Inês Carrilho

1.5k total citations
20 papers, 362 citations indexed

About

Inês Carrilho is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Inês Carrilho has authored 20 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Neurology and 5 papers in Physiology. Recurrent topics in Inês Carrilho's work include Histiocytic Disorders and Treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Inês Carrilho is often cited by papers focused on Histiocytic Disorders and Treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Inês Carrilho collaborates with scholars based in Portugal, United States and Spain. Inês Carrilho's co-authors include Teresa Temudo, Clara Barbot, Peter Huppke, José Pedro Vieira, Jorge Sequeiros, Pedro Cabral, Hendrik Rosewich, Sarah L. Sawyer, Robert Steinfeld and Maria José Fonseca and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Movement Disorders.

In The Last Decade

Inês Carrilho

18 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Inês Carrilho Portugal	8	162	153	79	75	59	20	362
Serena Galosi Italy	12	147 0.9×	136 0.9×	70 0.9×	16 0.2×	61 1.0×	38	328
Jared Cook United States	11	139 0.9×	36 0.2×	80 1.0×	50 0.7×	70 1.2×	17	314
Marcelo Miranda Chile	12	71 0.4×	30 0.2×	114 1.4×	59 0.8×	88 1.5×	35	313
A.E. Henneberg Germany	9	111 0.7×	40 0.3×	96 1.2×	26 0.3×	78 1.3×	17	357
Maria Teresa Dotti Italy	13	205 1.3×	60 0.4×	115 1.5×	39 0.5×	147 2.5×	18	400
Miguel Angel Pujana Spain	5	199 1.2×	217 1.4×	47 0.6×	35 0.5×	130 2.2×	7	420
Karin Kojima Japan	9	129 0.8×	105 0.7×	13 0.2×	65 0.9×	65 1.1×	18	311
Antonella Antenora Italy	13	163 1.0×	57 0.4×	145 1.8×	39 0.5×	210 3.6×	22	390
Svetlana Gataullina France	13	135 0.8×	172 1.1×	82 1.0×	36 0.5×	137 2.3×	22	527
Peter Henricus Maria Franciscus van Domburg Netherlands	9	169 1.0×	53 0.3×	155 2.0×	31 0.4×	44 0.7×	11	441

Countries citing papers authored by Inês Carrilho

Since Specialization

Citations

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

Fields of papers citing papers by Inês Carrilho

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inês Carrilho

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

20 of 20 papers shown

Chorão, Rui, et al.. (2023). Familial occipital lobe epilepsy associated with GABAA receptor variants. Seizure. 112. 139–142. 1 indexed citations

Temudo, Teresa, et al.. (2023). Cefaleas primarias con inicio en la infancia y la adolescencia: historia natural y factores pronósticos en una población portuguesa. Revista de Neurología. 76(1). 9–9. 1 indexed citations

Damásio, Joana, Diana Santos, Sara Morais, et al.. (2021). Congenital ataxia due to novel variant in ATP8A2 . Clinical Genetics. 100(1). 79–83. 6 indexed citations

Carrilho, Inês, et al.. (2018). Distonía temprana poco frecuente (DYT16) en una niña portuguesa. Revista de Neurología. 66(12). 434–434. 1 indexed citations

Lopes, Marta, et al.. (2018). Treatment of acute migraine and status migrainosus in pediatrics. SHILAP Revista de lepidopterología. 28(3). 132–140.

Melo, Cláudia, et al.. (2016). Idiopathic toe walking in children and adolescents. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 25(1). 27–34. 1 indexed citations

Melo, Cláudia, et al.. (2016). Marcha em pontas idiopática em idade pediátrica. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 1 indexed citations

Garrido, Cristina, et al.. (2014). Esclerosis tuberosa: caracterización clínica e intento de correlación fenotipo/genotipo. Anales de Pediatría. 81(5). 289–296. 7 indexed citations

Carrilho, Inês, et al.. (2014). Ataxia-Telangiectasia — Caso Clínico. SHILAP Revista de lepidopterología. 33(4). 283–286.

10.

Rosewich, Hendrik, Andreas Ohlenbusch, Peter Huppke, et al.. (2014). The expanding clinical and genetic spectrum of ATP1A3-related disorders. Neurology. 82(11). 945–955. 83 indexed citations

11.

Garrido, Cristina, et al.. (2014). Tuberous sclerosis: Clinical characteristics and their relationship to genotype/phenotype. Anales de Pediatría (English Edition). 81(5). 289–296. 6 indexed citations

12.

Damásio, Joana, Maria Isabel Leite, Estér Coutinho, et al.. (2013). Progressive Encephalomyelitis With Rigidity and Myoclonus. JAMA Neurology. 70(4). 498–498. 46 indexed citations

13.

Ríos, María del Carmen García, Clara Barbot, Pedro Sá Pinto, et al.. (2012). Síndrome de Sturge-Weber: variabilidad clínica y de neuroimagen. Anales de Pediatría. 77(6). 397–402. 1 indexed citations

14.

Santos, Mònica, Teresa Temudo, Teresa Kay, et al.. (2009). Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients. Journal of Child Neurology. 24(1). 49–55. 10 indexed citations

15.

Temudo, Teresa, Elisabete Ramos, Karin Ziliotto Dias, et al.. (2008). Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type. Movement Disorders. 23(10). 1384–1390. 66 indexed citations

16.

Temudo, Teresa, Inês Carrilho, Mònica Santos, et al.. (2008). Evaluation of CSF neurotransmitters and folate in 25 patients with Rett disorder and effects of treatment. Brain and Development. 31(1). 46–51. 42 indexed citations

17.

García‐Cazorla, Àngels, Sofia Duarte, Mercedes Serrano, et al.. (2008). Mitochondrial diseases mimicking neurotransmitter defects. Mitochondrion. 8(3). 273–278. 34 indexed citations

18.

Carrilho, Inês, António Guimarães, João Paulo Teixeira, et al.. (2008). Infantile neuroaxonal dystrophy: What's most important for the diagnosis?. European Journal of Paediatric Neurology. 12(6). 491–500. 43 indexed citations

19.

Sousa, Susana, et al.. (2007). Bilateral Perisylvian Polymicrogyria and Chromosome 1 Anomaly. Pediatric Neurology. 36(6). 418–420. 11 indexed citations

20.

Costa, Elı́sio, et al.. (2005). Múltiples factores de riesgo trombofílicos identificados en un lactante con accidente vascular cerebral. Revista de Neurología. 40(8). 479–479. 2 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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