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 7
- Genetics and Neurodevelopmental Disorders 2
- Congenital Ear and Nasal Anomalies 2
- BRCA gene mutations in cancer 1
- Genomics and Rare Diseases 1
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- Congenital heart defects research 5
- Chromatin Remodeling and Cancer 1
- Co-authors
- Merlin G. Butler (7 shared papers)Ann Genovese (1 shared paper)John M. Slattery (1 shared paper)Shirish Damle (1 shared paper)Michael J. Goldenthal (1 shared paper)Richard E. Frye (1 shared paper)Doreen Granpeesheh (1 shared paper)Agustín Legido (1 shared paper)
- Journals
- Journal of Pediatric Genetics (3 papers)Scientific Reports (1 paper)International Journal of Molecular Sciences (1 paper)Cytogenetic and Genome Research (1 paper)Clinical Pediatrics (1 paper)
- Partner nations
- United StatesJapan
In The Last Decade
Devin M. Cox
9 papers receiving 283 citations
Peers
Comparison fields: 5 of 43
- Genetics 238
- Developmental Neuroscience 16
- Pediatrics, Perinatology and Child Health 60
- Cognitive Neuroscience 48
- Molecular Biology 164
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 | 159 | |
| 2 | 2016 | 37 | |
| 3 | 2015 | 32 | |
| 4 | 2016 | 26 | |
| 5 | 2015 | 15 | |
| 6 | 2016 | 12 | |
| 7 | 2018 | 10 | |
| 8 | 2015 | 5 | |
| 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 299 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital Ear and Nasal Anomalies (2 papers), Immunodeficiency and Autoimmune Disorders (1 paper), BRCA gene mutations in cancer (1 paper), Genomics and Rare Diseases (1 paper) and Chromatin Remodeling and Cancer (1 paper). The work is most often cited by research in Genetics (238 citations), Developmental Neuroscience (16 citations), Pediatrics, Perinatology and Child Health (60 citations), Cognitive Neuroscience (48 citations) and Molecular Biology (164 citations). Devin M. Cox has collaborated with scholars based in United States and Japan. Frequent co-authors include Merlin G. Butler, Ann Genovese, John M. Slattery, Shirish Damle, Michael J. Goldenthal, Richard E. Frye, Doreen Granpeesheh, Agustín Legido, Stephen G. Kahler and Marie Tippett. Their work appears in journals such as Journal of Pediatric Genetics, Scientific Reports, International Journal of Molecular Sciences, Cytogenetic and Genome Research 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.