Andreas Rett
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 21
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 8
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- Metabolism and Genetic Disorders 7
- Co-authors
- Folker A. Hanefeld (1 shared paper)Bengt A. Hagberg (2 shared papers)Françoise Goutières (1 shared paper)John R. Wilson (1 shared paper)John M. Opitz (7 shared papers)James F. Reynolds (6 shared papers)Peter Riederer (4 shared papers)Mary Murphy (2 shared papers)
- Journals
- Brain and Development (8 papers)Human Genetics (5 papers)Journal of Neural Transmission (2 papers)Acta Neurologica Scandinavica (1 paper)Pain (1 paper)
- Partner nations
- AustriaUnited StatesGermany
In The Last Decade
Andreas Rett
53 papers receiving 1.6k citations
Andreas Rett's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 1.4k
- Cognitive Neuroscience 885
- Clinical Psychology 340
- Physiology 40
- Molecular Biology 578
Countries citing papers authored by Andreas Rett
This map shows the geographic impact of Andreas Rett'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 Andreas Rett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Rett more than expected).
Fields of papers citing papers by Andreas Rett
This network shows the impact of papers produced by Andreas Rett. 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 Andreas Rett. The network helps show where Andreas Rett may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Rett, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | [On a unusual brain atrophy syndrome in hyperammonemia in childhood]. Hit paper breakdown → | 1966 | 612 |
| 2 | 1985 | 243 | |
| 3 | 1986 | 103 | |
| 4 | 1986 | 72 | |
| 5 | 1985 | 62 | |
| 6 | 1985 | 57 | |
| 7 | 1976 | 49 | |
| 8 | 1987 | 47 | |
| 9 | 1986 | 43 | |
| 10 | 1975 | 28 | |
| 11 | 1990 | 26 | |
| 12 | 1975 | 24 | |
| 13 | 1986 | 23 | |
| 14 | 1968 | 22 | |
| 15 | 1987 | 22 | |
| 16 | 1986 | 21 | |
| 17 | 2016 | 19 | |
| 18 | 1979 | 18 | |
| 19 | 1978 | 15 | |
| 20 | 1976 | 13 |
About Andreas Rett
Andreas Rett is a scholar working on Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health, Psychiatry and Mental health and Cognitive Neuroscience, having authored 59 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (8 papers), Autism Spectrum Disorder Research (8 papers), Metabolism and Genetic Disorders (7 papers), Mitochondrial Function and Pathology (5 papers), Diet and metabolism studies (5 papers), Epilepsy research and treatment (3 papers) and Pharmaceutical studies and practices (3 papers). The work is most often cited by research in Genetics (1.4k citations), Cognitive Neuroscience (885 citations), Clinical Psychology (340 citations), Physiology (40 citations) and Molecular Biology (578 citations). Andreas Rett has collaborated with scholars based in Austria, United States and Germany. Frequent co-authors include Folker A. Hanefeld, Bengt A. Hagberg, Françoise Goutières, John R. Wilson, John M. Opitz, James F. Reynolds, Peter Riederer, Mary Murphy, Milly Andrle and Hugo W. Moser. Their work appears in journals such as Brain and Development, Human Genetics, Journal of Neural Transmission, Acta Neurologica Scandinavica and Pain.
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.