Gabriela Soares

4.1k total citations
29 papers, 370 citations indexed

About

Gabriela Soares is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Gabriela Soares has authored 29 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Gabriela Soares's work include Genetics and Neurodevelopmental Disorders (10 papers), Congenital heart defects research (6 papers) and Genomics and Rare Diseases (5 papers). Gabriela Soares is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Congenital heart defects research (6 papers) and Genomics and Rare Diseases (5 papers). Gabriela Soares collaborates with scholars based in Portugal, United States and Brazil. Gabriela Soares's co-authors include Fátima Lopes, Patrı́cia Maciel, Teresa Temudo, Joaquim Sá, Adam Ameur, Pedro Cabral, Ann‐Christine Syvänen, José Pedro Vieira, Ulf Gyllensten and Inger Jonasson and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Gabriela Soares

27 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gabriela Soares Portugal 10 191 175 38 34 30 29 370
Devon Lamb Thrush United States 10 218 1.1× 141 0.8× 54 1.4× 26 0.8× 27 0.9× 19 334
Qiuling Liu China 16 283 1.5× 223 1.3× 48 1.3× 25 0.7× 16 0.5× 54 552
Giulia Fragola United States 8 422 2.2× 168 1.0× 20 0.5× 17 0.5× 37 1.2× 10 546
Melanie Lacaria Canada 10 245 1.3× 179 1.0× 17 0.4× 15 0.4× 44 1.5× 15 399
Cláudia Vianna Maurer‐Morelli Brazil 16 224 1.2× 108 0.6× 111 2.9× 41 1.2× 13 0.4× 34 503
Parul Jayakar United States 15 383 2.0× 217 1.2× 99 2.6× 27 0.8× 22 0.7× 32 615
Yidi Wang United States 8 267 1.4× 62 0.4× 33 0.9× 34 1.0× 11 0.4× 14 429
Ranga N. Parthasarathy United States 12 198 1.0× 85 0.5× 21 0.6× 41 1.2× 7 0.2× 21 439
Jacek Lenart Poland 13 234 1.2× 45 0.3× 44 1.2× 17 0.5× 32 1.1× 28 389
Xiumin Wang China 12 282 1.5× 246 1.4× 8 0.2× 18 0.5× 30 1.0× 27 527

Countries citing papers authored by Gabriela Soares

Since Specialization
Citations

This map shows the geographic impact of Gabriela Soares'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 Gabriela Soares with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gabriela Soares more than expected).

Fields of papers citing papers by Gabriela Soares

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gabriela Soares. 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 Gabriela Soares. The network helps show where Gabriela Soares may publish in the future.

Co-authorship network of co-authors of Gabriela Soares

This figure shows the co-authorship network connecting the top 25 collaborators of Gabriela Soares. A scholar is included among the top collaborators of Gabriela Soares 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 Gabriela Soares. Gabriela Soares 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.
Soares, Gabriela, Rafael Izbicki, Željko Ivezić, et al.. (2024). The Quasar Catalogue for S-PLUS DR4 (QuCatS) and the estimation of photometric redshifts. Monthly Notices of the Royal Astronomical Society. 531(1). 327–339. 2 indexed citations
2.
Müller, Larissa, et al.. (2023). Multigenerational effects of co-exposure to dimethylarsinic acid and polystyrene microplastics on the nematode Caenorhabditis elegans. Environmental Science and Pollution Research. 30(36). 85359–85372. 7 indexed citations
3.
Soares, Gabriela, et al.. (2023). Biochemical and physiological effects of multigenerational exposure to spheric polystyrene microplastics in Caenorhabditis elegans. Environmental Science and Pollution Research. 30(26). 69307–69320. 5 indexed citations
4.
Abreu, María T., et al.. (2022). Genetic counseling and carrier screening in candidates for gamete donation at a Portuguese center. JBRA. 27(2). 180–184. 2 indexed citations
5.
Fachel, Flávia Nathiely Silveira, Gabriela Soares, Tony Silveira, et al.. (2020). Hydrogels containing soybean isoflavone aglycones-rich fraction-loaded nanoemulsions for wound healing treatment – in vitro and in vivo studies. Colloids and Surfaces B Biointerfaces. 196. 111301–111301. 22 indexed citations
6.
Soares, Gabriela, Cecília Silva, Rosário Santos, et al.. (2020). Two Compound Heterozygous Variants in SNX14 Cause Stereotypies and Dystonia in Autosomal Recessive Spinocerebellar Ataxia 20. Frontiers in Genetics. 11. 1038–1038. 3 indexed citations
7.
Soares, Gabriela, et al.. (2019). Platinum rechallenge in second-line treatment for endometrial carcinoma. European Journal of Gynaecological Oncology. 40(6). 963–963. 2 indexed citations
8.
Peter, Virginie G., Mathieu Quinodoz, Jorge Pinto‐Basto, et al.. (2019). The Liberfarb syndrome, a multisystem disorder affecting eye, ear, bone, and brain development, is caused by a founder pathogenic variant in the PISD gene. Genetics in Medicine. 21(12). 2734–2743. 35 indexed citations
9.
Soares, Gabriela, et al.. (2019). Subtelomeric Rearrangements: Presentation of 21 Probands with Emphasis on Familial Cases. Acta Médica Portuguesa. 32(7-8). 529–535. 1 indexed citations
10.
Jorge, Paula, Ana Gonçalves, Gabriela Soares, et al.. (2018). Classical fragile-X phenotype in a female infant disclosed by comprehensive genomic studies. BMC Medical Genetics. 19(1). 74–74. 6 indexed citations
11.
Lopes, Fátima, et al.. (2017). Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease. Frontiers in Genetics. 8. 143–143. 14 indexed citations
12.
Jenkinson, Emma M., John H. Livingston, Mary O’Driscoll, et al.. (2017). Comprehensive molecular screening strategy of OCLN in band‐like calcification with simplified gyration and polymicrogyria. Clinical Genetics. 93(2). 228–234. 8 indexed citations
13.
Paulo, Paula, Pedro Pinto, Ana Peixoto, et al.. (2017). Validation of a Next-Generation Sequencing Pipeline for the Molecular Diagnosis of Multiple Inherited Cancer Predisposing Syndromes. Journal of Molecular Diagnostics. 19(4). 502–513. 11 indexed citations
14.
Soares, Gabriela, et al.. (2017). Arthrogryposis multiplex congenita affecting a monochorionic diamniotic twin pregnancy. SHILAP Revista de lepidopterología. 27(4). 253–257. 1 indexed citations
15.
Lopes, Fátima, Mafalda Barbosa, Adam Ameur, et al.. (2016). Identification of novel genetic causes of Rett syndrome-like phenotypes. Journal of Medical Genetics. 53(3). 190–199. 126 indexed citations
16.
Lopes, Fátima, Mafalda Barbosa, Teresa Temudo, et al.. (2015). ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing. International Journal of Developmental Neuroscience. 47(Part_A). 99–99.
17.
Jorge, Paula, et al.. (2014). A 26-Year Experience in Chorionic Villus Sampling Prenatal Genetic Diagnosis. Journal of Clinical Medicine. 3(3). 838–848. 3 indexed citations
18.
David, D., Bárbara Marques, Cristina Ferreira, et al.. (2013). Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression. Human Genetics. 132(11). 1287–1299. 16 indexed citations
19.
Nogueira, Célia, Maria João Prata, Lúcia Lacerda, et al.. (2008). Molecular analysis of mucopolysaccharidosis type IIIB in Portugal: evidence of a single origin for a common mutation (R234C) in the Iberian Peninsula. Clinical Genetics. 73(3). 251–256. 15 indexed citations
20.
Møller, Rikke S., Margarida Pinto, Gabriela Soares, et al.. (2008). Mowat–Wilson syndrome: an underdiagnosed syndrome?. Clinical Genetics. 73(6). 579–584. 27 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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