Gerbert A. Jansen

2.6k total citations
41 papers, 1.9k citations indexed

About

Gerbert A. Jansen is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Gerbert A. Jansen has authored 41 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 24 papers in Clinical Biochemistry and 8 papers in Physiology. Recurrent topics in Gerbert A. Jansen's work include Peroxisome Proliferator-Activated Receptors (29 papers), Metabolism and Genetic Disorders (24 papers) and Adipose Tissue and Metabolism (6 papers). Gerbert A. Jansen is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (29 papers), Metabolism and Genetic Disorders (24 papers) and Adipose Tissue and Metabolism (6 papers). Gerbert A. Jansen collaborates with scholars based in Netherlands, United Kingdom and Belgium. Gerbert A. Jansen's co-authors include Ronald J. A. Wanders, Hans R. Waterham, Sacha Ferdinandusse, E.G. van Grunsven, Carlo W.T. van Roermund, P. Vreken, Ola H. Skjeldal, Matthew D. Lloyd, C. Jakobs and Simone Denis and has published in prestigious journals such as Nature Genetics, Bioinformatics and Annals of Neurology.

In The Last Decade

Gerbert A. Jansen

41 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gerbert A. Jansen Netherlands	21	1.5k	570	307	291	215	41	1.9k
Ronald S. Kaplan United States	25	1.4k 1.0×	518 0.9×	215 0.7×	272 0.9×	134 0.6×	46	1.8k
Rob Ofman Netherlands	28	1.8k 1.2×	714 1.3×	467 1.5×	374 1.3×	201 0.9×	64	2.2k
Guillermina Asins Spain	23	1.1k 0.7×	422 0.7×	495 1.6×	137 0.5×	190 0.9×	53	1.6k
Rita M. Kern United States	21	721 0.5×	390 0.7×	640 2.1×	559 1.9×	252 1.2×	29	1.9k
Wilhelm W. Just Germany	33	2.4k 1.6×	378 0.7×	565 1.8×	380 1.3×	220 1.0×	66	2.9k
Flavia Fontanesi United States	30	2.3k 1.5×	473 0.8×	184 0.6×	104 0.4×	198 0.9×	56	2.8k
Nanda M. Verhoeven‐Duif Netherlands	27	1.2k 0.8×	731 1.3×	354 1.2×	332 1.1×	223 1.0×	83	2.3k
Ian G. Jennings Australia	27	1.9k 1.3×	428 0.8×	425 1.4×	171 0.6×	113 0.5×	67	2.7k
Lioubov G. Korotchkina United States	27	1.6k 1.1×	706 1.2×	501 1.6×	1.1k 3.7×	452 2.1×	44	2.7k
Scott B. Vafai United States	13	2.7k 1.8×	703 1.2×	443 1.4×	142 0.5×	410 1.9×	15	3.3k

Countries citing papers authored by Gerbert A. Jansen

Since Specialization

Citations

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

Fields of papers citing papers by Gerbert A. Jansen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gerbert A. Jansen

This figure shows the co-authorship network connecting the top 25 collaborators of Gerbert A. Jansen. A scholar is included among the top collaborators of Gerbert A. Jansen 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 Gerbert A. Jansen. Gerbert A. Jansen 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

Stobbe, Miranda D., Gerbert A. Jansen, Perry D. Moerland, & Antoine H. C. van Kampen. (2012). Knowledge representation in metabolic pathway databases. Briefings in Bioinformatics. 15(3). 455–470. 18 indexed citations

Stobbe, Miranda D., Sander M. Houten, Gerbert A. Jansen, Antoine H. C. van Kampen, & Perry D. Moerland. (2011). Critical assessment of human metabolic pathway databases: a stepping stone for future integration. BMC Systems Biology. 5(1). 165–165. 47 indexed citations

Jansen, Gerbert A. & Ronald J. A. Wanders. (2006). Alpha-Oxidation. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1763(12). 1403–1412. 78 indexed citations

Gloerich, Jolein, Naomi van Vlies, Gerbert A. Jansen, et al.. (2005). A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways. Journal of Lipid Research. 46(4). 716–726. 66 indexed citations

Jansen, Gerbert A., Hans R. Waterham, & Ronald J. A. Wanders. (2004). Molecular basis of Refsum disease: Sequence variations in Phytanoyl-CoA Hydroxylase (PHYH) and the PTS2 receptor (PEX7). Human Mutation. 23(3). 209–218. 70 indexed citations

Mukherji, Mridul, Christopher J. Schofield, Anthony S. Wierzbicki, et al.. (2003). The chemical biology of branched-chain lipid metabolism. Progress in Lipid Research. 42(5). 359–376. 62 indexed citations

Wanders, Ronald J. A., Carlo W.T. van Roermund, Wouter F. Visser, et al.. (2003). Peroxisomal Fatty Acid Alpha-and Beta-Oxidation in Health and Disease: New insights. Advances in experimental medicine and biology. 544. 293–302. 18 indexed citations

Brink, Daan M. van den, Pedro Brites, Janet Haasjes, et al.. (2003). Identification of PEX7 as the Second Gene Involved in Refsum Disease. The American Journal of Human Genetics. 72(2). 471–477. 112 indexed citations

Brink, Daan M. van den, Pedro Brites, Janet Haasjes, et al.. (2003). Identification of PEX7 as the Second Gene Involved in Refsum Disease. Advances in experimental medicine and biology. 544. 69–70. 9 indexed citations

10.

Wanders, Ronald J. A., P. Vreken, Sacha Ferdinandusse, et al.. (2001). Peroxisomal fatty acid α- and β-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases. Biochemical Society Transactions. 29(2). 250–250. 199 indexed citations

11.

Wanders, Ronald J. A., Gerbert A. Jansen, & Ola H. Skjeldal. (2001). Refsum Disease, Peroxisomes and Phytanic Acid Oxidation: A Review. Journal of Neuropathology & Experimental Neurology. 60(11). 1021–1031. 71 indexed citations

12.

Zomer, Anna W.M., Bart van der Burg, Gerbert A. Jansen, et al.. (2000). Pristanic acid and phytanic acid: naturally occurring ligands for the nuclear receptor peroxisome proliferator-activated receptor α. Journal of Lipid Research. 41(11). 1801–1807. 132 indexed citations

13.

Jansen, Gerbert A.. (2000). Human phytanoyl-CoA hydroxylase: resolution of the gene structure and the molecular basis of Refsum's disease. Human Molecular Genetics. 9(8). 1195–1200. 55 indexed citations

14.

Wanders, Ronald J. A., E.G. van Grunsven, & Gerbert A. Jansen. (2000). Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid α- and β-oxidation systems in humans. Biochemical Society Transactions. 28(2). 141–149. 47 indexed citations

15.

Jansen, Gerbert A., Nanda M. Verhoeven, Simone Denis, et al.. (1999). Phytanic acid α-oxidation: identification of 2-hydroxyphytanoyl-CoA lyase in rat liver and its localisation in peroxisomes. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1440(2-3). 176–182. 22 indexed citations

16.

Jansen, Gerbert A., Sacha Ferdinandusse, Ola H. Skjeldal, et al.. (1998). Molecular basis of Refsum disease: Identification of new mutations in the phytanoyl‐CoA hydroxylase cDNA. Journal of Inherited Metabolic Disease. 21(3). 288–291. 9 indexed citations

17.

Ramaekers, V., et al.. (1997). Increased plasma malondialdehyde associated with cerebellar structural defects. Archives of Disease in Childhood. 77(3). 231–234. 10 indexed citations

18.

Jansen, Gerbert A., Sacha Ferdinandusse, Lodewijk IJlst, et al.. (1997). Refsum disease is caused by mutations in the phytanoyl–CoA hydroxylase gene. Nature Genetics. 17(2). 190–193. 221 indexed citations

19.

Jansen, Gerbert A., Stephanie J. Mihalik, Paul A. Watkins, et al.. (1996). Phytanoyl-CoA Hydroxylase Is Present in Human Liver, Located in Peroxisomes, and Deficient in Zellweger Syndrome: Direct, Unequivocal Evidence for the New, Revised Pathway of Phytanic Acid α-Oxidation in Humans. Biochemical and Biophysical Research Communications. 229(1). 205–210. 70 indexed citations

20.

Jansen, Gerbert A., et al.. (1996). Evidence against increased oxidative stress in fibroblasts from patients with non-superoxide-dismutase-1 mutant familial amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 139. 91–94. 10 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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