Soraia Melo

911 total citations
19 papers, 508 citations indexed

About

Soraia Melo is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Soraia Melo has authored 19 papers receiving a total of 508 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 3 papers in Oncology. Recurrent topics in Soraia Melo's work include Wnt/β-catenin signaling in development and cancer (9 papers), Cancer-related gene regulation (9 papers) and Hedgehog Signaling Pathway Studies (4 papers). Soraia Melo is often cited by papers focused on Wnt/β-catenin signaling in development and cancer (9 papers), Cancer-related gene regulation (9 papers) and Hedgehog Signaling Pathway Studies (4 papers). Soraia Melo collaborates with scholars based in Portugal, Spain and United States. Soraia Melo's co-authors include Raquel Seruca, Joana Figueiredo, Maria Sofia Fernandes, Patrı́cia Carneiro, Ana Moreira, Joana Simões‐Correia, Joana Paredes, Natércia Teixeira, Cristina Amaral and E. J. Tavares da Silva and has published in prestigious journals such as PLoS ONE, Scientific Reports and FEBS Letters.

In The Last Decade

Soraia Melo

19 papers receiving 504 citations

Peers

Soraia Melo

PFM

GENET

PRM

ONCOL

Alina Levy United States

Mandy Boer Netherlands

Ansu O. Perekatt United States

Soonweng Cho United States

Ira Kogan Israel

Wijnand Roessingh Netherlands

Danyi Zou China

Jinhui Wang United States

Rou Xu China

Janet I. Lee United States

Alina Levy United States

Soraia Melo

282 ×0.9

133 ×1.1

PFM

145 ×1.2

GENET

145 ×1.6

PRM

71 ×0.8

ONCOL

Citations per year, relative to Soraia Melo Soraia Melo (= 1×) peers Alina Levy

Countries citing papers authored by Soraia Melo

Since Specialization

Citations

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

Fields of papers citing papers by Soraia Melo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Soraia Melo

This figure shows the co-authorship network connecting the top 25 collaborators of Soraia Melo. A scholar is included among the top collaborators of Soraia Melo 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 Soraia Melo. Soraia Melo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

Melo, Soraia, Rui M. Ferreira, Patrı́cia Carneiro, et al.. (2024). E-cadherin variants associated with oral facial clefts trigger aberrant cell motility in a REG1A-dependent manner. Cell Communication and Signaling. 22(1). 152–152. 1 indexed citations

Melo, Soraia, José Rafael Bordin, Fátima Carneiro, et al.. (2023). The ECM and tissue architecture are major determinants of early invasion mediated by E-cadherin dysfunction. Communications Biology. 6(1). 1132–1132. 7 indexed citations

Fernandes, Maria Sofia, Ana Moreira, Soraia Melo, et al.. (2021). A machine learning approach for single cell interphase cell cycle staging. Scientific Reports. 11(1). 19278–19278. 5 indexed citations

Figueiredo, Joana, Fátima Mercadillo, Soraia Melo, et al.. (2021). Germline CDH1 G212E Missense Variant: Combining Clinical, In Vitro and In Vivo Strategies to Unravel Disease Burden. Cancers. 13(17). 4359–4359. 9 indexed citations

Moreira, Ana, Soraia Melo, Maria Sofia Fernandes, et al.. (2020). The Extracellular Matrix: An Accomplice in Gastric Cancer Development and Progression. Cells. 9(2). 394–394. 74 indexed citations

Figueiredo, Joana, Soraia Melo, Patrı́cia Carneiro, et al.. (2019). Clinical spectrum and pleiotropic nature of CDH1 germline mutations. Journal of Medical Genetics. 56(4). 199–208. 64 indexed citations

Perea, José, Soraia Melo, Fátima Mercadillo, et al.. (2018). Clinical and functional characterization of the CDH1 germline variant c.1679C>G in three unrelated families with hereditary diffuse gastric cancer. European Journal of Human Genetics. 26(9). 1348–1353. 6 indexed citations

Figueiredo, Joana, Maria Sofia Fernandes, Soraia Melo, et al.. (2018). Geometric compensation applied to image analysis of cell populations with morphological variability: a new role for a classical concept. Scientific Reports. 8(1). 10266–10266. 3 indexed citations

Melo, Soraia, Joana Figueiredo, Maria Sofia Fernandes, et al.. (2017). Predicting the Functional Impact of CDH1 Missense Mutations in Hereditary Diffuse Gastric Cancer. International Journal of Molecular Sciences. 18(12). 2687–2687. 30 indexed citations

10.

Fernandes, Maria Sofia, Soraia Melo, Sérgia Velho, et al.. (2016). Specific inhibition of p110α subunit of PI3K: putative therapeutic strategy forKRASmutant colorectal cancers. Oncotarget. 7(42). 68546–68558. 10 indexed citations

11.

Brito, Luciano Abreu, Guilherme Lopes Yamamoto, Soraia Melo, et al.. (2015). Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate. Human Mutation. 36(11). 1029–1033. 33 indexed citations

12.

Zhang, Liying, Ruben Bacares, Soraia Melo, et al.. (2014). The germline CDH1 c.48 G > C substitution contributes to cancer predisposition through generation of a pro-invasive mutation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 770. 106–111. 14 indexed citations

13.

Sanches, João, Joana Figueiredo, Martina Fonseca, et al.. (2014). Quantification of mutant E-cadherin using bioimaging analysis of in situ fluorescence microscopy. A new approach to CDH1 missense variants. European Journal of Human Genetics. 23(8). 1072–1079. 19 indexed citations

14.

Corso, Giovanni, Joana Figueiredo, Roberto Biffi, et al.. (2014). E-cadherin germline mutation carriers: clinical management and genetic implications. Cancer and Metastasis Reviews. 33(4). 1081–1094. 28 indexed citations

15.

Simões‐Correia, Joana, Soraia Melo, Joana Figueiredo, et al.. (2013). DNAJB4 molecular chaperone distinguishes WT from mutant E-cadherin, determining their fate in vitro and in vivo. Human Molecular Genetics. 23(8). 2094–2105. 22 indexed citations

16.

Vogelaar, Ingrid P., Joana Figueiredo, Iris A.L.M. van Rooij, et al.. (2012). Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts. Human Molecular Genetics. 22(5). 919–926. 47 indexed citations

17.

Amaral, Cristina, Margarida Borges, Soraia Melo, et al.. (2012). Apoptosis and Autophagy in Breast Cancer Cells following Exemestane Treatment. PLoS ONE. 7(8). e42398–e42398. 62 indexed citations

18.

Carneiro, Patrı́cia, Maria Sofia Fernandes, Joana Figueiredo, et al.. (2012). E‐cadherin dysfunction in gastric cancer ‐ Cellular consequences, clinical applications and open questions. FEBS Letters. 586(18). 2981–2989. 63 indexed citations

19.

Garziera, Marica, Vallì De Re, Silvano Geremia, et al.. (2012). A novel CDH1 germline missense mutation in a sporadic gastric cancer patient in north-east of Italy. Clinical and Experimental Medicine. 13(2). 149–157. 11 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.

Explore authors with similar magnitude of impact