Stacy Steinberg
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genetics and Neurodevelopmental Disorders
- Genetic and phenotypic traits in livestock
- Genomics and Rare Diseases
- Psychiatry and Mental health top 10%
- Migraine and Headache Studies
Papers in
- Genetics 7
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 2
- Genetic Associations and Epidemiology 2
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- DNA Repair Mechanisms 1
- Epigenetics and DNA Methylation 1
- Co-authors
- Hreinn Stefánsson (11 shared papers)Kāri Stefánsson (7 shared papers)Daníel F. Guðbjartsson (3 shared papers)Andrés Ingason (3 shared papers)Augustine Kong (3 shared papers)Michael L. Frigge (3 shared papers)Unnur Þorsteinsdóttir (2 shared papers)Guðmar Þorleifsson (1 shared paper)
- Journals
- Nature Genetics (2 papers)Journal of Learning Disabilities (1 paper)Addiction Biology (1 paper)European Journal of Neurology (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- IcelandDenmarkUnited Kingdom
In The Last Decade
Stacy Steinberg
14 papers receiving 791 citations
Peers
Comparison fields: 5 of 90
- Genetics 361
- Psychiatry and Mental health 100
- Otorhinolaryngology 26
- Biological Psychiatry 12
- Neurology 41
Countries citing papers authored by Stacy Steinberg
This map shows the geographic impact of Stacy Steinberg'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 Stacy Steinberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stacy Steinberg more than expected).
Fields of papers citing papers by Stacy Steinberg
This network shows the impact of papers produced by Stacy Steinberg. 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 Stacy Steinberg. The network helps show where Stacy Steinberg may publish in the future.
Co-authors
The 25 scholars most cited alongside Stacy Steinberg, 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 | 239 | |
| 2 | 2013 | 86 | |
| 3 | 2017 | 82 | |
| 4 | 2005 | 77 | |
| 5 | 2013 | 61 | |
| 6 | 1985 | 56 | |
| 7 | 2015 | 44 | |
| 8 | 2017 | 43 | |
| 9 | 2012 | 38 | |
| 10 | 2007 | 36 | |
| 11 | 2013 | 30 | |
| 12 | 2015 | 25 | |
| 13 | 1995 | 2 | |
| 14 | 2014 | 1 |
About Stacy Steinberg
Stacy Steinberg is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Developmental and Educational Psychology and Statistics and Probability, having authored 14 papers that have together received 820 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Migraine and Headache Studies (3 papers), Genomics and Rare Diseases (2 papers), Language Development and Disorders (2 papers), Genetic Associations and Epidemiology (2 papers), DNA Repair Mechanisms (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Genetics (361 citations), Psychiatry and Mental health (100 citations), Otorhinolaryngology (26 citations), Biological Psychiatry (12 citations) and Neurology (41 citations). Stacy Steinberg has collaborated with scholars based in Iceland, Denmark and United Kingdom. Frequent co-authors include Hreinn Stefánsson, Kāri Stefánsson, Daníel F. Guðbjartsson, Andrés Ingason, Augustine Kong, Michael L. Frigge, Unnur Þorsteinsdóttir, Guðmar Þorleifsson, Gísli Másson and Pall I. Olason. Their work appears in journals such as Nature Genetics, Journal of Learning Disabilities, Addiction Biology, European Journal of Neurology 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.