Laura Alías
Impact in
Papers in
- Genetics 21
- Neurogenetic and Muscular Disorders Research 21
- Genetics and Neurodevelopmental Disorders 2
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- RNA modifications and cancer 12
- Muscle Physiology and Disorders 2
- Cancer-related gene regulation 2
- Co-authors
- Eduardo F. Tizzano (23 shared papers)Sara Bernal (20 shared papers)Rebeca Martínez‐Hernández (12 shared papers)Pablo Fuentes‐Prior (5 shared papers)Francisco Javier Álvarez Rodríguez (4 shared papers)José M. Millán (4 shared papers)Concepción Hernández-Chico (4 shared papers)Ivon Cuscó (3 shared papers)
- Journals
- Neuromuscular Disorders (4 papers)European Journal of Human Genetics (3 papers)Journal of Neuropathology & Experimental Neurology (2 papers)Frontiers in Genetics (1 paper)Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (1 paper)
- Partner nations
- SpainArgentinaUnited States
In The Last Decade
Laura Alías
27 papers receiving 1.0k citations
Laura Alías's Hit Papers
Peers
Comparison fields: 5 of 51
- Genetics 953
- Surgery 397
- Molecular Biology 672
- Neurology 39
- Genetics 56
Countries citing papers authored by Laura Alías
This map shows the geographic impact of Laura Alías'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 Laura Alías with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Alías more than expected).
Fields of papers citing papers by Laura Alías
This network shows the impact of papers produced by Laura Alías. 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 Laura Alías. The network helps show where Laura Alías may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura Alías, 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 28 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 | 319 |
| 2 | 2008 | 137 | |
| 3 | 2009 | 82 | |
| 4 | 2012 | 75 | |
| 5 | 2011 | 56 | |
| 6 | 2020 | 38 | |
| 7 | 2014 | 34 | |
| 8 | 2013 | 32 | |
| 9 | 2021 | 32 | |
| 10 | 2011 | 29 | |
| 11 | 2015 | 29 | |
| 12 | 2018 | 29 | |
| 13 | 2011 | 28 | |
| 14 | 2010 | 25 | |
| 15 | 2016 | 18 | |
| 16 | 2004 | 15 | |
| 17 | 2010 | 14 | |
| 18 | 2007 | 13 | |
| 19 | 2011 | 11 | |
| 20 | 2021 | 10 |
About Laura Alías
Laura Alías is a scholar working on Genetics, Molecular Biology, Surgery, Genetics and Cell Biology, having authored 28 papers that have together received 1.1k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (21 papers), RNA modifications and cancer (12 papers), Congenital Anomalies and Fetal Surgery (9 papers), Genetics and Neurodevelopmental Disorders (2 papers), Muscle Physiology and Disorders (2 papers), Cardiac Structural Anomalies and Repair (2 papers), Cancer-related gene regulation (2 papers) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Genetics (953 citations), Surgery (397 citations), Molecular Biology (672 citations), Neurology (39 citations) and Genetics (56 citations). Laura Alías has collaborated with scholars based in Spain, Argentina and United States. Frequent co-authors include Eduardo F. Tizzano, Sara Bernal, Rebeca Martínez‐Hernández, Pablo Fuentes‐Prior, Francisco Javier Álvarez Rodríguez, José M. Millán, Concepción Hernández-Chico, Ivon Cuscó, Maite Calucho and Eva Also‐Rallo. Their work appears in journals such as Neuromuscular Disorders, European Journal of Human Genetics, Journal of Neuropathology & Experimental Neurology, Frontiers in Genetics and Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.
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.