David B. Everman
Impact in
- Developmental Biology top 2%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 23
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Connective tissue disorders research 3
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- Congenital heart defects research 3
- Hedgehog Signaling Pathway Studies 3
- Co-authors
- Fiorella Gurrieri (5 shared papers)Charles E. Schwartz (10 shared papers)Ramon Y. Birnbaum (2 shared papers)Nadav Ahituv (2 shared papers)Julie R. Jones (6 shared papers)Steven A. Skinner (4 shared papers)Nathaniel H. Robin (2 shared papers)Charles Fields (2 shared papers)
- Journals
- Human Molecular Genetics (3 papers)Journal of Cell Science (2 papers)Biochemical Pharmacology (1 paper)Disease Models & Mechanisms (1 paper)Genome Research (1 paper)
- Partner nations
- United StatesCanadaItaly
In The Last Decade
David B. Everman
38 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 100
- Developmental Biology 127
- Genetics 445
- Molecular Biology 641
- Pediatrics, Perinatology and Child Health 123
- Rheumatology 81
Countries citing papers authored by David B. Everman
This map shows the geographic impact of David B. Everman'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 David B. Everman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David B. Everman more than expected).
Fields of papers citing papers by David B. Everman
This network shows the impact of papers produced by David B. Everman. 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 David B. Everman. The network helps show where David B. Everman may publish in the future.
Co-authors
The 25 scholars most cited alongside David B. Everman, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 178 | |
| 2 | 2002 | 72 | |
| 3 | 2019 | 66 | |
| 4 | 2000 | 57 | |
| 5 | 2004 | 50 | |
| 6 | 2012 | 48 | |
| 7 | 2002 | 48 | |
| 8 | 2011 | 45 | |
| 9 | 2016 | 44 | |
| 10 | 2018 | 43 | |
| 11 | 2013 | 40 | |
| 12 | 2020 | 38 | |
| 13 | 1995 | 36 | |
| 14 | 2016 | 34 | |
| 15 | 2006 | 33 | |
| 16 | 2006 | 29 | |
| 17 | 2017 | 29 | |
| 18 | 2011 | 29 | |
| 19 | 2010 | 24 | |
| 20 | 2018 | 24 |
About David B. Everman
David B. Everman is a scholar working on Genetics, Molecular Biology, Developmental Biology, Pediatrics, Perinatology and Child Health and Physiology, having authored 41 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Congenital limb and hand anomalies (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Prenatal Screening and Diagnostics (5 papers), Genomics and Rare Diseases (4 papers), Congenital heart defects research (3 papers), Hedgehog Signaling Pathway Studies (3 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Developmental Biology (127 citations), Genetics (445 citations), Molecular Biology (641 citations), Pediatrics, Perinatology and Child Health (123 citations) and Rheumatology (81 citations). David B. Everman has collaborated with scholars based in United States, Canada and Italy. Frequent co-authors include Fiorella Gurrieri, Charles E. Schwartz, Ramon Y. Birnbaum, Nadav Ahituv, Julie R. Jones, Steven A. Skinner, Nathaniel H. Robin, Charles Fields, Shoa L. Clarke and E. Josephine Clowney. Their work appears in journals such as Human Molecular Genetics, Journal of Cell Science, Biochemical Pharmacology, Disease Models & Mechanisms and Genome Research.
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.