Stuart W. Tinker
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 3
-
- Prenatal Screening and Diagnostics 8
- Co-authors
- Stephanie L. Sherman (13 shared papers)Emily Graves Allen (9 shared papers)Sallie B. Freeman (6 shared papers)Claudine P. Torfs (5 shared papers)Eleanor Feingold (7 shared papers)Charlotte A. Hobbs (4 shared papers)Charlotte M. Druschel (4 shared papers)Marjorie H. Royle (4 shared papers)
- Journals
- Genetic Epidemiology (3 papers)Human Genetics (1 paper)Genetics in Medicine (1 paper)Behavior Genetics (1 paper)Public Health Reports (1 paper)
- Partner nations
- United States
In The Last Decade
Stuart W. Tinker
15 papers receiving 797 citations
Peers
Comparison fields: 5 of 63
- Pediatrics, Perinatology and Child Health 285
- Genetics 305
- Public Health, Environmental and Occupational Health 212
- Rheumatology 87
- Epidemiology 143
Countries citing papers authored by Stuart W. Tinker
This map shows the geographic impact of Stuart W. Tinker'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 Stuart W. Tinker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stuart W. Tinker more than expected).
Fields of papers citing papers by Stuart W. Tinker
This network shows the impact of papers produced by Stuart W. Tinker. 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 Stuart W. Tinker. The network helps show where Stuart W. Tinker may publish in the future.
Co-authors
The 25 scholars most cited alongside Stuart W. Tinker, 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 | 2008 | 234 | |
| 2 | 2008 | 141 | |
| 3 | 2007 | 69 | |
| 4 | 2010 | 67 | |
| 5 | 2008 | 50 | |
| 6 | 2011 | 46 | |
| 7 | 2013 | 43 | |
| 8 | 2013 | 42 | |
| 9 | 2011 | 38 | |
| 10 | 2011 | 35 | |
| 11 | 2008 | 31 | |
| 12 | 2009 | 25 | |
| 13 | 2014 | 16 | |
| 14 | 2013 | 16 | |
| 15 | 2004 | 14 |
About Stuart W. Tinker
Stuart W. Tinker is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Rheumatology, Public Health, Environmental and Occupational Health and Cognitive Neuroscience, having authored 15 papers that have together received 867 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (3 papers), Folate and B Vitamins Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (2 papers), Down syndrome and intellectual disability research (2 papers) and Biomedical Text Mining and Ontologies (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (285 citations), Genetics (305 citations), Public Health, Environmental and Occupational Health (212 citations), Rheumatology (87 citations) and Epidemiology (143 citations). Stuart W. Tinker has collaborated with scholars based in United States. Frequent co-authors include Stephanie L. Sherman, Emily Graves Allen, Sallie B. Freeman, Claudine P. Torfs, Eleanor Feingold, Charlotte A. Hobbs, Charlotte M. Druschel, Marjorie H. Royle, Paul A. Romitti and Tiffany Renee Oliver. Their work appears in journals such as Genetic Epidemiology, Human Genetics, Genetics in Medicine, Behavior Genetics and Public Health Reports.
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.