Ralf Triepels

1.4k total citations
16 papers, 1.1k citations indexed

About

Ralf Triepels is a scholar working on Molecular Biology, Clinical Biochemistry and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ralf Triepels has authored 16 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Clinical Biochemistry and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ralf Triepels's work include Mitochondrial Function and Pathology (13 papers), Metabolism and Genetic Disorders (10 papers) and ATP Synthase and ATPases Research (7 papers). Ralf Triepels is often cited by papers focused on Mitochondrial Function and Pathology (13 papers), Metabolism and Genetic Disorders (10 papers) and ATP Synthase and ATPases Research (7 papers). Ralf Triepels collaborates with scholars based in Netherlands, United States and Curacao. Ralf Triepels's co-authors include Jan Smeıtınk, Lambertus P. van den Heuvel, Roel Smeets, Jan Loeffen, J. M. F. Trijbels, Lambert van den Heuvel, J.M.F. Trijbels, Frans J.M. Trijbels, Markus Schuelke and Carin A. F. Buskens and has published in prestigious journals such as Journal of Biological Chemistry, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Ralf Triepels

16 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ralf Triepels Netherlands 13 1.0k 624 65 63 57 16 1.1k
Fabian Baertling Germany 17 882 0.9× 356 0.6× 60 0.9× 70 1.1× 58 1.0× 28 1.1k
Jan Smeitink Netherlands 13 1.1k 1.1× 587 0.9× 130 2.0× 68 1.1× 116 2.0× 13 1.3k
Susana Peralta United States 18 953 0.9× 329 0.5× 131 2.0× 70 1.1× 62 1.1× 29 1.1k
Ricarda Richter‐Dennerlein Germany 16 1.1k 1.1× 253 0.4× 86 1.3× 66 1.0× 38 0.7× 26 1.2k
Grzegorz J. Stępień France 9 656 0.6× 237 0.4× 85 1.3× 47 0.7× 36 0.6× 12 730
Florence Malka France 8 894 0.9× 351 0.6× 156 2.4× 52 0.8× 22 0.4× 10 997
Sofía García United States 13 722 0.7× 239 0.4× 153 2.4× 64 1.0× 36 0.6× 18 839
Katharina Danhauser Germany 12 615 0.6× 290 0.5× 48 0.7× 32 0.5× 72 1.3× 18 736
Reetta Hinttala Finland 16 455 0.4× 219 0.4× 56 0.9× 60 1.0× 90 1.6× 49 653
Roel Smeets Netherlands 22 1.9k 1.8× 1.0k 1.7× 95 1.5× 110 1.7× 129 2.3× 33 2.1k

Countries citing papers authored by Ralf Triepels

Since Specialization
Citations

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

Fields of papers citing papers by Ralf Triepels

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ralf Triepels

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

All Works

16 of 16 papers shown
1.
Riel, N.A.W. van, Simon W. Nienhuijs, Ralf Triepels, et al.. (2022). Assessment of Comorbidity in Bariatric Patients through a Biomarker-Based Model—A Multicenter Validation of the Metabolic Health Index. The Journal of Applied Laboratory Medicine. 7(5). 1062–1075. 2 indexed citations
2.
Loeber, J.G., Bert Elvers, Ralf Triepels, et al.. (2012). The influence of sex, gestational age, birth weight, blood transfusion, and timing of the heel prick on the pancreatitis‐associated protein concentration in newborn screening for cystic fibrosis. Journal of Inherited Metabolic Disease. 36(1). 147–154. 12 indexed citations
3.
Loeber, J.G., L.H. Elvers, Ralf Triepels, et al.. (2009). Cystic fibrosis Heelprick among a newbOrn Population in the Netherlands: the CHOPIN-study. Journal of Cystic Fibrosis. 8. S9–S9. 3 indexed citations
4.
Ugalde, Cristina, Ralf Triepels, Marieke J. H. Coenen, et al.. (2003). Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene. Annals of Neurology. 54(5). 665–669. 88 indexed citations
5.
Triepels, Ralf, Bonnie J. Hanson, Lambert P. van den Heuvel, et al.. (2001). Human Complex I Defects Can Be Resolved by Monoclonal Antibody Analysis into Distinct Subunit Assembly Patterns. Journal of Biological Chemistry. 276(12). 8892–8897. 58 indexed citations
6.
Triepels, Ralf, Lambertus P. van den Heuvel, J. M. F. Trijbels, & Jan Smeıtınk. (2001). Respiratory chain complex I deficiency. American Journal of Medical Genetics. 106(1). 37–45. 152 indexed citations
7.
Trijbels, J.M.F., et al.. (2000). Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects. Human Mutation. 15(2). 123–134. 237 indexed citations
8.
Triepels, Ralf, Jan Smeıtınk, Jan Loeffen, et al.. (2000). Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients. Human Genetics. 106(4). 385–391. 14 indexed citations
9.
Triepels, Ralf, Lambertus P. van den Heuvel, Jan Loeffen, et al.. (1999). Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I. Annals of Neurology. 45(6). 787–790. 164 indexed citations
10.
Loeffen, Jan, Roel Smeets, Jan Smeıtınk, et al.. (1999). The human NADH:ubiquinone oxidoreductase NDUFS5 (15kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I‐deficient patients. Journal of Inherited Metabolic Disease. 22(1). 19–28. 17 indexed citations
11.
Triepels, Ralf, Jan Smeıtınk, Jan Loeffen, et al.. (1999). The human nuclear‐encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathology. Journal of Inherited Metabolic Disease. 22(2). 163–173. 38 indexed citations
12.
Loeffen, Jan, Ralf Triepels, Lambertus P. van den Heuvel, et al.. (1998). cDNA of Eight Nuclear Encoded Subunits of NADH:Ubiquinone Oxidoreductase: Human Complex I cDNA Characterization Completed. Biochemical and Biophysical Research Communications. 253(2). 415–422. 61 indexed citations
13.
Loeffen, Jan, Lambert van den Heuvel, Roel Smeets, et al.. (1998). cDNA Sequence and Chromosomal Localization of the Remaining Three Human Nuclear Encoded Iron Sulphur Protein (IP) Subunits of Complex I: The Human IP Fraction Is Completed. Biochemical and Biophysical Research Communications. 247(3). 751–758. 19 indexed citations
14.
Triepels, Ralf, Lambert van den Heuvel, Jan Loeffen, et al.. (1998). The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patients. Human Genetics. 103(5). 557–563. 18 indexed citations
15.
Smeitink, Jan, Jan Loeffen, Roel Smeets, et al.. (1998). Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I. Human Genetics. 103(2). 245–250. 17 indexed citations
16.
Loeffen, Jan, Jan Smeıtınk, Ralf Triepels, et al.. (1998). The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh Syndrome. The American Journal of Human Genetics. 63(6). 1598–1608. 219 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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