Sabine A. Fuchs

5.1k total citations · 1 hit paper
56 papers, 1.9k citations indexed

About

Sabine A. Fuchs is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Sabine A. Fuchs has authored 56 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 9 papers in Genetics. Recurrent topics in Sabine A. Fuchs's work include Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Amino Acid Enzymes and Metabolism (8 papers). Sabine A. Fuchs is often cited by papers focused on Metabolism and Genetic Disorders (16 papers), Mitochondrial Function and Pathology (9 papers) and Amino Acid Enzymes and Metabolism (8 papers). Sabine A. Fuchs collaborates with scholars based in Netherlands, Germany and United Kingdom. Sabine A. Fuchs's co-authors include Ian B. Wilkinson, James Spratt, Gordon Murray, John R. Cockcroft, David J. Webb, Ruud Berger, Tom J. de Koning, Leo W. J. Klomp, Peter M. van Hasselt and Edward E. S. Nieuwenhuis and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Sabine A. Fuchs

56 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Reproducibility of pulse wave velocity and augmentation index measured by pulse wave analysis

1998 792 citations Ian B. Wilkinson, Sabine A. Fuchs et al. Journal of Hypertension profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sabine A. Fuchs Netherlands	18	760	653	251	214	201	56	1.9k
Daniel Petrovič Slovenia	26	517 0.7×	809 1.2×	74 0.3×	185 0.9×	262 1.3×	141	2.3k
Lawrence J. Druhan United States	29	496 0.7×	1.3k 1.9×	334 1.3×	84 0.4×	189 0.9×	71	3.0k
Maura Brioschi Italy	29	381 0.5×	818 1.3×	56 0.2×	108 0.5×	265 1.3×	75	1.9k
Margaret C. Cam United States	29	473 0.6×	988 1.5×	70 0.3×	84 0.4×	193 1.0×	57	2.5k
Isabelle Rémy‐Jouet France	22	492 0.6×	580 0.9×	202 0.8×	45 0.2×	235 1.2×	48	1.5k
Kyle S. McCommis United States	26	207 0.3×	1.1k 1.6×	188 0.7×	154 0.7×	224 1.1×	67	2.1k
Andreas Petry Germany	18	240 0.3×	750 1.1×	99 0.4×	78 0.4×	232 1.2×	44	1.9k
George Seki Japan	31	354 0.5×	1.7k 2.6×	173 0.7×	79 0.4×	392 2.0×	96	2.6k
Tomomi Matsuura Japan	18	310 0.4×	805 1.2×	84 0.3×	49 0.2×	240 1.2×	56	1.4k
Daniel L. Galvan United States	20	236 0.3×	1.4k 2.2×	64 0.3×	237 1.1×	148 0.7×	32	2.0k

Countries citing papers authored by Sabine A. Fuchs

Since Specialization

Citations

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

Fields of papers citing papers by Sabine A. Fuchs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabine A. Fuchs

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

All Works

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20 of 20 papers shown

Joore, Indi P., Wilbert P. Vermeij, Richard J. Rodenburg, et al.. (2025). Correction of pathogenic mitochondrial DNA in patient-derived disease models using mitochondrial base editors. PLoS Biology. 23(6). e3003207–e3003207. 2 indexed citations

Bui, Bich Ngoc, Arif Ibrahim Ardisasmita, Shari Mackens, et al.. (2024). Enrichment of cell cycle pathways in progesterone-treated endometrial organoids of infertile women compared to fertile women. Journal of Assisted Reproduction and Genetics. 41(9). 2405–2418. 3 indexed citations

Schene, Imre F., Marisa I. Mendes, Desirée E.C. Smith, et al.. (2024). Isoleucine-to-valine substitutions support cellular physiology during isoleucine deprivation. Nucleic Acids Research. 53(1). 1 indexed citations

Albada, Mirjam E. van, Pratik Shah, Terry G. J. Derks, et al.. (2023). Abnormal glucose homeostasis and fasting intolerance in patients with congenital porto-systemic shunts. Frontiers in Endocrinology. 14. 1190473–1190473. 2 indexed citations

Bui, Bich Ngoc, Arif Ibrahim Ardisasmita, Ewart Kuijk, et al.. (2023). An unbiased approach of molecular characterization of the endometrium: toward defining endometrial-based infertility. Human Reproduction. 39(2). 275–281. 3 indexed citations

Ferdinandusse, Sacha, Saskia N. van der Crabben, Eugènie Dekkers, et al.. (2023). Newborn screening for primary carnitine deficiency: who will benefit? – a retrospective cohort study. Journal of Medical Genetics. 60(12). 1177–1185. 7 indexed citations

Ardisasmita, Arif Ibrahim, Imre F. Schene, Indi P. Joore, et al.. (2022). A comprehensive transcriptomic comparison of hepatocyte model systems improves selection of models for experimental use. Communications Biology. 5(1). 1094–1094. 15 indexed citations

Schene, Imre F., Indi P. Joore, Remi Stevelink, et al.. (2022). Mutation-specific reporter for optimization and enrichment of prime editing. Nature Communications. 13(1). 1028–1028. 24 indexed citations

Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations

10.

Schene, Imre F., Arif Ibrahim Ardisasmita, Nalan Liv, et al.. (2021). The potential and limitations of intrahepatic cholangiocyte organoids to study inborn errors of metabolism. Journal of Inherited Metabolic Disease. 45(2). 353–365. 8 indexed citations

11.

Wiame, Elsa, Sabine A. Fuchs, Maarten P.G. Massink, et al.. (2021). NAA80 bi-allelic missense variants result in high-frequency hearing loss, muscle weakness and developmental delay. Brain Communications. 3(4). fcab256–fcab256. 17 indexed citations

12.

Molema, Femke, Hanneke A. Haijes, Mirian C. H. Janssen, et al.. (2020). High protein prescription in methylmalonic and propionic acidemia patients and its negative association with long-term outcome. Clinical Nutrition. 40(5). 3622–3630. 9 indexed citations

13.

Oostendorp, M. van, Lourens J.P. Nonkes, Edward E. S. Nieuwenhuis, et al.. (2020). Quantifying lymphocyte vacuolization serves as a measure of CLN3 disease severity. JIMD Reports. 54(1). 87–97. 7 indexed citations

14.

Shamseldin, Hanan E., Amal Alhashem, Mais Hashem, et al.. (2019). MDH1 deficiency is a metabolic disorder of the malate–aspartate shuttle associated with early onset severe encephalopathy. Human Genetics. 138(11-12). 1247–1257. 40 indexed citations

15.

Theunissen, Tom E. J., Rick Kamps, Alexandra T.M. Hendrickx, et al.. (2018). Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause. Frontiers in Genetics. 9. 400–400. 62 indexed citations

16.

Fuchs, Sabine A., Magdaléna Harakaľová, Gijs van Haaften, et al.. (2012). Application of exome sequencing in the search for genetic causes of rare disorders of copper metabolism. Metallomics. 4(7). 606–606. 6 indexed citations

17.

Moat, Stuart J., Rachel S. Carling, Michael Henderson, et al.. (2010). Multicentre age-related reference intervals for cerebrospinal fluid serine concentrations: Implications for the diagnosis and follow-up of serine biosynthesis disorders. Molecular Genetics and Metabolism. 101(2-3). 149–152. 8 indexed citations

18.

Fuchs, Sabine A., Martina M.J. de Barse, Floor Scheepers, et al.. (2008). Cerebrospinal fluid d-serine and glycine concentrations are unaltered and unaffected by olanzapine therapy in male schizophrenic patients. European Neuropsychopharmacology. 18(5). 333–338. 27 indexed citations

19.

Fuchs, Sabine A., Ronald H.B. Meyboom, Eugène van Puijenbroek, & Henk‐Jan Guchelaar. (2004). Use of angiotensin receptor antagonists in patients with ACE inhibitor induced angioedema. Pharmacy World & Science. 26(4). 191–192. 20 indexed citations

20.

Wilkinson, Ian B., et al.. (1998). The reproducibility of augmentation index measured using pulse wave analysis. Journal of Hypertension. 16. 4 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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