Flemming Wibrand

4.0k total citations · 1 hit paper
70 papers, 3.0k citations indexed

About

Flemming Wibrand is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Flemming Wibrand has authored 70 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 34 papers in Clinical Biochemistry and 13 papers in Physiology. Recurrent topics in Flemming Wibrand's work include Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (34 papers) and ATP Synthase and ATPases Research (12 papers). Flemming Wibrand is often cited by papers focused on Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (34 papers) and ATP Synthase and ATPases Research (12 papers). Flemming Wibrand collaborates with scholars based in Denmark, United States and Canada. Flemming Wibrand's co-authors include Morten Dunø, John Vissing, Henrik Daa Schrøder, Flemming Dela, Joachim Nielsen, Jørn Wulff Helge, Martin Hey‐Mogensen, Steen Larsen, Lars B. Nielsen and Robert Boushel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Flemming Wibrand

68 papers receiving 2.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects

2012 940 citations Steen Larsen, Joachim Nielsen et al. The Journal of Physiology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Flemming Wibrand Denmark	28	1.9k	872	809	395	201	70	3.0k
Frank N. Gellerich Germany	35	2.8k 1.5×	646 0.7×	984 1.2×	366 0.9×	689 3.4×	92	4.0k
Stephan Zierz Germany	34	2.0k 1.0×	801 0.9×	533 0.7×	215 0.5×	557 2.8×	175	3.6k
H.R. Scholte Netherlands	35	2.6k 1.4×	1.8k 2.1×	602 0.7×	351 0.9×	251 1.2×	100	3.7k
Martin Hey‐Mogensen Denmark	18	1.8k 0.9×	226 0.3×	1.3k 1.6×	465 1.2×	88 0.4×	22	3.0k
Alberto Casarin Italy	18	2.1k 1.1×	400 0.5×	412 0.5×	186 0.5×	209 1.0×	28	2.7k
Erin L. Seifert United States	33	2.2k 1.1×	260 0.3×	1.4k 1.7×	332 0.8×	269 1.3×	76	3.9k
W. Ruitenbeek Netherlands	33	3.7k 1.9×	2.3k 2.6×	644 0.8×	366 0.9×	412 2.0×	118	4.8k
Tianzheng Yu United States	20	2.0k 1.0×	471 0.5×	800 1.0×	218 0.6×	128 0.6×	39	2.8k
Monique Malgat France	21	1.9k 1.0×	682 0.8×	552 0.7×	94 0.2×	191 1.0×	40	2.5k
Rolf Wibom Sweden	38	5.5k 2.8×	1.6k 1.8×	1.5k 1.8×	458 1.2×	535 2.7×	80	6.8k

Countries citing papers authored by Flemming Wibrand

Since Specialization

Citations

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

Fields of papers citing papers by Flemming Wibrand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Flemming Wibrand

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

All Works

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20 of 20 papers shown

Thompson, Kyle, Emanuele Bellacchio, Courtney E. French, et al.. (2021). Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Human Molecular Genetics. 31(4). 523–534. 13 indexed citations

Wibrand, Flemming, et al.. (2019). Genotype and phenotype classification of 29 patients affected by Krabbe disease. JIMD Reports. 46(1). 35–45. 10 indexed citations

Vissing, Christoffer Rasmus, Morten Dunø, Flemming Wibrand, Mette Christensen, & John Vissing. (2019). Hydroxylated long-chain acylcarnitines are biomarkers of mitochondrial myopathy. The Journal of Clinical Endocrinology & Metabolism. 104(12). 5968–5976. 24 indexed citations

Fritzen, Andreas M., Kasper Højgaard Thybo, Christoffer Rasmus Vissing, et al.. (2019). Adaptations in Mitochondrial Enzymatic Activity Occurs Independent of Genomic Dosage in Response to Aerobic Exercise Training and Deconditioning in Human Skeletal Muscle. Cells. 8(3). 237–237. 27 indexed citations

Hansen, Dennis Lund, et al.. (2017). Splenomegaly – Diagnostic validity, work-up, and underlying causes. PLoS ONE. 12(11). e0186674–e0186674. 35 indexed citations

Jeppesen, Tina D., et al.. (2017). Mitochondrial DNA mutation load in a family with the m.8344A>G point mutation and lipomas: a case study. Clinical Case Reports. 5(12). 2034–2039. 1 indexed citations

Madsen, Karen L., et al.. (2017). Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report. BMC Musculoskeletal Disorders. 18(1). 419–419. 4 indexed citations

Grønborg, Sabine, Niklas Darín, María J. Miranda, et al.. (2016). Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling. JIMD Reports. 33. 69–77. 19 indexed citations

Saunders, Carol, Laurie D. Smith, Flemming Wibrand, et al.. (2015). CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria. The American Journal of Human Genetics. 96(2). 258–265. 44 indexed citations

10.

Dunø, Morten, Elsebet Østergaard, Kirstine Ravn, et al.. (2015). Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation. JIMD Reports. 25. 65–70. 4 indexed citations

11.

Ravn, Kirstine, Bitten Schönewolf‐Greulich, Rikke Middelhede Hansen, et al.. (2015). Neonatal mitochondrial hepatoencephalopathy caused by novel GFM1 mutations. SHILAP Revista de lepidopterología. 3. 5–10. 13 indexed citations

12.

Rasmussen, Jan, Allan M. Lund, Lotte Risom, et al.. (2014). Residual OCTN2 transporter activity, carnitine levels and symptoms correlate in patients with primary carnitine deficiency. Molecular Genetics and Metabolism Reports. 1. 241–248. 19 indexed citations

13.

Ghelli, Anna, Maria Antonietta Calvaruso, Luisa Iommarini, et al.. (2013). The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes. Human Molecular Genetics. 22(11). 2141–2151. 36 indexed citations

14.

Nouws, Jessica, Flemming Wibrand, Mariël van den Brand, et al.. (2013). A Patient with Complex I Deficiency Caused by a Novel ACAD9 Mutation Not Responding to Riboflavin Treatment. JIMD Reports. 12. 37–45. 23 indexed citations

15.

Larsen, Steen, Joachim Nielsen, Christina Hansen, et al.. (2012). Biomarkers of mitochondrial content in skeletal muscle of healthy young human subjects. The Journal of Physiology. 590(14). 3349–3360. 940 indexed citations breakdown →

16.

Østergaard, Elsebet, Morten Dunø, Lisbeth Birk Møller, et al.. (2012). Novel Mutations in the PC Gene in Patients with Type B Pyruvate Carboxylase Deficiency. JIMD Reports. 9. 1–5. 9 indexed citations

17.

Borch, Luise, Allan M. Lund, Flemming Wibrand, et al.. (2011). Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark. JIMD Reports. 3. 11–15. 10 indexed citations

18.

Jeppesen, Tina D., Morten Dunø, M. Schwartz, et al.. (2009). Short‐ and long‐term effects of endurance training in patients with mitochondrial myopathy. European Journal of Neurology. 16(12). 1336–1339. 35 indexed citations

19.

Wibrand, Flemming. (2004). A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum. Clinica Chimica Acta. 347(1-2). 89–96. 30 indexed citations

20.

Juel, Carsten & Flemming Wibrand. (1989). Lactate transport in isolated mouse muscles studied with a tracer technique—kinetics, stereospecificity, pH dependency and maximal capacity. Acta Physiologica Scandinavica. 137(1). 33–39. 34 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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