Pilar Cacheiro
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
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- Genetic Neurodegenerative Diseases
Papers in
- Genetics 12
- Genomics and Rare Diseases 10
- Genetics and Neurodevelopmental Disorders 1
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- Animal testing and alternatives 1
- Co-authors
- Damian P. Smedley (9 shared papers)Melissa Anne Haendel (1 shared paper)Hamed Haseli Mashhadi (2 shared papers)Helen E. Parkinson (3 shared papers)Robert J. Wilson (2 shared papers)Sara E. Wells (2 shared papers)Tudor Groza (1 shared paper)Violeta Muñoz‐Fuentes (1 shared paper)
- Journals
- Mammalian Genome (3 papers)Disease Models & Mechanisms (2 papers)Nucleic Acids Research (2 papers)Prenatal Diagnosis (1 paper)Nature Communications (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Pilar Cacheiro
25 papers receiving 1.1k citations
Pilar Cacheiro's Hit Papers
Peers
Comparison fields: 5 of 61
- Genetics 288
- Cellular and Molecular Neuroscience 82
- Sensory Systems 20
- Molecular Biology 156
- Pediatrics, Perinatology and Child Health 28
Countries citing papers authored by Pilar Cacheiro
This map shows the geographic impact of Pilar Cacheiro'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 Pilar Cacheiro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pilar Cacheiro more than expected).
Fields of papers citing papers by Pilar Cacheiro
This network shows the impact of papers produced by Pilar Cacheiro. 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 Pilar Cacheiro. The network helps show where Pilar Cacheiro may publish in the future.
Co-authors
The 25 scholars most cited alongside Pilar Cacheiro, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. Hit paper breakdown → | 2021 | 290 |
| 2 | The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease Hit paper breakdown → | 2022 | 254 |
| 3 | 2018 | 85 | |
| 4 | 2020 | 81 | |
| 5 | 2012 | 80 | |
| 6 | 2021 | 71 | |
| 7 | 2019 | 51 | |
| 8 | 2022 | 39 | |
| 9 | 2023 | 31 | |
| 10 | 2014 | 28 | |
| 11 | 2016 | 20 | |
| 12 | 2012 | 11 | |
| 13 | 2022 | 9 | |
| 14 | 2024 | 9 | |
| 15 | 2025 | 9 | |
| 16 | 2017 | 7 | |
| 17 | 2023 | 5 | |
| 18 | 2023 | 5 | |
| 19 | 2024 | 5 | |
| 20 | 2024 | 5 |
About Pilar Cacheiro
Pilar Cacheiro is a scholar working on Genetics, Small Animals, Cellular and Molecular Neuroscience, Molecular Biology and Neurology, having authored 27 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Genetics and Neurodevelopmental Disorders (1 paper), Animal testing and alternatives (1 paper), Migraine and Headache Studies (1 paper), Ion channel regulation and function (1 paper), Biomedical Text Mining and Ontologies (1 paper), Parkinson's Disease Mechanisms and Treatments (1 paper) and Genetic Neurodegenerative Diseases (1 paper). The work is most often cited by research in Genetics (288 citations), Cellular and Molecular Neuroscience (82 citations), Sensory Systems (20 citations), Molecular Biology (156 citations) and Pediatrics, Perinatology and Child Health (28 citations). Pilar Cacheiro has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Damian P. Smedley, Melissa Anne Haendel, Hamed Haseli Mashhadi, Helen E. Parkinson, Robert J. Wilson, Sara E. Wells, Tudor Groza, Violeta Muñoz‐Fuentes, Ann‐Marie Mallon and Piia Keskivali-Bond. Their work appears in journals such as Mammalian Genome, Disease Models & Mechanisms, Nucleic Acids Research, Prenatal Diagnosis and Nature Communications.
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.