Silvia Paracchini
Impact in
-
- Reading and Literacy Development
- Language Development and Disorders
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Forensic and Genetic Research
Papers in
- Genetics 42
- Genetics and Neurodevelopmental Disorders 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Dermatoglyphics and Human Traits 6
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- Reading and Literacy Development 19
- Language Development and Disorders 4
- Co-authors
- Anthony P. Monaco (27 shared papers)John Stein (19 shared papers)Thomas Scerri (13 shared papers)William M. Brandler (6 shared papers)A.J. Richardson (7 shared papers)Dianne F. Newbury (12 shared papers)Judith Schmitz (8 shared papers)Sebastian Ocklenburg (5 shared papers)
- Journals
- Human Molecular Genetics (6 papers)Genes Brain & Behavior (4 papers)PLoS ONE (4 papers)The American Journal of Human Genetics (4 papers)Human Genetics (3 papers)
- Partner nations
- United KingdomUnited StatesGermany
In The Last Decade
Silvia Paracchini
61 papers receiving 3.1k citations
Silvia Paracchini's Hit Papers
Peers
Comparison fields: 5 of 131
- Developmental and Educational Psychology 1.3k
- Genetics 1.5k
- Cognitive Neuroscience 976
- Statistics and Probability 341
- Anatomy 25
Countries citing papers authored by Silvia Paracchini
This map shows the geographic impact of Silvia Paracchini'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 Silvia Paracchini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Silvia Paracchini more than expected).
Fields of papers citing papers by Silvia Paracchini
This network shows the impact of papers produced by Silvia Paracchini. 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 Silvia Paracchini. The network helps show where Silvia Paracchini may publish in the future.
Co-authors
The 25 scholars most cited alongside Silvia Paracchini, 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 66 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Human handedness: A meta-analysis. Hit paper breakdown → | 2020 | 289 |
| 2 | 2006 | 203 | |
| 3 | 2004 | 190 | |
| 4 | 2010 | 162 | |
| 5 | 2004 | 157 | |
| 6 | 2004 | 156 | |
| 7 | 2006 | 127 | |
| 8 | 2011 | 125 | |
| 9 | 2007 | 115 | |
| 10 | 2013 | 115 | |
| 11 | 2013 | 109 | |
| 12 | 2006 | 106 | |
| 13 | 2008 | 103 | |
| 14 | 2010 | 101 | |
| 15 | 2009 | 81 | |
| 16 | 2014 | 77 | |
| 17 | 2014 | 63 | |
| 18 | 2002 | 60 | |
| 19 | 2007 | 50 | |
| 20 | 2021 | 48 |
About Silvia Paracchini
Silvia Paracchini is a scholar working on Genetics, Developmental and Educational Psychology, Molecular Biology, Cognitive Neuroscience and Statistics and Probability, having authored 66 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (22 papers), Reading and Literacy Development (19 papers), Hemispheric Asymmetry in Neuroscience (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Cognitive and developmental aspects of mathematical skills (8 papers), Dermatoglyphics and Human Traits (6 papers), Congenital heart defects research (4 papers) and Language Development and Disorders (4 papers). The work is most often cited by research in Developmental and Educational Psychology (1.3k citations), Genetics (1.5k citations), Cognitive Neuroscience (976 citations), Statistics and Probability (341 citations) and Anatomy (25 citations). Silvia Paracchini has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Anthony P. Monaco, John Stein, Thomas Scerri, William M. Brandler, A.J. Richardson, Dianne F. Newbury, Judith Schmitz, Sebastian Ocklenburg, Μαριέττα Παπαδάτου-Παστού and Joel B. Talcott. Their work appears in journals such as Human Molecular Genetics, Genes Brain & Behavior, PLoS ONE, The American Journal of Human Genetics and Human 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.