Dawn Earl

2.8k citations
15 papers · 544 · h-index 10

Impact in

  • Genetics top 5%
    • Craniofacial Disorders and Treatments
    • Cleft Lip and Palate Research
    • Genomic variations and chromosomal abnormalities
    • Neurogenetic and Muscular Disorders Research
    • Congenital Ear and Nasal Anomalies
    • Genetics and Neurodevelopmental Disorders
    • dental development and anomalies
    • RNA modifications and cancer

Papers in

    • Genomic variations and chromosomal abnormalities 3
    • Craniofacial Disorders and Treatments 3
    • Connective tissue disorders research 2
    • Genetics and Neurodevelopmental Disorders 1
    • Congenital heart defects research 2

Dawn Earl

14 papers receiving 508 citations

Peers

Dawn Earl
Comparison fields: 5 of 68
  • Genetics 326
  • Genetics 71
  • Molecular Biology 184
  • Developmental Biology 5
  • Otorhinolaryngology 9
Replace Beate Mitulla with:
Beate Mitulla Germany
Navid Almadani Iran
Josephine Wincent Sweden
Luciano Abreu Brito Brazil
Margo Whiteford United Kingdom
Thomas A. Maher United States
Janet M. Stewart United States
Heraldo Mendes Garmes Brazil
Ray E. Shenefelt United States
Maria Tereza Matias Baptista Brazil
Dawn Earl relative to Beate Mitulla Germany Beate Mitulla's profile →
Citations per field
00.5×3.4×
Beate Mitulla · 1×
Citations per year

Countries citing papers authored by Dawn Earl

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Dawn Earl Line = papers co-authored together Dawn Earl links everyone, so they are left out of the graph.

All Works

15 of 15 papers shown
#Work
1 2005138
2 200184
3 200575
4 201252
5 201244
6 201237
7 201330
8 201430
9 198325
10 20039
11 20228
12 20218
13 20163
14 20001
15 20250

About Dawn Earl

Dawn Earl is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine and Surgery, having authored 15 papers that have together received 544 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Craniofacial Disorders and Treatments (3 papers), Congenital heart defects research (2 papers), Connective tissue disorders research (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Soft tissue tumors and treatment (1 paper), Microgrid Control and Optimization (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (326 citations), Genetics (71 citations), Molecular Biology (184 citations), Developmental Biology (5 citations) and Otorhinolaryngology (9 citations). Dawn Earl has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include John M. Graham, Xiuqing Guo, Jeannie Kreutzman, Raymond Wang, Jinrui Cui, H.-J. Smith, D. Sloan Stribling, James M. Swanson, Jennifer E. Below and Elaine M. Faustman. Their work appears in journals such as The Journal of Pediatrics, European Journal of Human Genetics, The American Journal of Human Genetics, Genetics in Medicine and Human 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.

Explore authors with similar magnitude of impact