Sofia Dória
Impact in
- Reproductive Medicine top 10%
- Sperm and Testicular Function
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetic Syndromes and Imprinting 6
- Genetics and Neurodevelopmental Disorders 4
-
- Epigenetics and DNA Methylation 5
- Co-authors
- Filipa Carvalho (9 shared papers)Carla Ramalho (14 shared papers)Alberto Barros (13 shared papers)Mário Sousa (8 shared papers)Otília Brandão (5 shared papers)Alexandra Matias (4 shared papers)C. Joana Marques (7 shared papers)Guilherme da Silva Pereira (1 shared paper)
- Journals
- Journal of Assisted Reproduction and Genetics (5 papers)Epigenetics (2 papers)Gene (2 papers)Neuropediatrics (2 papers)Acta Paediatrica (2 papers)
- Partner nations
- PortugalUnited StatesUnited Kingdom
In The Last Decade
Sofia Dória
45 papers receiving 553 citations
Peers
Comparison fields: 5 of 63
- Reproductive Medicine 86
- Pediatrics, Perinatology and Child Health 163
- Obstetrics and Gynecology 46
- Genetics 176
- Cell Biology 61
Countries citing papers authored by Sofia Dória
This map shows the geographic impact of Sofia Dória'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 Sofia Dória with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sofia Dória more than expected).
Fields of papers citing papers by Sofia Dória
This network shows the impact of papers produced by Sofia Dória. 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 Sofia Dória. The network helps show where Sofia Dória may publish in the future.
Co-authors
The 25 scholars most cited alongside Sofia Dória, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 80 | |
| 2 | 2014 | 68 | |
| 3 | 2010 | 45 | |
| 4 | 2014 | 37 | |
| 5 | 2009 | 30 | |
| 6 | 2020 | 25 | |
| 7 | 2002 | 23 | |
| 8 | 2010 | 23 | |
| 9 | 2017 | 19 | |
| 10 | 2019 | 17 | |
| 11 | 2021 | 15 | |
| 12 | 2021 | 13 | |
| 13 | 2002 | 13 | |
| 14 | 2000 | 13 | |
| 15 | 2019 | 12 | |
| 16 | 2023 | 11 | |
| 17 | 2010 | 11 | |
| 18 | 2004 | 10 | |
| 19 | 2012 | 10 | |
| 20 | 2014 | 9 |
About Sofia Dória
Sofia Dória is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Genetics, having authored 50 papers that have together received 569 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (5 papers), Reproductive Biology and Fertility (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Advanced Electron Microscopy Techniques and Applications (2 papers). The work is most often cited by research in Reproductive Medicine (86 citations), Pediatrics, Perinatology and Child Health (163 citations), Obstetrics and Gynecology (46 citations), Genetics (176 citations) and Cell Biology (61 citations). Sofia Dória has collaborated with scholars based in Portugal, United States and United Kingdom. Frequent co-authors include Filipa Carvalho, Carla Ramalho, Alberto Barros, Mário Sousa, Otília Brandão, Alexandra Matias, C. Joana Marques, Guilherme da Silva Pereira, Daniela Cimini and Thomas Ried. Their work appears in journals such as Journal of Assisted Reproduction and Genetics, Epigenetics, Gene, Neuropediatrics and Acta Paediatrica.
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.