Ángeles Mencía

1.5k citations

22 papers · 951 indexed · h-index 14

Co-authors: Silvia Modamio‐Høybjør Miguel A. Moreno‐Pelayo Felipe Moreno Ignacio del Castillo Matías Morin Fernando Mayo Leticia Olavarrieta Luis A. Aguirre
Topics: Skin and Cellular Biology Research (7 papers)Hearing, Cochlea, Tinnitus, Genetics (5 papers)RNA Interference and Gene Delivery (5 papers)
Cited by: Sensory Systems Cancer Research Cell Biology
Journals: Proceedings of the National Academy of Sciences Nature Genetics The Journal of Immunology
Partner nations: Spain United Kingdom Germany

In The Last Decade

Ángeles Mencía

22 papers receiving 946 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Nonviral CRISPR/Cas9 mutagenesis for streamlined generation of mouse lung cancer models 2024 ·Proceedings of the National Academy of Sciences ·Irene Lara‐Sáez,Ángeles Mencía,(unknown),Yinghao Li,Marta García,Marta Oteo,Marta I. Gallego,Ana B. Enguita,(unknown),A Sigen,Wenxin Wang,Ramón Garcı́a-Escudero,Rodolfo Murillas,Mirentxu Santos	2
2	Preclinical model for phenotypic correction of dystrophic epidermolysis bullosa by in vivo CRISPR-Cas9 delivery using adenoviral vectors 2022 ·Molecular Therapy — Methods & Clinical Development ·Marta García,(unknown),(unknown),(unknown),Giandomenico Turchiano,(unknown),Adrian J. Thrasher,Fernando Larcher,Marcela Del Río,Rubén Hernández-Alcoceba,Marina Garín,Ángeles Mencía,Rodolfo Murillas	16
3	Non-viral delivery of CRISPR–Cas9 complexes for targeted gene editing via a polymer delivery system 2021 ·Gene Therapy ·Jonathan O’Keeffe Ahern,Irene Lara‐Sáez,Dezhong Zhou,Rodolfo Murillas,(unknown),Ángeles Mencía,Marta García,Darío Manzanares,Jennifer Lynch,Ruth Foley,Qian Xu,A Sigen,Fernando Larcher,Wenxin Wang	56
4	Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing 2021 ·Molecular Therapy ·(unknown),Ángeles Mencía,(unknown),Waracharee Srifa,Sriram Vaidyanathan,Rosa Romano,Marta García,(unknown),(unknown),Blanca Duarte,Matthew H. Porteus,Marcela Del Río,Fernando Larcher,Rodolfo Murillas	31
5	Efficient CRISPR-Cas9-Mediated Gene Ablation in Human Keratinocytes to Recapitulate Genodermatoses: Modeling of Netherton Syndrome 2020 ·Molecular Therapy — Methods & Clinical Development ·(unknown),(unknown),(unknown),Ángeles Mencía,Wei‐Li Di,Rodolfo Murillas,Sara Llames,Asunción Vicente,Marcela Del Río,Marta Carretero,Fernando Larcher	12
6	Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing 2019 ·Molecular Therapy ·(unknown),Ángeles Mencía,Marta García,Raúl Torres,Sandra Rodríguez,Marta Carretero,(unknown),Silvia Modamio‐Høybjør,(unknown),Carlos León,M.J. Escámez,Ingrid Haußer,Marcela Del Río,Rodolfo Murillas,Fernando Larcher	79
7	LB1544 Highly efficient, permanent ex vivo correction of RDEB via non-viral CRISPR/Cas9 excision of COL7A1 Exon 80 bearing a prevalent mutation 2018 ·Journal of Investigative Dermatology ·(unknown),Ángeles Mencía,Marcela Del Río,M.J. Escámez,Rosarelis Torres,(unknown),Rodolfo Murillas,Fernando Larcher	1
8	Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells 2018 ·Molecular Therapy — Nucleic Acids ·Ángeles Mencía,Cristina Chamorro,(unknown),Blanca Duarte,Almudena Holguín,Nuria Illera,Sara Llames,M.J. Escámez,Ingrid Haußer,Marcela Del Río,Fernando Larcher,Rodolfo Murillas	34
9	Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa Keratinocytes 2016 ·Molecular Therapy — Nucleic Acids ·Cristina Chamorro,Ángeles Mencía,(unknown),Blanca Duarte,Hildegard Büning,(unknown),Ingrid Haußer,Marcela Del Río,Fernando Larcher,Rodolfo Murillas	47
10	Identification of two rare and novel large deletions in ITGB4 gene causing epidermolysis bullosa with pyloric atresia 2016 ·Experimental Dermatology ·Ángeles Mencía,Marta García,Eva Jover,Sara Llames,A. Charlesworth,R. de Lucas,(unknown),(unknown),Pablo Coto,Marta D. Costa,Ángel Vera,(unknown),Rodolfo Murillas,Guerrino Meneguzzi,José L. Jorcano,Claudio J. Conti,M.J. Escámez,Marcela Del Río	11
11	In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment 2009 ·Human Molecular Genetics ·Matías Morin,Keith E. Bryan,Fernando Mayo,Richard J. Goodyear,Ángeles Mencía,Silvia Modamio‐Høybjør,Ignacio del Castillo,(unknown),Guy P. Richardson,Felipe Moreno,Peter A. Rubenstein,Miguel A. Moreno‐Pelayo	59
12	Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss 2009 ·Nature Genetics ·Ángeles Mencía,Silvia Modamio‐Høybjør,(unknown),Matías Morin,Fernando Mayo,Leticia Olavarrieta,Luis A. Aguirre,Ignacio del Castillo,Karen P. Steel,Tamás Dalmay,Felipe Moreno,Miguel A. Moreno‐Pelayo	421
13	Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene 2008 ·Journal of the Association for Research in Otolaryngology ·Miguel A. Moreno‐Pelayo,Richard J. Goodyear,Ángeles Mencía,Silvia Modamio‐Høybjør,P. Kevin Legan,Leticia Olavarrieta,Felipe Moreno,Guy P. Richardson	15
14	Differential Biological Role of CD3 Chains Revealed by Human Immunodeficiencies 2007 ·The Journal of Immunology ·María J. Recio,Miguel A. Moreno‐Pelayo,Sara Şebnem Kılıç,Alberto C. Guardo,Özden Sanal,Luis M. Allende,(unknown),Ángeles Mencía,Silvia Modamio‐Høybjør,Elena Seoane,José R. Regueiro	40
15	A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss 2007 ·The American Journal of Human Genetics ·Silvia Modamio‐Høybjør,Ángeles Mencía,Richard J. Goodyear,Ignacio del Castillo,Guy P. Richardson,Felipe Moreno,Miguel A. Moreno‐Pelayo	43
16	Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies 2007 ·Molecular Immunology ·Esther Mancebo,Miguel A. Moreno‐Pelayo,Ángeles Mencía,Oscar De La Calle-Martin,Luís M. Allende,Padma Sivadorai,Luba Kalaydjieva,Jaume Bertranpetit,Eliécer Coto,(unknown),Jesús Ruíz-Contreras,Estela Paz‐Artal	14
17	A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression 2007 ·Human Genetics ·Ángeles Mencía,Daniel González‐Nieto,Silvia Modamio‐Høybjør,Ainhoa Etxeberría,(unknown),(unknown),Ignacio del Castillo,Álvaro Villarroel,Felipe Moreno,Luis C. Barrio,Miguel A. Moreno‐Pelayo	42
18	Herpesvirus saimiri(HVS)-transformed T-cell lines: A method to study mucosal T cells in inflammatory bowel disease 2006 ·Scandinavian Journal of Gastroenterology ·Noemí Aguilera‐Montilla,(unknown),(unknown),Mercedes López‐Santalla,Cristina Rodríguez‐Juan,Ángeles Mencía,Gregorio Castellano,María Luisa Manzano,(unknown),(unknown),José Manuel Martín‐Villa	1
19	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 2004 ·Scandinavian Journal of Gastroenterology ·Noemí Aguilera‐Montilla,(unknown),(unknown),Mercedes López‐Santalla,Cristina Rodríguez‐Juan,Ángeles Mencía,Giancarlo Castellano,María Luisa Manzano,(unknown),(unknown),José Manuel Martín‐Villa	4
20	A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29 2003 ·Human Genetics ·Silvia Modamio‐Høybjør,Miguel A. Moreno‐Pelayo,Ángeles Mencía,Ignacio del Castillo,(unknown),(unknown),Mark Lathrop,Christine Petit,Felipe Moreno	18

About Ángeles Mencía

Ángeles Mencía is a scholar working on Sensory Systems, Immunology and Allergy and Cell Biology, having authored 22 papers that have together received 951 indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (7 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and RNA Interference and Gene Delivery (5 papers). The work is most often cited by research in Sensory Systems (237 citations), Cancer Research (305 citations) and Cell Biology (155 citations). Ángeles Mencía has collaborated with scholars based in Spain, United Kingdom and Germany. Frequent co-authors include Silvia Modamio‐Høybjør, Miguel A. Moreno‐Pelayo, Felipe Moreno, Ignacio del Castillo, Matías Morin, Fernando Mayo, Leticia Olavarrieta, Luis A. Aguirre, Karen P. Steel and Tamás Dalmay. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Immunology.

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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