Florence Pache

5.0k total citations
38 papers, 1.2k citations indexed

About

Florence Pache is a scholar working on Pathology and Forensic Medicine, Neurology and Rheumatology. According to data from OpenAlex, Florence Pache has authored 38 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Pathology and Forensic Medicine, 18 papers in Neurology and 11 papers in Rheumatology. Recurrent topics in Florence Pache's work include Multiple Sclerosis Research Studies (25 papers), Peripheral Neuropathies and Disorders (13 papers) and Systemic Lupus Erythematosus Research (10 papers). Florence Pache is often cited by papers focused on Multiple Sclerosis Research Studies (25 papers), Peripheral Neuropathies and Disorders (13 papers) and Systemic Lupus Erythematosus Research (10 papers). Florence Pache collaborates with scholars based in Germany, United States and Switzerland. Florence Pache's co-authors include Friedemann Paul, Klemens Ruprecht, Alexander U. Brandt, Judith Bellmann–Strobl, Norbert Suttorp, Bastian Opitz, Martin Witzenrath, Karolin Meixenberger, Anna Lacheta and Hanna Zimmermann and has published in prestigious journals such as The Journal of Immunology, PLoS ONE and Neurology.

In The Last Decade

Florence Pache

36 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Pache Germany 20 596 389 344 337 177 38 1.2k
Makbule Şenel Germany 20 635 1.1× 200 0.5× 420 1.2× 232 0.7× 259 1.5× 43 1.2k
Sergio Martínez‐Yélamos Spain 23 671 1.1× 165 0.4× 560 1.6× 144 0.4× 246 1.4× 86 1.5k
Mónica Marta United Kingdom 20 1.0k 1.8× 307 0.8× 368 1.1× 761 2.3× 266 1.5× 66 1.9k
John S. Tzartos Greece 15 788 1.3× 323 0.8× 340 1.0× 955 2.8× 231 1.3× 69 2.0k
Philipp Schwenkenbecher Germany 21 400 0.7× 146 0.4× 307 0.9× 117 0.3× 159 0.9× 56 902
Ilijas Jelčić Switzerland 20 473 0.8× 153 0.4× 427 1.2× 456 1.4× 142 0.8× 55 1.5k
Alexandros Tselis United States 21 729 1.2× 105 0.3× 472 1.4× 151 0.4× 242 1.4× 40 1.3k
Rafael Arroyo Spain 26 762 1.3× 356 0.9× 224 0.7× 611 1.8× 218 1.2× 76 1.7k
Hikoaki Fukaura Japan 13 489 0.8× 139 0.4× 301 0.9× 694 2.1× 162 0.9× 34 1.2k
Konstantin Balashov United States 21 891 1.5× 318 0.8× 196 0.6× 1.5k 4.4× 243 1.4× 40 2.3k

Countries citing papers authored by Florence Pache

Since Specialization
Citations

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

Fields of papers citing papers by Florence Pache

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Pache

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Pache. A scholar is included among the top collaborators of Florence Pache 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 Florence Pache. Florence Pache 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.
Pache, Florence, Carolin Otto, Katja Steinhagen, et al.. (2024). Broad Analysis of Serum and Intrathecal Antimicrobial Antibodies in Multiple Sclerosis Underscores Unique Role of Epstein-Barr Virus. Neurology Neuroimmunology & Neuroinflammation. 12(1). e200332–e200332. 1 indexed citations
2.
Otto, Carolin, Tatjana Schwarz, Lara M. Jeworowski, et al.. (2023). Humoral immune responses remain quantitatively impaired but improve qualitatively in anti-CD20-treated patients with multiple sclerosis after three or four COVID-19 vaccinations. Multiple Sclerosis Journal. 29(7). 884–888. 1 indexed citations
3.
Schwarz, Tatjana, Carolin Otto, Terry C. Jones, et al.. (2022). Preserved T cell responses to SARS-CoV-2 in anti-CD20 treated multiple sclerosis. Multiple Sclerosis Journal. 28(7). 1041–1050. 12 indexed citations
4.
Otto, Carolin, Helena Radbruch, Katja Steinhagen, et al.. (2022). Frequent intrathecal production of antibodies to the viral capsid antigen of Epstein-Barr virus in patients with central nervous system post-transplant lymphoproliferative disorder. Journal of Neuroimmunology. 369. 577902–577902. 2 indexed citations
5.
Steiner, Leon A, et al.. (2021). Oculomotor Nerve Palsy as a Presenting Symptom of Epstein-Barr Virus-Associated Infectious Mononucleosis: Case Report and Review of the Literature. Case Reports in Neurology. 13(3). 756–762. 3 indexed citations
6.
Pache, Florence, Marius Ringelstein, Orhan Aktaş, et al.. (2021). C3 and C4 complement levels in AQP4-IgG-positive NMOSD and in MOGAD. Journal of Neuroimmunology. 360. 577699–577699. 22 indexed citations
7.
Faissner, Simon, Sabrina Reinehr, Steffen Haupeltshofer, et al.. (2020). Binding patterns and functional properties of human antibodies to AQP4 and MOG on murine optic nerve and retina. Journal of Neuroimmunology. 342. 577194–577194. 3 indexed citations
8.
Grittner, Ulrike, René M. Gieß, Michael Scheel, et al.. (2019). Intrathecal IgM production is a strong risk factor for early conversion to multiple sclerosis. Neurology. 93(15). e1439–e1451. 35 indexed citations
9.
Mealy, Maureen A., Lawrence J. Cook, Florence Pache, et al.. (2018). Vaccines and the association with relapses in patients with neuromyelitis optica spectrum disorder. Multiple Sclerosis and Related Disorders. 23. 78–82. 28 indexed citations
10.
Thöne, Jan, Anna Stahl‐Pehe, Florence Pache, et al.. (2018). Ovarian Reserve in Women With Neuromyelitis Optica Spectrum Disorder. Frontiers in Neurology. 9. 446–446. 9 indexed citations
11.
12.
Pache, Florence, Judith Bellmann–Strobl, Janina Behrens, et al.. (2016). Neuromyelitis optica does not impact periventricular venous density versus healthy controls: a 7.0 Tesla MRI clinical study. Magnetic Resonance Materials in Physics Biology and Medicine. 29(3). 535–541. 10 indexed citations
13.
Schmidt, Felix, Hanna Zimmermann, Janine Mikolajczak, et al.. (2016). Severe structural and functional visual system damage leads to profound loss of vision-related quality of life in patients with neuromyelitis optica spectrum disorders. Multiple Sclerosis and Related Disorders. 11. 45–50. 76 indexed citations
14.
Ayzenberg, Ilya, Robert Hoepner, Kerstin Hellwig, et al.. (2016). Efficacy of glatiramer acetate in neuromyelitis optica spectrum disorder: a multicenter retrospective study. Journal of Neurology. 263(3). 575–582. 39 indexed citations
15.
Streitberger, Kaspar‐Josche, Andreas Fehlner, Florence Pache, et al.. (2016). Multifrequency magnetic resonance elastography of the brain reveals tissue degeneration in neuromyelitis optica spectrum disorder. European Radiology. 27(5). 2206–2215. 19 indexed citations
16.
Pache, Florence, Hanna Zimmermann, Carsten Finke, et al.. (2016). Brain parenchymal damage in neuromyelitis optica spectrum disorder – A multimodal MRI study. European Radiology. 26(12). 4413–4422. 51 indexed citations
17.
Fatykhova, Diana, Anne Rabes, Kunchur Guruprasad, et al.. (2015). Serotype 1 and 8 Pneumococci Evade Sensing by Inflammasomes in Human Lung Tissue. PLoS ONE. 10(8). e0137108–e0137108. 31 indexed citations
18.
Jarius, Sven, Friedemann Paul, Kaï Fechner, et al.. (2014). Aquaporin-4 antibody testing: direct comparison of M1-AQP4-DNA-transfected cells with leaky scanning versus M23-AQP4-DNA-transfected cells as antigenic substrate. Journal of Neuroinflammation. 11(1). 129–129. 24 indexed citations
19.
Meixenberger, Karolin, Florence Pache, Julia Eitel, et al.. (2009). Listeria monocytogenes -Infected Human Peripheral Blood Mononuclear Cells Produce IL-1β, Depending on Listeriolysin O and NLRP3. The Journal of Immunology. 184(2). 922–930. 157 indexed citations
20.
Bonsack, Charles, et al.. (2009). [Integration processes and clinical governance in the psychiatric network].. PubMed. 5(217). 1822–5. 3 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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