Barbara E. Stranger
Impact in
- Genetics top 0.2%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 2%
Papers in
- Genetics 47
- Genetic Associations and Epidemiology 32
- Genomic variations and chromosomal abnormalities 11
- Genetic Mapping and Diversity in Plants and Animals 9
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- Genomics and Chromatin Dynamics 12
- Gene expression and cancer classification 10
- Bioinformatics and Genomic Networks 6
- Co-authors
- Emmanouil T. Dermitzakis (17 shared papers)Claude Beazley (8 shared papers)Towfique Raj (18 shared papers)Catherine Ingle (6 shared papers)Antigone S. Dimas (7 shared papers)Stephen B. Montgomery (6 shared papers)Simon Tavaré (5 shared papers)Matthew S. Forrest (4 shared papers)
- Journals
- PLoS Genetics (8 papers)The American Journal of Human Genetics (6 papers)Science (3 papers)Proceedings of the National Academy of Sciences (3 papers)Human Molecular Genetics (3 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Barbara E. Stranger
70 papers receiving 7.6k citations
Barbara E. Stranger's Hit Papers
Peers
Comparison fields: 5 of 152
- Genetics 3.5k
- Cancer Research 750
- Molecular Biology 3.6k
- Immunology 1.0k
- Aging 53
Countries citing papers authored by Barbara E. Stranger
This map shows the geographic impact of Barbara E. Stranger'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 Barbara E. Stranger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara E. Stranger more than expected).
Fields of papers citing papers by Barbara E. Stranger
This network shows the impact of papers produced by Barbara E. Stranger. 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 Barbara E. Stranger. The network helps show where Barbara E. Stranger may publish in the future.
Co-authors
The 25 scholars most cited alongside Barbara E. Stranger, 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 71 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes Hit paper breakdown → | 2007 | 1276 |
| 2 | Population genomics of human gene expression Hit paper breakdown → | 2007 | 793 |
| 3 | 2009 | 495 | |
| 4 | 2005 | 384 | |
| 5 | 2010 | 372 | |
| 6 | 2012 | 355 | |
| 7 | 2012 | 308 | |
| 8 | 2010 | 300 | |
| 9 | 2013 | 195 | |
| 10 | 2013 | 188 | |
| 11 | 2010 | 186 | |
| 12 | 2018 | 182 | |
| 13 | 2019 | 164 | |
| 14 | 2015 | 159 | |
| 15 | 2014 | 158 | |
| 16 | 2007 | 133 | |
| 17 | 2004 | 116 | |
| 18 | 2008 | 113 | |
| 19 | 2013 | 110 | |
| 20 | 2007 | 101 |
About Barbara E. Stranger
Barbara E. Stranger is a scholar working on Genetics, Molecular Biology, Immunology, Neurology and Public Health, Environmental and Occupational Health, having authored 71 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (32 papers), Genomics and Chromatin Dynamics (12 papers), Genomic variations and chromosomal abnormalities (11 papers), Gene expression and cancer classification (10 papers), Genetic Mapping and Diversity in Plants and Animals (9 papers), T-cell and B-cell Immunology (6 papers), Immune Cell Function and Interaction (6 papers) and Bioinformatics and Genomic Networks (6 papers). The work is most often cited by research in Genetics (3.5k citations), Cancer Research (750 citations), Molecular Biology (3.6k citations), Immunology (1.0k citations) and Aging (53 citations). Barbara E. Stranger has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Emmanouil T. Dermitzakis, Claude Beazley, Towfique Raj, Catherine Ingle, Antigone S. Dimas, Stephen B. Montgomery, Simon Tavaré, Matthew S. Forrest, Christine Bird and Panos Deloukas. Their work appears in journals such as PLoS Genetics, The American Journal of Human Genetics, Science, Proceedings of the National Academy of Sciences and Human Molecular 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.