Marta Codina‐Solà
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
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- Autism Spectrum Disorder Research
Papers in
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- RNA modifications and cancer 3
- Mitochondrial Function and Pathology 2
- Genetics 6
- Neurogenetic and Muscular Disorders Research 5
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 2
- Co-authors
- Luis A. Pérez‐Jurado (4 shared papers)Ivon Cuscó (6 shared papers)Benjamín Rodríguez‐Santiago (2 shared papers)Guillermo Antiñolo (1 shared paper)M.P. Botella (1 shared paper)Javier Santoyo‐López (1 shared paper)Elisabeth Gabau (1 shared paper)Gemma Aznar‐Laín (1 shared paper)
- Journals
- Journal of Medical Genetics (4 papers)Genetics in Medicine (2 papers)Clinical Genetics (2 papers)Genes (2 papers)European Journal of Pediatrics (1 paper)
- Partner nations
- SpainUnited StatesUnited Kingdom
In The Last Decade
Marta Codina‐Solà
20 papers receiving 224 citations
Peers
Comparison fields: 5 of 52
- Genetics 108
- Cognitive Neuroscience 65
- Genetics 23
- Molecular Biology 83
- Developmental Neuroscience 4
Countries citing papers authored by Marta Codina‐Solà
This map shows the geographic impact of Marta Codina‐Solà'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 Codina‐Solà with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marta Codina‐Solà more than expected).
Fields of papers citing papers by Marta Codina‐Solà
This network shows the impact of papers produced by Marta Codina‐Solà. 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 Codina‐Solà. The network helps show where Marta Codina‐Solà may publish in the future.
Co-authors
The 25 scholars most cited alongside Marta Codina‐Solà, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 91 | |
| 2 | 2016 | 33 | |
| 3 | 2015 | 19 | |
| 4 | 2017 | 15 | |
| 5 | 2019 | 11 | |
| 6 | 2022 | 10 | |
| 7 | 2024 | 8 | |
| 8 | 2021 | 7 | |
| 9 | 2022 | 6 | |
| 10 | 2024 | 6 | |
| 11 | 2021 | 5 | |
| 12 | 2023 | 3 | |
| 13 | 2023 | 2 | |
| 14 | 2022 | 2 | |
| 15 | 2020 | 2 | |
| 16 | 2022 | 2 | |
| 17 | 2024 | 2 | |
| 18 | 2023 | 1 | |
| 19 | 2023 | 1 | |
| 20 | 2024 | 1 |
About Marta Codina‐Solà
Marta Codina‐Solà is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Cognitive Neuroscience, having authored 22 papers that have together received 227 indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (5 papers), Autism Spectrum Disorder Research (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), RNA modifications and cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Rare Diseases (2 papers), Family and Disability Support Research (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Genetics (108 citations), Cognitive Neuroscience (65 citations), Genetics (23 citations), Molecular Biology (83 citations) and Developmental Neuroscience (4 citations). Marta Codina‐Solà has collaborated with scholars based in Spain, United States and United Kingdom. Frequent co-authors include Luis A. Pérez‐Jurado, Ivon Cuscó, Benjamín Rodríguez‐Santiago, Guillermo Antiñolo, M.P. Botella, Javier Santoyo‐López, Elisabeth Gabau, Gemma Aznar‐Laín, Blanca Gener and Miguel Del Campo. Their work appears in journals such as Journal of Medical Genetics, Genetics in Medicine, Clinical Genetics, Genes and European Journal of Pediatrics.
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.