Francisco Martı́nez-Azorı́n

740 total citations
36 papers, 426 citations indexed

About

Francisco Martı́nez-Azorı́n is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Francisco Martı́nez-Azorı́n has authored 36 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Francisco Martı́nez-Azorı́n's work include Mitochondrial Function and Pathology (11 papers), RNA modifications and cancer (10 papers) and Metabolism and Genetic Disorders (7 papers). Francisco Martı́nez-Azorı́n is often cited by papers focused on Mitochondrial Function and Pathology (11 papers), RNA modifications and cancer (10 papers) and Metabolism and Genetic Disorders (7 papers). Francisco Martı́nez-Azorı́n collaborates with scholars based in Spain, United States and Netherlands. Francisco Martı́nez-Azorı́n's co-authors include Juan P. G. Ballesta, Elena Martín‐Hernández, María Elena Rodríguez‐García, Miguel Remacha, Miguel A. Martı́n, Joaquı́n Arenas, Juan C. Gómez‐Fernández, Francisco Fernández-Belda, Pilar Quijada‐Fraile and José A. Teruel and has published in prestigious journals such as Journal of Biological Chemistry, Biochemistry and Biochemical Journal.

In The Last Decade

Francisco Martı́nez-Azorı́n

35 papers receiving 420 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Francisco Martı́nez-Azorı́n Spain	14	320	73	71	49	42	36	426
Marta Díaz Spain	15	239 0.7×	72 1.0×	15 0.2×	92 1.9×	103 2.5×	25	503
Vladimir Mayorov United States	17	335 1.0×	98 1.3×	43 0.6×	60 1.2×	12 0.3×	32	553
Stefan J. Siira Australia	18	893 2.8×	53 0.7×	150 2.1×	32 0.7×	27 0.6×	29	989
Katsumi Kasashima Japan	14	772 2.4×	53 0.7×	88 1.2×	90 1.8×	36 0.9×	23	891
Teresa M. Buck United States	15	449 1.4×	63 0.9×	27 0.4×	55 1.1×	36 0.9×	28	602
Zhibo Wang China	17	634 2.0×	164 2.2×	97 1.4×	37 0.8×	10 0.2×	47	905
Daniella H. Hock Australia	13	268 0.8×	44 0.6×	75 1.1×	23 0.5×	9 0.2×	23	370
Jeffrey D. Thomas United States	10	558 1.7×	143 2.0×	16 0.2×	74 1.5×	29 0.7×	11	770
Monika Papworth United Kingdom	9	660 2.1×	72 1.0×	129 1.8×	17 0.3×	41 1.0×	13	746
Yoshihito Kishita Japan	14	589 1.8×	66 0.9×	240 3.4×	16 0.3×	30 0.7×	38	693

Countries citing papers authored by Francisco Martı́nez-Azorı́n

Since Specialization

Citations

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

Fields of papers citing papers by Francisco Martı́nez-Azorı́n

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Francisco Martı́nez-Azorı́n. 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 Francisco Martı́nez-Azorı́n. The network helps show where Francisco Martı́nez-Azorı́n may publish in the future.

Co-authorship network of co-authors of Francisco Martı́nez-Azorı́n

This figure shows the co-authorship network connecting the top 25 collaborators of Francisco Martı́nez-Azorı́n. A scholar is included among the top collaborators of Francisco Martı́nez-Azorı́n 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 Francisco Martı́nez-Azorı́n. Francisco Martı́nez-Azorı́n 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

Pignatti, Emanuele, Jesse Slone, Kay‐Sara Sauter, et al.. (2024). FDXR variants cause adrenal insufficiency and atypical sexual development. JCI Insight. 9(14). 3 indexed citations

Rodríguez‐García, María Elena, Aurelio Hernández‐Laín, Ana Arteche‐López, et al.. (2024). Expanding the genetic and phenotypic spectrum of congenital myasthenic syndrome: new homozygous VAMP1 splicing variants in 2 novel individuals. Journal of Human Genetics. 69(5). 187–196. 1 indexed citations

Rodríguez‐García, María Elena, Ana Martı́nez de Aragón, Jonathan D. Dinman, et al.. (2023). A novel de novo variant in CASK causes a severe neurodevelopmental disorder that masks the phenotype of a novel de novo variant in EEF2. Journal of Human Genetics. 68(8). 543–550. 5 indexed citations

Rodríguez‐García, María Elena, et al.. (2021). Characterization of a complex phenotype (fever-dependent recurrent acute liver failure and osteogenesis imperfecta) due to NBAS and P4HB variants. Molecular Genetics and Metabolism. 133(2). 201–210. 4 indexed citations

Rodríguez‐García, María Elena, et al.. (2021). New subtype of PCH1C caused by novel EXOSC8 variants in a 16-year-old Spanish patient. Neuromuscular Disorders. 31(8). 773–782. 1 indexed citations

Martín‐Hernández, Elena, María Elena Rodríguez‐García, Chun‐An Chen, et al.. (2018). Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation. Journal of Human Genetics. 63(4). 525–528. 22 indexed citations

Rodríguez‐García, María Elena, et al.. (2017). An innovative strategy to clone positive modifier genes of defects caused by mtDNA mutations: MRPS18C as suppressor gene of m.3946G>A mutation in MT-ND1 gene. Human Genetics. 136(7). 885–896. 4 indexed citations

Martín‐Hernández, Elena, María Elena Rodríguez‐García, Ana Camacho, et al.. (2016). New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy. Neurogenetics. 17(4). 259–263. 30 indexed citations

Rodríguez‐García, María Elena, Elena Martín‐Hernández, Ana Martı́nez de Aragón, et al.. (2015). First missense mutation outside of SERAC1 lipase domain affecting intracellular cholesterol trafficking. Neurogenetics. 17(1). 51–56. 5 indexed citations

10.

Castro‐Gago, Manuel, David Dacruz-Álvarez, Aitor Delmiro, et al.. (2014). Exome sequencing identifies a CHKB mutation in Spanish patient with Megaconial Congenital Muscular Dystrophy and mtDNA depletion. European Journal of Paediatric Neurology. 18(6). 796–800. 18 indexed citations

11.

Martı́nez-Azorı́n, Francisco, et al.. (2013). MUSCLE‐SPECIFIC OVEREXPRESSION OF THE CATALYTIC SUBUNIT OF DNA POLYMERASE γ INDUCES PUPAL LETHALITY IN Drosophila melanogaster. Archives of Insect Biochemistry and Physiology. 83(3). 127–137. 1 indexed citations

12.

Martı́nez-Azorı́n, Francisco, Miguel Remacha, Encarnación Martı́nez-Salas, & Juan P. G. Ballesta. (2008). Internal translation initiation on the foot‐and‐mouth disease virus IRES is affected by ribosomal stalk conformation. FEBS Letters. 582(20). 3029–3032. 19 indexed citations

13.

Martı́nez-Azorı́n, Francisco, et al.. (2007). Over‐expression of the catalytic core of mitochondrial DNA (mtDNA) polymerase in the nervous system of Drosophila melanogaster reduces median life span by inducing mtDNA depletion. Journal of Neurochemistry. 105(1). 165–176. 19 indexed citations

14.

Martı́nez-Azorı́n, Francisco. (2005). The Mitochondrial Ribomotor Hypothesis. IUBMB Life. 57(1). 27–30. 7 indexed citations

15.

Martı́nez-Azorı́n, Francisco. (2004). Cyclopiazonic acid reduces the coupling factor of the Ca²⁺‐ATPase acting on Ca²⁺ binding. FEBS Letters. 576(1-2). 73–76. 16 indexed citations

16.

Talamillo, Ana, Miguel Ángel Fernández‐Moreno, Francisco Martı́nez-Azorı́n, et al.. (2004). Expression of the Drosophila melanogaster ATP synthase α subunit gene is regulated by a transcriptional element containing GAF and Adf‐1 binding sites. European Journal of Biochemistry. 271(20). 4003–4013. 7 indexed citations

17.

Montoya, Julio, et al.. (2001). A study on the human mitochondrial RNA polymerase activity points to existence of a transcription factor B‐like protein. FEBS Letters. 503(1). 51–55. 12 indexed citations

18.

Enrı́quez, José Antonio, et al.. (1998). Sistema genético mitocondrial humano. Revista de Neurología. 26(S1). 21–21. 2 indexed citations

19.

Martı́nez-Azorı́n, Francisco, José A. Teruel, Francisco Fernández-Belda, & Juan C. Gómez‐Fernández. (1992). Effect of diethylstilbestrol and related compounds on the Ca(2+)-transporting ATPase of sarcoplasmic reticulum.. Journal of Biological Chemistry. 267(17). 11923–11929. 38 indexed citations

20.

Martı́nez-Azorı́n, Francisco, et al.. (1990). La Castellana, escenario de poder: del Palacio de Linares a la Torre de Picasso. Dialnet (Universidad de la Rioja).

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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