Elsebet Østergaard
Impact in
- Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
- Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Retinal Development and Disorders
Papers in
-
- Mitochondrial Function and Pathology 29
- ATP Synthase and ATPases Research 8
- RNA and protein synthesis mechanisms 7
- RNA modifications and cancer 6
- RNA regulation and disease 4
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- Metabolism and Genetic Disorders 12
- Co-authors
- Flemming Wibrand (20 shared papers)Morten Dunø (17 shared papers)Jes Olesen (3 shared papers)Eric A. Shoubridge (4 shared papers)Thomas Rosenberg (5 shared papers)Mustafa Batbayli (5 shared papers)Ernst Christensen (4 shared papers)Lise Lykke Thomsen (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)Human Molecular Genetics (5 papers)Journal of Inherited Metabolic Disease (5 papers)The American Journal of Human Genetics (5 papers)Neurology (3 papers)
- Partner nations
- DenmarkNetherlandsUnited Kingdom
In The Last Decade
Elsebet Østergaard
67 papers receiving 2.4k citations
Peers
Comparison fields: 5 of 102
- Clinical Biochemistry 754
- Molecular Biology 1.7k
- Psychiatry and Mental health 238
- Neurology 113
- Sensory Systems 59
Countries citing papers authored by Elsebet Østergaard
This map shows the geographic impact of Elsebet Østergaard'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 Elsebet Østergaard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elsebet Østergaard more than expected).
Fields of papers citing papers by Elsebet Østergaard
This network shows the impact of papers produced by Elsebet Østergaard. 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 Elsebet Østergaard. The network helps show where Elsebet Østergaard may publish in the future.
Co-authors
The 25 scholars most cited alongside Elsebet Østergaard, 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 69 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 175 | |
| 2 | 2007 | 159 | |
| 3 | 2007 | 153 | |
| 4 | 2010 | 128 | |
| 5 | 2005 | 119 | |
| 6 | 2003 | 106 | |
| 7 | 2012 | 104 | |
| 8 | 2004 | 104 | |
| 9 | 2002 | 98 | |
| 10 | 2013 | 94 | |
| 11 | 2011 | 67 | |
| 12 | 2020 | 61 | |
| 13 | 2008 | 57 | |
| 14 | 2017 | 57 | |
| 15 | 2011 | 53 | |
| 16 | 2010 | 52 | |
| 17 | 1994 | 52 | |
| 18 | A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases. | 2011 | 51 |
| 19 | 2015 | 50 | |
| 20 | 2020 | 50 |
About Elsebet Østergaard
Elsebet Østergaard is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Surgery and Pathology and Forensic Medicine, having authored 69 papers that have together received 2.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (29 papers), Metabolism and Genetic Disorders (12 papers), ATP Synthase and ATPases Research (8 papers), RNA and protein synthesis mechanisms (7 papers), RNA modifications and cancer (6 papers), Genomics and Rare Diseases (5 papers), Migraine and Headache Studies (4 papers) and RNA regulation and disease (4 papers). The work is most often cited by research in Clinical Biochemistry (754 citations), Molecular Biology (1.7k citations), Psychiatry and Mental health (238 citations), Neurology (113 citations) and Sensory Systems (59 citations). Elsebet Østergaard has collaborated with scholars based in Denmark, Netherlands and United Kingdom. Frequent co-authors include Flemming Wibrand, Morten Dunø, Jes Olesen, Eric A. Shoubridge, Thomas Rosenberg, Mustafa Batbayli, Ernst Christensen, Lise Lykke Thomsen, Richard J. Rodenburg and Michael Bjørn Russell. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, Journal of Inherited Metabolic Disease, The American Journal of Human Genetics and Neurology.
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.