Jordi Rambla

1.7k total citations
17 papers, 135 citations indexed

About

Jordi Rambla is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Jordi Rambla has authored 17 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Jordi Rambla's work include Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (4 papers) and Bioinformatics and Genomic Networks (4 papers). Jordi Rambla is often cited by papers focused on Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (4 papers) and Bioinformatics and Genomic Networks (4 papers). Jordi Rambla collaborates with scholars based in Spain, United Kingdom and United States. Jordi Rambla's co-authors include Arcadi Navarro, Michael Brudno, Marc Fiume, Dylan Spalding, Heidi L. Rehm, Anthony J. Brookes, Michael Baudis, Mark Thompson, Stephen T. Sherry and Anthony Philippakis and has published in prestigious journals such as Bioinformatics, PLoS ONE and Evolution.

In The Last Decade

Jordi Rambla

14 papers receiving 132 citations

Peers

Jordi Rambla

GENET

PHEOH

Sarah E. Ali‐Khan Canada

Emily Kirby Canada

Dylan Spalding United Kingdom

Sara Y. Nussbeck Germany

Jason Bobe United States

Karen Kennedy United Kingdom

William D. Duncan United States

Judit Kumuthini South Africa

Michael J. S. Beauvais Canada

Tom Clegg United States

Sarah E. Ali‐Khan Canada

Jordi Rambla

50 ×1.1

90 ×2.0

GENET

62 ×1.4

PHEOH

36 ×1.1

16 ×0.5

Citations per year, relative to Jordi Rambla Jordi Rambla (= 1×) peers Sarah E. Ali‐Khan

Countries citing papers authored by Jordi Rambla

Since Specialization

Citations

This map shows the geographic impact of Jordi Rambla'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 Jordi Rambla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jordi Rambla more than expected).

Fields of papers citing papers by Jordi Rambla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jordi Rambla. 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 Jordi Rambla. The network helps show where Jordi Rambla may publish in the future.

Co-authorship network of co-authors of Jordi Rambla

This figure shows the co-authorship network connecting the top 25 collaborators of Jordi Rambla. A scholar is included among the top collaborators of Jordi Rambla 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 Jordi Rambla. Jordi Rambla is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

García‐Lezana, Teresa, Maciej Bobowicz, Katrine Riklund, et al.. (2024). New implementation of data standards for AI in oncology: Experience from the EuCanImage project. GigaScience. 14.

Fromont, Lauren A., Mauricio Moldes, Michael Baudis, et al.. (2024). Twelve quick tips for deploying a Beacon. PLoS Computational Biology. 20(3). e1011817–e1011817.

Ruiz‐Serra, Victoria, Nataly Buslón, M. P. Morales, et al.. (2024). Analyzing sex imbalance in EGA and dbGaP biological databases: Recommendations for better practices. iScience. 27(10). 110831–110831.

Daniš, Daniel, Julius O.B. Jacobsen, Alex H. Wagner, et al.. (2023). Phenopacket-tools: Building and validating GA4GH Phenopackets. PLoS ONE. 18(5). e0285433–e0285433. 4 indexed citations

Rambla, Jordi, Michael Baudis, Tim Beck, et al.. (2022). Beacon v2 and Beacon networks: A “lingua franca” for federated data discovery in biomedical genomics, and beyond. Human Mutation. 43(6). 791–799. 22 indexed citations

Rueda, Manuel, et al.. (2022). Beacon v2 Reference Implementation: a toolkit to enable federated sharing of genomic and phenotypic data. Bioinformatics. 38(19). 4656–4657. 6 indexed citations

Dyke, Stephanie O. M., Victoria Nembaware, Nchangwi Syntia Munung, et al.. (2022). Consent Codes: Maintaining Consent in an Ever-expanding Open Science Ecosystem. Neuroinformatics. 21(1). 89–100. 1 indexed citations

Arnal, Magdalena, Giorgio Bini, Dietmar Fernández‐Orth, et al.. (2022). Machine learning methods applied to genotyping data capture interactions between single nucleotide variants in late onset Alzheimer's disease. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 14(1). e12300–e12300. 6 indexed citations

Fernández‐Orth, Dietmar, Manuel Rueda, Babita Singh, et al.. (2022). A quality control portal for sequencing data deposited at the European genome–phenome archive. Briefings in Bioinformatics. 23(3). 3 indexed citations

10.

Thorogood, Adrian, Heidi L. Rehm, Peter Goodhand, et al.. (2021). International federation of genomic medicine databases using GA4GH standards. Cell Genomics. 1(2). 100032–100032. 22 indexed citations

11.

Rafajlović, Marina, Jordi Rambla, Jeffrey L. Feder, Arcadi Navarro, & Rui Faria. (2021). Inversions and genomic differentiation after secondary contact: When drift contributes to maintenance, not loss, of differentiation. Evolution. 75(6). 1288–1303. 9 indexed citations

12.

Fernández‐Orth, Dietmar, Audald Lloret‐Villas, & Jordi Rambla. (2019). European Genome-Phenome Archive (EGA) - Granular Solutions for the Next 10 Years. 4–6. 2 indexed citations

13.

Farré, Xavier, Nino Spataro, Frédéric Haziza, Jordi Rambla, & Arcadi Navarro. (2019). Genome-phenome explorer (GePhEx): a tool for the visualization and interpretation of phenotypic relationships supported by genetic evidence. Bioinformatics. 36(3). 890–896. 3 indexed citations

14.

Barrachina, Sergio, Maribel Castillo, Enrique S. Quintana–Ort́ı, et al.. (2018). FaST-LMM for Two-Way Epistasis Tests on High-Performance Clusters. Journal of Computational Biology. 25(8). 862–870. 5 indexed citations

15.

Matalonga, Leslie, Óscar Martínez, Davide Piscia, et al.. (2018). ELIXIR Implementation Study End Report: Remote real-time visualization of human rare disease genomics data (RD-Connect) stored at the EGA. Faculty of 1000 Research Ltd. 7. 1216. 1 indexed citations

16.

Dyke, Stephanie O. M., Anthony Philippakis, Jordi Rambla, et al.. (2016). Consent Codes: Upholding Standard Data Use Conditions. PLoS Genetics. 12(1). e1005772–e1005772. 49 indexed citations

17.

Santpere, Gabriel, Elena Carnero‐Montoro, Natalia Petit, et al.. (2015). Analysis of Five Gene Sets in Chimpanzees Suggests Decoupling between the Action of Selection on Protein-Coding and on Noncoding Elements. Genome Biology and Evolution. 7(6). 1490–1505. 2 indexed citations

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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