Niels Gregersen

1.1k citations

28 papers · 935 indexed · h-index 14

Co-authors: Brage Storstein Andresen Peter Bross Lars Bolund Thomas J. Corydon Vibeke Winter Frank E. Frerman Per Hove Andreasen Nanna Cornelius
Topics: Metabolism and Genetic Disorders (13 papers)Mitochondrial Function and Pathology (7 papers)Peroxisome Proliferator-Activated Receptors (7 papers)
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: SHILAP Revista de lepidopterologíaBlood Journal of Molecular Biology
Partner nations: Denmark United States Poland

In The Last Decade

Niels Gregersen

28 papers receiving 907 citations

Peers

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

#	Work	Indexed citations
1	Fluxomic evidence for impaired contribution of short-chain acyl-CoA dehydrogenase to mitochondrial palmitate β-oxidation in symptomatic patients with ACADS gene susceptibility variants 2017 ·Clinica Chimica Acta ·Anne‐Frédérique Dessein,Monique Fontaine,Marie Joncquel-Chevalier Curt,Gilbert Briand,(unknown),Karine Mention-Mulliez,Dries Dobbelaere,Claire Douillard,Arnaud Lacour,(unknown),Delphine Lamireau,Magalie Barth,Marie-Christine Minot-Myhié,Alice Kuster,Pascale de Lonlay,Niels Gregersen,Cécile Acquaviva,Christine Vianey‐Saban,Jòseph Vamecq	10
2	CoQ10 as a modulator of mitochondrial dysfunction and maladaptive stress responses in chronic fatigue syndrome 2015 ·(unknown),Louise Brinth,Niels Gregersen,Rikke Katrine Jentoft Olsen	1
3	Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency 2012 ·Human Molecular Genetics ·Nanna Cornelius,Frank E. Frerman,Thomas J. Corydon,Johan Palmfeldt,Peter Bross,Niels Gregersen,Rikke Katrine Jentoft Olsen	68
4	Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 separated by a bidirectional promoter 2003 ·Human Genetics ·Jens Jacob Hansen,Peter Bross,Majken Westergaard,(unknown),Hans Eiberg,Anders D. Børglum,Jens Mogensen,Karsten Kristiansen,Lars Bolund,Niels Gregersen	8
5	Rare Disorders of Metabolism with Elevated Butyryl- and Isobutyryl-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening 2003 ·Pediatric Research ·Dwight D. Koeberl,Sarah P. Young,Niels Gregersen,Jerry Vockley,Wendy E. Smith,Daniel K. Benjamin,Yan An,(unknown),Shu Chaing,Deeksha Bali,Marie McDonald,Priya S. Kishnani,Ying-Tsong Chen,David S. Millington	68
6	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 2002 ·Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) ·Brage Storstein Andresen,Kristopher Nielsen,(unknown),Thomas J. Corydon,Jørgen Kjems,Adrian R. Krainer,(unknown),Lisbeth Dahl Schroeder,Niels Gregersen	1
7	Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype–phenotype relationship 2001 ·Human Mutation ·Niels Gregersen,Brage Storstein Andresen,Morten J. Corydon,Thomas J. Corydon,Rikke Katrine Jentoft Olsen,Lars Bolund,Peter Bross	4
8	Human and mouse mitochondrial orthologs of bacterial ClpX 2000 ·Mammalian Genome ·Thomas J. Corydon,(unknown),Cathrine Jespersgaard,Brage Storstein Andresen,Anders D. Børglum,Søren L. Pedersen,Lars Bolund,Niels Gregersen,Peter Bross	33
9	Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations 2000 ·European Journal of Pediatrics ·Niels Gregersen,Brage Storstein Andresen,Peter Bross	29
10	Characterization of mouse Clpp protease cDNA, gene, and protein 2000 ·Mammalian Genome ·Brage Storstein Andresen,Thomas J. Corydon,(unknown),Peter Bross,Lisbeth Dahl Schroeder,(unknown),Lars Bolund,Niels Gregersen	4
11	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 1998 ·Human Molecular Genetics ·Niels Gregersen	102
12	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 1997 ·Pediatric Research ·Kay Tanaka,Niels Gregersen,Antònia Ribes,Julie Kim,(unknown),Vibeke Winter,(unknown),Gemma Martínez,Thomas Deufel,(unknown),René Santer,(unknown),Ewa Pronicka,Aranka László,Stanislav Kmoch,Ivo Kremensky,(unknown),İ Özalp,Michinori Ito	54
13	Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia 1997 ·Human Mutation ·Henrik Kjærulf Jensen,Thomas Glasdam Jensen,Ole Færgeman,(unknown),Brage Storstein Andresen,Thomas J. Corydon,Per Hove Andreasen,(unknown),Finn Heath,Lars Bolund,Niels Gregersen	24
14	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 1997 ·Blood ·Kristian Sandvej,Jan W. Gratama,Mette Munch,Xiao‐ge Zhou,R. L. H. Bolhuis,Brage Storstein Andresen,Niels Gregersen,Stephen Hamilton‐Dutoit	33
15	Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families 1996 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·(unknown),Henrik Kjærulf Jensen,(unknown),Fernando Civeira,(unknown),Miguel Pocovı́,Niels Gregersen	8
16	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 1994 ·Biochemical Medicine and Metabolic Biology ·Peter Bross,Thomas G. Jensen,Brage Storstein Andresen,(unknown),Andreas Nandy,Steen Kølvraa,Sandro Ghisla,Ihab Rasched,Lars Bolund,Niels Gregersen	11
17	Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe 1993 ·Human Heredity ·Niels Gregersen,Vibeke Winter,Diana Curtis,Thomas Deufel,(unknown),Jan Hendrickx,(unknown),A Ponzone,Teresa Parrella,Riccardo Ponzone,(unknown),(unknown),(unknown),(unknown),Charles R. Roe,(unknown),(unknown),Brage Storstein Andresen,Peter Bross,Lars Bolund	55
18	Acyl-CoA-binding protein/diazepam-binding inhibitor gene and pseudogenes 1992 ·Journal of Molecular Biology ·Susanne Mandrup,René Hummel,(unknown),(unknown),Per Hove Andreasen,Niels Gregersen,Jens Knudsen,Karsten Kristiansen	106
19	Characterization of a disease‐causing Lys329 to Glu mutation in 16 patients with medium‐chain Acyl‐CoA dehydrogenase deficiency 1991 ·Journal of Inherited Metabolic Disease ·Niels Gregersen,Brage Storstein Andresen,Peter Bross,Vibeke Winter,N. Rüdiger,Stefan Engst,Sandro Ghisla,E. Christensen,Daniel Kelly,Arnold W. Strauss,(unknown),Lars Bolund,Alexandra I. F. Blakemore,David Curtis,Paul C. Engel	8
20	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 1991 ·Human Genetics ·Niels Gregersen,Brage Storstein Andresen,Peter Bross,Vibeke Winter,(unknown),Stefan Engst,(unknown),Daniel P. Kelly,(unknown),(unknown),Lars Bolund,Sandro Ghisla	63

About Niels Gregersen

Niels Gregersen is a scholar working on Clinical Biochemistry, Molecular Biology and Cancer Research, having authored 28 papers that have together received 935 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (7 papers) and Peroxisome Proliferator-Activated Receptors (7 papers). The work is most often cited by research in Clinical Biochemistry (535 citations), Biochemistry (70 citations) and Molecular Biology (630 citations). Niels Gregersen has collaborated with scholars based in Denmark, United States and Poland. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, Blood and Journal of Molecular Biology.

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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