Marta Bleda
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 45
- Genomics and Rare Diseases 27
- Genetics and Neurodevelopmental Disorders 8
- Genetic and Kidney Cyst Diseases 7
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- Pulmonary Hypertension Research and Treatments 13
- Co-authors
- Joaquı́n Dopazo (13 shared papers)Ignacio Medina (10 shared papers)Francisco Salavert (7 shared papers)Luz García‐Alonso (6 shared papers)José Carbonell‐Caballero (2 shared papers)Rubén R. Sánchez (4 shared papers)Roberto Alonso (3 shared papers)Joaquín Tárraga (3 shared papers)
- Journals
- Genetics in Medicine (11 papers)Scientific Reports (8 papers)Nature Communications (8 papers)The American Journal of Human Genetics (8 papers)Nucleic Acids Research (6 papers)
- Partner nations
- United KingdomUnited StatesSpain
In The Last Decade
Marta Bleda
103 papers receiving 6.2k citations
Marta Bleda's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 1.5k
- Cancer Research 463
- Pulmonary and Respiratory Medicine 1k
- Molecular Biology 2k
- Immunology 429
Countries citing papers authored by Marta Bleda
This map shows the geographic impact of Marta Bleda'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 Marta Bleda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marta Bleda more than expected).
Fields of papers citing papers by Marta Bleda
This network shows the impact of papers produced by Marta Bleda. 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 Marta Bleda. The network helps show where Marta Bleda may publish in the future.
Co-authors
The 25 scholars most cited alongside Marta Bleda, 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 105 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli Hit paper breakdown → | 2020 | 926 |
| 2 | Whole-genome sequencing of patients with rare diseases in a national health system Hit paper breakdown → | 2020 | 418 |
| 3 | 2016 | 382 | |
| 4 | Identification of rare sequence variation underlying heritable pulmonary arterial hypertension Hit paper breakdown → | 2018 | 294 |
| 5 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 6 | Substitution mutational signatures in whole-genome–sequenced cancers in the UK population Hit paper breakdown → | 2022 | 195 |
| 7 | 2016 | 179 | |
| 8 | 2020 | 179 | |
| 9 | 2019 | 178 | |
| 10 | 2018 | 174 | |
| 11 | 2018 | 155 | |
| 12 | Whole genome sequencing for the diagnosis of neurological repeat expansion disorders in the UK: a retrospective diagnostic accuracy and prospective clinical validation study Hit paper breakdown → | 2022 | 134 |
| 13 | 2017 | 114 | |
| 14 | 2021 | 106 | |
| 15 | 2019 | 102 | |
| 16 | 2020 | 101 | |
| 17 | 2015 | 100 | |
| 18 | 2020 | 83 | |
| 19 | Origins and impact of extrachromosomal DNA Hit paper breakdown → | 2024 | 82 |
| 20 | 2020 | 81 |
About Marta Bleda
Marta Bleda is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Cellular and Molecular Neuroscience, Cancer Research and Molecular Biology, having authored 105 papers that have together received 6.3k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (27 papers), Pulmonary Hypertension Research and Treatments (13 papers), Genetics and Neurodevelopmental Disorders (8 papers), Cancer Genomics and Diagnostics (8 papers), Genetic and Kidney Cyst Diseases (7 papers), Genetic Neurodegenerative Diseases (6 papers), Bioinformatics and Genomic Networks (5 papers) and Immunodeficiency and Autoimmune Disorders (5 papers). The work is most often cited by research in Genetics (1.5k citations), Cancer Research (463 citations), Pulmonary and Respiratory Medicine (1k citations), Molecular Biology (2k citations) and Immunology (429 citations). Marta Bleda has collaborated with scholars based in United Kingdom, United States and Spain. Frequent co-authors include Joaquı́n Dopazo, Ignacio Medina, Francisco Salavert, Luz García‐Alonso, José Carbonell‐Caballero, Rubén R. Sánchez, Roberto Alonso, Joaquín Tárraga, Matías Marín Falco and Cristina González. Their work appears in journals such as Genetics in Medicine, Scientific Reports, Nature Communications, The American Journal of Human Genetics and Nucleic Acids Research.
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.