Devin M. Cox
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
- Congenital Ear and Nasal Anomalies 2
- Genomics and Rare Diseases 1
- Genetic Syndromes and Imprinting 1
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- Congenital heart defects research 5
- Glycosylation and Glycoproteins Research 1
- Co-authors
- Merlin G. Butler (7 shared papers)Ann Genovese (1 shared paper)Doreen Granpeesheh (1 shared paper)John M. Slattery (1 shared paper)Shirish Damle (1 shared paper)Michael J. Goldenthal (1 shared paper)Agustín Legido (1 shared paper)Marie Tippett (1 shared paper)
- Journals
- Journal of Pediatric Genetics (3 papers)Cytogenetic and Genome Research (1 paper)International Journal of Molecular Sciences (1 paper)Scientific Reports (1 paper)Clinical Pediatrics (1 paper)
- Partner nations
- United StatesJapan
In The Last Decade
Devin M. Cox
9 papers receiving 298 citations
Peers
Comparison fields: 5 of 43
- Genetics 230
- Developmental Neuroscience 15
- Pediatrics, Perinatology and Child Health 44
- Cognitive Neuroscience 48
- Molecular Biology 141
Countries citing papers authored by Devin M. Cox
This map shows the geographic impact of Devin M. Cox'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 Devin M. Cox with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Devin M. Cox more than expected).
Fields of papers citing papers by Devin M. Cox
This network shows the impact of papers produced by Devin M. Cox. 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 Devin M. Cox. The network helps show where Devin M. Cox may publish in the future.
Co-authors
The 20 scholars most cited alongside Devin M. Cox, 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 | 2015 | 169 | |
| 2 | 2016 | 38 | |
| 3 | 2015 | 34 | |
| 4 | 2016 | 29 | |
| 5 | 2015 | 15 | |
| 6 | 2016 | 12 | |
| 7 | 2018 | 10 | |
| 8 | 2015 | 6 | |
| 9 | 2015 | 3 |
About Devin M. Cox
Devin M. Cox is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Developmental Neuroscience, having authored 9 papers that have together received 316 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Williams Syndrome Research (1 paper), Glycosylation and Glycoproteins Research (1 paper), Genomics and Rare Diseases (1 paper) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (230 citations), Developmental Neuroscience (15 citations), Pediatrics, Perinatology and Child Health (44 citations), Cognitive Neuroscience (48 citations) and Molecular Biology (141 citations). Devin M. Cox has collaborated with scholars based in United States and Japan. Frequent co-authors include Merlin G. Butler, Ann Genovese, Doreen Granpeesheh, John M. Slattery, Shirish Damle, Michael J. Goldenthal, Agustín Legido, Marie Tippett, Stephen G. Kahler and Richard E. Frye. Their work appears in journals such as Journal of Pediatric Genetics, Cytogenetic and Genome Research, International Journal of Molecular Sciences, Scientific Reports and Clinical Pediatrics.
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.