Paul Flicek
Impact in
- Genetics top 0.05%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Molecular Biology top 0.1%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
Papers in
- Genetics 53
- Genomics and Rare Diseases 19
- Genomic variations and chromosomal abnormalities 13
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- Genomics and Phylogenetic Studies 55
- Genomics and Chromatin Dynamics 33
- RNA and protein synthesis mechanisms 18
- Gene expression and cancer classification 17
- RNA Research and Splicing 16
- Co-authors
- Fiona CunninghamWilliam McLarenGraham R. S. RitchieLaurent GilSarah HuntAnja ThormannHarpreet Singh RiatSteven G. E. Marsh
- Journals
- Nucleic Acids Research (15 papers)Genome Research (13 papers)Genome biology (9 papers)Bioinformatics (5 papers)Database (5 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Paul Flicek
125 papers receiving 23.4k citations
Hit Papers
Peers
Comparison fields: 5 of 187
- Genetics 8.2k
- Molecular Biology 14.2k
- Immunology 3.9k
- Cancer Research 2.8k
- Aging 179
Countries citing papers authored by Paul Flicek
This map shows the geographic impact of Paul Flicek'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 Paul Flicek with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Flicek more than expected).
Fields of papers citing papers by Paul Flicek
This network shows the impact of papers produced by Paul Flicek. 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 Paul Flicek. The network helps show where Paul Flicek may publish in the future.
Co-authors
The 25 scholars most cited alongside Paul Flicek, 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 | 2023 | 5 | |
| 2 | Sequence locally, think globally: The Darwin Tree of Life Project Hit paper breakdown → | 2022 | 172 |
| 3 | 2021 | 16 | |
| 4 | 2021 | 62 | |
| 5 | 2021 | 9 | |
| 6 | 2021 | 13 | |
| 7 | 2020 | 73 | |
| 8 | 2017 | 95 | |
| 9 | 2016 | 15 | |
| 10 | 2016 | 15 | |
| 11 | 2016 | 17 | |
| 12 | The Ensembl Variant Effect Predictor Hit paper breakdown → | 2016 | 4020 |
| 13 | 2015 | 121 | |
| 14 | 2013 | 45 | |
| 15 | The NHGRI GWAS Catalog, a curated resource of SNP-trait associations Hit paper breakdown → | 2013 | 1850 |
| 16 | 2012 | 70 | |
| 17 | 2012 | 1 | |
| 18 | Five-Vertebrate ChIP-seq Reveals the Evolutionary Dynamics of Transcription Factor Binding Hit paper breakdown → | 2010 | 535 |
| 19 | 2010 | 291 | |
| 20 | 2003 | 76 |
About Paul Flicek
Paul Flicek is a scholar working on Genetics, Molecular Biology, Cancer Research, Plant Science and Aging, having authored 125 papers that have together received 23.7k indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (55 papers), Genomics and Chromatin Dynamics (33 papers), Chromosomal and Genetic Variations (24 papers), Genomics and Rare Diseases (19 papers), RNA and protein synthesis mechanisms (18 papers), Gene expression and cancer classification (17 papers), RNA Research and Splicing (16 papers) and Genomic variations and chromosomal abnormalities (13 papers). The work is most often cited by research in Genetics (8.2k citations), Molecular Biology (14.2k citations), Immunology (3.9k citations), Cancer Research (2.8k citations) and Aging (179 citations). Paul Flicek has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Fiona Cunningham, William McLaren, Graham R. S. Ritchie, Laurent Gil, Sarah Hunt, Anja Thormann, Harpreet Singh Riat, Steven G. E. Marsh, James Robinson and Duncan T. Odom. Their work appears in journals such as Nucleic Acids Research, Genome Research, Genome biology, Bioinformatics and Database.
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.