S. E. Olpin

6.7k total citations
81 papers, 3.0k citations indexed

About

S. E. Olpin is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, S. E. Olpin has authored 81 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Clinical Biochemistry, 53 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in S. E. Olpin's work include Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (33 papers) and Neonatal Health and Biochemistry (12 papers). S. E. Olpin is often cited by papers focused on Metabolism and Genetic Disorders (64 papers), Mitochondrial Function and Pathology (33 papers) and Neonatal Health and Biochemistry (12 papers). S. E. Olpin collaborates with scholars based in United Kingdom, United States and Denmark. S. E. Olpin's co-authors include N. T. Davies, N. J. Manning, R. J. Pollitt, Brage Storstein Andresen, Neyaz Alam, Morteza Pourfarzam, Chris Bates, Niels Gregersen, I.M. Leigh and Werner J.H. Koopman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and American Journal of Clinical Nutrition.

In The Last Decade

S. E. Olpin

81 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S. E. Olpin United Kingdom 31 1.9k 1.5k 548 320 303 81 3.0k
Elisabeth Holme Sweden 34 3.0k 1.6× 2.0k 1.3× 404 0.7× 298 0.9× 168 0.6× 80 4.1k
M. Brivet France 28 2.3k 1.2× 2.0k 1.3× 671 1.2× 196 0.6× 87 0.3× 88 3.3k
Ute Spiekerkoetter Germany 30 1.5k 0.8× 1.7k 1.1× 787 1.4× 483 1.5× 91 0.3× 111 2.6k
Rikke Katrine Jentoft Olsen Denmark 25 1.4k 0.8× 1.4k 0.9× 382 0.7× 360 1.1× 104 0.3× 66 2.1k
Gepke Visser Netherlands 30 1.3k 0.7× 1.2k 0.8× 891 1.6× 1.5k 4.6× 287 0.9× 109 3.6k
Toshihiro Ohura Japan 27 1.5k 0.8× 1.8k 1.2× 654 1.2× 691 2.2× 54 0.2× 90 3.0k
Fatima Djouadi France 30 1.9k 1.0× 661 0.4× 862 1.6× 87 0.3× 71 0.2× 64 2.8k
Klaus-Dieter Gerbitz Germany 30 1.7k 0.9× 1.1k 0.7× 305 0.6× 85 0.3× 96 0.3× 71 2.6k
Si Houn Hahn United States 27 1.2k 0.6× 801 0.5× 229 0.4× 203 0.6× 39 0.1× 81 2.4k
Alisa Gutman Israel 27 916 0.5× 746 0.5× 411 0.8× 188 0.6× 55 0.2× 84 1.8k

Countries citing papers authored by S. E. Olpin

Since Specialization
Citations

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

Fields of papers citing papers by S. E. Olpin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. E. Olpin. 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 S. E. Olpin. The network helps show where S. E. Olpin may publish in the future.

Co-authorship network of co-authors of S. E. Olpin

This figure shows the co-authorship network connecting the top 25 collaborators of S. E. Olpin. A scholar is included among the top collaborators of S. E. Olpin 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 S. E. Olpin. S. E. Olpin 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.
Schoeler, Natasha E., et al.. (2019). Biochemical assessment of patients following ketogenic diets for epilepsy: Current practice in the UK and Ireland. Epilepsia Open. 5(1). 73–79. 5 indexed citations
2.
Olpin, S. E., Brage Storstein Andresen, Aneal Khan, et al.. (2017). Fibroblast Fatty-Acid Oxidation Flux Assays Stratify Risk in Newborns with Presumptive-Positive Results on Screening for Very-Long Chain Acyl-CoA Dehydrogenase Deficiency. International Journal of Neonatal Screening. 3(1). 2–2. 5 indexed citations
3.
Manning, N. J., et al.. (2012). Determinants of urinary methylmalonic acid concentration in an elderly population in the United Kingdom. American Journal of Clinical Nutrition. 95(3). 686–693. 13 indexed citations
4.
5.
Morris, Andrew A. M., S. E. Olpin, Michael J. Bennett, et al.. (2012). Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency. JIMD Reports. 7. 27–29. 5 indexed citations
6.
Owen, E., Peter Berman, S. E. Olpin, et al.. (2010). Glutaric aciduria type 1 in South Africa—high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans. Molecular Genetics and Metabolism. 101(2-3). 178–182. 37 indexed citations
7.
O′Flaherty, Linda, Julie Adam, Lisa C. Heather, et al.. (2010). Dysregulation of hypoxia pathways in fumarate hydratase-deficient cells is independent of defective mitochondrial metabolism. Human Molecular Genetics. 19(19). 3844–3851. 81 indexed citations
8.
Maegawa, Gustavo, et al.. (2008). Interstitial deletion of 1p22.2p31.1 and medium‐chain acyl‐CoA dehydrogenase deficiency in a patient with global developmental delay. American Journal of Medical Genetics Part A. 146A(12). 1581–1586. 10 indexed citations
9.
Race, Valérie, Younès Achouri, Elsa Wiame, et al.. (2007). Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway. The American Journal of Human Genetics. 80(5). 931–937. 89 indexed citations
10.
Pourfarzam, Morteza, et al.. (2006). Consensus case definitions for MCADD among infants with presumptive positive newborn screening results. Journal of Inherited Metabolic Disease. 1 indexed citations
11.
Worthington, Helen V, S. E. Olpin, I Blumenthal, & Andrew A. M. Morris. (2006). Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency. Journal of Inherited Metabolic Disease. 30(1). 104–104. 4 indexed citations
12.
Patterson, Amanda, et al.. (2006). Carnitine transporter defect: Diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infants. Journal of Inherited Metabolic Disease. 29(5). 627–630. 47 indexed citations
13.
Olpin, S. E.. (2005). Fatty acid oxidation defects as a cause of neuromyopathic disease in infants and adults.. PubMed. 51(5-6). 289–306. 19 indexed citations
14.
Kinali, Maria, S. E. Olpin, Peter T. Clayton, et al.. (2004). Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy. European Journal of Paediatric Neurology. 8(4). 217–219. 2 indexed citations
15.
Olpin, S. E.. (2004). Implications of impaired ketogenesis in fatty acid oxidation disorders. Prostaglandins Leukotrienes and Essential Fatty Acids. 70(3). 293–308. 30 indexed citations
16.
Hargreaves, Iain P., Simon Heales, S. E. Olpin, J A Morgan-Hughes, & John M. Land. (2000). The diagnosis of carnitine palmitoyltransferase II deficiency is now possible in small skeletal muscle biopsies. Journal of Inherited Metabolic Disease. 23(4). 352–354. 3 indexed citations
17.
Andresen, Brage Storstein, S. E. Olpin, Ben J. H. M. Poorthuis, et al.. (1999). Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency. The American Journal of Human Genetics. 64(2). 479–494. 233 indexed citations
18.
Morris, Andrew A. M., et al.. (1998). Hepatic Mitochondrial 3-Hydroxy-3-Methylglutaryl-Coenzyme A Synthase Deficiency. Pediatric Research. 44(3). 392–396. 29 indexed citations
19.
Morris, A. A. M., S. E. Olpin, M. Brivet, et al.. (1998). A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype. The Journal of Pediatrics. 132(3). 514–516. 34 indexed citations
20.
Morris, Andrew A. M., S. E. Olpin, William G. van’t Hoff, Andrew Johnson, & J V Leonard. (1997). Renal tubular dysfunction in multiple acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 20(4). 604–605. 2 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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