Michael E. Weale
- Genetics top 0.5%
- Genetic Associations and Epidemiology 26
- Forensic and Genetic Research 14
- Genetic diversity and population structure 10
- Genetic Mapping and Diversity in Plants and Animals 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Neurology top 2%
- Psychiatry and Mental health top 2%
- Pharmacology top 1%
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- Gene expression and cancer classification 9
- Bioinformatics and Genomic Networks 8
- Co-authors
- David B. GoldsteinJohn HardyMark ThomasMina RytenNicholas WoodNeil BradmanAlice C. SmithDaniah Trabzuni
- Journals
- The American Journal of Human Genetics (5 papers)Nature Genetics (4 papers)European Journal of Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Michael E. Weale
94 papers receiving 5.9k citations
Hit Papers
Peers
Comparison fields: 5 of 169
- Genetics 2.7k
- Neurology 352
- Psychiatry and Mental health 585
- Pharmacology 330
- Pediatrics, Perinatology and Child Health 644
Countries citing papers authored by Michael E. Weale
This map shows the geographic impact of Michael E. Weale'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 Michael E. Weale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael E. Weale more than expected).
Fields of papers citing papers by Michael E. Weale
This network shows the impact of papers produced by Michael E. Weale. 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 Michael E. Weale. The network helps show where Michael E. Weale may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Michael E. Weale, 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 | 9 | |
| 2 | 2021 | 96 | |
| 3 | 2018 | 16 | |
| 4 | 2017 | 186 | |
| 5 | 2017 | 150 | |
| 6 | 2017 | 9 | |
| 7 | 2013 | 66 | |
| 8 | 2013 | 138 | |
| 9 | 2012 | 45 | |
| 10 | 2012 | 100 | |
| 11 | 2011 | 29 | |
| 12 | 2011 | 145 | |
| 13 | 2008 | 30 | |
| 14 | 2007 | 37 | |
| 15 | Common variation in the SCN1A gene is a risk factor for common forms of epilepsy associated with febrile seizures | 2004 | 8 |
| 16 | 2004 | 98 | |
| 17 | Rare deep-rooting Y chromosome lineages in humans | 2003 | 2 |
| 18 | 2002 | 77 | |
| 19 | 2001 | 110 | |
| 20 | 2001 | 51 |
About Michael E. Weale
Michael E. Weale is a scholar working on Genetics, Neurology and Molecular Biology, having authored 95 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (26 papers), Forensic and Genetic Research (14 papers), Genetic diversity and population structure (10 papers), Gene expression and cancer classification (9 papers), Bioinformatics and Genomic Networks (8 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), Genomics and Rare Diseases (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Genetics (2.7k citations), Neurology (352 citations) and Psychiatry and Mental health (585 citations). Michael E. Weale has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include David B. Goldstein, John Hardy, Mark Thomas, Mina Ryten, Nicholas Wood, Neil Bradman, Alice C. Smith, Daniah Trabzuni, Robert Walker and Colin Smith. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, European Journal of Human Genetics, Human Molecular Genetics and Journal of Neurochemistry.
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.