Justin Cotney
Impact in
- Molecular Biology top 5%
- Genomics and Chromatin Dynamics
- Mitochondrial Function and Pathology
- RNA Research and Splicing
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Epigenetics and DNA Methylation
- ATP Synthase and ATPases Research
- Developmental Neuroscience top 5%
Papers in
-
- Epigenetics and DNA Methylation 10
- Genomics and Chromatin Dynamics 9
- RNA modifications and cancer 7
- RNA Research and Splicing 6
- dental development and anomalies 6
- Genetics 21
- Cleft Lip and Palate Research 9
- Craniofacial Disorders and Treatments 9
- Genetic Syndromes and Imprinting 5
- Co-authors
- Gerald S. Shadel (7 shared papers)James P. Noonan (14 shared papers)Steven K. Reilly (6 shared papers)Jing Leng (6 shared papers)Jun Yin (4 shared papers)Zhibo Wang (2 shared papers)Pasko Rakić (3 shared papers)Albert E. Ayoub (3 shared papers)
- Journals
- Nature Communications (6 papers)Proceedings of the National Academy of Sciences (5 papers)Cell Reports (3 papers)Human Molecular Genetics (2 papers)Cell (2 papers)
- Partner nations
- United StatesGermanyChina
In The Last Decade
Justin Cotney
42 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 105
- Molecular Biology 1.6k
- Developmental Neuroscience 88
- Genetics 573
- Clinical Biochemistry 130
- Aging 18
Countries citing papers authored by Justin Cotney
This map shows the geographic impact of Justin Cotney'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 Justin Cotney with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Justin Cotney more than expected).
Fields of papers citing papers by Justin Cotney
This network shows the impact of papers produced by Justin Cotney. 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 Justin Cotney. The network helps show where Justin Cotney may publish in the future.
Co-authors
The 25 scholars most cited alongside Justin Cotney, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 212 | |
| 2 | 2015 | 183 | |
| 3 | 2012 | 157 | |
| 4 | 2013 | 145 | |
| 5 | 2012 | 104 | |
| 6 | 2011 | 102 | |
| 7 | 2007 | 93 | |
| 8 | 2013 | 84 | |
| 9 | 2007 | 79 | |
| 10 | 2010 | 75 | |
| 11 | 2018 | 73 | |
| 12 | 2020 | 69 | |
| 13 | 2009 | 68 | |
| 14 | 2011 | 67 | |
| 15 | 2006 | 65 | |
| 16 | 2018 | 48 | |
| 17 | 2013 | 47 | |
| 18 | 2019 | 46 | |
| 19 | 2015 | 34 | |
| 20 | 2017 | 32 |
About Justin Cotney
Justin Cotney is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Cognitive Neuroscience, having authored 44 papers that have together received 2.0k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (10 papers), Cleft Lip and Palate Research (9 papers), Craniofacial Disorders and Treatments (9 papers), Genomics and Chromatin Dynamics (9 papers), RNA modifications and cancer (7 papers), RNA Research and Splicing (6 papers), dental development and anomalies (6 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Molecular Biology (1.6k citations), Developmental Neuroscience (88 citations), Genetics (573 citations), Clinical Biochemistry (130 citations) and Aging (18 citations). Justin Cotney has collaborated with scholars based in United States, Germany and China. Frequent co-authors include Gerald S. Shadel, James P. Noonan, Steven K. Reilly, Jing Leng, Jun Yin, Zhibo Wang, Pasko Rakić, Albert E. Ayoub, Laura E. DeMare and Timothy E. Shutt. Their work appears in journals such as Nature Communications, Proceedings of the National Academy of Sciences, Cell Reports, Human Molecular Genetics and Cell.
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.