Hugo Vega

1.1k total citations
10 papers, 583 citations indexed

About

Hugo Vega is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Physiology. According to data from OpenAlex, Hugo Vega has authored 10 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 2 papers in Physiology. Recurrent topics in Hugo Vega's work include RNA Research and Splicing (3 papers), Genomics and Chromatin Dynamics (3 papers) and Lysosomal Storage Disorders Research (2 papers). Hugo Vega is often cited by papers focused on RNA Research and Splicing (3 papers), Genomics and Chromatin Dynamics (3 papers) and Lysosomal Storage Disorders Research (2 papers). Hugo Vega collaborates with scholars based in United States, Colombia and Japan. Hugo Vega's co-authors include Hans Joenje, Norio Sakai, Koji Inui, Hülya Kayserili, Quinten Waisfisz, Ethylin Wang Jabs, Miriam Gordillo, Itaru Yanagihara, Keiichi Ozono and Minoru Yamada and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS Biology.

In The Last Decade

Hugo Vega

9 papers receiving 575 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Hugo Vega	477	149	93	79	45	10	583
Lidia Lopez‐Serra	776 1.6×	194 1.3×	87 0.9×	69 0.9×	14 0.3×	12	861
Dario Nicetto	681 1.4×	82 0.6×	90 1.0×	35 0.4×	25 0.6×	10	770
M. Lutz	475 1.0×	185 1.2×	36 0.4×	38 0.5×	19 0.4×	10	542
Michael Stevens	443 0.9×	76 0.5×	24 0.3×	36 0.5×	19 0.4×	10	542
Nicholas Stong	330 0.7×	95 0.6×	46 0.5×	22 0.3×	157 3.5×	28	471
Lígia Tavares	477 1.0×	149 1.0×	40 0.4×	20 0.3×	20 0.4×	11	595
Rebecca Cullum	537 1.1×	151 1.0×	37 0.4×	63 0.8×	9 0.2×	18	700
Suzanne A. Hartford	686 1.4×	206 1.4×	84 0.9×	111 1.4×	13 0.3×	16	833
Stefania Purgato	460 1.0×	147 1.0×	213 2.3×	45 0.6×	15 0.3×	15	604
Kazutsune Yamagata	474 1.0×	48 0.3×	77 0.8×	32 0.4×	30 0.7×	21	538

Countries citing papers authored by Hugo Vega

Since Specialization

Citations

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

Fields of papers citing papers by Hugo Vega

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hugo Vega

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

All Works

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10 of 10 papers shown

Vega, Hugo, et al.. (2020). ESCO2 Spectrum Disorder.

Zhang, Yihan, Haigen Huang, Gexin Zhao, et al.. (2017). ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13. PLoS Genetics. 13(2). e1006481–e1006481. 45 indexed citations

Vega, Hugo, et al.. (2015). Stereoscopy and haptics human eye AR app. 4. 1–2. 1 indexed citations

Soemedi, Rachel, Hugo Vega, Judson Belmont, Sohini Ramachandran, & William G. Fairbrother. (2014). Genetic Variation and RNA Binding Proteins: Tools and Techniques to Detect Functional Polymorphisms. Advances in experimental medicine and biology. 825. 227–266. 10 indexed citations

Gordillo, Miriam, Hugo Vega, & Ethylin Wang Jabs. (2013). Table 1. [Summary Molecular Genetic Testing Used in Roberts Syndrome].. 1 indexed citations

Liu, Jinglan, Zhe Zhang, Masashige Bando, et al.. (2010). Genome-wide DNA methylation analysis in cohesin mutant human cell lines. Nucleic Acids Research. 38(17). 5657–5671. 17 indexed citations

Liu, Jinglan, Zhe Zhang, Masashige Bando, et al.. (2009). Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells. PLoS Biology. 7(5). e1000119–e1000119. 180 indexed citations

Vega, Hugo, et al.. (2006). [Colombian haplotypes of the Gaucher disease-causing N370S mutation may originate from a possible common ancestral haplotype].. PubMed. 26(3). 434–41. 3 indexed citations

Vega, Hugo, Quinten Waisfisz, Miriam Gordillo, et al.. (2005). Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion. Nature Genetics. 37(5). 468–470. 284 indexed citations

10.

Kato, Zenichiro, Seiji Fukuda, Shunji Tomatsu, et al.. (1997). A novel common missense mutation G301C in the N-acetylgalactosamine-6-sulfate sulfatase gene in mucopolysaccharidosis IVA. Human Genetics. 101(1). 97–101. 42 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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