Arrate Pereda

1.5k total citations
31 papers, 430 citations indexed

About

Arrate Pereda is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Arrate Pereda has authored 31 papers receiving a total of 430 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Arrate Pereda's work include Genetic Syndromes and Imprinting (16 papers), Genomics and Rare Diseases (7 papers) and Epigenetics and DNA Methylation (5 papers). Arrate Pereda is often cited by papers focused on Genetic Syndromes and Imprinting (16 papers), Genomics and Rare Diseases (7 papers) and Epigenetics and DNA Methylation (5 papers). Arrate Pereda collaborates with scholars based in Spain, Italy and France. Arrate Pereda's co-authors include Guiomar Pérez de Nanclares, D. S. Faber, Antoine Triller, Henri Korn, Agnès Linglart, Intza Garin, Francesca Marta Elli, Giovanna Mantovani, Luisa De Sanctis and Patrick Hanna and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Arrate Pereda

29 papers receiving 415 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Arrate Pereda Spain 12 279 242 68 42 36 31 430
Yeon‐Joo Kang United States 5 181 0.6× 102 0.4× 64 0.9× 12 0.3× 23 0.6× 6 371
Manuela Pendziwiat Germany 12 204 0.7× 103 0.4× 70 1.0× 18 0.4× 11 0.3× 21 379
Jean‐François Ouimette France 11 497 1.8× 231 1.0× 42 0.6× 22 0.5× 30 0.8× 15 601
Sandra Whalen France 13 268 1.0× 157 0.6× 59 0.9× 37 0.9× 33 0.9× 28 417
Monica Castro Varela Brazil 16 489 1.8× 754 3.1× 30 0.4× 167 4.0× 38 1.1× 24 928
Mingi Hong United States 16 458 1.6× 183 0.8× 61 0.9× 119 2.8× 72 2.0× 28 657
Wolfgang Hofmeister Sweden 12 194 0.7× 112 0.5× 54 0.8× 33 0.8× 31 0.9× 16 336
Ronald E. Haskell United States 9 203 0.7× 106 0.4× 55 0.8× 7 0.2× 39 1.1× 10 407
Tessa Walcher Germany 5 271 1.0× 87 0.4× 53 0.8× 17 0.4× 31 0.9× 5 430
Sofía Nasif Argentina 11 507 1.8× 96 0.4× 44 0.6× 9 0.2× 34 0.9× 12 712

Countries citing papers authored by Arrate Pereda

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Arrate Pereda

This figure shows the co-authorship network connecting the top 25 collaborators of Arrate Pereda. A scholar is included among the top collaborators of Arrate Pereda based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Arrate Pereda. Arrate Pereda is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Carcavilla, Atilano, Arrate Pereda, Mami Miyado, et al.. (2025). Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypes. European Journal of Endocrinology. 192(4). 364–372. 1 indexed citations
2.
Pereda, Arrate, et al.. (2024). Heterodisomy in the GNAS locus is also a cause of pseudohypoparathyroidism type 1B (iPPSD3). Frontiers in Endocrinology. 15. 1505244–1505244.
3.
Pereda, Arrate, et al.. (2024). Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune–Albright Syndrome (FD/MAS). Genes. 15(1). 120–120. 5 indexed citations
4.
Mantovani, Giovanna, Guiomar Pérez de Nanclares, Francesca Marta Elli, et al.. (2023). Growth patterns and outcomes of growth hormone therapy in patients with acrodysostosis. Journal of Endocrinological Investigation. 46(8). 1673–1684. 2 indexed citations
5.
Nanclares, Guiomar Pérez de, Harald Jüppner, Patrick Hanna, et al.. (2023). Recombinant growth hormone improves growth and adult height in patients with maternal inactivating GNAS mutations. European Journal of Endocrinology. 189(1). 123–131. 3 indexed citations
6.
Pereda, Arrate, et al.. (2023). Incidental finding at methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA): how to proceed?. Frontiers in Genetics. 14. 1274056–1274056. 1 indexed citations
7.
Pereda, Arrate, et al.. (2023). Frequency of de novo variants and parental mosaicism in families with inactivating PTH/PTHrP signaling disorder type 2. Frontiers in Endocrinology. 13. 1055431–1055431. 4 indexed citations
8.
Pereda, Arrate, et al.. (2023). Deficiencia de vitamina D en la edad adulta: presentación de 2 casos familiares de seudohipoparatiroidismo. Medicina Clínica. 161(11). 493–497. 2 indexed citations
9.
Eraña, Hasier, Beatriz San Millán, Jorge M. Charco, et al.. (2022). Description of the first Spanish case of Gerstmann–Sträussler–Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization. Journal of Neurology. 269(8). 4253–4263. 1 indexed citations
10.
Pereda, Arrate, et al.. (2021). Sporadic Creutzfeldt–Jakob disease with extremely long 14‐year survival period. European Journal of Neurology. 28(9). 2901–2906. 2 indexed citations
11.
Aguilera, Sergio, Ana B. de la Hoz, Olatz Villate, et al.. (2020). Hereditary Spastic Paraplegia and Intellectual Disability: Clinicogenetic Lessons From a Family Suggesting a Dual Genetics Diagnosis. Frontiers in Neurology. 11. 41–41. 1 indexed citations
12.
Pereda, Arrate, et al.. (2018). What to consider when pseudohypoparathyroidism is ruled out: iPPSD and differential diagnosis. BMC Medical Genetics. 19(1). 32–32. 1 indexed citations
13.
Pereda, Arrate, et al.. (2018). Transient neonatal diabetes mellitus and hypomethylation at additional imprinted loci: novel ZFP57 mutation and review on the literature. Acta Diabetologica. 56(3). 301–307. 24 indexed citations
14.
Elli, Francesca Marta, Arrate Pereda, Agnès Linglart, Guiomar Pérez de Nanclares, & Giovanna Mantovani. (2018). Parathyroid hormone resistance syndromes – Inactivating PTH/PTHrP signaling disorders (iPPSDs). Best Practice & Research Clinical Endocrinology & Metabolism. 32(6). 941–954. 14 indexed citations
15.
Briet, Claire, Arrate Pereda, Catherine Le Stunff, et al.. (2017). Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3. Human Molecular Genetics. 26(20). 3883–3894. 16 indexed citations
16.
Thomas‐Teinturier, Cécile, Arrate Pereda, Intza Garin, et al.. (2015). Report of two novel mutations in PTHLH associated with brachydactyly type E and literature review. American Journal of Medical Genetics Part A. 170(3). 734–742. 18 indexed citations
17.
Garin, Intza, Francesca Marta Elli, Agnès Linglart, et al.. (2015). Novel Microdeletions Affecting the GNAS Locus in Pseudohypoparathyroidism: Characterization of the Underlying Mechanisms. The Journal of Clinical Endocrinology & Metabolism. 100(4). E681–E687. 32 indexed citations
18.
Pereda, Arrate, Intza Garin, María García‐Barcina, et al.. (2013). Brachydactyly E: isolated or as a feature of a syndrome. Orphanet Journal of Rare Diseases. 8(1). 141–141. 31 indexed citations
19.
Pereda, Arrate, et al.. (2007). Orientación al diagnóstico y tratamiento del dolor abdominal crónico y dolor abdominal recurrente en el niño y adolescente. 27(1). 17–25.
20.

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.

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