Niels Gregersen

1.1k total citations
28 papers, 935 citations indexed

About

Niels Gregersen is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Niels Gregersen has authored 28 papers receiving a total of 935 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 4 papers in Surgery. Recurrent topics in Niels Gregersen's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Peroxisome Proliferator-Activated Receptors (7 papers). Niels Gregersen is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Peroxisome Proliferator-Activated Receptors (7 papers). Niels Gregersen collaborates with scholars based in Denmark, United States and Poland. Niels Gregersen's co-authors include Brage Storstein Andresen, Peter Bross, Lars Bolund, Thomas J. Corydon, Vibeke Winter, Frank E. Frerman, Per Hove Andreasen, Nanna Cornelius, Rikke Katrine Jentoft Olsen and R. L. H. Bolhuis and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Journal of Molecular Biology.

In The Last Decade

Niels Gregersen

28 papers receiving 907 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Niels Gregersen Denmark	14	630	535	176	127	121	28	935
Emmanuelle Sarzi France	17	1.6k 2.5×	865 1.6×	103 0.6×	73 0.6×	35 0.3×	25	1.7k
Johann Penzien Germany	14	268 0.4×	184 0.3×	76 0.4×	38 0.3×	59 0.5×	17	627
Hendrik Rosewich Germany	18	567 0.9×	137 0.3×	105 0.6×	56 0.4×	41 0.3×	34	857
A Ponzone Italy	16	366 0.6×	468 0.9×	98 0.6×	16 0.1×	127 1.0×	56	729
Yolanda Cámara Spain	19	1.5k 2.3×	448 0.8×	202 1.1×	34 0.3×	84 0.7×	35	1.7k
Alberto Blázquez Spain	18	750 1.2×	323 0.6×	129 0.7×	27 0.2×	185 1.5×	50	1.1k
Alan S. Lidsky United States	9	582 0.9×	577 1.1×	106 0.6×	24 0.2×	295 2.4×	10	855
Toshinobu Matsuura Japan	17	854 1.4×	386 0.7×	53 0.3×	82 0.6×	79 0.7×	44	1.3k
H. ter Laak Netherlands	19	634 1.0×	184 0.3×	129 0.7×	41 0.3×	64 0.5×	37	934
Shlomo Almashanu Israel	16	390 0.6×	271 0.5×	128 0.7×	13 0.1×	67 0.6×	45	838

Countries citing papers authored by Niels Gregersen

Since Specialization

Citations

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

Fields of papers citing papers by Niels Gregersen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niels Gregersen

This figure shows the co-authorship network connecting the top 25 collaborators of Niels Gregersen. A scholar is included among the top collaborators of Niels Gregersen 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 Niels Gregersen. Niels Gregersen 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

Dessein, Anne‐Frédérique, Monique Fontaine, Marie Joncquel-Chevalier Curt, et al.. (2017). Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants. Clinica Chimica Acta. 471. 101–106. 10 indexed citations

Brinth, Louise, et al.. (2015). CoQ10 as a modulator of mitochondrial dysfunction and maladaptive stress responses in chronic fatigue syndrome. 1 indexed citations

Cornelius, Nanna, Frank E. Frerman, Thomas J. Corydon, et al.. (2012). Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency. Human Molecular Genetics. 21(15). 3435–3448. 68 indexed citations

Hansen, Jens Jacob, Peter Bross, Majken Westergaard, et al.. (2003). Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter. Human Genetics. 112(4). 436–436. 8 indexed citations

Koeberl, Dwight D., Sarah P. Young, Niels Gregersen, et al.. (2003). Rare Disorders of Metabolism with Elevated Butyryl- and Isobutyryl-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening. Pediatric Research. 54(2). 219–223. 68 indexed citations

Andresen, Brage Storstein, Kristopher Nielsen, Thomas J. Corydon, et al.. (2002). Simple mutations in the coding region of three acyl-CoA dehydrogenase genes may lead to skipping of the constitutive exon due to disruption of potential splice enhancer sequences or mRNA secondary structures. Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory). 1 indexed citations

Gregersen, Niels, Brage Storstein Andresen, Morten J. Corydon, et al.. (2001). Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype–phenotype relationship. Human Mutation. 18(3). 169–169. 4 indexed citations

Corydon, Thomas J., Cathrine Jespersgaard, Brage Storstein Andresen, et al.. (2000). Human and mouse mitochondrial orthologs of bacterial ClpX. Mammalian Genome. 11(10). 899–905. 33 indexed citations

Gregersen, Niels, Brage Storstein Andresen, & Peter Bross. (2000). Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations. European Journal of Pediatrics. 159(S3). S213–S218. 29 indexed citations

10.

Andresen, Brage Storstein, Thomas J. Corydon, Peter Bross, et al.. (2000). Characterization of mouse Clpp protease cDNA, gene, and protein. Mammalian Genome. 11(4). 275–280. 4 indexed citations

11.

Gregersen, Niels. (1998). Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria. Human Molecular Genetics. 7(4). 619–627. 102 indexed citations

12.

Tanaka, Kay, Niels Gregersen, Antònia Ribes, et al.. (1997). A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey, and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA. Pediatric Research. 41(2). 201–209. 54 indexed citations

13.

Jensen, Henrik Kjærulf, Thomas Glasdam Jensen, Ole Færgeman, et al.. (1997). Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia. Human Mutation. 9(5). 437–444. 24 indexed citations

14.

Sandvej, Kristian, Jan W. Gratama, Mette Munch, et al.. (1997). Sequence Analysis of the Epstein-Barr Virus (EBV) Latent Membrane Protein-1 Gene and Promoter Region: Identification of Four Variants Among Wild-Type EBV Isolates. Blood. 90(1). 323–330. 33 indexed citations

15.

Jensen, Henrik Kjærulf, et al.. (1996). Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1316(1). 1–4. 8 indexed citations

16.

Bross, Peter, Thomas G. Jensen, Brage Storstein Andresen, et al.. (1994). Characterization of Wild-Type Human Medium-Chain Acyl-CoA Dehydrogenase (MCAD) and Mutant Enzymes Present in MCAD-Deficient Patients by Two-Dimensional Gel Electrophoresis: Evidence for Posttranslational Modification of the Enzyme. Biochemical Medicine and Metabolic Biology. 52(1). 36–44. 11 indexed citations

17.

Gregersen, Niels, Vibeke Winter, Diana Curtis, et al.. (1993). Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe. Human Heredity. 43(6). 342–350. 55 indexed citations

18.

Mandrup, Susanne, René Hummel, Per Hove Andreasen, et al.. (1992). Acyl-CoA-binding protein/diazepam-binding inhibitor gene and pseudogenes. Journal of Molecular Biology. 228(3). 1011–1022. 106 indexed citations

19.

Gregersen, Niels, Brage Storstein Andresen, Peter Bross, et al.. (1991). Characterization of a disease‐causing Lys329 to Glu mutation in 16 patients with medium‐chain Acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 14(3). 314–316. 8 indexed citations

20.

Gregersen, Niels, Brage Storstein Andresen, Peter Bross, et al.. (1991). Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli. Human Genetics. 86(6). 545–51. 63 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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