K E Davies
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
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- Epigenetics and DNA Methylation
- Muscle Physiology and Disorders
Papers in
-
- Muscle Physiology and Disorders 9
- RNA modifications and cancer 3
- DNA and Nucleic Acid Chemistry 3
- Genetics 7
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Cassandra L. Smith (1 shared paper)C R Cantor (1 shared paper)Karl J. A. McCullagh (1 shared paper)RA Hirst (1 shared paper)J. Weissenbach (2 shared papers)Lucy Bowden (2 shared papers)Wendy Dean (2 shared papers)Jörn Walter (2 shared papers)
- Journals
- The American Journal of Human Genetics (5 papers)Cytogenetic and Genome Research (3 papers)Aphasiology (2 papers)Neuromuscular Disorders (2 papers)Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics (1 paper)
- Partner nations
- United KingdomCanadaGermany
In The Last Decade
K E Davies
38 papers receiving 990 citations
Peers
Comparison fields: 5 of 104
- Genetics 405
- Molecular Biology 613
- Genetics 62
- Hematology 64
- Clinical Biochemistry 37
Countries citing papers authored by K E Davies
This map shows the geographic impact of K E Davies'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 K E Davies with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K E Davies more than expected).
Fields of papers citing papers by K E Davies
This network shows the impact of papers produced by K E Davies. 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 K E Davies. The network helps show where K E Davies may publish in the future.
Co-authors
The 25 scholars most cited alongside K E Davies, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Pulsed-field gel electrophoresis and the technology of large DNA molecules. | 1988 | 175 |
| 2 | 1998 | 92 | |
| 3 | Human genetic diseases : a practical approach | 1986 | 83 |
| 4 | 1989 | 80 | |
| 5 | 2000 | 79 | |
| 6 | 1987 | 74 | |
| 7 | 2003 | 73 | |
| 8 | Utrophin upregulation in Duchenne muscular dystrophy. | 2005 | 67 |
| 9 | Detection of single base changes in DNA : Ribonuclease cleavage and denaturing gradient gel electrophoresis | 1988 | 55 |
| 10 | 1989 | 54 | |
| 11 | 1996 | 37 | |
| 12 | Microdissection of the fragile X region. | 1990 | 32 |
| 13 | The turnover rate of muscle and liver protein in sheep. | 1975 | 23 |
| 14 | 2019 | 18 | |
| 15 | 1985 | 15 | |
| 16 | Genome rearrangement and stability | 1995 | 6 |
| 17 | Increased muscle lim protein expression associated with mild muscular dystrophy and with exercise | 2001 | 6 |
| 18 | Integrated dystrophin analysis using immunocytochemical, biochemical and genetic techniques. | 1990 | 6 |
| 19 | Genome maps and neurological disorders | 1993 | 5 |
| 20 | 1986 | 5 |
About K E Davies
K E Davies is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Cell Biology and Genetics, having authored 40 papers that have together received 1.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (9 papers), Neurobiology of Language and Bilingualism (5 papers), Nerve injury and regeneration (3 papers), Biotin and Related Studies (3 papers), Language Development and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), RNA modifications and cancer (3 papers) and DNA and Nucleic Acid Chemistry (3 papers). The work is most often cited by research in Genetics (405 citations), Molecular Biology (613 citations), Genetics (62 citations), Hematology (64 citations) and Clinical Biochemistry (37 citations). K E Davies has collaborated with scholars based in United Kingdom, Canada and Germany. Frequent co-authors include Cassandra L. Smith, C R Cantor, Karl J. A. McCullagh, RA Hirst, J. Weissenbach, Lucy Bowden, Wendy Dean, Jörn Walter, Wolf Reik and Val C. Sheffield. Their work appears in journals such as The American Journal of Human Genetics, Cytogenetic and Genome Research, Aphasiology, Neuromuscular Disorders and Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics.
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.