Clara Serra‐Juhé
- Genetics top 10%
- BRCA gene mutations in cancer 12
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 3
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- Ethics and Legal Issues in Pediatric Healthcare 5
- Prenatal Screening and Diagnostics 4
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- BRCA gene mutations in cancer 12
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 3
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- Ethics in medical practice 4
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- Congenital heart defects research 3
Clara Serra‐Juhé
23 papers receiving 531 citations
Peers
Comparison fields: 5 of 64
- Biological Psychiatry 25
- Genetics 254
- Pediatrics, Perinatology and Child Health 160
- Genetics 59
- Endocrine and Autonomic Systems 37
Countries citing papers authored by Clara Serra‐Juhé
This map shows the geographic impact of Clara Serra‐Juhé'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 Clara Serra‐Juhé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Clara Serra‐Juhé more than expected).
Fields of papers citing papers by Clara Serra‐Juhé
This network shows the impact of papers produced by Clara Serra‐Juhé. 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 Clara Serra‐Juhé. The network helps show where Clara Serra‐Juhé may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Clara Serra‐Juhé, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 6 | |
| 2 | 2023 | 9 | |
| 3 | 2020 | 1 | |
| 4 | 2020 | 2 | |
| 5 | 2019 | 39 | |
| 6 | 2019 | 30 | |
| 7 | 2019 | 20 | |
| 8 | 2018 | 26 | |
| 9 | 2017 | 15 | |
| 10 | 2017 | 26 | |
| 11 | 2017 | 8 | |
| 12 | 2017 | 29 | |
| 13 | 2017 | 13 | |
| 14 | 2015 | 94 | |
| 15 | 2015 | 22 | |
| 16 | 2013 | 13 | |
| 17 | 2012 | 18 | |
| 18 | 2012 | 21 | |
| 19 | 2011 | 69 | |
| 20 | 2009 | 73 |
About Clara Serra‐Juhé
Clara Serra‐Juhé is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and General Health Professions, having authored 23 papers that have together received 543 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (12 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Ethics and Legal Issues in Pediatric Healthcare (5 papers), Prenatal Screening and Diagnostics (4 papers), Ethics in medical practice (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Biological Psychiatry (25 citations), Genetics (254 citations) and Pediatrics, Perinatology and Child Health (160 citations). Clara Serra‐Juhé has collaborated with scholars based in Spain, Romania and Portugal. Frequent co-authors include Luis A. Pérez‐Jurado, Raquel Flores, Ivon Cuscó, Eduardo F. Tizzano, Núria Torán, Milena Paneque, Jesús Argente, Gabriel Ángel Martos‐Moreno, Ramona Moldovan and Benjamín Rodríguez‐Santiago. Their work appears in journals such as PLoS ONE, PLoS Genetics and International Journal of Obesity.
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.