N. Gregersen
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Molecular Biology top 5%
- Mitochondrial Function and Pathology
- Peroxisome Proliferator-Activated Receptors
- Biochemical and Molecular Research
- Metabolomics and Mass Spectrometry Studies
Papers in
-
- Peroxisome Proliferator-Activated Receptors 18
- Biochemical and Molecular Research 17
- Mitochondrial Function and Pathology 14
-
- Metabolism and Genetic Disorders 60
- Co-authors
- Steen Kølvraa (26 shared papers)Henrik Kjærulf Jensen (18 shared papers)Ole Færgeman (20 shared papers)Brage Storstein Andresen (23 shared papers)E. Christensen (10 shared papers)Peter Bross (15 shared papers)Peter S. Hansen (13 shared papers)P. Divry (4 shared papers)
In The Last Decade
N. Gregersen
106 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 104
- Clinical Biochemistry 1.6k
- Molecular Biology 2.0k
- Biochemistry 173
- Physiology 488
- Rheumatology 221
Countries citing papers authored by N. Gregersen
This map shows the geographic impact of N. 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 N. Gregersen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Gregersen more than expected).
Fields of papers citing papers by N. Gregersen
This network shows the impact of papers produced by N. 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 N. Gregersen. The network helps show where N. Gregersen may publish in the future.
Co-authors
The 25 scholars most cited alongside N. Gregersen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 107 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1997 | 197 | |
| 2 | 1982 | 142 | |
| 3 | 1987 | 129 | |
| 4 | Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus. | 1996 | 127 |
| 5 | 1982 | 108 | |
| 6 | 1991 | 94 | |
| 7 | 1996 | 86 | |
| 8 | 1990 | 84 | |
| 9 | 2006 | 82 | |
| 10 | 1992 | 74 | |
| 11 | 2008 | 70 | |
| 12 | 2006 | 70 | |
| 13 | High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing. | 1996 | 70 |
| 14 | 1983 | 70 | |
| 15 | 2001 | 68 | |
| 16 | 1996 | 63 | |
| 17 | 1980 | 60 | |
| 18 | 2004 | 59 | |
| 19 | 1998 | 57 | |
| 20 | 1985 | 56 |
About N. Gregersen
N. Gregersen is a scholar working on Molecular Biology, Clinical Biochemistry, Surgery, Physiology and Cell Biology, having authored 107 papers that have together received 3.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (60 papers), Lipoproteins and Cardiovascular Health (20 papers), Peroxisome Proliferator-Activated Receptors (18 papers), Biochemical and Molecular Research (17 papers), Mitochondrial Function and Pathology (14 papers), Diet and metabolism studies (14 papers), Amino Acid Enzymes and Metabolism (7 papers) and Muscle metabolism and nutrition (6 papers). The work is most often cited by research in Clinical Biochemistry (1.6k citations), Molecular Biology (2.0k citations), Biochemistry (173 citations), Physiology (488 citations) and Rheumatology (221 citations). N. Gregersen has collaborated with scholars based in Denmark, Poland and France. Frequent co-authors include Steen Kølvraa, Henrik Kjærulf Jensen, Ole Færgeman, Brage Storstein Andresen, E. Christensen, Peter Bross, Peter S. Hansen, P. Divry, L G Jensen and K. Rasmussen. Their work appears in journals such as Journal of Inherited Metabolic Disease, Clinical Genetics, Clinica Chimica Acta, Molecular Genetics and Metabolism and Pediatric Research.
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.