Aurora Pujol

23.2k total citations · 1 hit paper
114 papers, 4.6k citations indexed

About

Aurora Pujol is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Aurora Pujol has authored 114 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 40 papers in Physiology and 18 papers in Genetics. Recurrent topics in Aurora Pujol's work include Peroxisome Proliferator-Activated Receptors (52 papers), Adipose Tissue and Metabolism (28 papers) and Mitochondrial Function and Pathology (18 papers). Aurora Pujol is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (52 papers), Adipose Tissue and Metabolism (28 papers) and Mitochondrial Function and Pathology (18 papers). Aurora Pujol collaborates with scholars based in Spain, United States and France. Aurora Pujol's co-authors include Isidró Ferrer, Stéphane Fourcade, Agatha Schlüter, Montserrat Ruíz, Manuel Portero-Otı́n, Reinald Pamplona, Patrick Aubourg, Mariona Jové, Inderjit Singh and Jean‐Louis Mandel and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Aurora Pujol

111 papers receiving 4.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Accelerated biological aging in COVID-19 patients

2022 126 citations Laura Planas‐Serra, Aurora Pujol et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aurora Pujol Spain	41	3.3k	1.5k	713	472	416	114	4.6k
Brett H. Graham United States	36	3.3k 1.0×	835 0.6×	1.0k 1.5×	574 1.2×	253 0.6×	91	4.6k
Estela Área-Gómez United States	32	2.8k 0.8×	1.6k 1.1×	388 0.5×	153 0.3×	248 0.6×	64	4.2k
Linsey Stiles United States	23	3.1k 0.9×	1.2k 0.8×	611 0.9×	196 0.4×	171 0.4×	51	4.7k
Lynda D. Hester United States	28	3.3k 1.0×	938 0.6×	138 0.2×	175 0.4×	284 0.7×	34	5.0k
Francesc X. Soriano Spain	25	2.5k 0.7×	935 0.6×	279 0.4×	130 0.3×	373 0.9×	41	3.6k
Nicolle Sitte Germany	31	2.5k 0.8×	1.8k 1.2×	318 0.4×	149 0.3×	175 0.4×	39	4.3k
Marc Gleichmann United States	27	2.0k 0.6×	1.2k 0.8×	140 0.2×	203 0.4×	580 1.4×	40	3.9k
Tinna Stevnsner Denmark	37	3.6k 1.1×	748 0.5×	413 0.6×	501 1.1×	171 0.4×	83	4.9k
Marc Uldry Switzerland	20	3.0k 0.9×	2.7k 1.9×	159 0.2×	269 0.6×	172 0.4×	21	5.7k
Phillip W. Dickson Australia	32	1.7k 0.5×	484 0.3×	184 0.3×	235 0.5×	248 0.6×	77	3.7k

Countries citing papers authored by Aurora Pujol

Since Specialization

Citations

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

Fields of papers citing papers by Aurora Pujol

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurora Pujol

This figure shows the co-authorship network connecting the top 25 collaborators of Aurora Pujol. A scholar is included among the top collaborators of Aurora Pujol 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 Aurora Pujol. Aurora Pujol 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

Launay, Nathalie, Edgard Verdura, Gorka Fernández‐Eulate, et al.. (2024). Altered tubulin detyrosination due to SVBP malfunction induces cytokinesis failure and senescence, underlying a complex hereditary spastic paraplegia. Aging Cell. 24(1). e14355–e14355.

Mohan, Shruthi, Meredith Weaver, Irene De Biase, et al.. (2023). Evaluating the strength of evidence for genes implicated in peroxisomal disorders using the ClinGen clinical validity framework and providing updates to the peroxisomal disease nomenclature. Molecular Genetics and Metabolism. 139(3). 107604–107604.

Launay, Nathalie, Montserrat Ruíz, Laura Planas‐Serra, et al.. (2023). RINT1 deficiency disrupts lipid metabolism and underlies a complex hereditary spastic paraplegia. Journal of Clinical Investigation. 133(14). 7 indexed citations

Planas‐Serra, Laura, Nathalie Launay, Leire Goicoechea, et al.. (2023). Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity. Journal of Clinical Investigation. 133(10). 24 indexed citations

Ranea‐Robles, Pablo, Jorge Galino, Lluı́s Espinosa, et al.. (2021). Modulation of mitochondrial and inflammatory homeostasis through RIP140 is neuroprotective in an adrenoleukodystrophy mouse model. Neuropathology and Applied Neurobiology. 48(1). e12747–e12747. 9 indexed citations

Troya, Jesús, Paul Bastard, Laura Planas‐Serra, et al.. (2021). Neutralizing Autoantibodies to Type I IFNs in >10% of Patients with Severe COVID-19 Pneumonia Hospitalized in Madrid, Spain. Journal of Clinical Immunology. 41(5). 914–922. 71 indexed citations

Andrés‐Benito, Pol, Ellen Gelpí, Mariona Jové, et al.. (2020). Lipid alterations in human frontal cortex in ALS‐FTLD‐TDP43 proteinopathy spectrum are partly related to peroxisome impairment. Neuropathology and Applied Neurobiology. 47(4). 544–563. 15 indexed citations

Li, Rachel, Scott A. Turner, Richard H. van Jaarsveld, et al.. (2020). HNRNPH1 ‐related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndrome. Clinical Genetics. 98(1). 91–98. 18 indexed citations

Harting, Inga, Ingeborg Krägeloh‐Mann, Annette Bley, et al.. (2020). POLR3A variants with striatal involvement and extrapyramidal movement disorder. Neurogenetics. 21(2). 121–133. 26 indexed citations

10.

López‐Erauskin, Jone, Jorge Galino, Montserrat Ruíz, et al.. (2013). Impaired mitochondrial oxidative phosphorylation in the peroxisomal disease X-linked adrenoleukodystrophy. Human Molecular Genetics. 22(16). 3296–3305. 99 indexed citations

11.

Morató, Laia, Jorge Galino, Montserrat Ruíz, et al.. (2013). Pioglitazone halts axonal degeneration in a mouse model of X-linked adrenoleukodystrophy. Brain. 136(8). 2432–2443. 60 indexed citations

12.

Launay, Nathalie, Montserrat Ruíz, Stéphane Fourcade, et al.. (2013). Oxidative stress regulates the ubiquitin–proteasome system and immunoproteasome functioning in a mouse model of X-adrenoleukodystrophy. Brain. 136(3). 891–904. 38 indexed citations

13.

Dumont, Magali, Cliona Stack, Ceyhan Elipenahli, et al.. (2012). Bezafibrate administration improves behavioral deficits and tau pathology in P301S mice. Human Molecular Genetics. 21(23). 5091–5105. 64 indexed citations

14.

Galino, Jorge, Montserrat Ruíz, Stéphane Fourcade, et al.. (2011). Oxidative Damage Compromises Energy Metabolism in the Axonal Degeneration Mouse Model of X-Adrenoleukodystrophy. Antioxidants and Redox Signaling. 15(8). 2095–2107. 72 indexed citations

15.

Ferrer, Isidró, Irene López‐González, Margarita Carmona, et al.. (2011). Neurochemistry and the non-motor aspects of PD. Neurobiology of Disease. 46(3). 508–526. 68 indexed citations

16.

Fourcade, Stéphane, Montserrat Ruíz, Cristina Guilera, et al.. (2010). Valproic acid induces antioxidant effects in X-linked adrenoleukodystrophy. Human Molecular Genetics. 19(10). 2005–2014. 76 indexed citations

17.

Schlüter, Agatha, Stéphane Fourcade, Raymond Ripp, et al.. (2006). The Evolutionary Origin of Peroxisomes: An ER-Peroxisome Connection. Molecular Biology and Evolution. 23(4). 838–845. 132 indexed citations

18.

Ferrer, Isidró, Josef P. Kapfhammer, C. Hindelang, et al.. (2005). Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. Human Molecular Genetics. 14(23). 3565–3577. 86 indexed citations

19.

Pujol, Aurora, Isidró Ferrer, Carme Camps, et al.. (2004). Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy. Human Molecular Genetics. 13(23). 2997–3006. 158 indexed citations

20.

Guimarães, Carla P., Pedro Domíngues, Patrick Aubourg, et al.. (2004). Mouse liver PMP70 and ALDP: homomeric interactions prevail in vivo. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1689(3). 235–243. 45 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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