A. H. van Gennip

3.8k total citations
82 papers, 2.8k citations indexed

About

A. H. van Gennip is a scholar working on Molecular Biology, Clinical Biochemistry and Oncology. According to data from OpenAlex, A. H. van Gennip has authored 82 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 32 papers in Clinical Biochemistry and 19 papers in Oncology. Recurrent topics in A. H. van Gennip's work include Biochemical and Molecular Research (34 papers), Metabolism and Genetic Disorders (32 papers) and Neonatal Health and Biochemistry (16 papers). A. H. van Gennip is often cited by papers focused on Biochemical and Molecular Research (34 papers), Metabolism and Genetic Disorders (32 papers) and Neonatal Health and Biochemistry (16 papers). A. H. van Gennip collaborates with scholars based in Netherlands, United States and Germany. A. H. van Gennip's co-authors include André B. P. Kuilenburg, P. Vreken, Ronald J. A. Wanders, Henk van Lenthe, Henk Overmars, N.G.G.M. Abeling, M. Durán, Lodewijk IJlst, Albert H. Bootsma and Frits A. Wijburg and has published in prestigious journals such as Journal of Clinical Investigation, Analytical Biochemistry and Journal of Lipid Research.

In The Last Decade

A. H. van Gennip

82 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. H. van Gennip Netherlands 25 1.7k 840 829 303 257 82 2.8k
N. G. G. M. Abeling Netherlands 25 943 0.6× 566 0.7× 224 0.3× 231 0.8× 297 1.2× 84 2.0k
David S. Duch United States 25 1.2k 0.7× 461 0.5× 263 0.3× 94 0.3× 342 1.3× 62 2.6k
C. R. Scriver Canada 39 1.8k 1.1× 1.5k 1.8× 316 0.4× 575 1.9× 740 2.9× 128 4.3k
Masatoshi Tomi Japan 29 771 0.5× 239 0.3× 635 0.8× 530 1.7× 252 1.0× 87 2.2k
Shuhei Suzuki Japan 26 1.1k 0.6× 321 0.4× 509 0.6× 77 0.3× 207 0.8× 116 2.0k
David Watkins Canada 30 1.6k 1.0× 1.1k 1.3× 75 0.1× 298 1.0× 147 0.6× 99 3.0k
Rosalba Carrozzo Italy 38 4.0k 2.4× 1.5k 1.8× 129 0.2× 255 0.8× 418 1.6× 143 5.3k
Saskia B. Wortmann Netherlands 32 1.9k 1.1× 1.0k 1.2× 118 0.1× 137 0.5× 302 1.2× 122 2.7k
Laura Silvestri Italy 35 1.6k 1.0× 244 0.3× 176 0.2× 108 0.4× 794 3.1× 73 5.6k
Devin Oglesbee United States 29 1.9k 1.1× 905 1.1× 70 0.1× 367 1.2× 637 2.5× 87 3.1k

Countries citing papers authored by A. H. van Gennip

Since Specialization
Citations

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

Fields of papers citing papers by A. H. van Gennip

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. H. van Gennip. 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 A. H. van Gennip. The network helps show where A. H. van Gennip may publish in the future.

Co-authorship network of co-authors of A. H. van Gennip

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

All Works

20 of 20 papers shown
1.
Bierau, Jörgen, Jaap Bakker, Martijn Lindhout, & A. H. van Gennip. (2006). Determination of ITPase Activity in Erythrocyte Lysates Obtained for Determination of Tpmt Activity. Nucleosides Nucleotides & Nucleic Acids. 25(9-11). 1129–1132. 12 indexed citations
2.
Al‐Sannaa, Nouriya, et al.. (2005). Dihydropyrimidine dehydrogenase deficiency presenting at birth. Journal of Inherited Metabolic Disease. 28(5). 793–796. 14 indexed citations
3.
Valianpour, Fredoen, Ronald J. A. Wanders, Henk Overmars, et al.. (2003). Linoleic acid supplemention of Barth syndrome fibroblasts restores cardiolipin levels: implications for treatment. Journal of Lipid Research. 44(3). 560–566. 58 indexed citations
4.
Abeling, N.G.G.M., et al.. (2001). Mild learning difficulties and offending behaviour – is there a link with monoamine oxidase A deficiency?. Psychiatric Genetics. 11(3). 173–176. 2 indexed citations
5.
Kuilenburg, André B. P., Janet Haasjes, Dick J. Richel, et al.. (2000). Clinical implications of dihydropyrimidine dehydrogenase (DPD) deficiency in patients with severe 5-fluorouracil-associated toxicity: identification of new mutations in the DPD gene.. Data Archiving and Networked Services (DANS). 6(12). 4705–12. 307 indexed citations
6.
Bootsma, Albert H., Henk Overmars, Arno van Rooij, et al.. (1999). Rapid analysis of conjugated bile acids in plasma using electrospray tandem mass spectrometry: Application for selective screening of peroxisomal disorders. Journal of Inherited Metabolic Disease. 22(3). 307–310. 71 indexed citations
7.
Kuilenburg, André B. P., Henk van Lenthe, & A. H. van Gennip. (1999). A Radiochemical Assay for β-Ureidopropionase Using Radiolabeled N-Carbamyl-β-alanine Obtained via Hydrolysis of [2-14C]5,6-Dihydrouracil. Analytical Biochemistry. 272(2). 250–253. 18 indexed citations
8.
Abeling, N.G.G.M., et al.. (1998). Aromatic L‐amino acid decarboxylase deficiency: A new case with a mild clinical presentation and unexpected laboratory findings. Journal of Inherited Metabolic Disease. 21(3). 240–242. 29 indexed citations
9.
Gennip, A. H. van, et al.. (1997). Specification of the inhibitory action of MIBG on the respiratory chain by EPR scanning.. Data Archiving and Networked Services (DANS). 17(1A). 265–8. 1 indexed citations
10.
Lenders, Jacques W.M., Graeme Eisenhofer, N.G.G.M. Abeling, et al.. (1996). Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.. Journal of Clinical Investigation. 97(4). 1010–1019. 114 indexed citations
11.
Kuilenburg, André B. P., Henk van Lenthe, & A. H. van Gennip. (1996). Identification and tissue-specific expression of a NADH-dependent activity of dihydropyrimidine dehydrogenase in man.. PubMed. 16(1). 389–94. 20 indexed citations
12.
Meinsma, Rutger, Pedro M. Fernández‐Salguero, André B. P. Kuilenburg, A. H. van Gennip, & Frank J. Gonzalez. (1995). Human Polymorphism in Drug Metabolism: Mutation in the Dihydropyrimidine Dehydrogenase Gene Results in Exon Skipping and Thymine Uracilurea. DNA and Cell Biology. 14(1). 1–6. 104 indexed citations
13.
Gennip, A. H. van, N. G. G. M. Abeling, A. E. M. Stroomer, Henk Overmars, & H. D. Bakker. (1994). The detection of molybdenum cofactor deficiency: Clinical symptomatology and urinary metabolite profile. Journal of Inherited Metabolic Disease. 17(1). 142–145. 11 indexed citations
14.
Slingerland, Robbert J., et al.. (1993). Imbalance between the pyrimidine ribonucleotide pools of rat pheochromocytoma PC-12 cells. Pure Amsterdam UMC. 5. 315–319. 8 indexed citations
15.
Kal, Henk B., et al.. (1993). Treatment of the rat R-1 rhabdomyosarcoma with methotrexate and radiation; effects of timing on cell survival and tumour growth delay. Journal of Cancer Research and Clinical Oncology. 119(4). 215–220. 1 indexed citations
16.
Johnson, Jean L., K.V. Rajagopalan, R. B. H. Schutgens, et al.. (1991). Prenatal diagnosis of molybdenum cofactor deficiency by assay of sulphite oxidase activity in chorionic villus samples. Journal of Inherited Metabolic Disease. 14(6). 932–937. 29 indexed citations
17.
Gennip, A. H. van, et al.. (1991). The effect of molybdenum cofactor deficiency on the purine pattern of cerebrospinal fluid. Journal of Inherited Metabolic Disease. 14(3). 364–366. 2 indexed citations
18.
Wanders, R. J. A., Lodewijk IJlst, A. H. van Gennip, et al.. (1990). Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidation. Journal of Inherited Metabolic Disease. 13(3). 311–314. 106 indexed citations
19.
Jakobs, C., et al.. (1989). A new case of dihydropyrimidine dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 13(1). 121–124. 24 indexed citations
20.

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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