Francesc Palau

10.2k total citations
167 papers, 4.8k citations indexed

About

Francesc Palau is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Francesc Palau has authored 167 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 102 papers in Cellular and Molecular Neuroscience, 87 papers in Molecular Biology and 34 papers in Genetics. Recurrent topics in Francesc Palau's work include Genetic Neurodegenerative Diseases (71 papers), Hereditary Neurological Disorders (55 papers) and Mitochondrial Function and Pathology (45 papers). Francesc Palau is often cited by papers focused on Genetic Neurodegenerative Diseases (71 papers), Hereditary Neurological Disorders (55 papers) and Mitochondrial Function and Pathology (45 papers). Francesc Palau collaborates with scholars based in Spain, United States and United Kingdom. Francesc Palau's co-authors include Carmen Espinós, Juan J. Vílchez, Pilar González‐Cabo, Teresa Sevilla, Laia Pedrola, María José Chumillas, Amalia Capilla, A Cruz-Martı́nez, Yolanda Sanz and Gemma Castillejo and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Francesc Palau

161 papers receiving 4.6k citations

Peers

Francesc Palau
Lev G. Goldfarb United States
Timothy Vartanian United States
Robert O. Heuckeroth United States
Norman Latov United States
Andrea B. Huber Germany
Maria Lindahl Finland
Murray B. Bornstein United States
Tim Chataway Australia
Joan Goverman United States
Bao‐Guo Xiao China
Lev G. Goldfarb United States
Francesc Palau
Citations per year, relative to Francesc Palau Francesc Palau (= 1×) peers Lev G. Goldfarb

Countries citing papers authored by Francesc Palau

Since Specialization
Citations

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

Fields of papers citing papers by Francesc Palau

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesc Palau

This figure shows the co-authorship network connecting the top 25 collaborators of Francesc Palau. A scholar is included among the top collaborators of Francesc Palau 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 Francesc Palau. Francesc Palau 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.
Benito, Daniel Natera‐de, Carla Garcia‐Cabau, Cristina Jou, et al.. (2023). Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of Clinical and Translational Neurology. 10(3). 408–425. 7 indexed citations
2.
Cantarero, Lara, et al.. (2023). Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites. Biology Open. 12(4). 8 indexed citations
3.
León, Marian, Javier Prieto, Maria Micaela Molina‐Navarro, et al.. (2023). Rapid degeneration of iPSC-derived motor neurons lacking Gdap1 engages a mitochondrial-sustained innate immune response. Cell Death Discovery. 9(1). 217–217. 7 indexed citations
4.
Casas‐Alba, Dídac, et al.. (2022). Diagnostic strategies in patients with undiagnosed and rare diseases. 6. 322–332. 3 indexed citations
5.
Carrera‐García, Laura, et al.. (2022). Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease. 6. 333–352. 5 indexed citations
6.
Nuevo‐Tapioles, Cristina, Fulvio Santacatterina, Cristina Núñez de Arenas, et al.. (2021). Effective therapeutic strategies in a preclinical mouse model of Charcot–Marie–Tooth disease. Human Molecular Genetics. 30(24). 2441–2455. 5 indexed citations
7.
Esquerda, Montse, et al.. (2020). Ethical questions concerning newborn genetic screening. Clinical Genetics. 99(1). 93–98. 12 indexed citations
8.
González‐Sánchez, Paloma, Jorgina Satrústegui, Francesc Palau, & Araceli del Arco. (2019). Calcium Deregulation and Mitochondrial Bioenergetics in GDAP1-Related CMT Disease. International Journal of Molecular Sciences. 20(2). 403–403. 21 indexed citations
9.
Olivares, Marta, Alan W. Walker, Amalia Capilla, et al.. (2018). Gut microbiota trajectory in early life may predict development of celiac disease. Microbiome. 6(1). 36–36. 95 indexed citations
10.
Soldevilla, Beatriz, Clara Ibáñez, Fulvio Santacatterina, et al.. (2017). Plasma metabolome and skin proteins in Charcot-Marie-Tooth 1A patients. PLoS ONE. 12(6). e0178376–e0178376. 13 indexed citations
11.
Lupo, Vincenzo, Eduardo Calpena, Luca Bartesaghi, et al.. (2013). Sh3tc2 deficiency affects neuregulin‐1/ErbB signaling. Glia. 61(7). 1041–1051. 36 indexed citations
12.
Sevilla, Teresa, Dolores Martínez‐Rubio, Catalina Márquez-Vega, et al.. (2012). Genetics of the Charcot‐Marie‐Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy‐Russe in depth. Clinical Genetics. 83(6). 565–570. 25 indexed citations
13.
García‐Giménez, Jose Luis, Amparo Gimeno, Pilar González‐Cabo, et al.. (2011). Differential Expression of PGC-1α and Metabolic Sensors Suggest Age-Dependent Induction of Mitochondrial Biogenesis in Friedreich Ataxia Fibroblasts. PLoS ONE. 6(6). e20666–e20666. 40 indexed citations
14.
González‐Cabo, Pilar, Juan Cabello, Sergio Moreno, et al.. (2011). Disruption of the ATP-binding Cassette B7 (ABTM-1/ABCB7) Induces Oxidative Stress and Premature Cell Death in Caenorhabditis elegans. Journal of Biological Chemistry. 286(24). 21304–21314. 22 indexed citations
15.
González‐Cabo, Pilar, José Vicente Llorens, Francesc Palau, & María Dolores Moltó. (2009). Friedreich Ataxia: An Update on Animal Models, Frataxin Function and Therapies. Advances in experimental medicine and biology. 652. 247–261. 15 indexed citations
16.
Palau, Francesc, et al.. (2008). Gene symbol: SH3TC2. Disease: Charcot-Marie-Tooth type 4C.. PubMed. 124(3). 320–320. 1 indexed citations
17.
Vázquez‐Manrique, Rafael P., et al.. (2006). The frataxin-encoding operon of Caenorhabditis elegans shows complex structure and regulation. Genomics. 89(3). 392–401. 11 indexed citations
18.
Ahearn, Mary Ellen, Devin Dressman, Kemal O. Yariz, et al.. (2004). X-linked lethal infantile (XL)-SMA: new clinical information, variant phenotypes, and candidate disease gene studies.. mediaTUM (Technical University of Munich). 1 indexed citations
19.
20.
Moltó, María Dolores, Juan J. Vílchez, Massimo Pandolfo, et al.. (1994). Mapping of Friedreich's AtaxiaLocus by Identification ofRecombination Events in PatientsHomozygous by Descent. European Journal of Human Genetics. 2(4). 291–299. 8 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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