Niels Gregersen

1.1k citations

28 papers · 935 indexed · h-index 14

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders 13
Biochemistry top 10%
Molecular Biology
- Mitochondrial Function and Pathology 7
- Peroxisome Proliferator-Activated Receptors 7
- Biochemical and Molecular Research 5
- RNA and protein synthesis mechanisms 3
- Metabolomics and Mass Spectrometry Studies 2
- Coenzyme Q10 studies and effects 2
Rheumatology top 10%
Physiology
Surgery
- Lipoproteins and Cardiovascular Health 4

Co-authors: Brage Storstein Andresen Peter Bross Lars Bolund Thomas J. Corydon Vibeke Winter Frank E. Frerman Per Hove Andreasen Nanna Cornelius
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: SHILAP Revista de lepidopterología (1 paper)Blood (2 papers)Journal of Molecular Biology (1 paper)
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

The 25 scholars most cited alongside Niels Gregersen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Niels Gregersen Line = papers co-authored together Niels Gregersen links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
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 Clinica Chimica Acta ·Anne‐Frédérique Dessein,Monique Fontaine,Marie Joncquel-Chevalier Curt,Gilbert Briand,Claire Sechter,Karine Mention-Mulliez,Dries Dobbelaere,Claire Douillard,Arnaud Lacour,Isabelle Redonnet-Vernhet,Delphine Lamireau,Magalie Barth,Marie-Christine Minot-Myhié,Alice Kuster,Pascale de Lonlay,Niels Gregersen,Cécile Acquaviva,Christine Vianey‐Saban,Jòseph Vamecq	2017	10
2	CoQ10 as a modulator of mitochondrial dysfunction and maladaptive stress responses in chronic fatigue syndrome Signe Søes,Louise Brinth,Niels Gregersen,Rikke Katrine Jentoft Olsen	2015	1
3	Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency Human Molecular Genetics ·Nanna Cornelius,Frank E. Frerman,Thomas J. Corydon,Johan Palmfeldt,Peter Bross,Niels Gregersen,Rikke Katrine Jentoft Olsen	2012	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 Human Genetics ·Jens Jacob Hansen,Peter Bross,Majken Westergaard,Marit Nielsen,Hans Eiberg,Anders D. Børglum,Jens Mogensen,Karsten Kristiansen,Lars Bolund,Niels Gregersen	2003	8
5	Rare Disorders of Metabolism with Elevated Butyryl- and Isobutyryl-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening Pediatric Research ·Dwight D. Koeberl,Sarah P. Young,Niels Gregersen,Jerry Vockley,Wendy E. Smith,Daniel K. Benjamin,Yan An,S. D. Weavil,Shu Chaing,Deeksha Bali,Marie McDonald,Priya S. Kishnani,Ying-Tsong Chen,David S. Millington	2003	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 Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) ·Brage Storstein Andresen,Kristopher Nielsen,P. P. Madsen,Thomas J. Corydon,Jørgen Kjems,Adrian R. Krainer,O Elpeleg,Lisbeth Dahl Schroeder,Niels Gregersen	2002	1
7	Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype–phenotype relationship Human Mutation ·Niels Gregersen,Brage Storstein Andresen,Morten J. Corydon,Thomas J. Corydon,Rikke Katrine Jentoft Olsen,Lars Bolund,Peter Bross	2001	4
8	Human and mouse mitochondrial orthologs of bacterial ClpX Mammalian Genome ·Thomas J. Corydon,Mette Wilsbech,Cathrine Jespersgaard,Brage Storstein Andresen,Anders D. Børglum,Søren L. Pedersen,Lars Bolund,Niels Gregersen,Peter Bross	2000	33
9	Prevalent mutations in fatty acid oxidation disorders: diagnostic considerations European Journal of Pediatrics ·Niels Gregersen,Brage Storstein Andresen,Peter Bross	2000	29
10	Characterization of mouse Clpp protease cDNA, gene, and protein Mammalian Genome ·Brage Storstein Andresen,Thomas J. Corydon,Mette Wilsbech,Peter Bross,Lisbeth Dahl Schroeder,Tina F. Hindkjær,Lars Bolund,Niels Gregersen	2000	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 Human Molecular Genetics ·Niels Gregersen	1998	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 Pediatric Research ·Kay Tanaka,Niels Gregersen,Antònia Ribes,Julie Kim,Steen Kølvraa,Vibeke Winter,Hans Eiberg,Gemma Martínez,Thomas Deufel,Barbara Leifert,René Santer,Baudouin Francois,Ewa Pronicka,Aranka László,Stanislav Kmoch,Ivo Kremensky,Luba Kalaydjicva,İ Özalp,Michinori Ito	1997	54
13	Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia Human Mutation ·Henrik Kjærulf Jensen,Thomas Glasdam Jensen,Ole Færgeman,Lillian G. Jensen,Brage Storstein Andresen,Thomas J. Corydon,Per Hove Andreasen,Peter S. Hansen,Finn Heath,Lars Bolund,Niels Gregersen	1997	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 Blood ·Kristian Sandvej,Jan W. Gratama,Mette Munch,Xiao‐ge Zhou,R. L. H. Bolhuis,Brage Storstein Andresen,Niels Gregersen,Stephen Hamilton‐Dutoit	1997	33
15	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 ·Ana Cenarro,Henrik Kjærulf Jensen,E. Casao,Fernando Civeira,José González‐Bonillo,Miguel Pocovı́,Niels Gregersen	1996	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 Biochemical Medicine and Metabolic Biology ·Peter Bross,Thomas G. Jensen,Brage Storstein Andresen,M. Kjeldsen,Andreas Nandy,Steen Kølvraa,Sandro Ghisla,Ihab Rasched,Lars Bolund,Niels Gregersen	1994	11
17	Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe Human Heredity ·Niels Gregersen,Vibeke Winter,Diana Curtis,Thomas Deufel,Marion Mack,Jan Hendrickx,Patrick J. Willems,A Ponzone,Teresa Parrella,Riccardo Ponzone,Jia-Huan Ding,Wen Zhang,Yuan Tsang Chen,Stephen Kahler,Charles R. Roe,Steen K oslash lvraa,Katrine Schneiderman,Brage Storstein Andresen,Peter Bross,Lars Bolund	1993	55
18	Acyl-CoA-binding protein/diazepam-binding inhibitor gene and pseudogenes Journal of Molecular Biology ·Susanne Mandrup,René Hummel,Stig Ravn,Gurli Jensen,Per Hove Andreasen,Niels Gregersen,Jens Knudsen,Karsten Kristiansen	1992	106
19	Characterization of a disease‐causing Lys329 to Glu mutation in 16 patients with medium‐chain Acyl‐CoA dehydrogenase deficiency 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,S. Kølvraa,Lars Bolund,Alexandra I. F. Blakemore,David Curtis,Paul C. Engel	1991	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 Human Genetics ·Niels Gregersen,Brage Storstein Andresen,Peter Bross,Vibeke Winter,Niels R�diger,Stefan Engst,Ernst Christensen,Daniel P. Kelly,ArnoldW. Strauss,Steen K�lvraa,Lars Bolund,Sandro Ghisla	1991	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), Peroxisome Proliferator-Activated Receptors (7 papers), Biochemical and Molecular Research (5 papers), Lipoproteins and Cardiovascular Health (4 papers), RNA and protein synthesis mechanisms (3 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and Coenzyme Q10 studies and effects (2 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.

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