E. Holme

2.7k total citations
45 papers, 1.7k citations indexed

About

E. Holme is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, E. Holme has authored 45 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 35 papers in Clinical Biochemistry and 8 papers in Physiology. Recurrent topics in E. Holme's work include Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (24 papers) and ATP Synthase and ATPases Research (9 papers). E. Holme is often cited by papers focused on Metabolism and Genetic Disorders (35 papers), Mitochondrial Function and Pathology (24 papers) and ATP Synthase and ATPases Research (9 papers). E. Holme collaborates with scholars based in Sweden, Spain and United States. E. Holme's co-authors include Anders Oldfors, Sandra Lindstedt, Nils‐Göran Larsson, M. Tulinius, Göran K. Hansson, Yong Geng, David A. Clayton, Niklas Darín, A.‐R. Moslemi and Ulf Jodal and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation Research and Neurology.

In The Last Decade

E. Holme

45 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Holme Sweden 22 1.1k 926 303 262 139 45 1.7k
Nancy G. Kennaway United States 22 1.5k 1.4× 906 1.0× 166 0.5× 179 0.7× 120 0.9× 37 2.0k
Hélène Ogier de Baulny France 24 1.2k 1.1× 968 1.0× 290 1.0× 276 1.1× 201 1.4× 45 1.9k
Akira Ohtake Japan 27 1.9k 1.8× 1.1k 1.2× 226 0.7× 146 0.6× 318 2.3× 138 2.7k
Dorothea Haas Germany 26 1.2k 1.1× 483 0.5× 227 0.7× 159 0.6× 183 1.3× 67 1.7k
R. J. A. Wanders Netherlands 23 1.7k 1.5× 790 0.9× 318 1.0× 236 0.9× 71 0.5× 55 2.0k
Audrey Boutron France 21 1.2k 1.1× 627 0.7× 228 0.8× 230 0.9× 77 0.6× 47 1.6k
C. Charpentier France 26 1.2k 1.1× 1.0k 1.1× 285 0.9× 271 1.0× 148 1.1× 85 2.3k
N. G. Kennaway United States 18 838 0.8× 520 0.6× 137 0.5× 174 0.7× 101 0.7× 34 1.2k
Lewis Waber United States 14 552 0.5× 649 0.7× 898 3.0× 127 0.5× 135 1.0× 20 1.7k
Anaïs Brassier France 19 608 0.6× 389 0.4× 714 2.4× 175 0.7× 157 1.1× 84 1.7k

Countries citing papers authored by E. Holme

Since Specialization
Citations

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

Fields of papers citing papers by E. Holme

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Holme

This figure shows the co-authorship network connecting the top 25 collaborators of E. Holme. A scholar is included among the top collaborators of E. Holme 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 E. Holme. E. Holme 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.
Holme, E., et al.. (2009). Ekbom's syndrome of photomyoclonus, cerebellar ataxia and cervical lipoma is associated with the tRNALys A8344G mutation in mitochondrial DNA. Acta Neurologica Scandinavica. 92(5). 394–397. 14 indexed citations
2.
Darín, Niklas, et al.. (2007). M.P.1.12 Progressive encephalopathy and complex I deficiency associated with novel mutations in MTND1. Neuromuscular Disorders. 17(9-10). 771–771. 4 indexed citations
3.
Darín, Niklas, Gittan Kollberg, M. Tulinius, et al.. (2006). Mitochondrial myopathy with exercise intolerance and retinal dystrophy in a sporadic patient with a G583A mutation in the mt tRNAphe gene. Neuromuscular Disorders. 16(8). 504–506. 18 indexed citations
4.
Sperl, Wolfgang, Pavel Ješina, J Zeman, et al.. (2006). Deficiency of mitochondrial ATP synthase of nuclear genetic origin. Neuromuscular Disorders. 16(12). 821–829. 56 indexed citations
5.
Moslemi, A.‐R., et al.. (2005). Two New Mutations in theMTATP6Gene Associated with Leigh Syndrome. Neuropediatrics. 36(5). 314–318. 51 indexed citations
6.
Moslemi, A.‐R., Christopher Lindberg, Jens Toft, et al.. (2003). A novel mutation in the mitochondrial tRNAPhe gene associated with mitochondrial myopathy. Neuromuscular Disorders. 14(1). 46–50. 16 indexed citations
7.
Sakamoto, Osamu, Yoshiro Suzuki, Yoko Aoki, et al.. (2000). Diagnosis and molecular analysis of an atypical case of holocarboxylase synthetase deficiency. European Journal of Pediatrics. 159(1-2). 18–22. 18 indexed citations
8.
Cerone, R., et al.. (1997). Tyrosinemia type III: diagnosis and ten‐year follow‐up. Acta Paediatrica. 86(9). 1013–1015. 30 indexed citations
9.
Abrahamsson, Kate, E. Holme, Ulf Jodal, Sandra Lindstedt, & Ingalill Nordin. (1995). Effect of Short-Term Treatment with Pivalic Acid Containing Antibiotics on Serum Carnitine Concentration - A Risk Irrespective of Age. Biochemical and Molecular Medicine. 55(1). 77–79. 16 indexed citations
10.
Abrahamsson, Kate, Bengt O. Eriksson, E. Holme, et al.. (1994). Impaired Ketogenesis in Carnitine Depletion Caused by Short-Term Administration of Pivalic Acid Prodrug. Biochemical Medicine and Metabolic Biology. 52(1). 18–21. 27 indexed citations
11.
Larsson, Nils‐Göran, Anders Oldfors, E. Holme, & David A. Clayton. (1994). Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA Depletion. Biochemical and Biophysical Research Communications. 200(3). 1374–1381. 189 indexed citations
12.
Holme, E., Nils‐Göran Larsson, Anders Oldfors, et al.. (1993). Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.. PubMed. 52(3). 551–6. 85 indexed citations
13.
Holme, E., et al.. (1992). Effects of pivalic acid-containing prodrugs on carnitine homeostasis and on response to fasting in children. Scandinavian Journal of Clinical and Laboratory Investigation. 52(5). 361–372. 40 indexed citations
14.
Geng, Yong, Göran K. Hansson, & E. Holme. (1992). Interferon-gamma and tumor necrosis factor synergize to induce nitric oxide production and inhibit mitochondrial respiration in vascular smooth muscle cells.. Circulation Research. 71(5). 1268–1276. 225 indexed citations
15.
Riudor, E., et al.. (1991). Liver transplantation in two children with tyrosinaemia type I: Biochemical aspects. Journal of Inherited Metabolic Disease. 14(3). 281–284. 4 indexed citations
16.
Oldfors, Anders, Ing‐Marie Fyhr, E. Holme, Nils‐Göran Larsson, & M. Tulinius. (1990). Neuropathology in Kearns-Sayre syndrome. Acta Neuropathologica. 80(5). 541–546. 68 indexed citations
17.
Oldfors, Anders, et al.. (1989). Cytochromec oxidase deficiency in infancy. Acta Neuropathologica. 77(3). 267–275. 32 indexed citations
18.
Oldfors, Anders, M. Tulinius, E. Holme, et al.. (1987). Mitochondrial encephalomyopathy. Acta Neuropathologica. 74(3). 287–293. 13 indexed citations
19.
Lindblad, Bengt, et al.. (1986). Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitution. Journal of Inherited Metabolic Disease. 9(S2). 257–261. 3 indexed citations
20.
Greter, Joachim, J Gustafsson, & E. Holme. (1985). Pyruvate‐Carboxylase Deficiency with Urea Cycle Impairment. Acta Paediatrica. 74(6). 982–986. 15 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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