M. Durán
Impact in
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
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- Amino Acid Enzymes and Metabolism
Papers in
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- Metabolism and Genetic Disorders 8
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- Amino Acid Enzymes and Metabolism 2
- Co-authors
- Nenad Blau (1 shared paper)Albert H. Gennip (3 shared papers)Bwee Tien Poll‐The (4 shared papers)Isabel Tavares de Almeida (1 shared paper)Wim J. Kleijer (1 shared paper)Ronald Wanders (1 shared paper)M. Estela Rubio‐Gozalbo (1 shared paper)Jos P.N. Ruiter (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (1 paper)Pediatric Research (1 paper)American Journal of Medical Genetics (1 paper)Pure Amsterdam UMC (2 papers)Springer eBooks (1 paper)
- Partner nations
- NetherlandsGermanyItaly
In The Last Decade
M. Durán
10 papers receiving 105 citations
Peers
Comparison fields: 5 of 36
- Clinical Biochemistry 70
- Biochemistry 7
- Rheumatology 10
- Developmental Biology 1
- Molecular Biology 25
Countries citing papers authored by M. Durán
This map shows the geographic impact of M. Durán'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 M. Durán with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Durán more than expected).
Fields of papers citing papers by M. Durán
This network shows the impact of papers produced by M. Durán. 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 M. Durán. The network helps show where M. Durán may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Durán, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 89 | |
| 2 | 1997 | 6 | |
| 3 | Guanidino compounds in hyperargininaemia | 1992 | 4 |
| 4 | Mitochondrial energy metabolism. | 1996 | 2 |
| 5 | Treatment and molecular analysis of neonatal carnitine palmitoyltransferase II deficiency. | 1999 | 2 |
| 6 | Laboratory diagnosis of inherited metabolic disease | 2002 | 2 |
| 7 | Evaluation of the presence of premature atherosclerosis in adults with heterozygosity for cystathionine-beta-synthase deficiency. | 1996 | 1 |
| 8 | Dihydropyrimidinase deficiency and congenital microvillous atrophy: coincidence or genetic relation? | 1997 | 1 |
| 9 | Een kinderziekte op de volwassen leeftijd: fenylketonurie | 2000 | 1 |
| 10 | In vivo and in vitro studies on the interaction of valproic acid and metabolites with the leucine oxidative metabolism | 2007 | 1 |
| 11 | 2000 | 0 |
About M. Durán
M. Durán is a scholar working on Clinical Biochemistry, Biochemistry, Health Information Management, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 11 papers that have together received 109 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (8 papers), Amino Acid Enzymes and Metabolism (2 papers), Biochemical and Molecular Research (2 papers), Folate and B Vitamins Research (1 paper), Mitochondrial Function and Pathology (1 paper), Pharmacological Effects and Toxicity Studies (1 paper), Medical Coding and Health Information (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Clinical Biochemistry (70 citations), Biochemistry (7 citations), Rheumatology (10 citations), Developmental Biology (1 citation) and Molecular Biology (25 citations). M. Durán has collaborated with scholars based in Netherlands, Germany and Italy. Frequent co-authors include Nenad Blau, Albert H. Gennip, Bwee Tien Poll‐The, Isabel Tavares de Almeida, Wim J. Kleijer, Ronald Wanders, M. Estela Rubio‐Gozalbo, Jos P.N. Ruiter, Dick Lindhout and Frits A. Beemer. Their work appears in journals such as Journal of Inherited Metabolic Disease, Pediatric Research, American Journal of Medical Genetics, Pure Amsterdam UMC and Springer eBooks.
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.