Thomas Scerri
Impact in
-
- Reading and Literacy Development
- Language Development and Disorders
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 14
- Genetics and Neurodevelopmental Disorders 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genomics and Rare Diseases 2
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- Reading and Literacy Development 8
- Language Development and Disorders 3
- Co-authors
- Silvia Paracchini (13 shared papers)Anthony P. Monaco (12 shared papers)Gerd Schulte‐Körne (1 shared paper)John Stein (11 shared papers)Melanie Bahlo (10 shared papers)Andrew P. Morris (5 shared papers)A.J. Richardson (4 shared papers)Susan M. Ring (4 shared papers)
- Journals
- Human Molecular Genetics (3 papers)Molecular Psychiatry (3 papers)PLoS ONE (2 papers)PLoS Genetics (2 papers)Genes Brain & Behavior (1 paper)
- Partner nations
- United KingdomAustraliaUnited States
In The Last Decade
Thomas Scerri
24 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 97
- Developmental and Educational Psychology 734
- Genetics 749
- Statistics and Probability 205
- Cognitive Neuroscience 415
- Anatomy 16
Countries citing papers authored by Thomas Scerri
This map shows the geographic impact of Thomas Scerri'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 Thomas Scerri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Scerri more than expected).
Fields of papers citing papers by Thomas Scerri
This network shows the impact of papers produced by Thomas Scerri. 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 Thomas Scerri. The network helps show where Thomas Scerri may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Scerri, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 203 | |
| 2 | 2012 | 149 | |
| 3 | 2009 | 139 | |
| 4 | 2006 | 127 | |
| 5 | 2007 | 115 | |
| 6 | 2013 | 115 | |
| 7 | 2018 | 113 | |
| 8 | 2015 | 103 | |
| 9 | 2008 | 103 | |
| 10 | 2010 | 101 | |
| 11 | 2017 | 89 | |
| 12 | 2009 | 81 | |
| 13 | 2014 | 77 | |
| 14 | 2015 | 77 | |
| 15 | 2015 | 55 | |
| 16 | 2010 | 31 | |
| 17 | 2012 | 31 | |
| 18 | 2013 | 27 | |
| 19 | 2018 | 22 | |
| 20 | 2017 | 15 |
About Thomas Scerri
Thomas Scerri is a scholar working on Genetics, Developmental and Educational Psychology, Molecular Biology, Statistics and Probability and Cognitive Neuroscience, having authored 24 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Reading and Literacy Development (8 papers), Cognitive and developmental aspects of mathematical skills (4 papers), Language Development and Disorders (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Genomics and Rare Diseases (2 papers), Retinal Diseases and Treatments (2 papers) and Hemispheric Asymmetry in Neuroscience (2 papers). The work is most often cited by research in Developmental and Educational Psychology (734 citations), Genetics (749 citations), Statistics and Probability (205 citations), Cognitive Neuroscience (415 citations) and Anatomy (16 citations). Thomas Scerri has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Silvia Paracchini, Anthony P. Monaco, Gerd Schulte‐Körne, John Stein, Melanie Bahlo, Andrew P. Morris, A.J. Richardson, Susan M. Ring, Joel B. Talcott and William M. Brandler. Their work appears in journals such as Human Molecular Genetics, Molecular Psychiatry, PLoS ONE, PLoS Genetics and Genes Brain & Behavior.
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.