Ángeles Mencía

1.5k total citations
22 papers, 951 citations indexed

About

Ángeles Mencía is a scholar working on Molecular Biology, Cell Biology and Sensory Systems. According to data from OpenAlex, Ángeles Mencía has authored 22 papers receiving a total of 951 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Cell Biology and 5 papers in Sensory Systems. Recurrent topics in Ángeles Mencía's work include Skin and Cellular Biology Research (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and RNA Interference and Gene Delivery (5 papers). Ángeles Mencía is often cited by papers focused on Skin and Cellular Biology Research (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and RNA Interference and Gene Delivery (5 papers). Ángeles Mencía collaborates with scholars based in Spain, United Kingdom and Germany. Ángeles Mencía's co-authors include Silvia Modamio‐Høybjør, Miguel A. Moreno‐Pelayo, Felipe Moreno, Ignacio del Castillo, Fernando Mayo, Matías Morin, Leticia Olavarrieta, Luis A. Aguirre, Karen P. Steel and Tamás Dalmay and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Immunology.

In The Last Decade

Ángeles Mencía

22 papers receiving 946 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ángeles Mencía Spain 14 598 305 237 155 140 22 951
Silvia Modamio‐Høybjør Spain 9 470 0.8× 308 1.0× 279 1.2× 63 0.4× 78 0.6× 16 775
Johanna Thurlow United Kingdom 9 477 0.8× 142 0.5× 213 0.9× 70 0.5× 46 0.3× 11 911
Matías Morin Spain 12 529 0.9× 323 1.1× 262 1.1× 57 0.4× 83 0.6× 27 856
Fiorella C. Grandi United States 16 459 0.8× 115 0.4× 49 0.2× 54 0.3× 65 0.5× 27 891
Batiste Boëda France 10 471 0.8× 45 0.1× 291 1.2× 355 2.3× 47 0.3× 17 889
Junko Sakagami Japan 11 590 1.0× 67 0.2× 186 0.8× 160 1.0× 135 1.0× 13 1.4k
Cheuk T. Leung United States 7 540 0.9× 146 0.5× 237 1.0× 367 2.4× 88 0.6× 11 1.0k
Kevin J. Sonnemann United States 9 616 1.0× 35 0.1× 105 0.4× 307 2.0× 62 0.4× 10 949
Koko Urase Japan 19 776 1.3× 71 0.2× 70 0.3× 169 1.1× 138 1.0× 26 1.0k
Michael J. Hansen United States 15 810 1.4× 81 0.3× 47 0.2× 535 3.5× 254 1.8× 46 1.8k

Countries citing papers authored by Ángeles Mencía

Since Specialization
Citations

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

Fields of papers citing papers by Ángeles Mencía

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ángeles Mencía

This figure shows the co-authorship network connecting the top 25 collaborators of Ángeles Mencía. A scholar is included among the top collaborators of Ángeles Mencía 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 Ángeles Mencía. Ángeles Mencía 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.
Lara‐Sáez, Irene, Ángeles Mencía, Yinghao Li, et al.. (2024). Nonviral CRISPR/Cas9 mutagenesis for streamlined generation of mouse lung cancer models. Proceedings of the National Academy of Sciences. 121(28). e2322917121–e2322917121. 2 indexed citations
2.
García, Marta, Giandomenico Turchiano, Adrian J. Thrasher, et al.. (2022). Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectors. Molecular Therapy — Methods & Clinical Development. 27. 96–108. 16 indexed citations
3.
Ahern, Jonathan O’Keeffe, Irene Lara‐Sáez, Dezhong Zhou, et al.. (2021). Non-viral delivery of CRISPR–Cas9 complexes for targeted gene editing via a polymer delivery system. Gene Therapy. 29(3-4). 157–170. 56 indexed citations
4.
Mencía, Ángeles, Waracharee Srifa, Sriram Vaidyanathan, et al.. (2021). Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing. Molecular Therapy. 29(6). 2008–2018. 31 indexed citations
5.
Mencía, Ángeles, Wei‐Li Di, Rodolfo Murillas, et al.. (2020). Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome. Molecular Therapy — Methods & Clinical Development. 18. 280–290. 12 indexed citations
6.
Mencía, Ángeles, Marta García, Raúl Torres, et al.. (2019). Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing. Molecular Therapy. 27(5). 986–998. 79 indexed citations
7.
Mencía, Ángeles, Marcela Del Río, M.J. Escámez, et al.. (2018). LB1544 Highly efficient, permanent ex vivo correction of RDEB via non-viral CRISPR/Cas9 excision of COL7A1 Exon 80 bearing a prevalent mutation. Journal of Investigative Dermatology. 138(9). B13–B13. 1 indexed citations
8.
Mencía, Ángeles, Cristina Chamorro, Blanca Duarte, et al.. (2018). Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells. Molecular Therapy — Nucleic Acids. 11. 68–78. 34 indexed citations
9.
Chamorro, Cristina, Ángeles Mencía, Blanca Duarte, et al.. (2016). Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa Keratinocytes. Molecular Therapy — Nucleic Acids. 5. e307–e307. 47 indexed citations
10.
Mencía, Ángeles, Marta García, Eva Jover, et al.. (2016). Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia. Experimental Dermatology. 25(4). 269–274. 11 indexed citations
11.
Morin, Matías, Keith E. Bryan, Fernando Mayo, et al.. (2009). In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment. Human Molecular Genetics. 18(16). 3075–3089. 59 indexed citations
12.
Mencía, Ángeles, Silvia Modamio‐Høybjør, Matías Morin, et al.. (2009). Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss. Nature Genetics. 41(5). 609–613. 421 indexed citations
13.
Moreno‐Pelayo, Miguel A., Richard J. Goodyear, Ángeles Mencía, et al.. (2008). Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene. Journal of the Association for Research in Otolaryngology. 9(2). 202–214. 15 indexed citations
14.
Recio, María J., Miguel A. Moreno‐Pelayo, Sara Şebnem Kılıç, et al.. (2007). Differential Biological Role of CD3 Chains Revealed by Human Immunodeficiencies. The Journal of Immunology. 178(4). 2556–2564. 40 indexed citations
15.
Mancebo, Esther, Miguel A. Moreno‐Pelayo, Ángeles Mencía, et al.. (2007). Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies. Molecular Immunology. 45(2). 479–484. 14 indexed citations
16.
Modamio‐Høybjør, Silvia, Ángeles Mencía, Richard J. Goodyear, et al.. (2007). A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss. The American Journal of Human Genetics. 80(6). 1076–1089. 43 indexed citations
17.
Mencía, Ángeles, Daniel González‐Nieto, Silvia Modamio‐Høybjør, et al.. (2007). A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression. Human Genetics. 123(1). 41–53. 42 indexed citations
18.
Aguilera‐Montilla, Noemí, Mercedes López‐Santalla, Cristina Rodríguez‐Juan, et al.. (2006). Herpesvirus saimiri(HVS)-transformed T-cell lines: A method to study mucosal T cells in inflammatory bowel disease. Scandinavian Journal of Gastroenterology. 41(11). 1361–1363. 1 indexed citations
19.
Aguilera‐Montilla, Noemí, Mercedes López‐Santalla, Cristina Rodríguez‐Juan, et al.. (2004). Higher proliferative capacity of T lymphocytes from patients with Crohn disease than from ulcerative colitis is disclosed by use of Herpesvirus saimiri-transformed T-cell lines. Scandinavian Journal of Gastroenterology. 39(12). 1236–1242. 4 indexed citations
20.
Modamio‐Høybjør, Silvia, Miguel A. Moreno‐Pelayo, Ángeles Mencía, et al.. (2003). A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29. Human Genetics. 112(1). 24–28. 18 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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