Ivon Cuscó
Impact in
- Genetics top 1%
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 10%
- RNA modifications and cancer
- RNA Research and Splicing
- Congenital heart defects research
Papers in
-
- RNA modifications and cancer 11
- Congenital heart defects research 6
- Genetics 17
- Neurogenetic and Muscular Disorders Research 17
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 4
- Co-authors
- Eduardo F. Tizzano (23 shared papers)Luis A. Pérez‐Jurado (18 shared papers)Montserrat Baiget (11 shared papers)M. J. Barceló (9 shared papers)Raquel Flores (6 shared papers)Sara Bernal (4 shared papers)Laura Alías (3 shared papers)Pablo Fuentes‐Prior (3 shared papers)
- Journals
- PLoS ONE (3 papers)Human Mutation (3 papers)Neurology (3 papers)Neuromuscular Disorders (2 papers)Genome Research (2 papers)
- Partner nations
- SpainUnited StatesFrance
In The Last Decade
Ivon Cuscó
42 papers receiving 1.5k citations
Ivon Cuscó's Hit Papers
Peers
Comparison fields: 5 of 86
- Genetics 736
- Genetics 408
- Molecular Biology 843
- Developmental Neuroscience 35
- Cognitive Neuroscience 166
Countries citing papers authored by Ivon Cuscó
This map shows the geographic impact of Ivon Cuscó'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 Ivon Cuscó with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ivon Cuscó more than expected).
Fields of papers citing papers by Ivon Cuscó
This network shows the impact of papers produced by Ivon Cuscó. 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 Ivon Cuscó. The network helps show where Ivon Cuscó may publish in the future.
Co-authors
The 25 scholars most cited alongside Ivon Cuscó, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases Hit paper breakdown → | 2018 | 313 |
| 2 | 2015 | 99 | |
| 3 | 2015 | 91 | |
| 4 | 2005 | 87 | |
| 5 | 2009 | 87 | |
| 6 | 2009 | 76 | |
| 7 | 2014 | 74 | |
| 8 | 2008 | 56 | |
| 9 | 2018 | 50 | |
| 10 | 2012 | 48 | |
| 11 | 2005 | 41 | |
| 12 | 2019 | 38 | |
| 13 | 2020 | 38 | |
| 14 | 2003 | 38 | |
| 15 | 2001 | 36 | |
| 16 | 2012 | 35 | |
| 17 | 2004 | 34 | |
| 18 | 2016 | 33 | |
| 19 | 2021 | 31 | |
| 20 | 2008 | 27 |
About Ivon Cuscó
Ivon Cuscó is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Cognitive Neuroscience, having authored 43 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (17 papers), RNA modifications and cancer (11 papers), Genetics and Neurodevelopmental Disorders (8 papers), Congenital Anomalies and Fetal Surgery (7 papers), Congenital heart defects research (6 papers), Autism Spectrum Disorder Research (6 papers), Williams Syndrome Research (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Genetics (736 citations), Genetics (408 citations), Molecular Biology (843 citations), Developmental Neuroscience (35 citations) and Cognitive Neuroscience (166 citations). Ivon Cuscó has collaborated with scholars based in Spain, United States and France. Frequent co-authors include Eduardo F. Tizzano, Luis A. Pérez‐Jurado, Montserrat Baiget, M. J. Barceló, Raquel Flores, Sara Bernal, Laura Alías, Pablo Fuentes‐Prior, Maite Calucho and Concepción Hernández-Chico. Their work appears in journals such as PLoS ONE, Human Mutation, Neurology, Neuromuscular Disorders and Genome 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.