Luísa Coutinho Santos

645 total citations
11 papers, 372 citations indexed

About

Luísa Coutinho Santos is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Luísa Coutinho Santos has authored 11 papers receiving a total of 372 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Ophthalmology. Recurrent topics in Luísa Coutinho Santos's work include Retinal Development and Disorders (6 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Luísa Coutinho Santos is often cited by papers focused on Retinal Development and Disorders (6 papers), Genomics and Rare Diseases (2 papers) and Mitochondrial Function and Pathology (2 papers). Luísa Coutinho Santos collaborates with scholars based in Portugal, United Kingdom and Switzerland. Luísa Coutinho Santos's co-authors include Virginie G. Peter, Carlo Rivolta, Mathieu Quinodoz, Elias I. Traboulsi, Cameron F. Parsa, Ana Berta Sousa, Olof Sundin, Ethan M. Weinberg, Eduardo Silva and Irene H. Maumenee and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Luísa Coutinho Santos

11 papers receiving 363 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Luísa Coutinho Santos Portugal	7	219	161	141	66	36	11	372
Jenina Capasso United States	12	238 1.1×	103 0.6×	113 0.8×	45 0.7×	22 0.6×	36	316
Elena Schiff United Kingdom	10	300 1.4×	107 0.7×	134 1.0×	40 0.6×	54 1.5×	29	418
Delphine Blain United States	10	275 1.3×	189 1.2×	119 0.8×	90 1.4×	59 1.6×	24	432
Jan-Willem R. Pott Netherlands	8	293 1.3×	71 0.4×	176 1.2×	48 0.7×	28 0.8×	9	336
Zixi Sun China	11	224 1.0×	67 0.4×	110 0.8×	36 0.5×	32 0.9×	37	304
Hannah Verdin Belgium	14	317 1.4×	268 1.7×	69 0.5×	23 0.3×	26 0.7×	29	467
Anna M. Siemiatkowska Netherlands	14	392 1.8×	126 0.8×	216 1.5×	43 0.7×	64 1.8×	24	461
Xunlun Sheng China	14	386 1.8×	118 0.7×	249 1.8×	121 1.8×	61 1.7×	48	598
Tasneem P. Sharma United States	9	309 1.4×	55 0.3×	204 1.4×	113 1.7×	48 1.3×	17	473

Countries citing papers authored by Luísa Coutinho Santos

Since Specialization

Citations

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

Fields of papers citing papers by Luísa Coutinho Santos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luísa Coutinho Santos. 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 Luísa Coutinho Santos. The network helps show where Luísa Coutinho Santos may publish in the future.

Co-authorship network of co-authors of Luísa Coutinho Santos

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

All Works

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11 of 11 papers shown

Marques, João Pedro, et al.. (2025). Portuguese Society of Ophthalmology and Portuguese Society of Human Genetics Joint Clinical Practice Guidelines for Genetic Testing in Inherited Retinal Dystrophies. Clinical Genetics. 107(6). 600–611. 1 indexed citations

Vaz-Pereira, Sara, Lilianne Duarte, Ana Berta Sousa, et al.. (2024). Genetic profile of syndromic retinitis pigmentosa in Portugal. Graefe s Archive for Clinical and Experimental Ophthalmology. 262(6). 1883–1897. 5 indexed citations

Quinodoz, Mathieu, Marc Folcher, Siying Lin, et al.. (2024). Bi-allelic variants in COQ8B, a gene involved in the biosynthesis of coenzyme Q10, lead to non-syndromic retinitis pigmentosa. The American Journal of Human Genetics. 111(10). 2299–2306. 1 indexed citations

Marques, João Pedro, Luísa Coutinho Santos, Sara Vaz-Pereira, et al.. (2024). The socioeconomic epidemiology of inherited retinal diseases in Portugal. Orphanet Journal of Rare Diseases. 19(1). 151–151. 1 indexed citations

Peter, Virginie G., Mathieu Quinodoz, Katarina Cisarova, et al.. (2023). The first genetic landscape of inherited retinal dystrophies in Portuguese patients identifies recurrent homozygous mutations as a frequent cause of pathogenesis. PNAS Nexus. 2(3). pgad043–pgad043. 19 indexed citations

Quinodoz, Mathieu, Virginie G. Peter, Nicola Bedoni, et al.. (2021). AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data. Nature Communications. 12(1). 518–518. 85 indexed citations

Peter, Virginie G., Mathieu Quinodoz, Marta Soares, et al.. (2020). New clinical and molecular evidence linking mutations in ARSG to Usher syndrome type IV. Human Mutation. 42(3). 261–271. 25 indexed citations

Bedoni, Nicola, J Cunningham, Eric S. Tucker, et al.. (2019). Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. PLoS Genetics. 15(8). e1008315–e1008315. 20 indexed citations

Pinto, Rita M., et al.. (2013). Ritonavir and bull’s eye maculopathy: case report. SHILAP Revista de lepidopterología. 3. Doc01–Doc01. 10 indexed citations

10.

Sundin, Olof, Eduardo Silva, Sharola Dharmaraj, et al.. (2005). Extreme hyperopia is the result of null mutations inMFRP, which encodes a Frizzled-related protein. Proceedings of the National Academy of Sciences. 102(27). 9553–9558. 134 indexed citations

11.

Gerber, S., Jean‐Michel Rozet, Shinichiro Takezawa, et al.. (2000). The photoreceptor cell-specific nuclear receptor gene ( PNR ) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish Inquisition. Human Genetics. 107(3). 276–284. 71 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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