Laura Gort

2.0k total citations
67 papers, 1.3k citations indexed

About

Laura Gort is a scholar working on Physiology, Molecular Biology and Cell Biology. According to data from OpenAlex, Laura Gort has authored 67 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Physiology, 39 papers in Molecular Biology and 20 papers in Cell Biology. Recurrent topics in Laura Gort's work include Lysosomal Storage Disorders Research (41 papers), Cellular transport and secretion (17 papers) and Metabolism and Genetic Disorders (14 papers). Laura Gort is often cited by papers focused on Lysosomal Storage Disorders Research (41 papers), Cellular transport and secretion (17 papers) and Metabolism and Genetic Disorders (14 papers). Laura Gort collaborates with scholars based in Spain, United Kingdom and Portugal. Laura Gort's co-authors include Amparo Chabás, María Josep Coll, Antònia Ribes, Daniel Grinberg, Lluı̈sa Vilageliu, Rafael Artuch, Bru Cormand, Leslie Matalonga, Judit García‐Villoria and María José Coll and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Scientific Reports.

In The Last Decade

Laura Gort

66 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Gort Spain 24 758 629 282 275 247 67 1.3k
María Josep Coll Spain 19 703 0.9× 370 0.6× 153 0.5× 218 0.8× 158 0.6× 37 1.1k
N. U. Bosshard Switzerland 18 446 0.6× 338 0.5× 164 0.6× 223 0.8× 149 0.6× 27 972
Clare Beesley United Kingdom 17 607 0.8× 288 0.5× 123 0.4× 240 0.9× 189 0.8× 29 980
G. T. N. Besley United Kingdom 26 904 1.2× 948 1.5× 210 0.7× 250 0.9× 510 2.1× 87 1.9k
I Maire France 17 785 1.0× 341 0.5× 188 0.7× 228 0.8× 82 0.3× 85 1.2k
Jan Lukáš Germany 19 904 1.2× 435 0.7× 338 1.2× 323 1.2× 56 0.2× 56 1.3k
Jakub Sikora Czechia 20 487 0.6× 507 0.8× 186 0.7× 137 0.5× 71 0.3× 48 1.1k
Federica Deodato Italy 23 640 0.8× 801 1.3× 149 0.5× 114 0.4× 608 2.5× 55 1.7k
J. Ledvinová Czechia 20 1.4k 1.9× 500 0.8× 447 1.6× 325 1.2× 72 0.3× 53 1.7k
Wei‐Lien Chuang United States 18 797 1.1× 472 0.8× 371 1.3× 240 0.9× 59 0.2× 28 1.1k

Countries citing papers authored by Laura Gort

Since Specialization
Citations

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

Fields of papers citing papers by Laura Gort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Gort

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Gort. A scholar is included among the top collaborators of Laura Gort 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 Laura Gort. Laura Gort 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.
Arrabal, Luisa, Laura Gort, Judit García‐Villoria, et al.. (2023). Functional Evidence of CCDC186 as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations. International Journal of Molecular Sciences. 24(15). 12319–12319.
2.
Morén, Constanza, Francesc Josep García‐García, Alberto Blázquez, et al.. (2022). Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects. Antioxidants. 11(4). 741–741. 5 indexed citations
3.
Tort, Frederic, Laura Texidó, Cèlia Painous, et al.. (2022). Over-Mutated Mitochondrial, Lysosomal and TFEB-Regulated Genes in Parkinson’s Disease. Journal of Clinical Medicine. 11(6). 1749–1749. 4 indexed citations
4.
Álvarez‐Mora, María Isabel, Glòria Garrabou, Francisco García‐García, et al.. (2022). Bioenergetic and Autophagic Characterization of Skin Fibroblasts from C9orf72 Patients. Antioxidants. 11(6). 1129–1129. 5 indexed citations
5.
Arranz, José Antonio, Aída Ormazábal, Mireia del Toro, et al.. (2021). Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns. Orphanet Journal of Rare Diseases. 16(1). 195–195. 22 indexed citations
6.
García‐Silva, María Teresa, Luis Aldámiz‐Echevarría, Laura Gort, et al.. (2020). Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia. Mitochondrion. 55. 78–84. 4 indexed citations
7.
Heras, Javier de las, Elena García‐Arumí, José Antonio Arranz, et al.. (2020). Leigh syndrome associated with TRMU gene mutations. Molecular Genetics and Metabolism Reports. 26. 100690–100690. 4 indexed citations
8.
Tort, Frederic, Ranjani Parthasarathy, Judit García‐Villoria, et al.. (2020). Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution. Molecular Genetics and Metabolism. 131(3). 349–357. 11 indexed citations
9.
Ocón, Olga, et al.. (2020). Prenatal mucopolysaccharidosis VII: A novel pathogenic variant identified in GUSB gene. SHILAP Revista de lepidopterología. 9(2). 790–795. 5 indexed citations
10.
López, Rosa María, Laura Gort, José Luis Marı́n, et al.. (2020). An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations. Molecular Genetics and Metabolism Reports. 22. 100553–100553. 10 indexed citations
11.
12.
Gort, Laura, et al.. (2018). Galactosialidosis: nueva mutación de novo en el gen CTSA en un paciente afecto de la forma infantil tardía. Archivos Argentinos de Pediatria. 116(1). e88–e92. 1 indexed citations
13.
Sisinni, Luisa, Mercédes Pineda, María Josep Coll, et al.. (2018). Haematopoietic stem cell transplantation for mucopolysaccharidosis type VII: A case report. Pediatric Transplantation. 22(7). e13278–e13278. 16 indexed citations
14.
15.
O’Callaghan, María del Mar, et al.. (2013). Natural history of Sanfilippo syndrome in Spain. Orphanet Journal of Rare Diseases. 8(1). 189–189. 55 indexed citations
16.
Tiscórnia, Gustavo, Erika Lorenzo-Vivas, Leslie Matalonga, et al.. (2012). Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds. Human Molecular Genetics. 22(4). 633–645. 66 indexed citations
17.
Gort, Laura, et al.. (2012). GM2 gangliosidoses in Spain: Analysis of the HEXA and HEXB genes in 34 Tay–Sachs and 14 Sandhoff patients. Gene. 506(1). 25–30. 26 indexed citations
18.
19.
Cormand, Bru, Laura Gort, Cristina Campoy, et al.. (1998). Mutation analysis of Gaucher disease patients from Argentina: High prevalence of the RecNciI mutation. American Journal of Medical Genetics. 80(4). 343–351. 35 indexed citations
20.
Gort, Laura, Amparo Chabás, & María Josep Coll. (1998). Analysis of five mutations in 20 mucopolysaccharidosis type I patients: High prevalence of the W402X mutation. Human Mutation. 11(4). 332–333. 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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