Catherine E. Keegan
Impact in
Papers in
-
- Sexual Differentiation and Disorders 13
- Renal and related cancers 5
- Epigenetics and DNA Methylation 5
- Genetics 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
- Co-authors
- Gary D. Hammer (10 shared papers)Mark Hannibal (3 shared papers)Jeffrey W. Innis (5 shared papers)William A. Paznekas (1 shared paper)Simeon A. Boyadjiev (1 shared paper)Robert E. Shapiro (1 shared paper)Mary Beth Dinulos (1 shared paper)Ethylin Wang Jabs (1 shared paper)
- Journals
- Human Molecular Genetics (3 papers)Genetics in Medicine (3 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (3 papers)Journal of Pediatric and Adolescent Gynecology (2 papers)Mammalian Genome (2 papers)
- Partner nations
- United StatesPolandUnited Kingdom
In The Last Decade
Catherine E. Keegan
67 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 102
- Urology 165
- Aging 51
- Behavioral Neuroscience 94
- Genetics 703
- Molecular Biology 1.5k
Countries citing papers authored by Catherine E. Keegan
This map shows the geographic impact of Catherine E. Keegan'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 Catherine E. Keegan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine E. Keegan more than expected).
Fields of papers citing papers by Catherine E. Keegan
This network shows the impact of papers produced by Catherine E. Keegan. 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 Catherine E. Keegan. The network helps show where Catherine E. Keegan may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine E. Keegan, 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 68 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 488 | |
| 2 | 2007 | 151 | |
| 3 | 2008 | 140 | |
| 4 | 2002 | 138 | |
| 5 | 2009 | 97 | |
| 6 | 1994 | 97 | |
| 7 | 2014 | 87 | |
| 8 | 2002 | 77 | |
| 9 | 2004 | 58 | |
| 10 | 2015 | 52 | |
| 11 | 2015 | 50 | |
| 12 | 2018 | 44 | |
| 13 | 2007 | 42 | |
| 14 | 2017 | 42 | |
| 15 | 2018 | 40 | |
| 16 | 2016 | 40 | |
| 17 | 1995 | 36 | |
| 18 | 2020 | 34 | |
| 19 | 2002 | 34 | |
| 20 | 2013 | 32 |
About Catherine E. Keegan
Catherine E. Keegan is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Physiology and Urology, having authored 68 papers that have together received 2.3k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (13 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Telomeres, Telomerase, and Senescence (10 papers), Urological Disorders and Treatments (10 papers), Renal and related cancers (5 papers), Epigenetics and DNA Methylation (5 papers), Metabolism and Genetic Disorders (5 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Urology (165 citations), Aging (51 citations), Behavioral Neuroscience (94 citations), Genetics (703 citations) and Molecular Biology (1.5k citations). Catherine E. Keegan has collaborated with scholars based in United States, Poland and United Kingdom. Frequent co-authors include Gary D. Hammer, Mark Hannibal, Jeffrey W. Innis, William A. Paznekas, Simeon A. Boyadjiev, Robert E. Shapiro, Mary Beth Dinulos, Ethylin Wang Jabs, Bernd Wollnik and Otto Daniëls. Their work appears in journals such as Human Molecular Genetics, Genetics in Medicine, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Journal of Pediatric and Adolescent Gynecology and Mammalian Genome.
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.