Kenneth Morgan
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Inflammatory Bowel Disease
- Nephrology top 1%
- Parathyroid Disorders and Treatments
Papers in
- Genetics 61
- Inflammatory Bowel Disease 10
- Genetic Syndromes and Imprinting 9
- Evolution and Genetic Dynamics 8
- Genetics and Neurodevelopmental Disorders 8
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- Epigenetics and DNA Methylation 8
- Co-authors
- Takuya Fujiwara (23 shared papers)Webster K. Cavenee (3 shared papers)Alex Koufos (2 shared papers)Paul E. Grundy (2 shared papers)Danielle Malo (7 shared papers)Thomas J. Hudson (9 shared papers)Anna K. Naumova (10 shared papers)François Rousseau (3 shared papers)
- Journals
- Genomics (10 papers)The American Journal of Human Genetics (9 papers)The William and Mary Quarterly (5 papers)Genetics (5 papers)International Journal of Maritime History (5 papers)
- Partner nations
- CanadaUnited StatesUnited Kingdom
In The Last Decade
Kenneth Morgan
183 papers receiving 6.8k citations
Peers
Comparison fields: 5 of 175
- Genetics 2.2k
- Nephrology 354
- Molecular Biology 3.2k
- Cellular and Molecular Neuroscience 794
- Immunology 793
Countries citing papers authored by Kenneth Morgan
This map shows the geographic impact of Kenneth Morgan'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 Kenneth Morgan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kenneth Morgan more than expected).
Fields of papers citing papers by Kenneth Morgan
This network shows the impact of papers produced by Kenneth Morgan. 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 Kenneth Morgan. The network helps show where Kenneth Morgan may publish in the future.
Co-authors
The 25 scholars most cited alongside Kenneth Morgan, 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 203 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. | 1989 | 364 |
| 2 | 2006 | 326 | |
| 3 | 2000 | 299 | |
| 4 | Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome. | 1995 | 289 |
| 5 | 2007 | 249 | |
| 6 | 1994 | 226 | |
| 7 | 2004 | 209 | |
| 8 | 1988 | 209 | |
| 9 | 2003 | 196 | |
| 10 | 1998 | 195 | |
| 11 | 2002 | 188 | |
| 12 | 2000 | 164 | |
| 13 | 2000 | 152 | |
| 14 | 1994 | 148 | |
| 15 | Heritability of X chromosome--inactivation phenotype in a large family. | 1996 | 148 |
| 16 | 2005 | 128 | |
| 17 | 2000 | 127 | |
| 18 | 2005 | 124 | |
| 19 | 2007 | 113 | |
| 20 | 1997 | 113 |
About Kenneth Morgan
Kenneth Morgan is a scholar working on Genetics, Molecular Biology, Anthropology, Economics and Econometrics and Cellular and Molecular Neuroscience, having authored 203 papers that have together received 7.2k indexed citations. Recurring topics across this work include Colonialism, slavery, and trade (23 papers), Historical Economic and Social Studies (21 papers), Genetic Neurodegenerative Diseases (15 papers), Inflammatory Bowel Disease (10 papers), Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (8 papers), Evolution and Genetic Dynamics (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (2.2k citations), Nephrology (354 citations), Molecular Biology (3.2k citations), Cellular and Molecular Neuroscience (794 citations) and Immunology (793 citations). Kenneth Morgan has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Takuya Fujiwara, Webster K. Cavenee, Alex Koufos, Paul E. Grundy, Danielle Malo, Thomas J. Hudson, Anna K. Naumova, François Rousseau, Curtis Strobeck and Erwin Schurr. Their work appears in journals such as Genomics, The American Journal of Human Genetics, The William and Mary Quarterly, Genetics and International Journal of Maritime History.
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.