Laura Gort

2.0k citations

67 papers · 1.3k indexed · h-index 24

Co-authors: Amparo Chabás María Josep Coll Antònia Ribes Daniel Grinberg Lluı̈sa Vilageliu Rafael Artuch Bru Cormand Leslie Matalonga
Topics: Lysosomal Storage Disorders Research (41 papers)Cellular transport and secretion (17 papers)Metabolism and Genetic Disorders (14 papers)
Cited by: Clinical Biochemistry Physiology Cell Biology
Journals: SHILAP Revista de lepidopterologíaBrain Scientific Reports
Partner nations: Spain United Kingdom Portugal

In The Last Decade

Laura Gort

66 papers receiving 1.3k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Functional Evidence of CCDC186 as a New Disease-Associated Gene with Endocrine and Central Nervous System Alterations 2023 ·International Journal of Molecular Sciences ·Luisa Arrabal,(unknown),(unknown),Laura Gort,Judit García‐Villoria,S. Roldán,Frederic Tort,Antònia Ribes	0
2	Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects 2022 ·Antioxidants ·(unknown),Constanza Morén,Francesc Josep García‐García,Alberto Blázquez,(unknown),Ana Cortés,(unknown),Ester López‐Gallardo,Ester Lozano,(unknown),Laura Gort,Ester Tobías,Aitor Delmiro,Miguel A. Martı́n,Miguel Ángel Fernández‐Moreno,Eduardo Ruiz‐Pesini,Elena García‐Arumí,Juan Carlos Rodríguez‐Aguilera,Glòria Garrabou	5
3	Over-Mutated Mitochondrial, Lysosomal and TFEB-Regulated Genes in Parkinson’s Disease 2022 ·Journal of Clinical Medicine ·(unknown),(unknown),Frederic Tort,Laura Texidó,Cèlia Painous,Yaroslau Compta,Marı́a José Martı́,Antònia Ribes,Laura Gort	4
4	Bioenergetic and Autophagic Characterization of Skin Fibroblasts from C9orf72 Patients 2022 ·Antioxidants ·María Isabel Álvarez‐Mora,Glòria Garrabou,(unknown),Francisco García‐García,(unknown),(unknown),Laura Gort,Sergi Borrego‐Écija,Raquel Sánchez‐Valle,(unknown),(unknown),Laia Rodríguez‐Revenga	5
5	Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns 2021 ·Orphanet Journal of Rare Diseases ·(unknown),José Antonio Arranz,Aída Ormazábal,Mireia del Toro,Ángeles García‐Cazorla,Aleix Navarro‐Sastre,Rosa María López,(unknown),(unknown),(unknown),(unknown),(unknown),José Luis Marı́n,(unknown),Rafael Artuch,Frederic Tort,Laura Gort,(unknown),Judit García‐Villoria,Antònia Ribes	22
6	Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia 2020 ·Mitochondrion ·(unknown),María Teresa García‐Silva,Luis Aldámiz‐Echevarría,Laura Gort,Judit García‐Villoria,Frederic Tort,Antònia Ribes	4
7	Leigh syndrome associated with TRMU gene mutations 2020 ·Molecular Genetics and Metabolism Reports ·(unknown),(unknown),Javier de las Heras,(unknown),Elena García‐Arumí,(unknown),José Antonio Arranz,(unknown),(unknown),Ángel Sánchez‐Montáñez,Laura Gort,Frederic Tort,Mireia del Toro	4
8	Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution 2020 ·Molecular Genetics and Metabolism ·Frederic Tort,(unknown),Ranjani Parthasarathy,(unknown),(unknown),Judit García‐Villoria,Laura Gort,(unknown),Miguel A. Martı́n,Erika Fernández‐Vizarra,Massimo Zeviani,Antònia Ribes	11
9	Prenatal mucopolysaccharidosis VII: A novel pathogenic variant identified in GUSB gene 2020 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),(unknown),Olga Ocón,(unknown),Laura Gort,Francisca S. Molina	5
10	An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations 2020 ·Molecular Genetics and Metabolism Reports ·(unknown),Rosa María López,Laura Gort,(unknown),José Luis Marı́n,(unknown),Judit García‐Villoria,José Antonio Arranz,Mireia del Toro,Frederic Tort,(unknown),(unknown),(unknown),Antònia Ribes	10
11	Generation of two NAGLU-mutated homozygous cell lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo B syndrome 2019 ·Stem Cell Research ·(unknown),Mónica Cozar,Laura Gort,(unknown),Lluı̈sa Vilageliu,Daniel Grinberg,Isaac Canals	4
12	Galactosialidosis: nueva mutación de novo en el gen CTSA en un paciente afecto de la forma infantil tardía 2018 ·Archivos Argentinos de Pediatria ·(unknown),(unknown),Laura Gort,(unknown)	1
13	Haematopoietic stem cell transplantation for mucopolysaccharidosis type VII: A case report 2018 ·Pediatric Transplantation ·Luisa Sisinni,Mercédes Pineda,María Josep Coll,Laura Gort,Eulalia Turón‐Viñas,Montserrat Torrent,(unknown),(unknown),Isabel Badell	16
14	Lysosomal Acid Lipase Deficiency in 23 Spanish Patients: High Frequency of the Novel c.966+2T>G Mutation in Wolman Disease 2017 ·JIMD Reports ·(unknown),(unknown),(unknown),Ángela Arias,Laura Gort	9
15	Natural history of Sanfilippo syndrome in Spain 2013 ·Orphanet Journal of Rare Diseases ·(unknown),María del Mar O’Callaghan,Laura Gort,María José Coll,Mercédes Pineda	55
16	Neuronopathic Gaucher's disease: induced pluripotent stem cells for disease modelling and testing chaperone activity of small compounds 2012 ·Human Molecular Genetics ·Gustavo Tiscórnia,Erika Lorenzo-Vivas,Leslie Matalonga,Ina Berniakovich,Montserrat Barragán,Cristina Eguizábal,Laura Gort,Federico Gonzãlez,Carmen Ortiz Mellet,José M. Garcı́a Fernández,Antònia Ribes,Anna Veiga,Juan Carlos Izpisúa Belmonte	66
17	GM2 gangliosidoses in Spain: Analysis of the HEXA and HEXB genes in 34 Tay–Sachs and 14 Sandhoff patients 2012 ·Gene ·Laura Gort,Natalia de Olano,Judit Macías‐Vidal,(unknown)	26
18	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
19	Mutation analysis of Gaucher disease patients from Argentina: High prevalence of the RecNciI mutation 1998 ·American Journal of Medical Genetics ·Bru Cormand,(unknown),Laura Gort,Cristina Campoy,Mariana Blanco,N. Chamoles,(unknown),(unknown),Daniel Grinberg	35
20	Analysis of five mutations in 20 mucopolysaccharidosis type I patients: High prevalence of the W402X mutation 1998 ·Human Mutation ·Laura Gort,Amparo Chabás,María Josep Coll	21

About Laura Gort

Laura Gort is a scholar working on Clinical Biochemistry, Physiology and Cell Biology, having authored 67 papers that have together received 1.3k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (41 papers), Cellular transport and secretion (17 papers) and Metabolism and Genetic Disorders (14 papers). The work is most often cited by research in Clinical Biochemistry (247 citations), Physiology (758 citations) and Cell Biology (282 citations). Laura Gort has collaborated with scholars based in Spain, United Kingdom and Portugal. Frequent 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. Their work appears in journals such as SHILAP Revista de lepidopterología, Brain and Scientific Reports.

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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