Michael E. Weale
Impact in
Papers in
- Genetics 47
- Genetic Associations and Epidemiology 24
- Forensic and Genetic Research 14
- Genetic diversity and population structure 9
- Genetic Mapping and Diversity in Plants and Animals 6
- Genomic variations and chromosomal abnormalities 5
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- Gene expression and cancer classification 7
- Bioinformatics and Genomic Networks 6
- RNA Research and Splicing 5
- Co-authors
- Mina Ryten (17 shared papers)John Hardy (17 shared papers)David B. Goldstein (11 shared papers)Mark Thomas (21 shared papers)Neil Bradman (20 shared papers)Daniah Trabzuni (13 shared papers)Colin Smith (11 shared papers)Robert Walker (11 shared papers)
- Journals
- The American Journal of Human Genetics (4 papers)Human Genetics (3 papers)PLoS ONE (3 papers)Human Molecular Genetics (3 papers)European Journal of Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
Michael E. Weale
90 papers receiving 5.6k citations
Michael E. Weale's Hit Papers
Peers
Comparison fields: 5 of 163
- Genetics 2.3k
- Neurology 308
- Psychiatry and Mental health 445
- Pharmacology 262
- Pediatrics, Perinatology and Child Health 477
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-authors
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
Showing the 20 most-cited of 91 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 488 | |
| 2 | Genetic variability in the regulation of gene expression in ten regions of the human brain Hit paper breakdown → | 2014 | 416 |
| 3 | 2001 | 335 | |
| 4 | 2013 | 219 | |
| 5 | 2017 | 191 | |
| 6 | 2003 | 184 | |
| 7 | 2012 | 173 | |
| 8 | 2017 | 166 | |
| 9 | 2006 | 161 | |
| 10 | 2005 | 161 | |
| 11 | 2013 | 158 | |
| 12 | 2017 | 152 | |
| 13 | 2011 | 147 | |
| 14 | 2013 | 139 | |
| 15 | 2002 | 123 | |
| 16 | 2004 | 116 | |
| 17 | 2001 | 110 | |
| 18 | 2009 | 105 | |
| 19 | 2015 | 102 | |
| 20 | 2012 | 100 |
About Michael E. Weale
Michael E. Weale is a scholar working on Genetics, Molecular Biology, Physiology, Immunology and Neurology, having authored 91 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (24 papers), Forensic and Genetic Research (14 papers), Genetic diversity and population structure (9 papers), Gene expression and cancer classification (7 papers), Genetic Mapping and Diversity in Plants and Animals (6 papers), Bioinformatics and Genomic Networks (6 papers), RNA Research and Splicing (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). The work is most often cited by research in Genetics (2.3k citations), Neurology (308 citations), Psychiatry and Mental health (445 citations), Pharmacology (262 citations) and Pediatrics, Perinatology and Child Health (477 citations). Michael E. Weale has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Mina Ryten, John Hardy, David B. Goldstein, Mark Thomas, Neil Bradman, Daniah Trabzuni, Colin Smith, Robert Walker, Alice C. Smith and Adaikalavan Ramasamy. Their work appears in journals such as The American Journal of Human Genetics, Human Genetics, PLoS ONE, Human Molecular Genetics and European Journal of Human Genetics.
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.