M. Durán

12.1k total citations
263 papers, 6.2k citations indexed

About

M. Durán is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, M. Durán has authored 263 papers receiving a total of 6.2k indexed citations (citations by other indexed papers that have themselves been cited), including 162 papers in Molecular Biology, 149 papers in Clinical Biochemistry and 43 papers in Physiology. Recurrent topics in M. Durán's work include Metabolism and Genetic Disorders (149 papers), Biochemical and Molecular Research (55 papers) and Mitochondrial Function and Pathology (35 papers). M. Durán is often cited by papers focused on Metabolism and Genetic Disorders (149 papers), Biochemical and Molecular Research (55 papers) and Mitochondrial Function and Pathology (35 papers). M. Durán collaborates with scholars based in Netherlands, Spain and United States. M. Durán's co-authors include S.K. Wadman, D. Ketting, L. Dorland, Ronald J. A. Wanders, L. Bruinvis, Bwee Tien Poll‐The, F. A. Beemer, Lodewijk IJlst, J.P. Kamerling and C. Jakobs and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

M. Durán

252 papers receiving 6.0k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
M. Durán 3.8k 3.0k 929 831 774 263 6.2k
Stephen I. Goodman 4.8k 1.3× 4.5k 1.5× 898 1.0× 1.1k 1.4× 662 0.9× 177 7.4k
Marinus Durán 3.0k 0.8× 2.1k 0.7× 1.1k 1.2× 634 0.8× 657 0.8× 102 5.3k
C. Jakobs 3.2k 0.8× 2.8k 0.9× 1.2k 1.3× 896 1.1× 931 1.2× 218 7.1k
Nicola Longo 3.4k 0.9× 3.3k 1.1× 1.9k 2.0× 742 0.9× 715 0.9× 197 6.1k
Michael J. Bennett 4.1k 1.1× 2.4k 0.8× 1.8k 2.0× 491 0.6× 925 1.2× 185 7.5k
William J. Rhead 2.5k 0.7× 2.6k 0.9× 1.3k 1.4× 486 0.6× 657 0.8× 111 4.5k
Ruud Berger 2.9k 0.8× 1.3k 0.4× 1.0k 1.1× 1.2k 1.5× 524 0.7× 152 7.4k
Jürgen G. Okun 3.3k 0.9× 2.2k 0.7× 865 0.9× 687 0.8× 420 0.5× 144 5.3k
Stefan Kölker 3.9k 1.0× 4.2k 1.4× 955 1.0× 938 1.1× 895 1.2× 218 6.3k
Lawrence Sweetman 3.0k 0.8× 2.7k 0.9× 1.0k 1.1× 514 0.6× 545 0.7× 180 5.5k

Countries citing papers authored by M. Durán

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of M. Durán

This figure shows the co-authorship network connecting the top 25 collaborators of M. Durán. A scholar is included among the top collaborators of M. Durán 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 M. Durán. M. Durán 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.
Durán, M., et al.. (2025). Efficacy of erector spinae plane block for postoperative pain management: A meta-analysis and trial sequential analysis of randomized controlled trials. Journal of Clinical Anesthesia. 103. 111831–111831. 2 indexed citations
2.
3.
Infante, Mar, et al.. (2022). Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?. International Journal of Molecular Sciences. 23(19). 11499–11499. 8 indexed citations
4.
IJlst, Lodewijk, M. Durán, Lodewyk J. Mienie, et al.. (2013). Inhibition of N-acetylglutamate synthase by various monocarboxylic and dicarboxylic short-chain coenzyme A esters and the production of alternative glutamate esters. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(12). 2510–2516. 29 indexed citations
5.
Pérez‐Cabornero, Lucía, et al.. (2013). Evaluating the Effect of Unclassified Variants Identified in MMR Genes Using Phenotypic Features, Bioinformatics Prediction, and RNA Assays. Journal of Molecular Diagnostics. 15(3). 380–390. 6 indexed citations
6.
García-González, María Asunción, et al.. (2012). Lynch syndrome diagnostics: decision-making process for germ-line testing. Clinical & Translational Oncology. 14(4). 254–262. 2 indexed citations
7.
Pérez‐Cabornero, Lucía, et al.. (2011). Frequency of Rearrangements in Lynch Syndrome Cases Associated with MSH2 : Characterization of a New Deletion Involving both EPCAM and the 5′ Part of MSH2. Cancer Prevention Research. 4(10). 1556–1562. 24 indexed citations
8.
Pérez‐Cabornero, Lucía, Mar Infante, Eladio A. Velasco, et al.. (2011). Characterization of New Founder Alu-Mediated Rearrangements in MSH2 Gene Associated with a Lynch Syndrome Phenotype. Cancer Prevention Research. 4(10). 1546–1555. 15 indexed citations
9.
Sanz, David J., Alberto Acedo, Mar Infante, et al.. (2010). A High Proportion of DNA Variants of BRCA1 and BRCA2 Is Associated with Aberrant Splicing in Breast/Ovarian Cancer Patients. Clinical Cancer Research. 16(6). 1957–1967. 84 indexed citations
10.
Xunclà, Mar, Célia Bádenas, M. Durán, et al.. (2010). Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses. Reproductive BioMedicine Online. 21(4). 560–565. 7 indexed citations
11.
Peters, Bart D., M. Durán, Charles B.L.M. Majoie, et al.. (2009). Polyunsaturated fatty acids and brain white matter anisotropy in recent-onset schizophrenia: A preliminary study. Prostaglandins Leukotrienes and Essential Fatty Acids. 81(1). 61–63. 28 indexed citations
12.
Abeling, N.G.G.M., M. Durán, Hester I. Bakker, et al.. (2006). Sepiapterin reductase deficiency an autosomal recessive DOPA-responsive dystonia. Molecular Genetics and Metabolism. 89(1-2). 116–120. 40 indexed citations
13.
Gloerich, Jolein, Naomi van Vlies, Gerbert A. Jansen, et al.. (2005). A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways. Journal of Lipid Research. 46(4). 716–726. 66 indexed citations
14.
Mancini, Grazia M.S., Coriene E. Catsman‐Berrevoets, I.F.M. de Coo, et al.. (2004). Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X‐linked mental retardation in two unrelated Dutch families. American Journal of Medical Genetics Part A. 132A(3). 288–295. 45 indexed citations
15.
Bosch, Annet M., H. R. Waterham, M. Durán, & H. D. Bakker. (2003). Een premature tweeling met icterus, stollingsstoornissen en een E. coli-sepsis. Data Archiving and Networked Services (DANS). 28. 341–343.
16.
Durán, M., et al.. (2002). El poblado ibérico del Turó de Les Maleses (Montcada i Reixac, Barcelona). Balance de las campañas 2000-2002. Dialnet (Universidad de la Rioja). 177–184.
17.
Donckerwolcke, R. A., M. Durán, Jan Smeıtınk, et al.. (1994). Rate-Dependent Distal Renal Tubular Acidosis and Carnitine Palmitoyltransferase I Deficiency. Pediatric Research. 36(5). 582–587. 29 indexed citations
18.
Fuchshuber, Arno, Terttu Suormala, B. Roth, et al.. (1993). Holocarboxylase synthetase deficiency: Early diagnosis and management of a new case. European Journal of Pediatrics. 152(5). 446–449. 17 indexed citations
19.
Zachwieja, J, R. A. Donckerwolcke, M. Durán, & J. Maciejewski. (1992). Carnitine deficiency and hyperlipidemia in hemodialyzed patients Effect of amino acids supplementation. Pediatric Nephrology. 6(5). 186. 1 indexed citations
20.
Endres, W., et al.. (1988). Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency. European Journal of Pediatrics. 148(3). 246–249. 26 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

Breakdown of academic impact, for papers by Stephen I. Goodman Breakdown of academic impact, for papers by Marinus Durán Breakdown of academic impact, for papers by C. Jakobs Breakdown of academic impact, for papers by Nicola Longo Breakdown of academic impact, for papers by Michael J. Bennett Breakdown of academic impact, for papers by William J. Rhead Breakdown of academic impact, for papers by Ruud Berger Breakdown of academic impact, for papers by Jürgen G. Okun Breakdown of academic impact, for papers by Stefan Kölker Breakdown of academic impact, for papers by Lawrence Sweetman
Rankless by CCL
2026