Dalila Pinto
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- High Altitude and Hypoxia
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 31
- Genomic variations and chromosomal abnormalities 17
- Genetics and Neurodevelopmental Disorders 16
- Genomics and Rare Diseases 7
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- Autism Spectrum Disorder Research 10
- Co-authors
- Stephen W. Scherer (19 shared papers)Christian R. Marshall (6 shared papers)Péter Szatmári (5 shared papers)Wendy Roberts (3 shared papers)James S. Sutcliffe (3 shared papers)Bridget A. Fernandez (1 shared paper)Jennifer Skaug (1 shared paper)Lonnie Zwaigenbaum (1 shared paper)
- Journals
- Epilepsia (4 papers)Journal of Neurodevelopmental Disorders (3 papers)Scientific Reports (2 papers)PLoS ONE (2 papers)Human Molecular Genetics (2 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
Dalila Pinto
46 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 120
- Genetics 1.8k
- Cognitive Neuroscience 811
- Gastroenterology 96
- Cellular and Molecular Neuroscience 340
- Molecular Biology 1.2k
Countries citing papers authored by Dalila Pinto
This map shows the geographic impact of Dalila Pinto'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 Dalila Pinto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dalila Pinto more than expected).
Fields of papers citing papers by Dalila Pinto
This network shows the impact of papers produced by Dalila Pinto. 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 Dalila Pinto. The network helps show where Dalila Pinto may publish in the future.
Co-authors
The 25 scholars most cited alongside Dalila Pinto, 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 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 499 | |
| 2 | 2010 | 434 | |
| 3 | 2010 | 412 | |
| 4 | 2010 | 217 | |
| 5 | 2007 | 169 | |
| 6 | 2010 | 148 | |
| 7 | 2016 | 130 | |
| 8 | 2008 | 117 | |
| 9 | 2014 | 103 | |
| 10 | 2011 | 89 | |
| 11 | 2004 | 77 | |
| 12 | 2010 | 76 | |
| 13 | 2004 | 64 | |
| 14 | 2010 | 47 | |
| 15 | 2012 | 43 | |
| 16 | 2020 | 43 | |
| 17 | 2013 | 42 | |
| 18 | 2014 | 38 | |
| 19 | 2010 | 33 | |
| 20 | 2014 | 31 |
About Dalila Pinto
Dalila Pinto is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Cancer Research and Rheumatology, having authored 46 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (16 papers), Autism Spectrum Disorder Research (10 papers), Genomics and Rare Diseases (7 papers), Chromosomal and Genetic Variations (4 papers), Glycogen Storage Diseases and Myoclonus (4 papers), Epilepsy research and treatment (3 papers) and Single-cell and spatial transcriptomics (2 papers). The work is most often cited by research in Genetics (1.8k citations), Cognitive Neuroscience (811 citations), Gastroenterology (96 citations), Cellular and Molecular Neuroscience (340 citations) and Molecular Biology (1.2k citations). Dalila Pinto has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Stephen W. Scherer, Christian R. Marshall, Péter Szatmári, Wendy Roberts, James S. Sutcliffe, Bridget A. Fernandez, Jennifer Skaug, Lonnie Zwaigenbaum, John B. Vincent and Rainald Moessner. Their work appears in journals such as Epilepsia, Journal of Neurodevelopmental Disorders, Scientific Reports, PLoS ONE 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.