Sofia Dória

858 total citations
49 papers, 541 citations indexed

About

Sofia Dória is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sofia Dória has authored 49 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 21 papers in Molecular Biology and 19 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sofia Dória's work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Sofia Dória is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (14 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (10 papers). Sofia Dória collaborates with scholars based in Portugal, United Kingdom and United States. Sofia Dória's co-authors include Filipa Carvalho, Carla Ramalho, Alberto Barros, Mário Sousa, Otília Brandão, Alexandra Matias, C. Joana Marques, Elsa Logarinho, Aaron Mattingly and Jordi Camps and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Developmental Biology.

In The Last Decade

Sofia Dória

45 papers receiving 529 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Sofia Dória Portugal 13 244 208 196 108 99 49 541
Rachel Michaelson‐Cohen Israel 12 201 0.8× 170 0.8× 81 0.4× 135 1.3× 156 1.6× 39 525
Mariana F.A. Funari Brazil 17 368 1.5× 400 1.9× 91 0.5× 119 1.1× 76 0.8× 35 736
Lu Luo China 12 225 0.9× 85 0.4× 107 0.5× 189 1.8× 164 1.7× 39 539
Malgorzata Gasperowicz Canada 10 254 1.0× 78 0.4× 155 0.8× 43 0.4× 25 0.3× 15 488
Jodi D. Hoffman United States 18 215 0.9× 365 1.8× 119 0.6× 48 0.4× 11 0.1× 33 654
Michiharu Horikawa Japan 12 151 0.6× 43 0.2× 53 0.3× 203 1.9× 197 2.0× 22 451
Hadas Grossman Israel 12 201 0.8× 45 0.2× 31 0.2× 152 1.4× 154 1.6× 17 473
Anna Newlin United States 12 147 0.6× 210 1.0× 96 0.5× 41 0.4× 37 0.4× 17 425
Daniela Bettio Italy 12 169 0.7× 277 1.3× 235 1.2× 90 0.8× 39 0.4× 35 535
Dianne Vassmer United States 7 197 0.8× 151 0.7× 37 0.2× 98 0.9× 46 0.5× 7 520

Countries citing papers authored by Sofia Dória

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Sofia Dória

This figure shows the co-authorship network connecting the top 25 collaborators of Sofia Dória. A scholar is included among the top collaborators of Sofia Dória based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sofia Dória. Sofia Dória is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dória, Sofia, et al.. (2025). A protocol for karyotyping and genetic editing of induced pluripotent stem cells with homology-directed repair mediated CRISPR/Cas9. Biology Methods and Protocols. 10(1). bpaf018–bpaf018. 1 indexed citations
2.
Sobral, Daniel, et al.. (2024). Transcriptomic analysis and epigenetic regulators in human oocytes at different stages of oocyte meiotic maturation. Developmental Biology. 519. 55–64. 2 indexed citations
3.
Almeida, Carolina, et al.. (2024). Impact of copy number variants in epilepsy plus neurodevelopment disorders. Seizure. 117. 6–12. 2 indexed citations
4.
Dória, Sofia, et al.. (2024). Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease. ˜The œNephron journals/Nephron journals. 148(8). 578–583. 2 indexed citations
5.
6.
Pinho, Maria João, et al.. (2023). Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature. European Journal of Medical Genetics. 66(10). 104827–104827. 2 indexed citations
7.
Grangeia, Ana, et al.. (2023). Copy number variations on chromosome 2: impact on human phenotype, a cross-sectional study. Porto Biomedical Journal. 8(1). e198–e198.
8.
Lopes, Susana M. Chuva de Sousa, et al.. (2023). The role of DNA hydroxymethylation and TET enzymes in placental development and pregnancy outcome. Clinical Epigenetics. 15(1). 66–66. 10 indexed citations
9.
Souto, Selma B., et al.. (2023). Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients. Revista Internacional de Andrología. 21(3). 100349–100349.
10.
Dória, Sofia, et al.. (2020). 12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?. BMC Medical Genomics. 13(1). 2–2. 4 indexed citations
11.
Silva, Joaquina, et al.. (2019). Reproductive success of assisted reproductive technology in couples with chromosomal abnormalities. Journal of Assisted Reproduction and Genetics. 36(7). 1471–1479. 12 indexed citations
12.
Rocha, Gustavo, Susana Pissarra, Henrique Soares, et al.. (2017). Neonatal dilated cardiomyopathy. Revista Portuguesa de Cardiologia. 36(3). 201–214. 19 indexed citations
13.
Carvalho, Filipa, et al.. (2014). Relevance of genomic imprinting in intrauterine human growth expression of CDKN1C, H19, IGF2, KCNQ1 and PHLDA2 imprinted genes. Journal of Assisted Reproduction and Genetics. 31(10). 1361–1368. 36 indexed citations
14.
Dória, Sofia, Carolina Almeida, Maria João Pinho, et al.. (2012). Inv21p12q22del21q22 and intellectual disability. Gene. 517(1). 120–124. 1 indexed citations
15.
Dória, Sofia, Mário Sousa, Susana Fernandes, et al.. (2010). Gene expression pattern of IGF2 , PHLDA2 , PEG10 and CDKN1C imprinted genes in spontaneous miscarriages or fetal deaths. Epigenetics. 5(5). 444–450. 43 indexed citations
16.
Dória, Sofia, et al.. (2010). Application of touch FISH in the study of mosaic tetraploidy and maternal cell contamination in pregnancy losses. Journal of Assisted Reproduction and Genetics. 27(11). 657–662. 11 indexed citations
17.
Dória, Sofia, Carla Ramalho, Otília Brandão, et al.. (2010). Aneuploidies detection in miscarriages and fetal deaths using multiplex ligation-dependent probe amplification: an alternative for speeding up results?. European Journal of Obstetrics & Gynecology and Reproductive Biology. 153(2). 151–155. 21 indexed citations
18.
Rocha, Gustavo, et al.. (2004). New findings in partial trisomy 16q: clinical report. Acta Paediatrica. 93(6). 852–854. 9 indexed citations
19.
Lima, Margarida, José Manuel Lopes, Sofia Dória, et al.. (2002). Chronic Eosinophilic Leukaemia Presenting with Erythroderma, Mild Eosinophilia and Hyper-IgE: Clinical, Immunological and Cytogenetic Features and Therapeutic Approach. Acta Haematologica. 107(2). 108–112. 20 indexed citations
20.
Cerveira, Nuno, Susana Ferreira, Sofia Dória, et al.. (2000). Detection of prognostic significant translocations in childhood acute lymphoblastic leukaemia by one‐step multiplex reverse transcription polymerase chain reaction. British Journal of Haematology. 109(3). 638–640. 12 indexed citations

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.

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