Astrid M. Vicente

15.1k total citations
72 papers, 1.7k citations indexed

About

Astrid M. Vicente is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Astrid M. Vicente has authored 72 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 28 papers in Cognitive Neuroscience and 24 papers in Molecular Biology. Recurrent topics in Astrid M. Vicente's work include Autism Spectrum Disorder Research (28 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Genomic variations and chromosomal abnormalities (8 papers). Astrid M. Vicente is often cited by papers focused on Autism Spectrum Disorder Research (28 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Genomic variations and chromosomal abnormalities (8 papers). Astrid M. Vicente collaborates with scholars based in Portugal, Mozambique and United Kingdom. Astrid M. Vicente's co-authors include Catarina Correia, Guiomar Oliveira, Carla Marques, Teresa S. Miguel, Assunção Ataíde, Hugo Martiniano, Constantin Fesel, Celeste Bento, Marta Barreto and Sofia A. Oliveira and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Astrid M. Vicente

69 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Astrid M. Vicente Portugal	20	664	631	497	234	198	72	1.7k
Yuichiro Watanabe Japan	25	390 0.6×	293 0.5×	642 1.3×	134 0.6×	231 1.2×	110	2.2k
Melanie A. Carless United States	28	490 0.7×	550 0.9×	1.0k 2.1×	163 0.7×	301 1.5×	81	2.7k
Lisa J. Strug Canada	26	606 0.9×	310 0.5×	523 1.1×	94 0.4×	569 2.9×	81	2.2k
Mina Tabrizi Iran	28	217 0.3×	356 0.6×	686 1.4×	438 1.9×	657 3.3×	75	2.4k
Anna C. Need United States	26	1.3k 2.0×	353 0.6×	1.1k 2.3×	110 0.5×	284 1.4×	33	3.0k
Thomas Bettecken Germany	22	379 0.6×	204 0.3×	786 1.6×	56 0.2×	211 1.1×	53	2.0k
Beth Wilmot United States	22	319 0.5×	227 0.4×	711 1.4×	123 0.5×	277 1.4×	70	2.0k
John P. Hussman United States	11	400 0.6×	473 0.7×	309 0.6×	47 0.2×	96 0.5×	14	964
Nina Mononen Finland	30	501 0.8×	100 0.2×	954 1.9×	183 0.8×	232 1.2×	88	2.4k
Silvia Pellegrini Italy	29	272 0.4×	271 0.4×	1.0k 2.0×	57 0.2×	119 0.6×	80	2.6k

Countries citing papers authored by Astrid M. Vicente

Since Specialization

Citations

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

Fields of papers citing papers by Astrid M. Vicente

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Astrid M. Vicente. 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 Astrid M. Vicente. The network helps show where Astrid M. Vicente may publish in the future.

Co-authorship network of co-authors of Astrid M. Vicente

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

All Works

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20 of 20 papers shown

Pezzullo, Angelo Maria, Péter Pikó, Markus Perola, et al.. (2025). A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utility. Journal of Clinical Epidemiology. 181. 111729–111729. 1 indexed citations

Rasga, Célia, et al.. (2024). Bridging Genetic Insights with Neuroimaging in Autism Spectrum Disorder—A Systematic Review. International Journal of Molecular Sciences. 25(9). 4938–4938. 4 indexed citations

Rasga, Célia, Hugo Martiniano, Cátia Café, et al.. (2023). Evidence for an association of prenatal exposure to particulate matter with clinical severity of Autism Spectrum Disorder. Environmental Research. 228. 115795–115795. 10 indexed citations

Rasga, Célia, Cátia Café, Frederico Duque, et al.. (2023). Prevalence of Autism Spectrum Disorder in the Centro region of Portugal: a population based study of school age children within the ASDEU project. Frontiers in Psychiatry. 14. 1148184–1148184. 2 indexed citations

Rasga, Célia, et al.. (2020). Prevalência da perturbação do espectro do autismo na região Centro de Portugal: um estudo no âmbito do projeto ASDEU. Scientific Repository of the National Health Institute Doutor Ricardo Jorge (Instituto Nacional de Saúde Doutor Ricardo Jorge). 9(27). 47–51.

Rasga, Célia, et al.. (2020). Saúde mental em tempos da pandemia da COVID-19 : abordagem metodológica utilizada no projeto SM-COVID19. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 9. 40–45. 1 indexed citations

Martiniano, Hugo, et al.. (2018). Identifying disease genes using machine learning and gene functional similarities, assessed through Gene Ontology. PLoS ONE. 13(12). e0208626–e0208626. 60 indexed citations

Almeida, Joana, Susana Mouga, Ana Beleza‐Meireles, et al.. (2017). Copy number variations in chromosome 16p13.11-The neurodevelopmental clinical spectrum. Current Pediatric Research. 21(1). 116–129. 5 indexed citations

Gaio, Vânia, Baltazar Nunes, Aida Fernandes, et al.. (2015). Pharmacogenetic Profile of a South Portuguese Population: Results from the Pilot Study of the European Health Examination Survey in Portugal. Public Health Genomics. 18(3). 139–150. 3 indexed citations

10.

Correia, Catarina, Guiomar Oliveira, & Astrid M. Vicente. (2014). Protein Interaction Networks Reveal Novel Autism Risk Genes within GWAS Statistical Noise. PLoS ONE. 9(11). e112399–e112399. 15 indexed citations

11.

Oliveira, Bárbara, Inês C. Conceição, Cátia Café, et al.. (2013). Synaptic Transmission: Looking for Clues to Autism Spectrum Disorders (ASD) Etiology in Copy Number Variants Containing Synaptic Genes. Postgraduate Medicine. 96(1). 37–50. 1 indexed citations

12.

Fesel, Constantin, Marta Barreto, Ricardo C. Ferreira, et al.. (2012). Compensatory T-Cell Regulation in Unaffected Relatives of SLE Patients, and Opposite IL-2/CD25-Mediated Effects Suggested by Coreferentiality Modeling. PLoS ONE. 7(3). e33992–e33992. 29 indexed citations

13.

Manso, Helena, Tiago Krug, João Sobral, et al.. (2011). Variants within the nitric oxide synthase 1 gene are associated with stroke susceptibility. Atherosclerosis. 220(2). 443–448. 21 indexed citations

14.

Manso, Helena, Tiago Krug, João Sobral, et al.. (2010). Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after stroke. BMC Medical Genetics. 11(1). 40–40. 57 indexed citations

15.

Branco, Cláudia C., et al.. (2009). Linkage disequilibrium and diversity for three genomic regions in Azoreans and mainland Portuguese. Genetics and Molecular Biology. 32(2). 220–226. 2 indexed citations

16.

Barreto, Marta, Ricardo C. Ferreira, Maria Francisca Moraes‐Fontes, et al.. (2009). Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFβ gene variants. BMC Immunology. 10(1). 5–5. 69 indexed citations

17.

Oliveira, Guiomar, Assunção Ataíde, Carla Marques, et al.. (2007). Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions. Developmental Medicine & Child Neurology. 49(10). 726–733. 87 indexed citations

18.

Barreto, Marta, Eugénia Santos, Ricardo C. Ferreira, et al.. (2004). Evidence for CTLA4 as a susceptibility gene for systemic lupus erythematosus. European Journal of Human Genetics. 12(8). 620–626. 105 indexed citations

19.

Fesel, Constantin, T.R.A. Macedo, Celeste Bento, et al.. (2004). Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism. Molecular Psychiatry. 9(3). 264–271. 101 indexed citations

20.

Basile, Vincenzo S., Astrid M. Vicente, John A. Martignetti, et al.. (1998). Assignment<footref rid="foot01"><sup>1</sup></footref> of the human BC200 RNA gene (BCYRN1) to chromosome 2p16 by radiation hybrid mapping. Cytogenetic and Genome Research. 82(3-4). 271–272. 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.

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