Felix de Rooij

444 total citations
9 papers, 385 citations indexed

About

Felix de Rooij is a scholar working on Molecular Biology, Rheumatology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Felix de Rooij has authored 9 papers receiving a total of 385 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Rheumatology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Felix de Rooij's work include Porphyrin Metabolism and Disorders (9 papers), Heme Oxygenase-1 and Carbon Monoxide (8 papers) and Folate and B Vitamins Research (6 papers). Felix de Rooij is often cited by papers focused on Porphyrin Metabolism and Disorders (9 papers), Heme Oxygenase-1 and Carbon Monoxide (8 papers) and Folate and B Vitamins Research (6 papers). Felix de Rooij collaborates with scholars based in France, Netherlands and Switzerland. Felix de Rooij's co-authors include Bernard Grandchamp, Y Nordmann, Jean‐Charles Deybach, C. Picat, Xuefan Gu, Gardi Voortman, Peter J. Wilson, C. Beaumont, Marie Hélène Delfau and J.H.P. Wilson and has published in prestigious journals such as Nucleic Acids Research, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Felix de Rooij

9 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Felix de Rooij France 9 361 184 110 29 29 9 385
X. Schneider‐Yin Switzerland 8 337 0.9× 103 0.6× 116 1.1× 116 4.0× 22 0.8× 12 374
Eliane Sardh Sweden 13 467 1.3× 94 0.5× 217 2.0× 90 3.1× 17 0.6× 30 486
Martin D. Kafina United States 6 126 0.3× 29 0.2× 13 0.1× 19 0.7× 17 0.6× 8 190
Juliet Yuen United States 5 31 0.1× 50 0.3× 46 0.4× 25 0.9× 9 0.3× 9 137
Juliana Teo Australia 6 103 0.3× 39 0.2× 7 0.1× 9 0.3× 17 0.6× 11 194
Gordon J. Hildick-Smith United States 7 121 0.3× 15 0.1× 12 0.1× 10 0.3× 22 0.8× 9 204
Yuwei Jin China 10 260 0.7× 26 0.1× 14 0.1× 7 0.2× 55 1.9× 27 307
Hannah Mandel Israel 5 155 0.4× 27 0.1× 10 0.1× 15 0.5× 8 0.3× 6 252
M. Tuchman United States 7 141 0.4× 8 0.0× 37 0.3× 9 0.3× 43 1.5× 8 238
Aisha Al Shamsi United Arab Emirates 6 67 0.2× 13 0.1× 9 0.1× 11 0.4× 18 0.6× 13 129

Countries citing papers authored by Felix de Rooij

Since Specialization
Citations

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

Fields of papers citing papers by Felix de Rooij

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Felix de Rooij. 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 Felix de Rooij. The network helps show where Felix de Rooij may publish in the future.

Co-authorship network of co-authors of Felix de Rooij

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

All Works

9 of 9 papers shown
1.
Ducamp, Sarah, Xiaoye Schneider‐Yin, Felix de Rooij, et al.. (2012). Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP). Human Molecular Genetics. 22(7). 1280–1288. 42 indexed citations
2.
Gu, Xuefan, Felix de Rooij, Gardi Voortman, et al.. (1994). Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis. Human Genetics. 93(1). 47–52. 38 indexed citations
3.
Gu, Xuefan, et al.. (1993). High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria. Human Genetics. 91(2). 128–130. 53 indexed citations
4.
Gu, Xuefan, Felix de Rooij, M. Bruyland, et al.. (1993). Two novel mutations of the porphobilinogen deaminase gene in acute intermittent porphyria. Human Molecular Genetics. 2(10). 1735–1736. 24 indexed citations
5.
Rooij, Felix de, et al.. (1992). High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria.. PubMed. 51(3). 660–5. 32 indexed citations
6.
Verneuil, Hubert de, Francine Bourgeois, Felix de Rooij, et al.. (1992). Characterization of a new mutation (R292G) and a deletion at the human uroporphyrinogen decarboxylase locus in two patients with hepatoerythropoietic porphyria. Human Genetics. 89(5). 548–52. 25 indexed citations
7.
Bourgeois, F., Xuefan Gu, Jean‐Charles Deybach, et al.. (1992). Denaturing Gradient Gel Electrophoresis for Rapid Detection of Latent Carriers of a Subtype of Acute Intermittent Porphyria with Normal Erythrocyte Porphobilinogen Deaminase Activity. Clinical Chemistry. 38(1). 93–95. 23 indexed citations
8.
Delfau, Marie Hélène, C. Picat, Felix de Rooij, et al.. (1991). Molecular heterogeneity of acute intermittent porphyria: identification of four additional mutations resulting in the CRIM-negative subtype of the disease.. PubMed. 49(2). 421–8. 42 indexed citations
9.
Grandchamp, Bernard, C. Picat, Felix de Rooij, et al.. (1989). A point mutation G—A in exon 12 of the porphoblllnogen deaminase gene results in exon skipping and is responsible for acute intermittent porphyria. Nucleic Acids Research. 17(16). 6637–6649. 106 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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