Allan Bayat
Impact in
- Psychiatry and Mental health top 5%
- Epilepsy research and treatment
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 47
- Genetics and Neurodevelopmental Disorders 26
- Genomics and Rare Diseases 24
- Genomic variations and chromosomal abnormalities 8
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- Congenital heart defects research 10
- Mitochondrial Function and Pathology 6
- Co-authors
- Rikke Steensbjerre Møller (17 shared papers)Helle Hjalgrim (1 shared paper)Guido Rubboli (6 shared papers)Marie-Laure Bouchy Jacobsson (1 shared paper)Christina Dühring Fenger (6 shared papers)Konstantinos Kamperis (1 shared paper)Sofia Douzgou (1 shared paper)Bronwyn A. Kerr (1 shared paper)
- Journals
- Genetics in Medicine (11 papers)Epilepsia (10 papers)Clinical Genetics (8 papers)European Journal of Human Genetics (5 papers)Neurology Genetics (4 papers)
- Partner nations
- DenmarkUnited StatesItaly
In The Last Decade
Allan Bayat
100 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 103
- Psychiatry and Mental health 275
- Genetics 516
- Clinical Biochemistry 76
- Molecular Biology 655
- Cellular and Molecular Neuroscience 164
Countries citing papers authored by Allan Bayat
This map shows the geographic impact of Allan Bayat'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 Allan Bayat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Allan Bayat more than expected).
Fields of papers citing papers by Allan Bayat
This network shows the impact of papers produced by Allan Bayat. 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 Allan Bayat. The network helps show where Allan Bayat may publish in the future.
Co-authors
The 25 scholars most cited alongside Allan Bayat, 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 108 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 105 | |
| 2 | 2018 | 93 | |
| 3 | 2017 | 83 | |
| 4 | 2018 | 73 | |
| 5 | 2021 | 72 | |
| 6 | 2018 | 70 | |
| 7 | 2019 | 65 | |
| 8 | Nitrous oxide provides safe and effective analgesia for minor paediatric procedures--a systematic review. | 2013 | 51 |
| 9 | 2020 | 46 | |
| 10 | 2016 | 40 | |
| 11 | 2021 | 34 | |
| 12 | 2022 | 32 | |
| 13 | 2022 | 31 | |
| 14 | 2022 | 31 | |
| 15 | 2022 | 30 | |
| 16 | 2023 | 30 | |
| 17 | 2022 | 28 | |
| 18 | 2023 | 27 | |
| 19 | 2019 | 24 | |
| 20 | 2021 | 23 |
About Allan Bayat
Allan Bayat is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Clinical Biochemistry and Epidemiology, having authored 108 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (26 papers), Genomics and Rare Diseases (24 papers), Congenital heart defects research (10 papers), Epilepsy research and treatment (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (6 papers) and Fetal and Pediatric Neurological Disorders (5 papers). The work is most often cited by research in Psychiatry and Mental health (275 citations), Genetics (516 citations), Clinical Biochemistry (76 citations), Molecular Biology (655 citations) and Cellular and Molecular Neuroscience (164 citations). Allan Bayat has collaborated with scholars based in Denmark, United States and Italy. Frequent co-authors include Rikke Steensbjerre Møller, Helle Hjalgrim, Guido Rubboli, Marie-Laure Bouchy Jacobsson, Christina Dühring Fenger, Konstantinos Kamperis, Sofia Douzgou, Bronwyn A. Kerr, Troels Herlin and Laura Roos. Their work appears in journals such as Genetics in Medicine, Epilepsia, Clinical Genetics, European Journal of Human Genetics and Neurology 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.