Sigrid Fuchs

1.7k total citations
35 papers, 790 citations indexed

About

Sigrid Fuchs is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Sigrid Fuchs has authored 35 papers receiving a total of 790 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Physiology. Recurrent topics in Sigrid Fuchs's work include Genomic variations and chromosomal abnormalities (5 papers), Retinal Development and Disorders (5 papers) and Neurological diseases and metabolism (4 papers). Sigrid Fuchs is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Retinal Development and Disorders (5 papers) and Neurological diseases and metabolism (4 papers). Sigrid Fuchs collaborates with scholars based in Germany, United States and Netherlands. Sigrid Fuchs's co-authors include Andreas Gal, Mitsuru Nakazawa, Makoto Tamai, Y. Oguchi, Marion A. Maw, H. G. Doerr, GC Korenke, D. H. Hunneman, E. Schwinger and Rainer König and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Sigrid Fuchs

33 papers receiving 769 citations

Peers

Sigrid Fuchs
Felix Tonagel Germany
Piotr Stawiński Poland
Shanaz Pasha United Kingdom
Denis A. Akkad Germany
Christian Hamel France
Christine Briggs United States
Wojciech Wiszniewski United States
Katharina Steindl Switzerland
Agnès Guichet France
Arif O. Khan Saudi Arabia
Felix Tonagel Germany
Sigrid Fuchs
Citations per year, relative to Sigrid Fuchs Sigrid Fuchs (= 1×) peers Felix Tonagel

Countries citing papers authored by Sigrid Fuchs

Since Specialization
Citations

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

Fields of papers citing papers by Sigrid Fuchs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sigrid Fuchs

This figure shows the co-authorship network connecting the top 25 collaborators of Sigrid Fuchs. A scholar is included among the top collaborators of Sigrid Fuchs 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 Sigrid Fuchs. Sigrid Fuchs 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.
Fuchs, Sigrid, et al.. (2025). Generation of a biallelic NRAP-knockout mutant from a human iPSC line. Stem Cell Research. 88. 103829–103829.
2.
Lisfeld, Jasmin, Christopher M. Grochowski, Alex Hastie, et al.. (2024). A combination of long- and short-read genomics reveals frequent p-arm breakpoints within chromosome 21 complex genomic rearrangements. SHILAP Revista de lepidopterología. 2. 101863–101863. 2 indexed citations
3.
Fuchs, Sigrid, et al.. (2021). The acrocentric part of der(Y)t(Y;acro)(q12;p1?2) contains D15Z1 sequences in the majority of cases. Human Genome Variation. 8(1). 32–32. 1 indexed citations
4.
Sismani, Carolina, Athina Theodosiou, Maria Syrrou, et al.. (2020). Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Journal of Human Genetics. 65(9). 783–795. 9 indexed citations
5.
Lüttgen, Sabine, Sigrid Fuchs, Holger Thiele, et al.. (2020). Two novel cases further expand the phenotype of TOR1AIP1-associated nuclear envelopathies. Human Genetics. 139(4). 483–498. 12 indexed citations
6.
Hu, Xiaomeng, Nigel G. Kooreman, Alessia Gravina, et al.. (2020). The H-Y Antigen in Embryonic Stem Cells Causes Rejection in Syngeneic Female Recipients. Stem Cells and Development. 29(18). 1179–1189. 7 indexed citations
7.
Petkov, Stoyan, Orr Shomroni, Thomas Lingner, et al.. (2018). Immortalization of common marmoset monkey fibroblasts by piggyBac transposition of hTERT. PLoS ONE. 13(9). e0204580–e0204580. 11 indexed citations
8.
Rau, Isabella, Sigrid Fuchs, Hiram Larangeira de Almeida, et al.. (2014). Clinical spectrum of females with HCCS mutation: from no clinical signs to a neonatal lethal form of the microphthalmia with linear skin defects (MLS) syndrome. Orphanet Journal of Rare Diseases. 9(1). 53–53. 21 indexed citations
9.
Kortüm, Fanny, Sigrid Fuchs, Beate Albrecht, et al.. (2011). Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies. Molecular Syndromology. 2(1). 27–34. 7 indexed citations
10.
11.
Timmann, Christian, Sigrid Fuchs, Christian Thoma, et al.. (2004). Promoter haplotypes of the interleukin-10 gene influence proliferation of peripheral blood cells in response to helminth antigen. Genes and Immunity. 5(4). 256–260. 16 indexed citations
12.
13.
Asmus, Friedrich, Alexander Zimprich, Markus Naumann, et al.. (2001). Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families. Annals of Neurology. 49(1). 121–124. 30 indexed citations
14.
Nakazawa, Mitsuru, Yuko Wada, Sigrid Fuchs, Andreas Gal, & Makoto Tamai. (1997). OGUCHI DISEASE. Retina. 17(1). 17–22. 34 indexed citations
15.
Korenke, GC, Ekkehard Wilichowski, D. H. Hunneman, et al.. (1996). Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype. Annals of Neurology. 40(2). 254–257. 83 indexed citations
16.
Fuchs, Sigrid, et al.. (1996). Three novel and two recurrent mutations of the Norrie disease gene in patients with Norrie syndrome. Human Mutation. 8(1). 85–88. 10 indexed citations
17.
Fuchs, Sigrid, et al.. (1995). Missense mutation (Arg121Trp) in the norrie disease gene associated with X-linked exudative vitreoretinopathy. Human Mutation. 6(3). 257–259. 27 indexed citations
18.
Fuchs, Sigrid, M. J. Denton, Eberhart Zrenner, et al.. (1994). Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 3(7). 1203–1203. 28 indexed citations
19.
Fuchs, Sigrid, et al.. (1994). A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease. Human Molecular Genetics. 3(4). 655–656. 16 indexed citations
20.
Wullich, Bernd, et al.. (1991). Mosaic tetraploidy in a liveborn infant with features of the DiGeorge anomaly. Clinical Genetics. 40(5). 353–357. 15 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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