Simone M. Sauter

655 total citations
11 papers, 465 citations indexed

About

Simone M. Sauter is a scholar working on Cellular and Molecular Neuroscience, Neurology and Genetics. According to data from OpenAlex, Simone M. Sauter has authored 11 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 5 papers in Neurology and 4 papers in Genetics. Recurrent topics in Simone M. Sauter's work include Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simone M. Sauter is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Simone M. Sauter collaborates with scholars based in Germany, Austria and Poland. Simone M. Sauter's co-authors include Jürgen Neesen, Wolfgang Engel, Ashraf U. Mannan, Walter Paulus, Thomas Liehr, Barbara Zoll, Heike Starke, Moneef Shoukier, Iris Bartels and Luitgard M. Neumann and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and European Journal of Neurology.

In The Last Decade

Simone M. Sauter

11 papers receiving 451 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 M. Sauter Germany 9 279 170 116 114 111 11 465
Jean Welssenbach France 8 176 0.6× 82 0.5× 69 0.6× 50 0.4× 232 2.1× 8 387
Eric J. Meershoek Netherlands 10 252 0.9× 100 0.6× 24 0.2× 73 0.6× 160 1.4× 11 434
N. Ravisé France 14 345 1.2× 95 0.6× 29 0.3× 56 0.5× 298 2.7× 30 585
Е. Л. Дадали Russia 10 454 1.6× 208 1.2× 79 0.7× 152 1.3× 260 2.3× 115 760
Bart W. Nieuwenhuijsen United States 10 367 1.3× 110 0.6× 58 0.5× 99 0.9× 329 3.0× 11 632
James R. Lupski United States 8 202 0.7× 72 0.4× 39 0.3× 30 0.3× 140 1.3× 8 378
Andrzej Kochański Poland 14 490 1.8× 184 1.1× 62 0.5× 126 1.1× 287 2.6× 73 706
Esra Battaloğlu Türkiye 14 229 0.8× 126 0.7× 45 0.4× 58 0.5× 231 2.1× 33 457
Jenea M. Bin Canada 12 233 0.8× 151 0.9× 19 0.2× 81 0.7× 343 3.1× 16 637
Jens P. Magnusson Sweden 8 176 0.6× 213 1.3× 44 0.4× 41 0.4× 320 2.9× 8 620

Countries citing papers authored by Simone M. Sauter

Since Specialization
Citations

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

Fields of papers citing papers by Simone M. Sauter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone M. Sauter

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

All Works

11 of 11 papers shown
1.
Klimpe, Sven, Arne Zibat, Ulrich Zechner, et al.. (2010). Evaluating the effect of spastin splice mutations by quantitative allele‐specific expression assay. European Journal of Neurology. 18(1). 99–105. 6 indexed citations
2.
Shoukier, Moneef, et al.. (2008). Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia. European Journal of Human Genetics. 17(2). 187–194. 67 indexed citations
3.
Sauter, Simone M., Detlef Böhm, Iris Bartels, et al.. (2007). Partial trisomy of distal 19q detected by quantitative real‐time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. American Journal of Medical Genetics Part A. 143A(10). 1091–1099. 9 indexed citations
4.
Mannan, Ashraf U., et al.. (2006). ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia. The American Journal of Human Genetics. 79(2). 351–357. 107 indexed citations
5.
Bartels, Iris, et al.. (2006). An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype. European Journal of Medical Genetics. 50(2). 133–138. 42 indexed citations
6.
7.
Sauter, Simone M., Thomas Liehr, Peter Burfeind, et al.. (2005). Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay. American Journal of Medical Genetics Part A. 137A(1). 59–64. 7 indexed citations
8.
Sauter, Simone M., Peter Burfeind, Anja Weise, et al.. (2003). Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter → p12.2)[10]. American Journal of Medical Genetics Part A. 120A(4). 533–536. 22 indexed citations
9.
Sauter, Simone M., Wolfgang Engel, Luitgard M. Neumann, J. Kunze, & Jürgen Neesen. (2003). Novel mutations in theAtlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to theSPG3A locus. Human Mutation. 23(1). 98–98. 46 indexed citations
10.
Sauter, Simone M., Bianca Miterski, Sven Klimpe, et al.. (2002). Mutation analysis of thespastingene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia. Human Mutation. 20(2). 127–132. 74 indexed citations
11.
Bruch, Jochen, Gudrun Wöhr, Richard E. Hautmann, et al.. (1998). Chromosomal changes during progression of transitional cell carcinoma of the bladder and delineation of the amplified interval on chromosome arm 8q. Genes Chromosomes and Cancer. 23(2). 167–174. 40 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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