Fátima Lopes

3.2k total citations
14 papers, 334 citations indexed

About

Fátima Lopes is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Fátima Lopes has authored 14 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Fátima Lopes's work include Genetics and Neurodevelopmental Disorders (8 papers), Chromosomal and Genetic Variations (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Fátima Lopes is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Chromosomal and Genetic Variations (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Fátima Lopes collaborates with scholars based in Portugal, United States and Netherlands. Fátima Lopes's co-authors include Patrı́cia Maciel, Marisa Haenni, Tânia Ribeiro, Gabriela Soares, Benoît Zuber, Jacques Dubochet, Philippe Moreillon, José Pedro Vieira, Teresa Temudo and Mafalda Barbosa and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Bacteriology and Journal of Medical Genetics.

In The Last Decade

Fátima Lopes

13 papers receiving 317 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fátima Lopes Portugal	9	192	173	36	30	25	14	334
Laura Huopaniemi Finland	9	169 0.9×	89 0.5×	38 1.1×	26 0.9×	27 1.1×	14	359
Yi‐Liang Wei China	13	267 1.4×	217 1.3×	15 0.4×	9 0.3×	16 0.6×	28	486
Qian Pan China	10	298 1.6×	86 0.5×	45 1.3×	16 0.5×	15 0.6×	56	485
William Skarnes United Kingdom	6	370 1.9×	197 1.1×	23 0.6×	47 1.6×	20 0.8×	6	487
Peggy Winzenburger United States	7	189 1.0×	96 0.6×	47 1.3×	30 1.0×	31 1.2×	10	434
Haopeng Yu China	13	315 1.6×	95 0.5×	15 0.4×	56 1.9×	16 0.6×	25	719
Ana Gonçalves Portugal	12	184 1.0×	88 0.5×	22 0.6×	12 0.4×	16 0.6×	32	392
Rini Pauly United States	9	171 0.9×	90 0.5×	19 0.5×	29 1.0×	11 0.4×	31	335
Kathleen G. Banks Canada	8	197 1.0×	100 0.6×	33 0.9×	4 0.1×	22 0.9×	11	271
Guosong Qin China	11	379 2.0×	188 1.1×	13 0.4×	8 0.3×	17 0.7×	17	497

Countries citing papers authored by Fátima Lopes

Since Specialization

Citations

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

Fields of papers citing papers by Fátima Lopes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fátima Lopes

This figure shows the co-authorship network connecting the top 25 collaborators of Fátima Lopes. A scholar is included among the top collaborators of Fátima Lopes 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 Fátima Lopes. Fátima Lopes 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:

14 of 14 papers shown

Silva, Jorge Diogo Da, Marta D. Costa, Bruno Almeida, et al.. (2021). Case Report: A Novel GNB1 Mutation Causes Global Developmental Delay With Intellectual Disability and Behavioral Disorders. Frontiers in Neurology. 12. 735549–735549. 8 indexed citations

Lopes, Fátima, et al.. (2020). A spontaneous cervical epidural hematoma mimicking a stroke – A case report. Surgical Neurology International. 11. 157–157. 7 indexed citations

Martins, André F., et al.. (2020). Benefícios do exercício físico intradialítico: revisão sistemática. SHILAP Revista de lepidopterología. 3(2). 44–54. 1 indexed citations

Lopes, Fátima, Gabriela Soares, Clara D.M. van Karnebeek, et al.. (2019). The Role of AKT3 Copy Number Changes in Brain Abnormalities and Neurodevelopmental Disorders: Four New Cases and Literature Review. Frontiers in Genetics. 10. 58–58. 8 indexed citations

Lopes, Fátima, J Gauthier, Virginie Saillour, et al.. (2018). Refining the phenotype associated with biallelic DNAJC21 mutations. Clinical Genetics. 94(2). 252–258. 26 indexed citations

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

Lopes, Fátima, Sally Ann Lynch, Arminda Jorge, et al.. (2017). The contribution of 7q33 copy number variations for intellectual disability. Neurogenetics. 19(1). 27–40. 2 indexed citations

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

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.

10.

Vieira, José Pedro, Fátima Lopes, Anabela Silva‐Fernandes, et al.. (2015). Variant Rett syndrome in a girl with a pericentric X‐chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene. International Journal of Developmental Neuroscience. 46(1). 82–87. 24 indexed citations

11.

Wen, Jiadi, Fátima Lopes, Gabriela Soares, et al.. (2013). Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2. Orphanet Journal of Rare Diseases. 8(1). 100–100. 21 indexed citations

12.

Kjeldsen, Kasper Urup, Fátima Lopes, Kjeld Ingvorsen, et al.. (2009). Biocorrosion and biofilm formation in a nutrient limited heating system subjected to alternating microaerophilic conditions. Biofouling. 25(8). 727–737. 8 indexed citations

13.

Zuber, Benoît, Marisa Haenni, Tânia Ribeiro, et al.. (2006). Granular Layer in the Periplasmic Space of Gram-Positive Bacteria and Fine Structures ofEnterococcus gallinarumandStreptococcus gordoniiSepta Revealed by Cryo-Electron Microscopy of Vitreous Sections. Journal of Bacteriology. 188(18). 6652–6660. 77 indexed citations

14.

Dervaux, Alain, et al.. (2001). [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].. PubMed. 27(2). 194–7. 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.

Explore authors with similar magnitude of impact