Steve McCarroll
Impact in
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- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Schizophrenia research and treatment
Papers in
- Genetics 3
- Genetic Associations and Epidemiology 3
- Genomics and Rare Diseases 1
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- Congenital heart defects research 1
- Co-authors
- Daniel J. Weiner (1 shared paper)Patrick F. Sullivan (1 shared paper)Rachita Yadav (1 shared paper)Emi Ling (1 shared paper)Jennifer E. McDowell (1 shared paper)Ney Alliey‐Rodriguez (2 shared papers)Rebekka Lencer (1 shared paper)Godfrey D. Pearlson (2 shared papers)
- Partner nations
- United StatesDenmarkGermany
In The Last Decade
Steve McCarroll
3 papers receiving 4 citations
Peers
Comparison fields: 4 of 4
- Genetics 4
- Psychiatry and Mental health 1
- Cognitive Neuroscience 1
- Molecular Biology 2
Countries citing papers authored by Steve McCarroll
This map shows the geographic impact of Steve McCarroll'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 Steve McCarroll with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steve McCarroll more than expected).
Fields of papers citing papers by Steve McCarroll
This network shows the impact of papers produced by Steve McCarroll. 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 Steve McCarroll. The network helps show where Steve McCarroll may publish in the future.
Co-authors
The 25 scholars most cited alongside Steve McCarroll, 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 | 2022 | 2 | |
| 2 | 2017 | 1 | |
| 3 | 2019 | 1 | |
| 4 | 2017 | 0 |
About Steve McCarroll
Steve McCarroll is a scholar working on Genetics, Molecular Biology, Experimental and Cognitive Psychology, Infectious Diseases and Organic Chemistry, having authored 4 papers that have together received 4 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (3 papers), Congenital heart defects research (1 paper), Cognitive Abilities and Testing (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Genetics (4 citations), Psychiatry and Mental health (1 citation), Cognitive Neuroscience (1 citation), Molecular Biology (2 citations) and Infectious Diseases (0 citations). Steve McCarroll has collaborated with scholars based in United States, Denmark and Germany. Frequent co-authors include Daniel J. Weiner, Patrick F. Sullivan, Rachita Yadav, Emi Ling, Jennifer E. McDowell, Ney Alliey‐Rodriguez, Rebekka Lencer, Godfrey D. Pearlson, Francesco Lescai and Kyle Satterstrom. Their work appears in journals such as Schizophrenia Bulletin and European Neuropsychopharmacology.
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.