Arrate Pereda
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Developmental Biology top 10%
Papers in
- Genetics 26
- Genetic Syndromes and Imprinting 23
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- Congenital heart defects research 4
- Prion Diseases and Protein Misfolding 3
- Metabolism, Diabetes, and Cancer 2
- Co-authors
- Guiomar Pérez de Nanclares (30 shared papers)D. S. Faber (1 shared paper)Henri Korn (1 shared paper)Antoine Triller (1 shared paper)Intza Garin (9 shared papers)Agnès Linglart (8 shared papers)Giovanna Mantovani (8 shared papers)Francesca Marta Elli (6 shared papers)
In The Last Decade
Arrate Pereda
42 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 67
- Genetics 653
- Developmental Biology 24
- Nephrology 63
- Molecular Biology 517
- Cellular and Molecular Neuroscience 74
Countries citing papers authored by Arrate Pereda
This map shows the geographic impact of Arrate Pereda'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 Arrate Pereda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arrate Pereda more than expected).
Fields of papers citing papers by Arrate Pereda
This network shows the impact of papers produced by Arrate Pereda. 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 Arrate Pereda. The network helps show where Arrate Pereda may publish in the future.
Co-authors
The 25 scholars most cited alongside Arrate Pereda, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 220 | |
| 2 | 2016 | 109 | |
| 3 | 2012 | 95 | |
| 4 | 1992 | 93 | |
| 5 | 2016 | 62 | |
| 6 | 2018 | 42 | |
| 7 | 2020 | 42 | |
| 8 | 2013 | 36 | |
| 9 | 2022 | 35 | |
| 10 | 2015 | 35 | |
| 11 | 1993 | 33 | |
| 12 | 2022 | 33 | |
| 13 | 2018 | 29 | |
| 14 | 2022 | 26 | |
| 15 | 2015 | 24 | |
| 16 | 2017 | 18 | |
| 17 | 2018 | 16 | |
| 18 | 2022 | 15 | |
| 19 | 2020 | 15 | |
| 20 | 2020 | 13 |
About Arrate Pereda
Arrate Pereda is a scholar working on Genetics, Molecular Biology, Surgery, Neurology and Genetics, having authored 44 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (23 papers), Congenital heart defects research (4 papers), Prion Diseases and Protein Misfolding (3 papers), Thyroid and Parathyroid Surgery (2 papers), Neurological diseases and metabolism (2 papers), Bone Tumor Diagnosis and Treatments (2 papers), Metabolism, Diabetes, and Cancer (2 papers) and Bone health and treatments (2 papers). The work is most often cited by research in Genetics (653 citations), Developmental Biology (24 citations), Nephrology (63 citations), Molecular Biology (517 citations) and Cellular and Molecular Neuroscience (74 citations). Arrate Pereda has collaborated with scholars based in Spain, France and Italy. Frequent co-authors include Guiomar Pérez de Nanclares, D. S. Faber, Henri Korn, Antoine Triller, Intza Garin, Agnès Linglart, Giovanna Mantovani, Francesca Marta Elli, Luisa De Sanctis and Patrick Hanna. Their work appears in journals such as European Journal of Endocrinology, The Journal of Clinical Endocrinology & Metabolism, Clinical Epigenetics, Genes and Frontiers in Endocrinology.
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.