Dawn Earl
Impact in
- Genetics top 5%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
- Neurogenetic and Muscular Disorders Research
-
- dental development and anomalies
- Hedgehog Signaling Pathway Studies
Papers in
- Genetics 9
- Connective tissue disorders research 3
- Cleft Lip and Palate Research 3
- Craniofacial Disorders and Treatments 3
- Genomic variations and chromosomal abnormalities 3
-
- Congenital heart defects research 3
- Co-authors
- John M. Graham (5 shared papers)Xiuqing Guo (2 shared papers)Jeannie Kreutzman (2 shared papers)Raymond Wang (1 shared paper)Jinrui Cui (1 shared paper)H.-J. Smith (1 shared paper)D. Sloan Stribling (1 shared paper)Elaine M. Faustman (2 shared papers)
- Journals
- The Journal of Pediatrics (3 papers)The American Journal of Human Genetics (2 papers)European Journal of Human Genetics (2 papers)Journal of Pharmacology and Experimental Therapeutics (1 paper)American Journal of Medical Genetics Part C Seminars in Medical Genetics (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Dawn Earl
14 papers receiving 502 citations
Peers
Comparison fields: 5 of 74
- Genetics 347
- Genetics 84
- Molecular Biology 245
- Developmental Biology 5
- Otorhinolaryngology 10
Countries citing papers authored by Dawn Earl
This map shows the geographic impact of Dawn Earl'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 Dawn Earl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dawn Earl more than expected).
Fields of papers citing papers by Dawn Earl
This network shows the impact of papers produced by Dawn Earl. 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 Dawn Earl. The network helps show where Dawn Earl may publish in the future.
Co-authors
The 25 scholars most cited alongside Dawn Earl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 137 | |
| 2 | 2001 | 84 | |
| 3 | 2005 | 73 | |
| 4 | 2012 | 52 | |
| 5 | 2012 | 44 | |
| 6 | 2012 | 37 | |
| 7 | 2013 | 30 | |
| 8 | 2014 | 28 | |
| 9 | 1983 | 25 | |
| 10 | 2003 | 9 | |
| 11 | 2022 | 8 | |
| 12 | 2021 | 8 | |
| 13 | 2016 | 3 | |
| 14 | 2000 | 1 | |
| 15 | 2025 | 0 |
About Dawn Earl
Dawn Earl is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Pathology and Forensic Medicine and Surgery, having authored 15 papers that have together received 539 indexed citations. Recurring topics across this work include Connective tissue disorders research (3 papers), Cleft Lip and Palate Research (3 papers), Craniofacial Disorders and Treatments (3 papers), Congenital heart defects research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Reconstructive Facial Surgery Techniques (1 paper), Biochemical Analysis and Sensing Techniques (1 paper) and Veterinary Pharmacology and Anesthesia (1 paper). The work is most often cited by research in Genetics (347 citations), Genetics (84 citations), Molecular Biology (245 citations), Developmental Biology (5 citations) and Otorhinolaryngology (10 citations). Dawn Earl has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include John M. Graham, Xiuqing Guo, Jeannie Kreutzman, Raymond Wang, Jinrui Cui, H.-J. Smith, D. Sloan Stribling, Elaine M. Faustman, James M. Swanson and Jay Shendure. Their work appears in journals such as The Journal of Pediatrics, The American Journal of Human Genetics, European Journal of Human Genetics, Journal of Pharmacology and Experimental Therapeutics and American Journal of Medical Genetics Part C Seminars in Medical 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.