G. Schrakamp

1.2k total citations
23 papers, 859 citations indexed

About

G. Schrakamp is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, G. Schrakamp has authored 23 papers receiving a total of 859 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 5 papers in Physiology. Recurrent topics in G. Schrakamp's work include Peroxisome Proliferator-Activated Receptors (20 papers), Metabolism and Genetic Disorders (16 papers) and Folate and B Vitamins Research (4 papers). G. Schrakamp is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (20 papers), Metabolism and Genetic Disorders (16 papers) and Folate and B Vitamins Research (4 papers). G. Schrakamp collaborates with scholars based in Netherlands, France and United States. G. Schrakamp's co-authors include H. van den Bosch, Ronald J. A. Wanders, R. B. H. Schutgens, H. S. A. Heymans, J. M. Tager, R. B. H. Schutgens, Joseph M. Tager, W. H. H. Tegelaers, Milan Kos and A. J. Meijer and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Journal of Lipid Research and Clinica Chimica Acta.

In The Last Decade

G. Schrakamp

23 papers receiving 824 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
G. Schrakamp Netherlands	14	768	477	192	143	68	23	859
D G Brocks Germany	10	359 0.5×	194 0.4×	205 1.1×	115 0.8×	58 0.9×	15	637
Raymond K. Tan United States	4	260 0.3×	114 0.2×	105 0.5×	47 0.3×	29 0.4×	8	496
Ermelinda Santos Silva Portugal	12	288 0.4×	97 0.2×	83 0.4×	43 0.3×	42 0.6×	44	688
Tatsuya Kishimoto Japan	10	659 0.9×	45 0.1×	167 0.9×	123 0.9×	37 0.5×	15	836
Shawn S. Badal United States	9	630 0.8×	151 0.3×	88 0.5×	31 0.2×	366 5.4×	15	918
Josef Pfeilschifter Switzerland	7	196 0.3×	38 0.1×	101 0.5×	45 0.3×	59 0.9×	8	407
Maria Alessandra Maitan Italy	6	253 0.3×	92 0.2×	85 0.4×	34 0.2×	28 0.4×	7	416
Brenda S. Chan United States	9	183 0.2×	48 0.1×	32 0.2×	79 0.6×	23 0.3×	9	543
Ainhoa Iglesias–Ara Spain	16	536 0.7×	39 0.1×	63 0.3×	51 0.4×	156 2.3×	26	846
A Yoshida United States	13	404 0.5×	52 0.1×	145 0.8×	54 0.4×	58 0.9×	18	744

Countries citing papers authored by G. Schrakamp

Since Specialization

Citations

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

Fields of papers citing papers by G. Schrakamp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Schrakamp

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

Bosch, H. van den, et al.. (1993). Ether lipid synthesis and its deficiency in peroxisomal disorders. Biochimie. 75(3-4). 183–189. 36 indexed citations

Schutgens, R. B. H., G. Schrakamp, Ronald J. A. Wanders, et al.. (1989). Prenatal and perinatal diagnosis of peroxisomal disorders. Journal of Inherited Metabolic Disease. 12(S1). 118–134. 32 indexed citations

Wanders, R. J. A., R. B. H. Schutgens, Bwee Tien Poll‐The, et al.. (1988). Peroxisomal functions in classical Refsum's disease: Comparison with the infantile form of Refsum's disease. Journal of the Neurological Sciences. 84(2-3). 147–155. 11 indexed citations

Schrakamp, G., et al.. (1988). Aberration in de novo ether lipid biosynthesis in peroxisomal disorders.. PubMed. 282. 139–50. 10 indexed citations

Schrakamp, G., Casper G. Schalkwijk, R. B. H. Schutgens, et al.. (1988). Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors.. Journal of Lipid Research. 29(3). 325–334. 70 indexed citations

Wanders, R. J. A., R. B. H. Schutgens, G. Schrakamp, et al.. (1987). Generalized loss of peroxisomal functions in neonatal adrenoleukodystrophy: Implications for Pre‐ and postnatal detection and relationship to X‐linked adrenoleukodystrophy. Journal of Inherited Metabolic Disease. 10(S2). 225–228. 1 indexed citations

Schutgens, R. B. H., Ronald J. A. Wanders, H. S. A. Heymans, et al.. (1987). Zellweger syndrome: Biochemical procedures in diagnosis, prevention and treatment. Journal of Inherited Metabolic Disease. 10(S1). 33–45. 9 indexed citations

Schutgens, R. B. H., R. J. A. Wanders, H. S. A. Heymans, et al.. (1987). Genetic Diseases Caused by Peroxisomal Dysfunction. Enzyme. 38(1-4). 161–176. 12 indexed citations

Wanders, Ronald J. A., R. B. H. Schutgens, G. Schrakamp, et al.. (1986). Deficiency of dihydroxyacetonephosphate acyltransferase and catalase‐containing particles in patients with infantile refsum's disease. Journal of Inherited Metabolic Disease. 9(S2). 325–328. 5 indexed citations

10.

Wanders, Ronald J. A., G. Schrakamp, H. van den Bosch, et al.. (1986). Pre‐ and postnatal diagnosis of the cerebrohepato‐renal (Zellweger) syndrome via a simple method directly demonstrating the presence of absence of peroxisomes in cultured skin fibroblasts, amniocytes or chorionic villi fibroblasts. Journal of Inherited Metabolic Disease. 9(S2). 317–320. 9 indexed citations

11.

Wanders, Ronald J. A., R. B. H. Schutgens, G. Schrakamp, et al.. (1986). Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal β-oxidation enzyme proteins. European Journal of Pediatrics. 145(3). 172–175. 26 indexed citations

12.

Wanders, R. J. A., Carlo W.T. van Roermund, H. van den Bosch, et al.. (1986). Peroxisomal β-oxidation of palmitoyl-CoA in human liver homogenates and its deficiency in the cerebro-hepato-renal (Zellweger) syndrome. Clinica Chimica Acta. 159(1). 1–10. 50 indexed citations

13.

Schrakamp, G., R. B. H. Schutgens, Ronald J. A. Wanders, et al.. (1985). Alkyl dihydroxyacetone phosphate synthase in human fibroblasts and its deficiency in Zellweger syndrome.. Journal of Lipid Research. 26(7). 867–873. 62 indexed citations

14.

Poll‐The, Bwee Tien, Jean‐Marie Saudubray, H. Ogier, et al.. (1985). Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction. Journal of Inherited Metabolic Disease. 9(2). 169–174. 57 indexed citations

15.

Wanders, Ronald J. A., et al.. (1985). Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test. Clinica Chimica Acta. 151(3). 217–221. 13 indexed citations

16.

Schutgens, R. B. H., H. S. A. Heymans, R. J. A. Wanders, H. van den Bosch, & G. Schrakamp. (1985). Prenatal diagnosis of the cerebro‐hepato‐renal (Zellweger) syndrome by detection of an impaired plasmalogen biosynthesis. Journal of Inherited Metabolic Disease. 8(S2). 153–154. 8 indexed citations

17.

Schutgens, R. B. H., G. Schrakamp, R. J. A. Wanders, et al.. (1985). The cerebro‐hepato‐renal (Zellweger) syndrome: Prenatal detection based on impaired biosynthesis of plasmalogens. Prenatal Diagnosis. 5(5). 337–344. 19 indexed citations

18.

Schutgens, R. B. H., et al.. (1984). Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome. Biochemical and Biophysical Research Communications. 120(1). 179–184. 154 indexed citations

19.

Wanders, Ronald J. A., Milan Kos, A. J. Meijer, et al.. (1984). Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome. Biochemical and Biophysical Research Communications. 123(3). 1054–1061. 166 indexed citations

20.

Schrakamp, G., et al.. (1982). Localization of glycerophosphate acyltransferase in Escherichia coli. Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 713(2). 285–291. 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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