Karin Schäferhoff

537 total citations
20 papers, 348 citations indexed

About

Karin Schäferhoff is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Karin Schäferhoff has authored 20 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Karin Schäferhoff's work include Genomic variations and chromosomal abnormalities (6 papers), Retinal Development and Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Karin Schäferhoff is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Retinal Development and Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Karin Schäferhoff collaborates with scholars based in Germany, Italy and Austria. Karin Schäferhoff's co-authors include Andreas Freund, Günter Jäger, Michael Löffler, Ralf Takors, Michael Bonin, Ute Grasshoff, Andreas Tzschach, Angelika Rieß, Olaf Rieß and Anna Jauch and has published in prestigious journals such as Neurology, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Karin Schäferhoff

19 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin Schäferhoff Germany 10 248 81 67 55 36 20 348
Tamar Dvash Israel 9 407 1.6× 36 0.4× 91 1.4× 59 1.1× 43 1.2× 9 469
Olympia E. Psathaki Germany 13 452 1.8× 50 0.6× 60 0.9× 49 0.9× 13 0.4× 31 595
Anna Manfredi Italy 11 400 1.6× 66 0.8× 171 2.6× 24 0.4× 57 1.6× 19 477
Yotam Menuchin-Lasowski Israel 9 280 1.1× 92 1.1× 63 0.9× 22 0.4× 44 1.2× 10 396
Madalena Carido Germany 11 506 2.0× 168 2.1× 29 0.4× 106 1.9× 81 2.3× 15 615
Sarah Wassmer United States 7 411 1.7× 46 0.6× 178 2.7× 19 0.3× 55 1.5× 18 565
Sylvie Janssens Belgium 8 263 1.1× 39 0.5× 49 0.7× 13 0.2× 15 0.4× 8 323
Vincent T. Ciavatta United States 14 340 1.4× 148 1.8× 29 0.4× 20 0.4× 108 3.0× 28 529
Xuetao Bai United States 10 218 0.9× 80 1.0× 60 0.9× 8 0.1× 14 0.4× 17 421
Maren Haase Germany 4 248 1.0× 56 0.7× 170 2.5× 33 0.6× 10 0.3× 10 389

Countries citing papers authored by Karin Schäferhoff

Since Specialization
Citations

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

Fields of papers citing papers by Karin Schäferhoff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Schäferhoff

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Schäferhoff. A scholar is included among the top collaborators of Karin Schäferhoff 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 Karin Schäferhoff. Karin Schäferhoff 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.
Merle, David A., Susanne Kohl, Karin Schäferhoff, et al.. (2024). An Atypical Mild Phenotype of Autosomal Recessive RPE65-Associated Retinitis Pigmentosa. Klinische Monatsblätter für Augenheilkunde. 241(3). 266–271. 2 indexed citations
2.
Kohl, Susanne, et al.. (2023). An early onset cone dystrophy due to CEP290 mutation: a case report. Documenta Ophthalmologica. 147(3). 203–209.
3.
Zeltner, Lena, Karin Schäferhoff, Theresia Zuleger, et al.. (2022). A Novel, Apparently Silent Variant in MFSD8 Causes Neuronal Ceroid Lipofuscinosis with Marked Intrafamilial Variability. International Journal of Molecular Sciences. 23(4). 2271–2271. 7 indexed citations
4.
Kuehlewein, Laura, Ditta Zobor, Katarína Štingl, et al.. (2021). Clinical Phenotype of PDE6B-Associated Retinitis Pigmentosa. International Journal of Molecular Sciences. 22(5). 2374–2374. 18 indexed citations
5.
Weisschuh, Nicole, Valerio Marino, Karin Schäferhoff, et al.. (2021). Mutations at a split codon in the GTPase-encoding domain of OPA1 cause dominant optic atrophy through different molecular mechanisms. Human Molecular Genetics. 31(5). 761–774. 6 indexed citations
6.
Kellner, Ulrich, Nicole Weisschuh, Silke Weinitz, et al.. (2021). Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant. International Journal of Molecular Sciences. 22(4). 2089–2089. 6 indexed citations
7.
Mau‐Holzmann, Ulrike A., Sylke Singer, Angelika Rieß, et al.. (2020). Pre‐ and postnatal findings in a patient with a recombinant chromosome rec(8)(qter→q21.11::p23.3→qter) due to a paternal pericentric inversion inv(8)(p23.3q21.11) and review of the literature. American Journal of Medical Genetics Part A. 182(11). 2680–2684. 2 indexed citations
8.
Park, Joohyun, Karin Schäferhoff, Luigi Janiri, et al.. (2019). Novel HIVEP2 Variants in Patients with Intellectual Disability. Molecular Syndromology. 10(4). 195–201. 7 indexed citations
9.
Leonhardt, Ines, Karin Schäferhoff, Michael Bonin, et al.. (2017). Specific and Novel microRNAs Are Regulated as Response to Fungal Infection in Human Dendritic Cells. Frontiers in Microbiology. 8. 270–270. 26 indexed citations
10.
Löffler, Michael, et al.. (2017). Switching between nitrogen and glucose limitation: Unraveling transcriptional dynamics in Escherichia coli. Journal of Biotechnology. 258. 2–12. 19 indexed citations
11.
Löffler, Michael, Günter Jäger, Karin Schäferhoff, et al.. (2017). Transcriptional response of Escherichia coli to ammonia and glucose fluctuations. Microbial Biotechnology. 10(4). 858–872. 32 indexed citations
12.
Löffler, Michael, et al.. (2016). Engineering E. coli for large-scale production – Strategies considering ATP expenses and transcriptional responses. Metabolic Engineering. 38. 73–85. 71 indexed citations
13.
Soehn, Anne S., Tim W. Rattay, Stefanie Beck‐Wödl, et al.. (2016). Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H /SPG35 in 4 families. Neurology. 87(2). 186–191. 21 indexed citations
14.
Kehrer, Martin, Karin Schäferhoff, Michael Bonin, et al.. (2015). Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies. American Journal of Medical Genetics Part A. 167(10). 2406–2410. 6 indexed citations
15.
Rieß, Angelika, Ute Grasshoff, Karin Schäferhoff, et al.. (2013). Xq22.3–q23 deletion including ACSL4 in a patient with intellectual disability. American Journal of Medical Genetics Part A. 161(4). 860–864. 32 indexed citations
16.
Kehrer, Martin, Sylke Singer, Ute Grasshoff, et al.. (2013). 12q24.33 deletion: Report of a patient with intellectual disability and review of the literature. American Journal of Medical Genetics Part A. 161(6). 1409–1413. 1 indexed citations
17.
Tzschach, Andreas, Ute Grasshoff, Karin Schäferhoff, et al.. (2012). Interstitial 9q34.11–q34.13 deletion in a patient with severe intellectual disability, hydrocephalus, and cleft lip/palate. American Journal of Medical Genetics Part A. 158A(7). 1709–1712. 6 indexed citations
18.
Michalakis, Stylianos, Karin Schäferhoff, Isabella Spiwoks‐Becker, et al.. (2012). Characterization of neurite outgrowth and ectopic synaptogenesis in response to photoreceptor dysfunction. Cellular and Molecular Life Sciences. 70(10). 1831–1847. 34 indexed citations
19.
Rieß, Angelika, Ute Grasshoff, Karin Schäferhoff, et al.. (2012). Interstitial 3p25.3–p26.1 deletion in a patient with intellectual disability. American Journal of Medical Genetics Part A. 158A(10). 2587–2590. 11 indexed citations
20.
Willmann, Gabriel, Karin Schäferhoff, M. Dominik Fischer, et al.. (2011). Gene Expression Profiling of the Retina after Transcorneal Electrical Stimulation in Wild-type Brown Norway Rats. Investigative Ophthalmology & Visual Science. 52(10). 7529–7529. 41 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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