Arrate Pereda
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- Epigenetics and DNA Methylation 5
- Congenital heart defects research 5
- Metabolism, Diabetes, and Cancer 3
- Genetics 21
- Genetic Syndromes and Imprinting 16
- Genomics and Rare Diseases 7
- Blood disorders and treatments 3
- Co-authors
- Guiomar Pérez de Nanclares (27 shared papers)Henri Korn (1 shared paper)Antoine Triller (1 shared paper)D. S. Faber (1 shared paper)Agnès Linglart (9 shared papers)Intza Garin (8 shared papers)Giovanna Mantovani (9 shared papers)Francesca Marta Elli (6 shared papers)
In The Last Decade
Arrate Pereda
29 papers receiving 415 citations
Peers
Comparison fields: 5 of 57
- Genetics 242
- Developmental Biology 14
- Molecular Biology 279
- Cellular and Molecular Neuroscience 68
- Pediatrics, Perinatology and Child Health 42
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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 87 | |
| 2 | 2016 | 54 | |
| 3 | 2018 | 36 | |
| 4 | 2015 | 32 | |
| 5 | 2013 | 31 | |
| 6 | 1993 | 30 | |
| 7 | 2022 | 29 | |
| 8 | 2018 | 24 | |
| 9 | 2015 | 18 | |
| 10 | 2017 | 16 | |
| 11 | 2018 | 14 | |
| 12 | 2020 | 13 | |
| 13 | 2020 | 10 | |
| 14 | 2021 | 7 | |
| 15 | 2024 | 5 | |
| 16 | 2023 | 4 | |
| 17 | 2023 | 3 | |
| 18 | 2023 | 2 | |
| 19 | 2021 | 2 | |
| 20 | 2023 | 2 |
About Arrate Pereda
Arrate Pereda is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Surgery and Oncology, having authored 31 papers that have together received 430 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (16 papers), Genomics and Rare Diseases (7 papers), Epigenetics and DNA Methylation (5 papers), Congenital heart defects research (5 papers), Metabolism, Diabetes, and Cancer (3 papers), Prenatal Screening and Diagnostics (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Blood disorders and treatments (3 papers). The work is most often cited by research in Genetics (242 citations), Developmental Biology (14 citations), Molecular Biology (279 citations), Cellular and Molecular Neuroscience (68 citations) and Pediatrics, Perinatology and Child Health (42 citations). Arrate Pereda has collaborated with scholars based in Spain, Italy and France. Frequent co-authors include Guiomar Pérez de Nanclares, Henri Korn, Antoine Triller, D. S. Faber, Agnès Linglart, Intza Garin, Giovanna Mantovani, Francesca Marta Elli, Luisa De Sanctis and Patrick Hanna. Their work appears in journals such as European Journal of Endocrinology, Genes, The Journal of Clinical Endocrinology & Metabolism, Frontiers in Endocrinology and Clinical Epigenetics.
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.