Daniela Karall
Impact in
- Clinical Biochemistry top 0.02%
- Metabolism and Genetic Disorders
- Biochemistry top 5%
Papers in
-
- Metabolism and Genetic Disorders 86
- Genetics 17
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 5
- Co-authors
- Sabine Scholl‐Bürgi (81 shared papers)Martina Huemer (12 shared papers)Edda Haberlandt (27 shared papers)Johannes Häberle (11 shared papers)Martin S. Lindner (3 shared papers)Marjorie Dixon (2 shared papers)René Santer (3 shared papers)Carlo Dionisi‐Vici (3 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (28 papers)Orphanet Journal of Rare Diseases (12 papers)Neuropediatrics (7 papers)The American Journal of Human Genetics (5 papers)Scientific Reports (4 papers)
- Partner nations
- AustriaGermanySwitzerland
In The Last Decade
Daniela Karall
155 papers receiving 5.8k citations
Daniela Karall's Hit Papers
Peers
Comparison fields: 5 of 124
- Clinical Biochemistry 3.6k
- Biochemistry 131
- Molecular Biology 918
- Psychiatry and Mental health 252
- Genetics 382
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 165 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia Hit paper breakdown → | 2014 | 506 |
| 2 | Suggested guidelines for the diagnosis and management of urea cycle disorders Hit paper breakdown → | 2012 | 461 |
| 3 | Suggested guidelines for the diagnosis and management of urea cycle disorders: First revision Hit paper breakdown → | 2019 | 329 |
| 4 | The Genetic Landscape and Epidemiology of Phenylketonuria Hit paper breakdown → | 2020 | 262 |
| 5 | 2015 | 200 | |
| 6 | Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision Hit paper breakdown → | 2021 | 184 |
| 7 | 2015 | 182 | |
| 8 | 2009 | 180 | |
| 9 | 2016 | 166 | |
| 10 | 2009 | 148 | |
| 11 | 2013 | 142 | |
| 12 | 2009 | 135 | |
| 13 | 2012 | 123 | |
| 14 | 2014 | 96 | |
| 15 | 2015 | 94 | |
| 16 | 2015 | 91 | |
| 17 | 2007 | 83 | |
| 18 | 2016 | 78 | |
| 19 | 2015 | 76 | |
| 20 | 2011 | 72 |
About Daniela Karall
Daniela Karall is a scholar working on Clinical Biochemistry, Genetics, Physiology, Psychiatry and Mental health and Molecular Biology, having authored 165 papers that have together received 6k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (86 papers), Mitochondrial Function and Pathology (12 papers), Diet and metabolism studies (8 papers), Epilepsy research and treatment (8 papers), Lysosomal Storage Disorders Research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (5 papers) and Congenital Heart Disease Studies (5 papers). The work is most often cited by research in Clinical Biochemistry (3.6k citations), Biochemistry (131 citations), Molecular Biology (918 citations), Psychiatry and Mental health (252 citations) and Genetics (382 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, Martin S. Lindner, Marjorie Dixon, René Santer, Carlo Dionisi‐Vici, Aude Servais and Alberto Burlina. Their work appears in journals such as Journal of Inherited Metabolic Disease, Orphanet Journal of Rare Diseases, Neuropediatrics, The American Journal of Human Genetics and Scientific Reports.
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.