Inga Knudsen

738 total citations
13 papers, 588 citations indexed

About

Inga Knudsen is a scholar working on Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Inga Knudsen has authored 13 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Inga Knudsen's work include Metabolism and Genetic Disorders (12 papers), Biochemical and Molecular Research (9 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). Inga Knudsen is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Biochemical and Molecular Research (9 papers) and Peroxisome Proliferator-Activated Receptors (6 papers). Inga Knudsen collaborates with scholars based in Denmark, United States and Netherlands. Inga Knudsen's co-authors include Brage Storstein Andresen, Peter Bross, Niels Gregersen, Szabolcs Udvari, Vibeke Winter, Edwin W. Naylor, Shawn E. McCandless, Dianne M. Frazier, Lars Bolund and Linda P. O’Reilly and has published in prestigious journals such as FEBS Letters, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Inga Knudsen

13 papers receiving 573 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inga Knudsen Denmark 11 463 448 103 94 90 13 588
Mercedes Martínez‐Pardo Spain 16 589 1.3× 559 1.2× 85 0.8× 165 1.8× 191 2.1× 35 782
Keow Giak Sim Australia 12 399 0.9× 335 0.7× 112 1.1× 105 1.1× 94 1.0× 13 512
Jamiyan Purevsuren Japan 14 384 0.8× 373 0.8× 78 0.8× 55 0.6× 75 0.8× 25 513
W. Oostheim Netherlands 13 266 0.6× 398 0.9× 64 0.6× 35 0.4× 60 0.7× 16 550
A. Green United Kingdom 11 305 0.7× 179 0.4× 81 0.8× 46 0.5× 107 1.2× 28 415
Y Okano Japan 13 440 1.0× 315 0.7× 51 0.5× 176 1.9× 80 0.9× 17 507
A. E. M. Stroomer Netherlands 10 185 0.4× 271 0.6× 74 0.7× 80 0.9× 61 0.7× 13 445
S Scheibenreiter Austria 10 267 0.6× 176 0.4× 135 1.3× 30 0.3× 58 0.6× 35 416
Sandesh C.S. Nagamani United States 10 279 0.6× 180 0.4× 96 0.9× 42 0.4× 60 0.7× 16 385
Darius J. Adams United States 10 328 0.7× 328 0.7× 76 0.7× 64 0.7× 102 1.1× 17 464

Countries citing papers authored by Inga Knudsen

Since Specialization
Citations

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

Fields of papers citing papers by Inga Knudsen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inga Knudsen

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

All Works

13 of 13 papers shown
1.
Pedersen, Christina B., Claus Bischoff, Ernst Christensen, et al.. (2006). Variations in IBD (ACAD8) in Children with Elevated C4-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening. Pediatric Research. 60(3). 315–320. 26 indexed citations
2.
Olsen, Rikke Katrine Jentoft, Brage Storstein Andresen, Ernst Christensen, et al.. (2005). DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiency. Prenatal Diagnosis. 25(1). 60–64. 4 indexed citations
3.
Kibæk, Maria, Xavier Roca, Ravi Sachidanandam, et al.. (2005). Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping. Human Genetics. 118(6). 680–690. 33 indexed citations
4.
Olsen, Rikke Katrine Jentoft, Morteza Pourfarzam, A. A. M. Morris, et al.. (2004). Lipid‐storage myopathy and respiratory insufficiency due to ETFQO mutations in a patient with late‐onset multiple acyl‐CoA dehydrogenation deficiency. Journal of Inherited Metabolic Disease. 27(5). 671–678. 31 indexed citations
5.
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7.
Andresen, Brage Storstein, Peter Bross, Szabolcs Udvari, et al.. (1997). The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?. Human Molecular Genetics. 6(5). 695–707. 105 indexed citations
8.
Andresen, Brage Storstein, Christine Vianey‐Saban, Peter Bross, et al.. (1996). The mutational spectrum in very long‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 19(2). 169–172. 35 indexed citations
9.
Bross, Peter, Brage Storstein Andresen, Inga Knudsen, Torben A. Kruse, & Niels Gregersen. (1995). Human ClpP protease: cDNA sequence, tissue‐specific expression and chromosomal assignment of the gene. FEBS Letters. 377(2). 249–252. 46 indexed citations
10.
Andresen, Brage Storstein, Peter Bross, Inga Knudsen, et al.. (1995). Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency.. PubMed. 220. 9–25. 13 indexed citations
11.
Andresen, Brage Storstein, Peter Bross, Inga Knudsen, et al.. (1994). Medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency due to heterozygosity for the common mutation and an allele resulting in low levels of MCAD mRNA. Journal of Inherited Metabolic Disease. 17(3). 275–278. 1 indexed citations
12.
Andresen, Brage Storstein, Peter Bross, Inga Knudsen, et al.. (1994). Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene.. PubMed. 54(6). 975–88. 25 indexed citations
13.
Andresen, Brage Storstein, Peter Bross, Thomas G. Jensen, et al.. (1993). A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).. PubMed. 53(3). 730–9. 35 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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