Loreto Martorell

5.0k total citations
73 papers, 1.4k citations indexed

About

Loreto Martorell is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Loreto Martorell has authored 73 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 28 papers in Genetics and 24 papers in Cellular and Molecular Neuroscience. Recurrent topics in Loreto Martorell's work include Genetic Neurodegenerative Diseases (23 papers), Mitochondrial Function and Pathology (19 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Loreto Martorell is often cited by papers focused on Genetic Neurodegenerative Diseases (23 papers), Mitochondrial Function and Pathology (19 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Loreto Martorell collaborates with scholars based in Spain, United States and United Kingdom. Loreto Martorell's co-authors include Montserrat Baiget, Keith Johnson, Adolfo López de Munaín, Darren G. Monckton, Rafael Artuch, Ana María Cobo, Josep Gámez, Catherine Boucher, Aurora Sánchez and J J Poza and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Loreto Martorell

70 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Loreto Martorell Spain 22 1.0k 735 366 333 92 73 1.4k
Pedro Mancías United States 15 750 0.7× 809 1.1× 149 0.4× 380 1.1× 228 2.5× 37 1.7k
P S Harper United Kingdom 15 856 0.8× 613 0.8× 378 1.0× 283 0.8× 56 0.6× 35 1.3k
A. Löfgren Belgium 18 1.1k 1.1× 878 1.2× 187 0.5× 304 0.9× 164 1.8× 37 1.8k
Elisabeth Rosser United Kingdom 17 657 0.6× 301 0.4× 347 0.9× 173 0.5× 138 1.5× 35 1.1k
V. Volpini Spain 17 571 0.6× 369 0.5× 222 0.6× 167 0.5× 167 1.8× 33 996
Horia Stanescu United Kingdom 18 536 0.5× 251 0.3× 185 0.5× 90 0.3× 130 1.4× 42 1.3k
Francesca Madia Italy 18 351 0.3× 290 0.4× 292 0.8× 438 1.3× 95 1.0× 62 1.0k
Yoshihisa Takiyama Japan 30 1.7k 1.7× 1.6k 2.2× 170 0.5× 693 2.1× 106 1.2× 139 2.4k
Lamei Yuan China 19 551 0.5× 133 0.2× 268 0.7× 249 0.7× 74 0.8× 83 1.0k
Jacquie Greenberg South Africa 18 927 0.9× 575 0.8× 187 0.5× 244 0.7× 135 1.5× 44 1.3k

Countries citing papers authored by Loreto Martorell

Since Specialization
Citations

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

Fields of papers citing papers by Loreto Martorell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Loreto Martorell

This figure shows the co-authorship network connecting the top 25 collaborators of Loreto Martorell. A scholar is included among the top collaborators of Loreto Martorell 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 Loreto Martorell. Loreto Martorell 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.
2.
Martorell, Loreto, et al.. (2023). Tamaño de repeticiones CTG no aumentado en la transmisión de un padre con alelo expandido: falsa sospecha de fenómeno de contracción. SHILAP Revista de lepidopterología. 4(2). 190–194. 1 indexed citations
3.
Roldán, Mónica, Lluı́s Armengol, Marcos Frías, et al.. (2023). Advanced Optical Microscopy: Unveiling Functional Insights Regarding a Novel PPP2R1A Variant and Its Unreported Phenotype. International Journal of Molecular Sciences. 24(18). 13699–13699.
4.
Hector, S.P., et al.. (2023). Lateralized overgrowth as a guiding sign of abdominal neoplasms for pediatric orthopedic surgeons. Joint Diseases and Related Surgery. 34(1). 3–8. 2 indexed citations
5.
Ricart, Sílvia, Loreto Martorell, Judith Armstrong, et al.. (2023). Coexistence of junctional epidermolysis bullosa, autosomal recessive deafness type 57, and Angelman syndrome: A case report. SHILAP Revista de lepidopterología. 11(4). e7275–e7275. 2 indexed citations
6.
Tamura, Norito, Shota Sakai, Loreto Martorell, et al.. (2021). Intellectual-disability-associated mutations in the ceramide transport protein gene CERT1 lead to aberrant function and subcellular distribution. Journal of Biological Chemistry. 297(5). 101338–101338. 12 indexed citations
7.
Benito, Daniel Natera‐de, C. Ortez, Cristina Jou, et al.. (2020). The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort. Pediatric Neurology. 115. 50–65. 13 indexed citations
8.
Rodríguez‐Pazos, L., Laura Fachal, A. Martín‐Santiago, et al.. (2020). Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation. PLoS ONE. 15(2). e0229025–e0229025. 10 indexed citations
9.
Frongia, A., Daniel Natera‐de Benito, C. Ortez, et al.. (2019). Salbutamol tolerability and efficacy in patients with spinal muscular atrophy type II. Neuromuscular Disorders. 29(7). 517–524. 16 indexed citations
10.
Casas‐Alba, Dídac, et al.. (2017). Pseudohypoaldosteronism types I and II: little more than a name in common. Journal of Pediatric Endocrinology and Metabolism. 30(5). 597–601. 14 indexed citations
11.
Torres‐Torronteras, Javier, María José Mansilla, Sílvia Casacuberta‐Serra, et al.. (2014). Thymidine phosphorylase is both a therapeutic and a suicide gene in a murine model of mitochondrial neurogastrointestinal encephalomyopathy. Gene Therapy. 21(7). 673–681. 7 indexed citations
12.
Ulate-Campos, Adriana, Carmen Fons, Jaume Campistol, et al.. (2014). Hemiplejía alternante de la infancia: estudio del gen ATP1A3 en 16 pacientes. Medicina Clínica. 143(1). 25–28. 2 indexed citations
13.
Yrigollen, Carolyn M., Loreto Martorell, Blythe Durbin‐Johnson, et al.. (2014). AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission. Journal of Neurodevelopmental Disorders. 6(1). 24–24. 82 indexed citations
14.
Martorell, Loreto, Mireia Tondo, Ferran J Garcia-Fructuoso, et al.. (2012). Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia. Clinical Rheumatology. 31(11). 1611–1615. 5 indexed citations
15.
Romanelli, Valeria, Víctor Martínez‐Glez, Mario F. Fraga, et al.. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics. 19(4). 416–421. 36 indexed citations
16.
Tondo, Mireia, et al.. (2011). Predisposition to epilepsy in fragile X syndrome: Does the Val66Met polymorphism in the BDNF gene play a role?. Epilepsy & Behavior. 22(3). 581–583. 11 indexed citations
17.
Carretero, Pablo, et al.. (2009). Síndrome de Griscelli-Prunieras: a propósito de dos casos. Anales de Pediatría. 70(2). 164–167. 6 indexed citations
18.
Munaín, Adolfo López de, Ana María Cobo, Amets Sáenz, et al.. (1996). Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy. Genetic Epidemiology. 13(5). 483–487. 12 indexed citations
19.
Emparanza, José Ignacio, et al.. (1994). Anticipation in Myotonic Dystrophy: A Parental-Sex-Related Phenomenon. Neuroepidemiology. 13(1-2). 75–78. 9 indexed citations
20.
Cobo, A.M., et al.. (1993). Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters. Human Molecular Genetics. 2(6). 711–715. 21 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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