Daniela Karall
Impact in
- Clinical Biochemistry top 0.1%
- Metabolism and Genetic Disorders
- Biochemistry top 1%
- Amino Acid Enzymes and Metabolism
Papers in
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- Metabolism and Genetic Disorders 59
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- Mitochondrial Function and Pathology 25
- Co-authors
- Sabine Scholl‐Bürgi (82 shared papers)Martina Huemer (12 shared papers)Edda Haberlandt (27 shared papers)Johannes Häberle (12 shared papers)Marjorie Dixon (3 shared papers)Carlo Dionisi‐Vici (3 shared papers)Alberto Burlina (2 shared papers)Vicente Rubio (2 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (15 papers)Orphanet Journal of Rare Diseases (9 papers)Neuropediatrics (6 papers)Scientific Reports (3 papers)European Journal of Medical Genetics (3 papers)
- Partner nations
- AustriaGermanySwitzerland
In The Last Decade
Daniela Karall
116 papers receiving 2.7k citations
Daniela Karall's Hit Papers
Peers
Comparison fields: 5 of 113
- Clinical Biochemistry 1.4k
- Biochemistry 292
- Rheumatology 275
- Pediatrics, Perinatology and Child Health 343
- Physiology 432
Countries citing papers authored by Daniela Karall
This map shows the geographic impact of Daniela Karall'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 Daniela Karall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Karall more than expected).
Fields of papers citing papers by Daniela Karall
This network shows the impact of papers produced by Daniela Karall. 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 Daniela Karall. The network helps show where Daniela Karall may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela Karall, 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 128 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 436 | |
| 2 | Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision Hit paper breakdown → | 2019 | 284 |
| 3 | 2016 | 162 | |
| 4 | 2009 | 128 | |
| 5 | 2015 | 82 | |
| 6 | 2014 | 77 | |
| 7 | 2007 | 74 | |
| 8 | 2015 | 67 | |
| 9 | 2009 | 60 | |
| 10 | 2015 | 54 | |
| 11 | 2015 | 45 | |
| 12 | 2017 | 41 | |
| 13 | 2008 | 40 | |
| 14 | 2009 | 39 | |
| 15 | 2008 | 38 | |
| 16 | 2010 | 38 | |
| 17 | 2015 | 35 | |
| 18 | 2016 | 31 | |
| 19 | 2020 | 30 | |
| 20 | 2015 | 30 |
About Daniela Karall
Daniela Karall is a scholar working on Clinical Biochemistry, Molecular Biology, Physiology, Genetics and Pediatrics, Perinatology and Child Health, having authored 128 papers that have together received 2.8k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (59 papers), Mitochondrial Function and Pathology (25 papers), Diet and metabolism studies (18 papers), Pharmacological Effects and Toxicity Studies (7 papers), Glycogen Storage Diseases and Myoclonus (6 papers), Amino Acid Enzymes and Metabolism (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Childhood Cancer Survivors' Quality of Life (5 papers). The work is most often cited by research in Clinical Biochemistry (1.4k citations), Biochemistry (292 citations), Rheumatology (275 citations), Pediatrics, Perinatology and Child Health (343 citations) and Physiology (432 citations). Daniela Karall has collaborated with scholars based in Austria, Germany and Switzerland. Frequent co-authors include Sabine Scholl‐Bürgi, Martina Huemer, Edda Haberlandt, Johannes Häberle, Marjorie Dixon, Carlo Dionisi‐Vici, Alberto Burlina, Vicente Rubio, Martin Lindner and Anupam Chakrapani. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Neuropediatrics, Scientific Reports and European Journal of Medical 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.