Simone Schimpf

1.0k total citations
12 papers, 711 citations indexed

About

Simone Schimpf is a scholar working on Molecular Biology, Immunology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Simone Schimpf has authored 12 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Immunology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Simone Schimpf's work include Mitochondrial Function and Pathology (10 papers), ATP Synthase and ATPases Research (9 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Simone Schimpf is often cited by papers focused on Mitochondrial Function and Pathology (10 papers), ATP Synthase and ATPases Research (9 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Simone Schimpf collaborates with scholars based in Germany, Italy and United States. Simone Schimpf's co-authors include Bernd Wissinger, Valério Carelli, Maria Lucia Valentino, Marcello Pinti, Michela Rugolo, Andrea Cossarizza, Claudia Zanna, Anna Ghelli, Richard J. Youle and Anna Maria Porcelli and has published in prestigious journals such as Brain, Annals of Neurology and Ophthalmology.

In The Last Decade

Simone Schimpf

12 papers receiving 709 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simone Schimpf Germany 8 668 188 92 92 67 12 711
P Kjer Denmark 10 701 1.0× 85 0.5× 113 1.2× 109 1.2× 39 0.6× 12 822
Svitlana Yablonska United States 7 391 0.6× 32 0.2× 175 1.9× 76 0.8× 83 1.2× 10 512
Sylvia Cherninkova Bulgaria 7 260 0.4× 70 0.4× 214 2.3× 13 0.1× 12 0.2× 20 448
Patrick Yu Wai Man United Kingdom 5 543 0.8× 223 1.2× 44 0.5× 8 0.1× 20 0.3× 6 592
Rocío Sánchez-Alcudia Spain 14 339 0.5× 118 0.6× 40 0.4× 9 0.1× 15 0.2× 18 418
Takuro Fujimaki Japan 14 335 0.5× 29 0.2× 56 0.6× 19 0.2× 25 0.4× 26 462
Aïcha Bouaita France 5 345 0.5× 111 0.6× 50 0.5× 7 0.1× 30 0.4× 5 390
Marjan E. Steenweg Netherlands 11 509 0.8× 160 0.9× 42 0.5× 43 0.5× 88 1.3× 16 621
Phillippa J. Carling United Kingdom 8 232 0.3× 56 0.3× 78 0.8× 24 0.3× 62 0.9× 10 344
Shunji Nakatake Japan 18 494 0.7× 21 0.1× 52 0.6× 84 0.9× 18 0.3× 29 714

Countries citing papers authored by Simone Schimpf

Since Specialization
Citations

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

Fields of papers citing papers by Simone Schimpf

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Schimpf

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

All Works

12 of 12 papers shown
1.
Fuhrmann, Nico, Simone Schimpf, York Kamenisch, et al.. (2010). Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy. Molecular Neurodegeneration. 5(1). 25–25. 15 indexed citations
2.
Barboni, Piero, Michele Carbonelli, Giacomo Savini, et al.. (2010). OPA1 Mutations Associated with Dominant Optic Atrophy Influence Optic Nerve Head Size. Ophthalmology. 117(8). 1547–1553. 41 indexed citations
3.
Lodi, Raffaele, Caterina Tonon, Maria Lucia Valentino, et al.. (2010). Defective Mitochondrial Adenosine Triphosphate Production in Skeletal Muscle From Patients With Dominant Optic Atrophy Due to OPA1 Mutations. Archives of Neurology. 68(1). 67–73. 26 indexed citations
4.
Carelli, Valério, Simone Schimpf, Maria Lucia Valentino, et al.. (2007). Dominant Optic Atrophy (DOA) and Sensorineural Hearing Loss: Clinical, Biochemical, Spectroscopic and Molecular Genetic Study of a Large Italian Pedigree Linked to a New Locus on Chromosome 16. Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna). 68. 4 indexed citations
5.
Zanna, Claudia, Anna Ghelli, Anna Maria Porcelli, et al.. (2007). OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. Brain. 131(2). 352–367. 248 indexed citations
6.
Leo‐Kottler, Beate, et al.. (2007). Autosomal-dominant erbliche Optikusatrophie vs. Lebersche Optikusneuropathie – Wie kann man sie unterscheiden?. Der Ophthalmologe. 104(12). 1060–1065. 3 indexed citations
7.
Schimpf, Simone, Nico Fuhrmann, Simone Schaich, & Bernd Wissinger. (2007). Comprehensive cDNA study and quantitative transcript analysis of mutantOPA1transcripts containing premature termination codons. Human Mutation. 29(1). 106–112. 33 indexed citations
8.
Alavi, Marcel V., Stefanie Bette, Simone Schimpf, et al.. (2006). A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy. Brain. 130(4). 1029–1042. 207 indexed citations
9.
Schimpf, Simone, Simone Schaich, & Bernd Wissinger. (2005). Activation of cryptic splice sites is a frequent splicing defect mechanism caused by mutations in exon and intron sequences of the OPA1 gene. Human Genetics. 118(6). 767–771. 19 indexed citations
10.
Lodi, Raffaele, Caterina Tonon, Maria Lucia Valentino, et al.. (2005). Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy. American Journal of Ophthalmology. 139(2). 401–401. 4 indexed citations
11.
Lodi, Raffaele, Caterina Tonon, Maria Lucia Valentino, et al.. (2004). Deficit of in vivo mitochondrial ATP production in OPA1‐related dominant optic atrophy. Annals of Neurology. 56(5). 719–723. 109 indexed citations
12.
Long, Jeffrey C., et al.. (1996). Alcoholism genetics in a native American tribe. Psychiatric Genetics. 6(3). 162–162. 2 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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