10.
Schlaudraff, Falk, et al.. (2014). Orchestrated increase of dopamine and PARK mRNAs but not miR-133b in dopamine neurons in Parkinson's disease. Neurobiology of Aging. 35(10). 2302–2315. 38 indexed citations
11.
Parlato, Rosanna, et al.. (2014). Regulation of proliferation and histone acetylation in embryonic neural precursors by CREB/CREM signaling. PubMed. 1(1). e970883–e970883. 3 indexed citations
12.
13.
Elstner, Matthias, Sarina Müller, Falk Schlaudraff, et al.. (2011). Neuromelanin, neurotransmitter status and brainstem location determine the differential vulnerability of catecholaminergic neurons to mitochondrial DNA deletions. Molecular Brain. 4(1). 43–43. 38 indexed citations
14.
Rolyan, Harshvardhan, Annika Scheffold, Annette Heinrich, et al.. (2011). Telomere shortening reduces Alzheimer’s disease amyloid pathology in mice. Brain. 134(7). 2044–2056. 79 indexed citations
15.
Aguado, Carolina, José Colón, Francisco Ciruela, et al.. (2007). Cell type‐specific subunit composition of G protein‐gated potassium channels in the cerebellum. Journal of Neurochemistry. 105(2). 497–511. 65 indexed citations
16.
Tricarico, Domenico, Antonietta Mele, Birgit Liss, et al.. (2007). Reduced expression of Kir6.2/SUR2A subunits explains KATP deficiency in K+-depleted rats. Neuromuscular Disorders. 18(1). 74–80. 18 indexed citations
17.
Ramı́rez, Alfredo, André Heimbach, Jan Gründemann, et al.. (2006). Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nature Genetics. 38(10). 1184–1191. 881 indexed citations breakdown →
18.
Liss, Birgit & Jochen Roeper. (2001). A role for neuronal KATP channels in metabolic control of the seizure gate. Trends in Pharmacological Sciences. 22(12). 599–601. 18 indexed citations
19.
Liss, Birgit, Axel Neu, & Jochen Roeper. (1999). The weaver mouse gain-of-function phenotype of dopaminergic midbrain neurons is determined by coactivation of wvGirk2 and K-ATP channels.. PubMed. 19(20). 8839–48. 48 indexed citations
20.
Liss, Birgit, et al.. (1999). Alternative sulfonylurea receptor expression defines metabolic sensitivity of K-ATP channels in dopaminergic midbrain neurons. The EMBO Journal. 18(4). 833–846. 198 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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