Dèlia Yubero

1.1k total citations
35 papers, 422 citations indexed

About

Dèlia Yubero is a scholar working on Molecular Biology, Genetics and Electrical and Electronic Engineering. According to data from OpenAlex, Dèlia Yubero has authored 35 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 12 papers in Genetics and 10 papers in Electrical and Electronic Engineering. Recurrent topics in Dèlia Yubero's work include Mitochondrial Function and Pathology (12 papers), Coenzyme Q10 studies and effects (12 papers) and Advanced battery technologies research (10 papers). Dèlia Yubero is often cited by papers focused on Mitochondrial Function and Pathology (12 papers), Coenzyme Q10 studies and effects (12 papers) and Advanced battery technologies research (10 papers). Dèlia Yubero collaborates with scholars based in Spain, United Kingdom and Italy. Dèlia Yubero's co-authors include Rafael Artuch, Raquel Montero, Àngels García‐Cazorla, Plácido Navas, Iain P. Hargreaves, Julio Montoya, Francesc Palau, Viruna Neergheen, Judith Armstrong and Antònia Ribes and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Dèlia Yubero

32 papers receiving 420 citations

Peers

Countries citing papers authored by Dèlia Yubero

Since Specialization

Citations

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

Fields of papers citing papers by Dèlia Yubero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dèlia Yubero

This figure shows the co-authorship network connecting the top 25 collaborators of Dèlia Yubero. A scholar is included among the top collaborators of Dèlia Yubero 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 Dèlia Yubero. Dèlia Yubero 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	Personalised genomic strategies improve diagnostic yield in inherited retinal dystrophies: a stepwise, patient-centred approach 2025 ·Eye ·(unknown), (unknown), Jaume Català‐Mora, (unknown), Dèlia Yubero, (unknown), Frans P.M. Cremers, (unknown), José M. Millán, Gema García‐García, (unknown), Luís Arias, Estefanía Cobos, (unknown)	0
2	Exploring Plasma Coenzyme Q10 Status in Paediatric Dyslipidaemia 2024 ·Antioxidants ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ángela Arias, (unknown), Dèlia Yubero, Mireia Tondo, Carlos Santos‐Ocaña, (unknown), Rafael Artuch	1
3	Improving Diagnostic Precision: Phenotype-Driven Analysis Uncovers a Maternal Mosaicism in an Individual with RYR1 -Congenital Myopathy 2024 ·Journal of Neuromuscular Diseases ·(unknown), Leslie Matalonga, Loreto Martorell, Anna Codina, C. Ortez, Laura Carrera‐García, J. Expósito, Dèlia Yubero, Janet Hoenicka, Cristina Jou, Francesc Palau, Sergi Beltrán, Hanns Lochmüller, Ana Töpf, A. Nascimento, Daniel Natera‐de Benito	1
4	Woolly hair in tricho‐dento‐osseous syndrome 2023 ·Pediatric Dermatology ·(unknown), (unknown), (unknown), Lluís Brunet‐Llobet, Marta Ivars, Dèlia Yubero, Ofer Sarig, Liron Malki, A. Peled, Eli Sprecher, Eulàlia Baselga	0
5	The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1 2022 ·Clinical Genetics ·(unknown), Dèlia Yubero, Fátima Leal, María L. Couce, (unknown), Eduardo López‐Laso, Àngels García‐Cazorla, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Magdalena Ugarte, Rafael Artuch, Belén Pérez	6
6	Molecular Modelling Hurdle in the Next-Generation Sequencing Era 2022 ·International Journal of Molecular Sciences ·Guerau Fernández, Dèlia Yubero, Francesc Palau, Judith Armstrong	0
7	Pediatric Gaucher disease with intermediate type 2–3 phenotype associated with parkinsonian features and levodopa responsiveness 2021 ·Parkinsonism & Related Disorders ·Alejandra Darling, Pilar Irún, Pilar Giraldo, Judith Armstrong, Laura Gort, (unknown), Dèlia Yubero, (unknown), Aída Ormazábal, Rafael Artuch, Àngels García‐Cazorla, Mar O’Callaghan	3
8	The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort 2020 ·Pediatric Neurology ·Daniel Natera‐de Benito, C. Ortez, Cristina Jou, C. Jimenez‐Mallebrera, Anna Codina, Laura Carrera‐García, J. Expósito, Sergi César, Loreto Martorell, P. Gallano, Lidia González‐Quereda, Daniel Cuadras, J. Colomer, Dèlia Yubero, Francesc Palau, A. Nascimento	13
9	Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome 2020 ·Frontiers in Genetics ·Sonia Emperador, (unknown), (unknown), (unknown), (unknown), Dèlia Yubero, Ana Fernández‐Marmiesse, (unknown), Juan Darío Ortigoza‐Escobar, (unknown), Eduardo Ruiz‐Pesini, Àngels García‐Cazorla, Mercedes Gil‐Campos, Rafael Artuch, Julio Montoya, M. Pilar Bayona‐Bafaluy	9
10	Plasma coenzyme Q10 status is impaired in selected genetic conditions 2019 ·Scientific Reports ·Raquel Montero, Dèlia Yubero, (unknown), Marı́a Julieta González, Jaume Campistol, María del Mar O’Callaghan, Mercè Pineda, (unknown), (unknown), Guerau Fernández, Julio Montoya, Eduardo Ruiz‐Pesini, (unknown), Viruna Neergheen, Àngels García‐Cazorla, Plácido Navas, Iain P. Hargreaves, Rafael Artuch	28
11	Infectious stress triggers a POLG-related mitochondrial disease 2019 ·Neurogenetics ·(unknown), Sonia Emperador, (unknown), Eduardo Ruiz‐Pesini, Dèlia Yubero, Àngels García‐Cazorla, Rafael Artuch, Julio Montoya, M. Pilar Bayona‐Bafaluy	11
12	Cerebrospinal fluid monoamines, pterins, and folate in patients with mitochondrial diseases: systematic review and hospital experience 2018 ·Journal of Inherited Metabolic Disease ·(unknown), Marta Molero-Luís, Aída Ormazábal, Raquel Montero, Cristina Sierra, Antònia Ribes, Julio Montoya, Eduardo Ruiz‐Pesini, Mar O’Callaghan, (unknown), A. Nascimento, Francesc Palau, Judith Armstrong, Dèlia Yubero, Juan Darío Ortigoza‐Escobar, Àngels García‐Cazorla, Rafael Artuch	12
13	Targeted Next Generation Sequencing in Patients with Inborn Errors of Metabolism 2016 ·PLoS ONE ·Dèlia Yubero, Núria Brandi, Aída Ormazábal, Àngels García‐Cazorla, Belén Pérez‐Dueñas, Jaime Campistol, Antònia Ribes, Francesc Palau, Rafael Artuch, Judith Armstrong, (unknown)	39
14	A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities 2016 ·Scientific Reports ·Dèlia Yubero, Aritz Adín, Raquel Montero, Cristina Jou, C. Jimenez‐Mallebrera, Àngels García‐Cazorla, A. Nascimento, (unknown), Julio Montoya, Laura Gort, Plácido Navas, Antònia Ribes, M. D. Ugarte, Rafael Artuch	45
15	Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q10 content 2015 ·European Journal of Human Genetics ·Claudio Asencio, María Hernández, Paz Briones, Julio Montoya, Ana Cortés, Sonia Emperador, (unknown), Eduardo Ruiz‐Pesini, Dèlia Yubero, Raquel Montero, Mercédes Pineda, (unknown), María Alcázar‐Fabra, Leonardo Salviati, Rafael Artuch, Plácido Navas	13
16	Mutation loads in different tissues from six pathogenic mtDNA point mutations 2015 ·Mitochondrion ·(unknown), Sonia Emperador, Mercè Pineda, Ester López‐Gallardo, Raquel Montero, Dèlia Yubero, Cristina Jou, C. Jimenez‐Mallebrera, A. Nascimento, Isidró Ferrer, Àngels García‐Cazorla, Eduardo Ruiz‐Pesini, Julio Montoya, Rafael Artuch	11
17	BACE-1, PS-1 and sAPPβ Levels Are Increased in Plasma from Sporadic Inclusion Body Myositis Patients: Surrogate Biomarkers among Inflammatory Myopathies 2015 ·Molecular Medicine ·Marc Catalán‐García, Glòria Garrabou, Constanza Morén, Mariona Guitart‐Mampel, (unknown), (unknown), José M. Gallego‐Escuredo, Dèlia Yubero, Francesc Villarroya, Raquel Montero, Albert Selva-O’Callaghan, Francesc Cardellach, Josep M. Grau	12
18	Molecular diagnosis of coenzyme Q₁₀deficiency 2015 ·Expert Review of Molecular Diagnostics ·Dèlia Yubero, Raquel Montero, Judith Armstrong, Carmen Espinós, Francesc Palau, Carlos Santos‐Ocaña, Leonardo Salviati, Plácido Navas, Rafael Artuch	14
19	Association between coenzyme Q10 and glucose transporter (GLUT1) deficiency 2014 ·BMC Pediatrics ·Dèlia Yubero, Mar O’Callaghan, Raquel Montero, Aída Ormazábal, Judith Armstrong, Carmen Espinós, (unknown), Cristina Jou, (unknown), (unknown), María V. Cascajo, (unknown), Paz Briones, C. Jimenez‐Mallebrera, Mercédes Pineda, Plácido Navas, Rafael Artuch	12
20	Biochemical Diagnosis of Coenzyme Q<sub>10</sub> Deficiency 2014 ·Molecular Syndromology ·Dèlia Yubero, Raquel Montero, Rafael Artuch, John M. Land, Simon Heales, Iain P. Hargreaves	34

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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