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 7
- Co-authors
- Stephanie L. Sherman (13 shared papers)Emily G. Allen (9 shared papers)Claudine P. Torfs (5 shared papers)Eleanor Feingold (7 shared papers)Sallie B. Freeman (5 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 Mutation (1 paper)Birth Defects Research Part A Clinical and Molecular Teratology (1 paper)Human Molecular Genetics (1 paper)PLoS Genetics (1 paper)
- Partner nations
- United States
In The Last Decade
Stuart W. Tinker
15 papers receiving 729 citations
Peers
Comparison fields: 5 of 64
- Pediatrics, Perinatology and Child Health 302
- Genetics 298
- Public Health, Environmental and Occupational Health 209
- Rheumatology 90
- Epidemiology 190
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 | 204 | |
| 2 | 2008 | 130 | |
| 3 | 2010 | 63 | |
| 4 | 2007 | 60 | |
| 5 | 2011 | 46 | |
| 6 | 2013 | 41 | |
| 7 | 2013 | 39 | |
| 8 | 2011 | 35 | |
| 9 | 2011 | 35 | |
| 10 | 2008 | 28 | |
| 11 | 2008 | 27 | |
| 12 | 2009 | 23 | |
| 13 | 2013 | 17 | |
| 14 | 2004 | 14 | |
| 15 | 2014 | 14 |
About Stuart W. Tinker
Stuart W. Tinker is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cognitive Neuroscience and Epidemiology, having authored 15 papers that have together received 776 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (7 papers), Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers), Folate and B Vitamins Research (3 papers), Congenital Heart Disease Studies (3 papers), Chromosomal and Genetic Variations (3 papers) and Esophageal and GI Pathology (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (302 citations), Genetics (298 citations), Public Health, Environmental and Occupational Health (209 citations), Rheumatology (90 citations) and Epidemiology (190 citations). Stuart W. Tinker has collaborated with scholars based in United States. Frequent co-authors include Stephanie L. Sherman, Emily G. Allen, Claudine P. Torfs, Eleanor Feingold, Sallie B. Freeman, Charlotte A. Hobbs, Charlotte M. Druschel, Marjorie H. Royle, Paul A. Romitti and Tiffany Oliver. Their work appears in journals such as Genetic Epidemiology, Human Mutation, Birth Defects Research Part A Clinical and Molecular Teratology, Human Molecular Genetics and PLoS Genetics.
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.