Pilar Cacheiro
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 12
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 3
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- Biomedical Text Mining and Ontologies 7
- Bioinformatics and Genomic Networks 5
- CRISPR and Genetic Engineering 3
- Single-cell and spatial transcriptomics 3
- Co-authors
- Damian P. Smedley (9 shared papers)Melissa Anne Haendel (1 shared paper)Robert J. Wilson (3 shared papers)Helen E. Parkinson (3 shared papers)Sara Wells (2 shared papers)Violeta Muñoz‐Fuentes (1 shared paper)Federico López (2 shared papers)Aaron McCoy (1 shared paper)
- Journals
- Mammalian Genome (3 papers)Disease Models & Mechanisms (2 papers)Nucleic Acids Research (2 papers)Journal of the Neurological Sciences (1 paper)Nature (1 paper)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Pilar Cacheiro
26 papers receiving 1.1k citations
Pilar Cacheiro's Hit Papers
Peers
Comparison fields: 5 of 109
- Genetics 408
- Aging 18
- Molecular Biology 548
- Cellular and Molecular Neuroscience 115
- Cancer Research 73
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 28 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 | 241 |
| 3 | 2018 | 84 | |
| 4 | 2020 | 78 | |
| 5 | 2012 | 78 | |
| 6 | 2021 | 69 | |
| 7 | 2019 | 51 | |
| 8 | 2022 | 39 | |
| 9 | 2023 | 31 | |
| 10 | 2014 | 28 | |
| 11 | 2016 | 19 | |
| 12 | 2012 | 11 | |
| 13 | 2022 | 8 | |
| 14 | 2017 | 7 | |
| 15 | 2024 | 7 | |
| 16 | 2025 | 7 | |
| 17 | 2023 | 5 | |
| 18 | 2024 | 5 | |
| 19 | 2024 | 5 | |
| 20 | 2023 | 4 |
About Pilar Cacheiro
Pilar Cacheiro is a scholar working on Genetics, Molecular Biology, Cancer Research, Pediatrics, Perinatology and Child Health and Cellular and Molecular Neuroscience, having authored 28 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Biomedical Text Mining and Ontologies (7 papers), Bioinformatics and Genomic Networks (5 papers), CRISPR and Genetic Engineering (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Single-cell and spatial transcriptomics (3 papers), Cancer Genomics and Diagnostics (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (408 citations), Aging (18 citations), Molecular Biology (548 citations), Cellular and Molecular Neuroscience (115 citations) and Cancer Research (73 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, Robert J. Wilson, Helen E. Parkinson, Sara Wells, Violeta Muñoz‐Fuentes, Federico López, Aaron McCoy, Piia Keskivali-Bond and Anthony Frost. Their work appears in journals such as Mammalian Genome, Disease Models & Mechanisms, Nucleic Acids Research, Journal of the Neurological Sciences and Nature.
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.