Isabel Alonso

2.8k total citations
76 papers, 1.6k citations indexed

About

Isabel Alonso is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Isabel Alonso has authored 76 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 40 papers in Cellular and Molecular Neuroscience and 15 papers in Neurology. Recurrent topics in Isabel Alonso's work include Genetic Neurodegenerative Diseases (36 papers), Mitochondrial Function and Pathology (27 papers) and Migraine and Headache Studies (12 papers). Isabel Alonso is often cited by papers focused on Genetic Neurodegenerative Diseases (36 papers), Mitochondrial Function and Pathology (27 papers) and Migraine and Headache Studies (12 papers). Isabel Alonso collaborates with scholars based in Portugal, Brazil and United States. Isabel Alonso's co-authors include Jorge Sequeiros, Isabel Silveira, Paula Coutinho, Alda Sousa, José Barros, Carolina Lemos, Diana Santos, Laura Bannach Jardim, Assunção Tuna and Ricardo Taipa and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Isabel Alonso

75 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabel Alonso Portugal 24 889 776 400 348 218 76 1.6k
Jonas Alex Morales Saute Brazil 24 724 0.8× 832 1.1× 498 1.2× 187 0.5× 80 0.4× 78 1.3k
Patricia Kramer United States 15 848 1.0× 927 1.2× 853 2.1× 270 0.8× 299 1.4× 21 1.9k
Emilia Bellone Italy 24 681 0.8× 1.0k 1.3× 787 2.0× 405 1.2× 176 0.8× 100 1.8k
Velina Guergueltcheva Bulgaria 23 899 1.0× 561 0.7× 408 1.0× 213 0.6× 176 0.8× 52 1.6k
Hiroyuki Morino Japan 20 685 0.8× 564 0.7× 494 1.2× 216 0.6× 124 0.6× 78 1.2k
Fátima Ferreirinha Portugal 20 591 0.7× 446 0.6× 139 0.3× 246 0.7× 70 0.3× 47 1.4k
Ali Benomar Morocco 21 1.5k 1.7× 1.7k 2.2× 709 1.8× 346 1.0× 143 0.7× 69 2.3k
Denise M. Kay United States 25 736 0.8× 534 0.7× 1.2k 2.9× 525 1.5× 294 1.3× 54 2.4k
Ilaria Guella Canada 20 454 0.5× 255 0.3× 438 1.1× 152 0.4× 274 1.3× 45 1.3k
Rong Xue China 16 800 0.9× 424 0.5× 195 0.5× 237 0.7× 106 0.5× 23 1.5k

Countries citing papers authored by Isabel Alonso

Since Specialization
Citations

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

Fields of papers citing papers by Isabel Alonso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabel Alonso

This figure shows the co-authorship network connecting the top 25 collaborators of Isabel Alonso. A scholar is included among the top collaborators of Isabel Alonso 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 Isabel Alonso. Isabel Alonso 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.
2.
Fortuna, Ana María, et al.. (2023). An SPG7 mutation as a novel cause of monogenic progressive muscular atrophy. Neurological Sciences. 44(9). 3303–3305. 1 indexed citations
3.
4.
Alonso, Isabel, et al.. (2022). PRKRAP1 Pseudogene Complicating the Diagnosis of Young‐Onset Dystonia Due to PRKRA Gene Disease‐Causing Variants (DYT‐PRKRA). Movement Disorders Clinical Practice. 9(5). 703–706. 1 indexed citations
5.
Alonso, Isabel, et al.. (2022). As associações de doenças raras em Portugal: Uma fonte importante de apoio psicossocial. Psicologia. 36(2). 108–118. 1 indexed citations
6.
Alves‐Ferreira, Miguel, Jorge Sequeiros, Alda Sousa, et al.. (2021). A genetic interaction of NRXN2 with GABRE, SYT1 and CASK in migraine patients: a case-control study. The Journal of Headache and Pain. 22(1). 57–57. 5 indexed citations
7.
Santos, Diana, Teresa Coelho, Miguel Alves‐Ferreira, et al.. (2019). C1QA and C1QC modify age‐at‐onset in familial amyloid polyneuropathy patients. Annals of Clinical and Translational Neurology. 6(4). 748–754. 13 indexed citations
8.
Alonso, Isabel, et al.. (2019). Diagnostic yield of next-generation sequencing applied to neurological disorders. Journal of Clinical Neuroscience. 67. 14–18. 17 indexed citations
9.
Pereira, Susana, Esmeralda Rodrigues, Laura Vilarinho, et al.. (2018). Mitochondrial Encephalopathy: First Portuguese Report of a VARS2 Causative Variant. JIMD Reports. 42. 113–119. 9 indexed citations
10.
Matilla‐Dueñas, Antoni, Marc Corral‐Juan, Agustí Rodríguez‐Palmero, et al.. (2017). Rare Neurodegenerative Diseases: Clinical and Genetic Update. Advances in experimental medicine and biology. 1031. 443–496. 30 indexed citations
11.
Santos, Diana, Maria João Santos, Miguel Alves‐Ferreira, et al.. (2017). mtDNA copy number associated with age of onset in familial amyloid polyneuropathy. Journal of Neurology Neurosurgery & Psychiatry. 89(3). 300–304. 18 indexed citations
12.
Brás, José, Isabel Alonso, Clara Barbot, et al.. (2015). Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4. The American Journal of Human Genetics. 96(3). 474–479. 93 indexed citations
13.
Porto, Graça, Pierre Brissot, Dorine W. Swinkels, et al.. (2015). EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). European Journal of Human Genetics. 24(4). 479–495. 59 indexed citations
14.
Pereira‐Monteiro, José, José Barros, Jorge Sequeiros, et al.. (2013). Interaction between γ-Aminobutyric Acid A Receptor Genes: New Evidence in Migraine Susceptibility. PLoS ONE. 8(9). e74087–e74087. 18 indexed citations
15.
Pereira, Maria Luiza Saraiva, Tailise Conte Gheno, Gabriel Vasata Furtado, et al.. (2013). Spinocerebellar Ataxia Type 10: Haplotype Analyses in 15 Brazilian and Peruvian Families (P05.044). Neurology. 80(7_supplement). 1 indexed citations
16.
Loureiro, José Leal, Jorge Pinto‐Basto, Ana M. Lopes, et al.. (2012). Alu elements mediate large SPG11 gene rearrangements: further spatacsin mutations. Genetics in Medicine. 14(1). 143–151. 21 indexed citations
17.
Lemos, Carolina, Isabel Alonso, José Barros, et al.. (2012). Assessing Risk Factors for Migraine: Differences in Gender Transmission. PLoS ONE. 7(11). e50626–e50626. 19 indexed citations
18.
Almeida, Teresa, Isabel Alonso, Sandra Martins, et al.. (2009). Ancestral Origin of the ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10 (SCA10). PLoS ONE. 4(2). e4553–e4553. 39 indexed citations
19.
González‐Lois, Carmen, et al.. (2001). Small Cell Carcinoma of the KidneyA Case Report and Review of the Literature. Archives of Pathology & Laboratory Medicine. 125(6). 796–798. 9 indexed citations
20.
Silveira, Isabel, Isabel Alonso, Laura Guimarães, et al.. (2000). High Germinal Instability of the (CTG)n at the SCA8 Locus of Both Expanded and Normal Alleles. The American Journal of Human Genetics. 66(3). 830–840. 61 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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