Inga Knudsen
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
-
- Mitochondrial Function and Pathology
- Biochemical and Molecular Research
- Peroxisome Proliferator-Activated Receptors
Papers in
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- Biochemical and Molecular Research 9
- Peroxisome Proliferator-Activated Receptors 6
- Mitochondrial Function and Pathology 5
- Metabolomics and Mass Spectrometry Studies 2
- RNA and protein synthesis mechanisms 2
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- Metabolism and Genetic Disorders 12
- Co-authors
- Brage Storstein Andresen (13 shared papers)Peter Bross (9 shared papers)Niels Gregersen (6 shared papers)Szabolcs Udvari (2 shared papers)Vibeke Winter (6 shared papers)Steen Kølvraa (5 shared papers)Shawn E. McCandless (1 shared paper)Paul C. Engel (1 shared paper)
- Journals
- Journal of Inherited Metabolic Disease (3 papers)The American Journal of Human Genetics (2 papers)FEBS Letters (1 paper)Pediatric Research (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- DenmarkUnited StatesNetherlands
In The Last Decade
Inga Knudsen
13 papers receiving 573 citations
Peers
Comparison fields: 5 of 52
- Clinical Biochemistry 463
- Molecular Biology 448
- Rheumatology 94
- Pediatrics, Perinatology and Child Health 103
- Biochemistry 32
Countries citing papers authored by Inga Knudsen
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
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-authors
The 25 scholars most cited alongside Inga Knudsen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 180 | |
| 2 | 1997 | 105 | |
| 3 | 2000 | 54 | |
| 4 | 1995 | 46 | |
| 5 | 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). | 1993 | 35 |
| 6 | 1996 | 35 | |
| 7 | 2005 | 33 | |
| 8 | 2004 | 31 | |
| 9 | 2006 | 26 | |
| 10 | Disease-causing mutations in exon 11 of the medium-chain acyl-CoA dehydrogenase gene. | 1994 | 25 |
| 11 | Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency. | 1995 | 13 |
| 12 | 2005 | 4 | |
| 13 | 1994 | 1 |
About Inga Knudsen
Inga Knudsen is a scholar working on Molecular Biology, Clinical Biochemistry, Cardiology and Cardiovascular Medicine, Endocrinology, Diabetes and Metabolism and Nutrition and Dietetics, having authored 13 papers that have together received 588 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (12 papers), Biochemical and Molecular Research (9 papers), Peroxisome Proliferator-Activated Receptors (6 papers), Mitochondrial Function and Pathology (5 papers), Metabolomics and Mass Spectrometry Studies (2 papers), RNA and protein synthesis mechanisms (2 papers), Trace Elements in Health (1 paper) and Viral Infections and Immunology Research (1 paper). The work is most often cited by research in Clinical Biochemistry (463 citations), Molecular Biology (448 citations), Rheumatology (94 citations), Pediatrics, Perinatology and Child Health (103 citations) and Biochemistry (32 citations). Inga Knudsen has collaborated with scholars based in Denmark, United States and Netherlands. Frequent co-authors include Brage Storstein Andresen, Peter Bross, Niels Gregersen, Szabolcs Udvari, Vibeke Winter, Steen Kølvraa, Shawn E. McCandless, Paul C. Engel, Linda P. O’Reilly and Edwin W. Naylor. Their work appears in journals such as Journal of Inherited Metabolic Disease, The American Journal of Human Genetics, FEBS Letters, Pediatric Research and Human Molecular Genetics.
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.