Graça Fialho

894 total citations
17 papers, 159 citations indexed

About

Graça Fialho is a scholar working on Sensory Systems, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Graça Fialho has authored 17 papers receiving a total of 159 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Sensory Systems, 11 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in Graça Fialho's work include Hearing, Cochlea, Tinnitus, Genetics (14 papers), Connexins and lens biology (10 papers) and Hearing Loss and Rehabilitation (5 papers). Graça Fialho is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (14 papers), Connexins and lens biology (10 papers) and Hearing Loss and Rehabilitation (5 papers). Graça Fialho collaborates with scholars based in Portugal, United Kingdom and Brazil. Graça Fialho's co-authors include Helena Caria, Tiago Matos, O Dias, Mário Andrea, David P. Kelsell, Trond Aasen, Marília Antunes, Joana Rita Chora, Derek J. Hoare and Haúla F. Haider and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Hearing Research.

In The Last Decade

Graça Fialho

16 papers receiving 154 citations

Peers

Graça Fialho

NEURO

EAS

Małgorzata Mueller‐Malesińska Poland

Birgit Haack Germany

Saima Anwar Pakistan

Jaime Gallo‐Terán Spain

Mark Houseman United Kingdom

Khadijeh Jalalvand Iran

M. Cruz Tapia Spain

Xuezhong Liu United States

Linyi Xie China

Sebastian Gießelmann Germany

Małgorzata Mueller‐Malesińska Poland

Graça Fialho

117 ×1.1

111 ×1.2

47 ×1.2

NEURO

23 ×0.8

25 ×0.9

EAS

Citations per year, relative to Graça Fialho Graça Fialho (= 1×) peers Małgorzata Mueller‐Malesińska

Countries citing papers authored by Graça Fialho

Since Specialization

Citations

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

Fields of papers citing papers by Graça Fialho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Graça Fialho

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

All Works

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17 of 17 papers shown

Haider, Haúla F., Sara Ribeiro, Derek J. Hoare, et al.. (2021). Quality of Life and Psychological Distress in Portuguese Older Individuals with Tinnitus. Brain Sciences. 11(7). 953–953. 4 indexed citations

Haider, Haúla F., Marília Antunes, Agnieszka J. Szczepek, et al.. (2017). Biomarkers of Presbycusis and Tinnitus in a Portuguese Older Population. Frontiers in Aging Neuroscience. 9. 346–346. 13 indexed citations

Lourenço, Vera L., et al.. (2016). Genetic Basis of Nonsyndromic Sensorineural Hearing Loss in the Sub-Saharan African Island Population of São Tomé and Príncipe: The Role of the DFNB1 Locus?. OMICS A Journal of Integrative Biology. 20(8). 449–455. 2 indexed citations

Escada, Pedro, et al.. (2016). Caratterizzazione della mutazione SLC26A4 c.918+2T>C e report di una nuova variante potenzialmente a rischio. Acta Otorhinolaryngologica Italica. 36(3). 233–238.

Matos, Tiago, et al.. (2015). The controversial p.Met34Thr variant in GJB2 gene: Two siblings, one genotype, two phenotypes. International Journal of Pediatric Otorhinolaryngology. 79(8). 1316–1319. 3 indexed citations

Matos, Tiago, et al.. (2014). WFS1 and non-syndromic low-frequency sensorineural hearing loss: A novel mutation in a Portuguese case. Gene. 538(2). 288–291. 13 indexed citations

Matos, Tiago, Helena Caria, Joana Rita Chora, et al.. (2013). Spectrum and frequency ofGJB2mutations in a cohort of 264 Portuguese nonsyndromic sensorineural hearing loss patients. International Journal of Audiology. 52(7). 466–471. 16 indexed citations

Chora, Joana Rita, et al.. (2012). A novel p.Leu213X mutation in GJB2 gene in a Portuguese family. International Journal of Pediatric Otorhinolaryngology. 77(1). 89–91. 1 indexed citations

Chora, Joana Rita, Tiago Matos, Raquel Ferreira, et al.. (2012). Two Portuguese Cochlear Implanted Dizygotic Twins: A Case Report. SHILAP Revista de lepidopterología. 2012. 1–5. 1 indexed citations

10.

Matos, Tiago, O Dias, Mário Andrea, et al.. (2011). Novel splice-site mutation c.1615-2A>G (IVS14-2A>G) in the SLC26A4 gene causing Pendred syndrome in a consanguineous Portuguese family. American Journal of Medical Genetics Part A. 155(4). 924–927. 4 indexed citations

11.

Matos, Tiago, Helena Caria, Rita Cascão, et al.. (2011). Assessing Noncoding Sequence Variants of GJB2 for Hearing Loss Association. SHILAP Revista de lepidopterología. 2011. 1–8. 8 indexed citations

12.

Chora, Joana Rita, et al.. (2010). DFNB1-associated deafness in Portuguese cochlear implant users: Prevalence and impact on oral outcome. International Journal of Pediatric Otorhinolaryngology. 74(10). 1135–1139. 19 indexed citations

13.

Matos, Tiago, et al.. (2009). The Controversial p.Arg127His Mutation in GJB2 : Report on Three Portuguese Hearing Loss Family Cases. Genetic Testing and Molecular Biomarkers. 14(1). 141–144. 13 indexed citations

14.

Matos, Tiago, Helena Caria, Trond Aasen, et al.. (2008). A novel M163L mutation in connexin 26 causing cell death and associated with autosomal dominant hearing loss. Hearing Research. 240(1-2). 87–92. 29 indexed citations

15.

Caria, Helena, Tiago Matos, Rui Oliveira Soares, et al.. (2005). A7445G mtDNA mutation present in a Portuguese family exhibiting hereditary deafness and palmoplantar keratoderma. Journal of the European Academy of Dermatology and Venereology. 19(4). 455–458. 13 indexed citations

16.

Fialho, Graça, et al.. (1983). Inbreeding studies in Brasilian schoolchildren. American Journal of Medical Genetics. 16(3). 331–355. 15 indexed citations

17.

Freire‐Maia, N., et al.. (1970). Inbreeding Load, as Estimated with Sib Control, in a Portuguese Population. Human Heredity. 20(3). 248–251. 5 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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