Cornelis Jakobs

17.4k total citations
225 papers, 12.0k citations indexed

About

Cornelis Jakobs is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, Cornelis Jakobs has authored 225 papers receiving a total of 12.0k indexed citations (citations by other indexed papers that have themselves been cited), including 139 papers in Clinical Biochemistry, 93 papers in Molecular Biology and 56 papers in Rheumatology. Recurrent topics in Cornelis Jakobs's work include Metabolism and Genetic Disorders (139 papers), Folate and B Vitamins Research (50 papers) and Amino Acid Enzymes and Metabolism (44 papers). Cornelis Jakobs is often cited by papers focused on Metabolism and Genetic Disorders (139 papers), Folate and B Vitamins Research (50 papers) and Amino Acid Enzymes and Metabolism (44 papers). Cornelis Jakobs collaborates with scholars based in Netherlands, United States and Germany. Cornelis Jakobs's co-authors include Eduard A. Struys, Gajja S. Salomons, Nanda M. Verhoeven, K. Michael Gibson, Coen D.A. Stehouwer, Erwin E. W. Jansen, Marjo S. van der Knaap, Mirjam M. C. Wamelink, Isabel Tavares de Almeida and Markus Ralser and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Cornelis Jakobs

224 papers receiving 11.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cornelis Jakobs Netherlands	62	5.4k	4.4k	2.5k	2.1k	1.6k	225	12.0k
John T. Brosnan Canada	53	3.1k 0.6×	2.1k 0.5×	2.1k 0.8×	2.4k 1.1×	1.2k 0.8×	166	9.3k
Nenad Blau Switzerland	62	7.5k 1.4×	8.4k 1.9×	2.3k 0.9×	3.9k 1.8×	1.9k 1.1×	339	14.5k
Jerry Vockley United States	60	7.0k 1.3×	5.8k 1.3×	1.1k 0.4×	3.1k 1.5×	694 0.4×	318	11.3k
Dennis E. Vance Canada	69	8.5k 1.6×	1.9k 0.4×	1.8k 0.7×	3.1k 1.5×	3.2k 1.9×	238	16.4k
C. Jakobs Netherlands	42	3.2k 0.6×	2.8k 0.6×	1.5k 0.6×	1.2k 0.5×	896 0.5×	218	7.1k
Manuel Palacı́n Spain	67	10.7k 2.0×	3.2k 0.7×	659 0.3×	3.6k 1.7×	5.8k 3.5×	255	17.1k
Inderjit Singh United States	68	8.3k 1.5×	2.0k 0.5×	684 0.3×	4.1k 1.9×	1.4k 0.8×	344	15.6k
Suzanne R. Thorpe United States	70	5.2k 1.0×	10.3k 2.3×	882 0.4×	4.2k 2.0×	948 0.6×	165	19.1k
Margaret E. Brosnan Canada	46	2.3k 0.4×	1.4k 0.3×	1.8k 0.7×	1.7k 0.8×	918 0.6×	114	7.0k
Stephen I. Goodman United States	47	4.8k 0.9×	4.5k 1.0×	739 0.3×	898 0.4×	1.1k 0.7×	177	7.4k

Countries citing papers authored by Cornelis Jakobs

Since Specialization

Citations

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

Fields of papers citing papers by Cornelis Jakobs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cornelis Jakobs

This figure shows the co-authorship network connecting the top 25 collaborators of Cornelis Jakobs. A scholar is included among the top collaborators of Cornelis Jakobs 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 Cornelis Jakobs. Cornelis Jakobs 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:

20 of 20 papers shown

Oliveira, Renata L. de, Paula Garcia, Isabel Fineza, et al.. (2013). Pyridoxine‐dependent epilepsy due to antiquitin deficiency: achieving a favourable outcome. Epileptic Disorders. 15(4). 400–406. 18 indexed citations

Ndika, Joseph, et al.. (2013). Cloning and characterization of the promoter regions from the parent and paralogous creatine transporter genes. Gene. 533(2). 488–493. 6 indexed citations

Bok, Levinus A., Feico J. J. Halbertsma, Saskia Houterman, et al.. (2012). Long‐term outcome in pyridoxine‐dependent epilepsy. Developmental Medicine & Child Neurology. 54(9). 849–854. 76 indexed citations

Engqvist, Martin K. M., Katrin Weber, Erwin E. W. Jansen, et al.. (2011). Plant d-2-Hydroxyglutarate Dehydrogenase Participates in the Catabolism of Lysine Especially during Senescence. Journal of Biological Chemistry. 286(13). 11382–11390. 61 indexed citations

Hartmann, Hans, et al.. (2011). Status epilepticus in a neonate treated with pyridoxine because of a familial recurrence risk for antiquitin deficiency: pyridoxine toxicity?. Developmental Medicine & Child Neurology. 53(12). 1150–1153. 18 indexed citations

Bjursell, Magnus, Henk J. Blom, Martin Engvall, et al.. (2011). Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function. The American Journal of Human Genetics. 89(4). 507–515. 91 indexed citations

Rosenberg, Efraim H., Lígia S. Almeida, Tjitske Kleefstra, et al.. (2010). Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database. European Journal of Human Genetics. 19(1). 56–63. 15 indexed citations

Kamp, Jiddeke M. van de, Efraim H. Rosenberg, Arjan P.M. de Brouwer, et al.. (2008). Detection of low-level somatic and germline mosaicism by denaturing high-performance liquid chromatography in a EURO-MRX family with SLC6A8 deficiency. Neurogenetics. 9(3). 183–190. 25 indexed citations

Ralser, Markus, Mirjam M. C. Wamelink, Axel Kowald, et al.. (2007). Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress. Journal of Biology. 6(4). 10–10. 470 indexed citations

10.

Goodwin, Amy, Roland R. Griffiths, Phillip R. Brown, et al.. (2006). Chronic intragastric administration of gamma-butyrolactone produces physical dependence in baboons. Psychopharmacology. 189(1). 71–82. 19 indexed citations

11.

Mills, Philippa B., Eduard A. Struys, Cornelis Jakobs, et al.. (2006). Mutations in antiquitin in individuals with pyridoxine-dependent seizures. Nature Medicine. 12(3). 307–309. 392 indexed citations

12.

Stam, Frank, Coen van Guldener, Piet M. ter Wee, et al.. (2004). Effect of folic acid on methionine and homocysteine metabolism in end-stage renal disease. Kidney International. 67(1). 259–264. 21 indexed citations

13.

Huck, Jojanneke H.J., Nanda M. Verhoeven, Eduard A. Struys, et al.. (2004). Ribose-5-Phosphate Isomerase Deficiency: New Inborn Error in the Pentose Phosphate Pathway Associated with a Slowly Progressive Leukoencephalopathy. The American Journal of Human Genetics. 74(4). 745–751. 99 indexed citations

14.

Platt, Simon R., Cornelis Jakobs, Nanda M. Verhoeven, et al.. (2003). l-2-Hydroxyglutaric Aciduria in Staffordshire Bull Terriers. Journal of Veterinary Internal Medicine. 17(4). 551–551. 4 indexed citations

15.

Platt, Simon R., Cornelis Jakobs, Nanda M. Verhoeven, et al.. (2003). L-2-Hydroxyglutaric Aciduria in Staffordshire Bull Terriers. Journal of Veterinary Internal Medicine. 17(4). 551–556. 28 indexed citations

16.

Lopriore, Enrico, Reinoud J. B. J. Gemke, Nanda M. Verhoeven, et al.. (2001). Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome. European Journal of Pediatrics. 160(2). 101–104. 30 indexed citations

17.

Hoogeveen, Ellen K., Pieter J. Kostense, Agnes Jager, et al.. (1998). Serum homocysteine level and protein intake are related to risk of microalbuminuria: The Hoorn Study. Kidney International. 54(1). 203–209. 124 indexed citations

18.

Mandel, Hanna, Benjamin Brenner, Moshe Berant, et al.. (1996). Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis. New England Journal of Medicine. 334(12). 763–768. 203 indexed citations

19.

Craigen, William J., Cornelis Jakobs, Elizabeth A. Sekul, et al.. (1994). d-2-Hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction. Pediatric Neurology. 10(1). 49–53. 26 indexed citations

20.

Kok, Rob, et al.. (1987). Stable isotope dilution analysis of pipecolic acid in cerebrospinal fluid, plasma, urine and amniotic fluid using electron capture negative ion mass fragmentography. Clinica Chimica Acta. 168(2). 143–152. 41 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.

Explore authors with similar magnitude of impact