Sergio Lois

1.6k total citations
23 papers, 543 citations indexed

About

Sergio Lois is a scholar working on Molecular Biology, Nutrition and Dietetics and Genetics. According to data from OpenAlex, Sergio Lois has authored 23 papers receiving a total of 543 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 4 papers in Nutrition and Dietetics and 3 papers in Genetics. Recurrent topics in Sergio Lois's work include RNA modifications and cancer (6 papers), Epigenetics and DNA Methylation (5 papers) and RNA Research and Splicing (4 papers). Sergio Lois is often cited by papers focused on RNA modifications and cancer (6 papers), Epigenetics and DNA Methylation (5 papers) and RNA Research and Splicing (4 papers). Sergio Lois collaborates with scholars based in Spain, France and Sri Lanka. Sergio Lois's co-authors include Xavier de la Cruz, Marian A. Martínez‐Balbás, Sara Sánchez-Molina, Juan Carlos Triviño, Javier Benı́tez, Anna Díez-Villanueva, Miguel A. Peinado, Izaskun Mallona, Elvira Carrió and Mònica Suelves and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Current Biology.

In The Last Decade

Sergio Lois

23 papers receiving 535 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sergio Lois Spain 12 421 83 54 46 37 23 543
Miranda Kleijn Netherlands 15 597 1.4× 48 0.6× 62 1.1× 24 0.5× 36 1.0× 24 788
Kathryn E. Dickerson United States 10 602 1.4× 119 1.4× 79 1.5× 73 1.6× 49 1.3× 23 786
Isabel Peixeiro Portugal 4 423 1.0× 33 0.4× 38 0.7× 28 0.6× 21 0.6× 5 496
Christian Schuberth Germany 12 533 1.3× 72 0.9× 28 0.5× 64 1.4× 41 1.1× 17 793
Poshen B. Chen United States 11 805 1.9× 114 1.4× 131 2.4× 28 0.6× 18 0.5× 16 900
Mintie Pu United States 7 659 1.6× 129 1.6× 31 0.6× 27 0.6× 16 0.4× 10 750
Wai Shan Yuen Australia 11 381 0.9× 51 0.6× 27 0.5× 16 0.3× 66 1.8× 16 570
H. Shuen Lo United States 6 522 1.2× 191 2.3× 61 1.1× 61 1.3× 15 0.4× 7 647
Wenxuan Yin China 13 332 0.8× 75 0.9× 16 0.3× 24 0.5× 51 1.4× 29 432
Andrea Harničarová Czechia 10 520 1.2× 65 0.8× 34 0.6× 59 1.3× 6 0.2× 11 601

Countries citing papers authored by Sergio Lois

Since Specialization
Citations

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

Fields of papers citing papers by Sergio Lois

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sergio Lois

This figure shows the co-authorship network connecting the top 25 collaborators of Sergio Lois. A scholar is included among the top collaborators of Sergio Lois 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 Sergio Lois. Sergio Lois 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.
Carbonell, Diego, Sergio Lois, Gabriela Rodríguez‐Macías, et al.. (2021). Next Generation Cytogenetics in Myeloid Hematological Neoplasms: Detection of CNVs and Translocations. Cancers. 13(12). 3001–3001. 3 indexed citations
2.
Garrido-Godino, Ana I., Olga Rodríguez‐Galán, Antonio Jordán‐Pla, et al.. (2020). Prefoldin-like Bud27 influences the transcription of ribosomal components and ribosome biogenesis in Saccharomyces cerevisiae. RNA. 26(10). 1360–1379. 12 indexed citations
3.
Harpaz, Nofar, et al.. (2020). ミオシンVからのカーゴ放出はカーゴアダプターをリン酸化し,ユビキチン化する平行経路の収束を必要とする【JST・京大機械翻訳】. Current Biology. 30(22). 4399–4412. 2 indexed citations
4.
Lois, Sergio, et al.. (2019). RNA-Seq Perspectives to Improve Clinical Diagnosis. Frontiers in Genetics. 10. 1152–1152. 66 indexed citations
5.
Fueyo, Raquel, Conchi Estarás, Sergio Lois, et al.. (2018). Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation. Nucleic Acids Research. 46(7). 3351–3365. 22 indexed citations
6.
Fueyo, Raquel, Sergio Lois, Laia Bosch‐Presegué, et al.. (2017). The histone demethylase PHF8 is a molecular safeguard of the IFNγ response. Nucleic Acids Research. 45(7). gkw1346–gkw1346. 15 indexed citations
7.
Jordà, Mireia, Anna Díez-Villanueva, Izaskun Mallona, et al.. (2016). The epigenetic landscape of Alu repeats delineates the structural and functional genomic architecture of colon cancer cells. Genome Research. 27(1). 118–132. 42 indexed citations
8.
Carrió, Elvira, Anna Díez-Villanueva, Sergio Lois, et al.. (2015). Deconstruction of DNA Methylation Patterns During Myogenesis Reveals Specific Epigenetic Events in the Establishment of the Skeletal Muscle Lineage. Stem Cells. 33(6). 2025–2036. 51 indexed citations
9.
Joshi, Ricky S., Maya Shvartsman, Erica L. Moran, et al.. (2015). Functional consequences of transferrin receptor‐2 mutations causing hereditary hemochromatosis type 3. Molecular Genetics & Genomic Medicine. 3(3). 221–232. 16 indexed citations
10.
Alsina, Laia, Roger Colobrán, Mariona Fernández de Sevilla, et al.. (2014). Novel and atypical splicing mutation in a compound heterozygous UNC13D defect presenting in Familial Hemophagocytic Lymphohistiocytosis triggered by EBV infection. Clinical Immunology. 153(2). 292–297. 5 indexed citations
11.
Colobrán, Roger, Sergio Lois, Xavier de la Cruz, et al.. (2013). Identification and characterization of a novel splice site mutation in the SERPING1 gene in a family with hereditary angioedema. Clinical Immunology. 150(2). 143–148. 8 indexed citations
12.
Morata, Jordi, et al.. (2013). The Relationship between Gene Isoform Multiplicity, Number of Exons and Protein Divergence. PLoS ONE. 8(8). e72742–e72742. 4 indexed citations
13.
Lois, Sergio, et al.. (2013). Prediction of pathological mutations in proteins: the challenge of integrating sequence conservation and structure stability principles. Wiley Interdisciplinary Reviews Computational Molecular Science. 4(3). 249–268. 16 indexed citations
14.
Morata, Jordi, et al.. (2012). Characterization of the impact of alternative splicing on protein dynamics: The cases of glutathione S‐transferase and ectodysplasin‐A isoforms. Proteins Structure Function and Bioinformatics. 80(9). 2235–2249. 5 indexed citations
15.
16.
Álvarez, Víctor H., et al.. (2009). Comparative Lipid Composition Study in Farmed and Wild Blackspot Seabream (Pagellus bogaraveo). Czech Journal of Food Sciences. 27(Special Issue 1). S274–S276. 5 indexed citations
17.
Lois, Sergio, et al.. (2008). Preservation of protein clefts in comparative models. BMC Structural Biology. 8(1). 2–2. 10 indexed citations
18.
Lois, Sergio, et al.. (2007). The functional modulation of epigenetic regulators by alternative splicing. BMC Genomics. 8(1). 252–252. 15 indexed citations
19.
Medina, Isabel, Sergio Lois, Daneida Lizárraga, et al.. (2006). Functional Fatty Fish Supplemented with Grape Procyanidins. Antioxidant and Proapoptotic Properties on Colon Cell Lines. Journal of Agricultural and Food Chemistry. 54(10). 3598–3603. 9 indexed citations
20.
Cruz, Xavier de la, Sergio Lois, Sara Sánchez-Molina, & Marian A. Martínez‐Balbás. (2005). Do protein motifs read the histone code?. BioEssays. 27(2). 164–175. 195 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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