Greg Elgar
Impact in
- Molecular Biology top 2%
- Genomics and Chromatin Dynamics
- Genomics and Phylogenetic Studies
- RNA and protein synthesis mechanisms
- Developmental Biology and Gene Regulation
- RNA Research and Splicing
- Genetics top 1%
- Animal Genetics and Reproduction
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Genomics and Chromatin Dynamics 34
- RNA and protein synthesis mechanisms 22
- Genomics and Phylogenetic Studies 19
- Developmental Biology and Gene Regulation 16
- Congenital heart defects research 11
- Genetics 33
- Animal Genetics and Reproduction 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 10
- Co-authors
- Tanya Vavouri (10 shared papers)Sydney Brenner (13 shared papers)Adam Woolfe (8 shared papers)Debbie K. Goode (15 shared papers)Byrappa Venkatesh (3 shared papers)Samuel Aparício (3 shared papers)Heather Callaway (9 shared papers)Gayle K. McEwen (7 shared papers)
- Journals
- Gene (11 papers)Trends in Genetics (5 papers)Mammalian Genome (5 papers)Genomics (5 papers)PLoS ONE (5 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Greg Elgar
111 papers receiving 4.3k citations
Hit Papers
Peers
Comparison fields: 5 of 122
- Molecular Biology 3.3k
- Genetics 1.3k
- Aging 45
- Plant Science 951
- Cancer Research 311
Countries citing papers authored by Greg Elgar
This map shows the geographic impact of Greg Elgar'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 Greg Elgar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Greg Elgar more than expected).
Fields of papers citing papers by Greg Elgar
This network shows the impact of papers produced by Greg Elgar. 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 Greg Elgar. The network helps show where Greg Elgar may publish in the future.
Co-authors
The 25 scholars most cited alongside Greg Elgar, 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 111 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development Hit paper breakdown → | 2004 | 723 |
| 2 | Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome Hit paper breakdown → | 1993 | 479 |
| 3 | 1996 | 134 | |
| 4 | 2008 | 128 | |
| 5 | 2012 | 122 | |
| 6 | 1995 | 116 | |
| 7 | 2022 | 107 | |
| 8 | 1998 | 99 | |
| 9 | 2016 | 88 | |
| 10 | 2006 | 84 | |
| 11 | 2007 | 83 | |
| 12 | 1996 | 80 | |
| 13 | 1999 | 73 | |
| 14 | 2002 | 73 | |
| 15 | 2009 | 71 | |
| 16 | 1999 | 70 | |
| 17 | 1998 | 69 | |
| 18 | 2003 | 69 | |
| 19 | 2005 | 62 | |
| 20 | 1996 | 61 |
About Greg Elgar
Greg Elgar is a scholar working on Molecular Biology, Genetics, Plant Science, Immunology and Cellular and Molecular Neuroscience, having authored 111 papers that have together received 4.4k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (34 papers), Chromosomal and Genetic Variations (22 papers), RNA and protein synthesis mechanisms (22 papers), Animal Genetics and Reproduction (22 papers), Genomics and Phylogenetic Studies (19 papers), Developmental Biology and Gene Regulation (16 papers), Congenital heart defects research (11 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). The work is most often cited by research in Molecular Biology (3.3k citations), Genetics (1.3k citations), Aging (45 citations), Plant Science (951 citations) and Cancer Research (311 citations). Greg Elgar has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Tanya Vavouri, Sydney Brenner, Adam Woolfe, Debbie K. Goode, Byrappa Venkatesh, Samuel Aparício, Heather Callaway, Gayle K. McEwen, Yvonne J. K. Edwards and Melody S. Clark. Their work appears in journals such as Gene, Trends in Genetics, Mammalian Genome, Genomics and PLoS ONE.
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.