Daniela Choukair
Impact in
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- Growth Hormone and Insulin-like Growth Factors
- Pituitary Gland Disorders and Treatments
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- Metabolism and Genetic Disorders
Papers in
- Genetics 16
- Genomics and Rare Diseases 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
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- Growth Hormone and Insulin-like Growth Factors 6
- Thyroid Disorders and Treatments 3
- Co-authors
- Markus Bettendorf (18 shared papers)Burkhard Tönshoff (5 shared papers)Georg F. Hoffmann (12 shared papers)Lorenz Uhlmann (2 shared papers)Anja Sander (1 shared paper)Ulrike Hügel (1 shared paper)Egbert Schulze (2 shared papers)Corinna Grasemann (7 shared papers)
- Journals
- Hormone Research in Paediatrics (6 papers)Orphanet Journal of Rare Diseases (2 papers)Clinical Endocrinology (2 papers)Pediatric Rheumatology (1 paper)Journal of Inherited Metabolic Disease (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Daniela Choukair
28 papers receiving 216 citations
Peers
Comparison fields: 5 of 68
- Endocrinology, Diabetes and Metabolism 72
- Clinical Biochemistry 21
- Speech and Hearing 18
- Genetics 70
- Health Informatics 2
Countries citing papers authored by Daniela Choukair
This map shows the geographic impact of Daniela Choukair'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 Choukair with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Choukair more than expected).
Fields of papers citing papers by Daniela Choukair
This network shows the impact of papers produced by Daniela Choukair. 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 Choukair. The network helps show where Daniela Choukair may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela Choukair, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 29 | |
| 2 | 2018 | 21 | |
| 3 | 2016 | 17 | |
| 4 | 2017 | 16 | |
| 5 | 2019 | 15 | |
| 6 | 2023 | 13 | |
| 7 | 2021 | 13 | |
| 8 | 2020 | 10 | |
| 9 | 2015 | 10 | |
| 10 | 2020 | 10 | |
| 11 | 2019 | 9 | |
| 12 | 2023 | 8 | |
| 13 | 2022 | 7 | |
| 14 | 2021 | 6 | |
| 15 | 2015 | 5 | |
| 16 | 2022 | 4 | |
| 17 | 2023 | 4 | |
| 18 | 2013 | 4 | |
| 19 | 2022 | 4 | |
| 20 | 2021 | 2 |
About Daniela Choukair
Daniela Choukair is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 32 papers that have together received 217 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Growth Hormone and Insulin-like Growth Factors (6 papers), Sexual Differentiation and Disorders (6 papers), Childhood Cancer Survivors' Quality of Life (6 papers), Adolescent and Pediatric Healthcare (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Thyroid Disorders and Treatments (3 papers) and Child and Adolescent Health (3 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (72 citations), Clinical Biochemistry (21 citations), Speech and Hearing (18 citations), Genetics (70 citations) and Health Informatics (2 citations). Daniela Choukair has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Markus Bettendorf, Burkhard Tönshoff, Georg F. Hoffmann, Lorenz Uhlmann, Anja Sander, Ulrike Hügel, Egbert Schulze, Corinna Grasemann, Peter Burgard and Ioana Inta. Their work appears in journals such as Hormone Research in Paediatrics, Orphanet Journal of Rare Diseases, Clinical Endocrinology, Pediatric Rheumatology and Journal of Inherited Metabolic Disease.
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.