Elisabeth Stögmann

18.3k total citations
67 papers, 1.2k citations indexed

About

Elisabeth Stögmann is a scholar working on Psychiatry and Mental health, Molecular Biology and Physiology. According to data from OpenAlex, Elisabeth Stögmann has authored 67 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Psychiatry and Mental health, 17 papers in Molecular Biology and 15 papers in Physiology. Recurrent topics in Elisabeth Stögmann's work include Dementia and Cognitive Impairment Research (21 papers), Alzheimer's disease research and treatments (13 papers) and Epilepsy research and treatment (7 papers). Elisabeth Stögmann is often cited by papers focused on Dementia and Cognitive Impairment Research (21 papers), Alzheimer's disease research and treatments (13 papers) and Epilepsy research and treatment (7 papers). Elisabeth Stögmann collaborates with scholars based in Austria, Germany and Italy. Elisabeth Stögmann's co-authors include Fritz Zimprich, Alexander Zimprich, Christoph Baumgartner, Johann Lehrner, Andreas Gleiß, Christian Baumgärtner, Peter Dal‐Bianco, Eduard Auff, Eva Assem‐Hilger and Gisela Pußwald and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Elisabeth Stögmann

61 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Stögmann Austria 19 515 245 213 204 177 67 1.2k
Christine Soufflet France 20 492 1.0× 298 1.2× 417 2.0× 284 1.4× 148 0.8× 48 1.5k
Masumi Ito Japan 21 429 0.8× 445 1.8× 231 1.1× 206 1.0× 67 0.4× 77 1.3k
Mi‐Sun Yum South Korea 22 637 1.2× 256 1.0× 386 1.8× 264 1.3× 33 0.2× 110 1.4k
Edda Haberlandt Austria 25 641 1.2× 371 1.5× 477 2.2× 217 1.1× 45 0.3× 89 1.7k
Kyoung Heo South Korea 22 790 1.5× 129 0.5× 563 2.6× 362 1.8× 132 0.7× 88 1.4k
Yuguang Guan China 18 339 0.7× 423 1.7× 170 0.8× 192 0.9× 53 0.3× 95 1.4k
Y Bureau Canada 18 194 0.4× 168 0.7× 163 0.8× 179 0.9× 64 0.4× 85 1.3k
Iris E. Martínez‐Juárez Mexico 19 607 1.2× 139 0.6× 323 1.5× 252 1.2× 57 0.3× 60 1000
Nerses Bebek Türkiye 22 964 1.9× 187 0.8× 515 2.4× 404 2.0× 78 0.4× 126 1.5k
Gudrun Gröppel Austria 19 759 1.5× 104 0.4× 414 1.9× 199 1.0× 45 0.3× 40 1.1k

Countries citing papers authored by Elisabeth Stögmann

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Stögmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Stögmann

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Stögmann. A scholar is included among the top collaborators of Elisabeth Stögmann 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 Elisabeth Stögmann. Elisabeth Stögmann 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.
Matt, Eva, et al.. (2025). Ultrasound Neuromodulation With Transcranial Pulse Stimulation in Alzheimer Disease. JAMA Network Open. 8(2). e2459170–e2459170. 8 indexed citations
2.
3.
Klotz, Sigrid, Theresa König, Lukas Haider, et al.. (2024). Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation. Annals of Clinical and Translational Neurology. 11(6). 1579–1589. 1 indexed citations
4.
Wurm, Raphael, Suriya Prausmüller, Markus Ponleitner, et al.. (2024). Serum Markers of Neurodegeneration Are Strongly Linked to Heart Failure Severity and Outcome. JACC Heart Failure. 12(6). 1073–1085. 7 indexed citations
5.
Wurm, Raphael, Theresa König, Patrick Altmann, et al.. (2024). Real‐world performance of plasma p‐tau181 in a heterogeneous memory clinic cohort. Annals of Clinical and Translational Neurology. 11(8). 1988–1998. 3 indexed citations
6.
König, Theresa, Raphael Wurm, Evelyn Berger–Sieczkowski, et al.. (2023). Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genes. Human Genomics. 17(1). 55–55. 1 indexed citations
7.
König, Theresa, Raphael Wurm, Christoph Hotzy, et al.. (2022). C9orf72 repeat length might influence clinical sub-phenotypes in dementia patients. Neurobiology of Disease. 175. 105927–105927. 6 indexed citations
8.
Schernhammer, Eva, et al.. (2022). Homocysteine – A predictor for five year-mortality in patients with subjective cognitive decline, mild cognitive impairment and Alzheimer's dementia. Experimental Gerontology. 172. 112045–112045. 7 indexed citations
9.
König, Theresa, Raphael Wurm, Patrick Altmann, et al.. (2022). Real-world applicability of glial fibrillary acidic protein and neurofilament light chain in Alzheimer’s disease. Frontiers in Aging Neuroscience. 14. 887498–887498. 16 indexed citations
10.
Stögmann, Elisabeth, et al.. (2021). Neuropsychological prediction of dementia using the neuropsychological test battery Vienna – A retrospective study. SHILAP Revista de lepidopterología. 5. 100028–100028. 3 indexed citations
11.
König, Theresa, Martina Pigliautile, Jon Arambarri, et al.. (2021). User experience and acceptance of a device assisting persons with dementia in daily life: a multicenter field study. Aging Clinical and Experimental Research. 34(4). 869–879. 10 indexed citations
12.
Stögmann, Elisabeth, et al.. (2020). Individual cognitive changes in subjective cognitive decline, mild cognitive impairment and Alzheimer’s disease using the reliable change index methodology. Wiener klinische Wochenschrift. 133(19-20). 1064–1069. 5 indexed citations
13.
Rommer, Paulus, Johannes Zschocke, Brian Fowler, et al.. (2017). Manifestations of neurological symptoms and thromboembolism in adults with MTHFR-deficiency. Journal of the Neurological Sciences. 383. 123–127. 8 indexed citations
14.
Stögmann, Elisabeth. (2013). Autosomal recessive cortical myoclonic tremor and epilepsy: Association with a mutation in the potassium channel associated gene CNTN2. Journal of the Neurological Sciences. 333. e19–e19. 3 indexed citations
15.
Stögmann, Elisabeth, Eva M. Reinthaler, Salwa El Tawil, et al.. (2013). Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain. 136(4). 1155–1160. 51 indexed citations
16.
Hilger, Eva, Eva M. Reinthaler, Elisabeth Stögmann, et al.. (2012). Lack of Association Between ABCC2 Gene Variants and Treatment Response in Epilepsy. Pharmacogenomics. 13(2). 185–190. 32 indexed citations
17.
Assem‐Hilger, Eva, Rupert Lanzenberger, Markus Savli, et al.. (2010). Central serotonin 1A receptor binding in temporal lobe epilepsy: A [carbonyl-11C]WAY-100635 PET study. Epilepsy & Behavior. 19(3). 467–473. 29 indexed citations
18.
Djamshidian, Atbin, Jochen Schaefer, Dietrich Haubenberger, et al.. (2009). A novel mutation in the VCP gene (G157R) in a german family with inclusion‐body myopathy with paget disease of bone and frontotemporal dementia. Muscle & Nerve. 39(3). 389–391. 51 indexed citations
19.
Stögmann, Elisabeth, Shadi Tawil, Janine Wagenstaller, et al.. (2008). A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosis. Neurogenetics. 10(1). 73–77. 28 indexed citations
20.
Stögmann, Elisabeth, Alexander Zimprich, Christoph Baumgartner, et al.. (2002). A functional polymorphism in the prodynorphin gene promotor is associated with temporal lobe epilepsy. Annals of Neurology. 51(2). 260–263. 79 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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