Saskia J.G. Hoefs

1.4k total citations · 1 hit paper
9 papers, 1.1k citations indexed

About

Saskia J.G. Hoefs is a scholar working on Molecular Biology, Clinical Biochemistry and Infectious Diseases. According to data from OpenAlex, Saskia J.G. Hoefs has authored 9 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 1 paper in Infectious Diseases. Recurrent topics in Saskia J.G. Hoefs's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (3 papers). Saskia J.G. Hoefs is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (3 papers). Saskia J.G. Hoefs collaborates with scholars based in Netherlands, Germany and Belgium. Saskia J.G. Hoefs's co-authors include Chang Qing, Joost G.J. Hoenderop, René J.M. Bindels, Catalin N. Topala, Annemiete W. van der Kemp, Jan Smeıtınk, Leo Nijtmans, Richard J. Rodenburg, Lambert P. van den Heuvel and Peter H.G.M. Willems and has published in prestigious journals such as Science, Cell Metabolism and The American Journal of Human Genetics.

In The Last Decade

Saskia J.G. Hoefs

9 papers receiving 1.1k 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.

The ß-Glucuronidase Klotho Hydrolyzes and Activates the TRPV5 Channel

2005 502 citations Chang Qing, Saskia J.G. Hoefs et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Saskia J.G. Hoefs Netherlands	8	707	326	293	238	146	9	1.1k
Éva Dizin Switzerland	15	446 0.6×	150 0.5×	29 0.1×	115 0.5×	62 0.4×	19	768
Diana L. Fitzpatrick United States	8	430 0.6×	15 0.0×	419 1.4×	102 0.4×	115 0.8×	8	947
Xianglan Quan South Korea	9	245 0.3×	149 0.5×	33 0.1×	44 0.2×	40 0.3×	15	497
Paola Capuano Switzerland	15	435 0.6×	595 1.8×	12 0.0×	287 1.2×	308 2.1×	20	899
Bernardo Ortega United States	9	466 0.7×	226 0.7×	4 0.0×	169 0.7×	136 0.9×	13	728
Catalin N. Topala Netherlands	11	411 0.6×	425 1.3×	6 0.0×	234 1.0×	328 2.2×	11	949
Sudarsan Rajan United States	15	774 1.1×	9 0.0×	68 0.2×	39 0.2×	58 0.4×	20	1.0k
Mariela Méndez United States	13	296 0.4×	55 0.2×	12 0.0×	83 0.3×	25 0.2×	20	564
Antonio S. Gomes United States	5	416 0.6×	120 0.4×	8 0.0×	27 0.1×	188 1.3×	6	793
Iván Villegas United States	2	328 0.5×	548 1.7×	5 0.0×	106 0.4×	51 0.3×	3	768

Countries citing papers authored by Saskia J.G. Hoefs

Since Specialization

Citations

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

Fields of papers citing papers by Saskia J.G. Hoefs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Saskia J.G. Hoefs. 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 Saskia J.G. Hoefs. The network helps show where Saskia J.G. Hoefs may publish in the future.

Co-authorship network of co-authors of Saskia J.G. Hoefs

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Kasper, Lydia, Axel Franke, Selene Mogavero, et al.. (2016). Role of the fungal peptide toxin Candidalysin in macrophage damage and inflammatory response. 59. 3 indexed citations

2.

Hoefs, Saskia J.G., Richard J. Rodenburg, Jan Smeıtınk, & Lambert P. van den Heuvel. (2012). Molecular base of biochemical complex I deficiency. Mitochondrion. 12(5). 520–532. 32 indexed citations

3.

Hoefs, Saskia J.G., Francjan J. van Spronsen, Leo Nijtmans, et al.. (2010). NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease. European Journal of Human Genetics. 19(3). 270–274. 70 indexed citations

4.

Hoefs, Saskia J.G., Ola H. Skjeldal, Richard J. Rodenburg, et al.. (2010). Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies. Molecular Genetics and Metabolism. 100(3). 251–256. 45 indexed citations

5.

Nouws, Jessica, Leo Nijtmans, Sander M. Houten, et al.. (2010). Acyl-CoA Dehydrogenase 9 Is Required for the Biogenesis of Oxidative Phosphorylation Complex I. Cell Metabolism. 12(3). 283–294. 154 indexed citations

6.

Saada, Ann, Rutger O. Vogel, Saskia J.G. Hoefs, et al.. (2009). Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease. The American Journal of Human Genetics. 84(6). 718–727. 135 indexed citations

7.

Hoefs, Saskia J.G., Cindy E. Dieteren, Richard J. Rodenburg, et al.. (2009). Baculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency. Human Mutation. 30(7). E728–E736. 41 indexed citations

8.

Hoefs, Saskia J.G., Cindy E. Dieteren, Felix Distelmaier, et al.. (2008). NDUFA2 Complex I Mutation Leads to Leigh Disease. The American Journal of Human Genetics. 82(6). 1306–1315. 103 indexed citations

9.

Qing, Chang, Saskia J.G. Hoefs, Annemiete W. van der Kemp, et al.. (2005). The ß-Glucuronidase Klotho Hydrolyzes and Activates the TRPV5 Channel. Science. 310(5747). 490–493. 502 indexed citations breakdown →

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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