Ryan N. Traylor
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
-
- Congenital heart defects research 2
- Epigenetics and DNA Methylation 1
- Cancer-related gene regulation 1
- Gene expression and cancer classification 1
- Co-authors
- Jill A. Rosenfeld (6 shared papers)Lisa G. Shaffer (6 shared papers)Blake C. Ballif (5 shared papers)Erawati V. Bawle (2 shared papers)Sarah Alliman (2 shared papers)Allen N. Lamb (2 shared papers)Trilochan Sahoo (1 shared paper)Richard Person (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Molecular Cytogenetics (1 paper)PEDIATRICS (1 paper)Prenatal Diagnosis (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesAustraliaGermany
In The Last Decade
Ryan N. Traylor
7 papers receiving 473 citations
Peers
Comparison fields: 5 of 47
- Genetics 376
- Pediatrics, Perinatology and Child Health 115
- Molecular Biology 279
- Cancer Research 55
- Genetics 30
Countries citing papers authored by Ryan N. Traylor
This map shows the geographic impact of Ryan N. Traylor'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 Ryan N. Traylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ryan N. Traylor more than expected).
Fields of papers citing papers by Ryan N. Traylor
This network shows the impact of papers produced by Ryan N. Traylor. 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 Ryan N. Traylor. The network helps show where Ryan N. Traylor may publish in the future.
Co-authors
The 25 scholars most cited alongside Ryan N. Traylor, 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 | 2010 | 236 | |
| 2 | 2012 | 82 | |
| 3 | 2009 | 54 | |
| 4 | 2012 | 37 | |
| 5 | 2011 | 33 | |
| 6 | 2012 | 31 | |
| 7 | 2010 | 21 |
About Ryan N. Traylor
Ryan N. Traylor is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health and Hematology, having authored 7 papers that have together received 494 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Immunodeficiency and Autoimmune Disorders (1 paper), Epigenetics and DNA Methylation (1 paper), Hippo pathway signaling and YAP/TAZ (1 paper), Cancer-related gene regulation (1 paper) and Gene expression and cancer classification (1 paper). The work is most often cited by research in Genetics (376 citations), Pediatrics, Perinatology and Child Health (115 citations), Molecular Biology (279 citations), Cancer Research (55 citations) and Genetics (30 citations). Ryan N. Traylor has collaborated with scholars based in United States, Australia and Germany. Frequent co-authors include Jill A. Rosenfeld, Lisa G. Shaffer, Blake C. Ballif, Erawati V. Bawle, Sarah Alliman, Allen N. Lamb, Trilochan Sahoo, Richard Person, Angela L. Duker and Sangeetha Mahadevan. Their work appears in journals such as European Journal of Human Genetics, Molecular Cytogenetics, PEDIATRICS, Prenatal Diagnosis and PLoS ONE.
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.