Paz Briones

4.0k total citations
70 papers, 2.7k citations indexed

About

Paz Briones is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Paz Briones has authored 70 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 61 papers in Molecular Biology, 30 papers in Clinical Biochemistry and 16 papers in Biochemistry. Recurrent topics in Paz Briones's work include Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (30 papers) and Glycosylation and Glycoproteins Research (14 papers). Paz Briones is often cited by papers focused on Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (30 papers) and Glycosylation and Glycoproteins Research (14 papers). Paz Briones collaborates with scholars based in Spain, Netherlands and United States. Paz Briones's co-authors include Rafael Artuch, Antònia Ribes, Mercè Pineda, Manuel Palacı́n, Xavier Testar, António Zorzano, Marc Liesa, Marta Camps, Sara Pich and Daniel Q. Bach and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Paz Briones

70 papers receiving 2.6k citations

Peers

Countries citing papers authored by Paz Briones

Since Specialization

Citations

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

Fields of papers citing papers by Paz Briones

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paz Briones

This figure shows the co-authorship network connecting the top 25 collaborators of Paz Briones. A scholar is included among the top collaborators of Paz Briones 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 Paz Briones. Paz Briones 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	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
2	Expanding the clinical phenotypes of MT-ATP6 mutations 2014 ·Human Molecular Genetics ·Ester López‐Gallardo, Sonia Emperador, Abelardo Solano, (unknown), (unknown), Manuel J. López‐Pérez, Paz Briones, Mercédes Pineda, Rafael Artuch, Elena Barraquer, Ivonne Jericó, Eduardo Ruiz‐Pesini, Julio Montoya	32
3	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
4	Survival transcriptome in the coenzyme Q ₁₀ deficiency syndrome is acquired by epigenetic modifications: a modelling study for human coenzyme Q ₁₀ deficiencies 2013 ·BMJ Open ·Daniel J.M. Fernández‐Ayala, (unknown), Sandra Jiménez-Gancedo, María V. Cascajo, (unknown), Salvatore DiMauro, Michio Hirano, Paz Briones, Rafael Artuch, Rafael de Cabo, Leonardo Salviati, Plácido Navas	16
5	Coenzyme Q₁₀‐responsive ataxia: 2‐year‐treatment follow‐up 2010 ·Movement Disorders ·Mercè Pineda, Raquel Montero, (unknown), (unknown), Ana Mas, Carmen Espinós, Dolores Martínez‐Rubio, Francesc Palau, Plácido Navas, Paz Briones, Rafael Artuch	39
6	An update on the molecular analysis of classical galactosaemia patients diagnosed in Spain and Portugal: 7 new mutations in 17 new families 2009 ·Medicina Clínica ·Laura Gort, Ester Quintana, (unknown), Lidia González‐Quereda, Tania López-Hernández, Paz Briones	4
7	Analysis of Coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes 2008 ·Clinical Biochemistry ·Raquel Montero, José A. Sánchez‐Alcázar, Paz Briones, María Hernández, Mario D. Cordero, Eva Trevisson, Leonardo Salviati, Mercè Pineda, Àngels García‐Cazorla, Plácido Navas, Rafael Artuch	58
8	X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy 2007 ·Annals of Neurology ·Daniel Fernández-Moreira, Cristina Ugalde, Roel Smeets, Richard J. Rodenburg, Eduardo López‐Laso, (unknown), Paz Briones, Miguel A. Martı́n, Jan Smeıtınk, Joaquı́n Arenas	105
9	Characterization of two unusual truncating PMM2 mutations in two CDG-Ia patients 2007 ·Molecular Genetics and Metabolism ·Els Schollen, Liesbeth Keldermans, François Foulquier, Paz Briones, Amparo Chabás, Félix Sánchez‐Valverde, Maciej Adamowicz, Ewa Pronicka, Ron A. Wevers, Gert Matthijs	34
10	Creatine transporter deficiency: Prevalence among patients with mental retardation and pitfalls in metabolite screening 2007 ·Clinical Biochemistry ·Ángela Arias, (unknown), Carmen Fons, (unknown), Judit García‐Villoria, Aída Ormazábal, Pilar Póo, Mercè Pineda, María Antònia Vilaseca, Jaume Campistol, Paz Briones, Teresa Pàmpols, Gajja S. Salomons, Antònia Ribes, Rafael Artuch	51
11	Clinical, biochemical and molecular aspects of cerebellar ataxia and Coenzyme Q10 deficiency 2007 ·The Cerebellum ·Raquel Montero, Mercè Pineda, (unknown), M. Antònia Vilaseca, Paz Briones, José A. Sánchez‐Alcázar, Plácido Navas, Rafael Artuch	46
12	Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation 2006 ·Journal of the Neurological Sciences ·Rafael Artuch, Gloria Brea‐Calvo, Paz Briones, (unknown), (unknown), Carmen Espinós, Jordi Corral, Vı́ctor Volpini, Antònia Ribes, Antoni L. Andreu, Francesc Palau, José A. Sánchez‐Alcázar, Plácido Navas, Mercè Pineda	74
13	The Charcot–Marie–Tooth type 2A gene product, Mfn2, up-regulates fuel oxidation through expression of OXPHOS system 2005 ·Human Molecular Genetics ·Sara Pich, Daniel Q. Bach, Paz Briones, Marc Liesa, Marta Camps, Xavier Testar, Manuel Palacı́n, António Zorzano	365
14	Congenital Disorder of Glycosylation Type Ia Revealed by Hypertransaminasemia and Failure To Thrive in a Young Boy with Normal Neurodevelopment 2005 ·Journal of Pediatric Gastroenterology and Nutrition ·(unknown), Àngels García‐Cazorla, (unknown), Rafael Artuch, (unknown), María Antònia Vilaseca, Paz Briones, (unknown)	1
15	Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion 2005 ·Annals of Neurology ·Merçè Pineda, Aída Ormazábal, Ester López‐Gallardo, A. Nascimento, Abelardo Solano, María Dolores Herrero, María Antònia Vilaseca, Paz Briones, Lourdes Ibáñez, Julio Montoya, Rafael Artuch	119
16	Exercise intolerance resulting: from a muscle-restricted mutation in the mitochondrial tRNA^Leu(CUN)gene 2001 ·Annals of Medicine ·Cristòfol Vives-Bauzá, Josep Gámez, (unknown), Paz Briones, (unknown), Abelardo Solano, Julio Montoya, Antoni L. Andreu	20
17	Oxygen consumption measurement in lymphocytes for the diagnosis of pediatric patients with oxidative phosphorylation diseases 2000 ·Clinical Biochemistry ·Rafael Artuch, Catrina Colomé, (unknown), (unknown), Paz Briones, Julio Montoya, María Antònia Vilaseca, Mercè Pineda	9
18	Identification and characterization of mutations in patients with holocarboxylase synthetase deficiency 1999 ·Human Genetics ·Yoko Aoki, (unknown), Osamu Sakamoto, Masahiro Hiratsuka, (unknown), (unknown), Paz Briones, Terttu Suormala, E. R. Baumgartner, Yoichi Suzuki, Kuniaki Narisawa	19
19	Multiple Endocrine Involvement in Two Pediatric Patients with Kearns-Sayre Syndrome 1998 ·Hormone Research in Paediatrics ·Rafael Artuch, (unknown), (unknown), María Antònia Vilaseca, Jaume Colomer, Carme Valls, (unknown), (unknown), Adolf Pou, Paz Briones, Julio Montoya, Merçè Pineda	36
20	An atypical French form of pyruvate carboxylase deficiency 1995 ·Brain and Development ·Mercè Pineda, Jaume Campistol, Marina Vilaseca, Paz Briones, Antònia Ribes, Teresa Temudo, M. Pons, V. Cusí, M. O. Rolland	15

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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