Laura Turpín‐Fenoll

576 total citations
26 papers, 424 citations indexed

About

Laura Turpín‐Fenoll is a scholar working on Neurology, Epidemiology and Cognitive Neuroscience. According to data from OpenAlex, Laura Turpín‐Fenoll has authored 26 papers receiving a total of 424 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 12 papers in Epidemiology and 8 papers in Cognitive Neuroscience. Recurrent topics in Laura Turpín‐Fenoll's work include Parkinson's Disease Mechanisms and Treatments (12 papers), Restless Legs Syndrome Research (12 papers) and Sleep and Wakefulness Research (7 papers). Laura Turpín‐Fenoll is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (12 papers), Restless Legs Syndrome Research (12 papers) and Sleep and Wakefulness Research (7 papers). Laura Turpín‐Fenoll collaborates with scholars based in Spain and Germany. Laura Turpín‐Fenoll's co-authors include Jorge Millán‐Pascual, Elena Garcı́a-Martı́n, José A. G. Agúndez, Félix Javier Jiménez‐Jiménez, José Francisco Plaza‐Nieto, Hortensia Alonso‐Navarro, E García-Albea, Antonio Oliviero, E. Botía Paniagua and Nicolas Lang and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Laura Turpín‐Fenoll

26 papers receiving 423 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Turpín‐Fenoll Spain	13	138	138	107	101	94	26	424
José Francisco Plaza‐Nieto Spain	13	187 1.4×	140 1.0×	27 0.3×	88 0.9×	87 0.9×	29	434
Ibán Aldecoa Spain	13	336 2.4×	118 0.9×	58 0.5×	73 0.7×	24 0.3×	48	564
Mojdeh Ghabaee Iran	13	50 0.4×	66 0.5×	27 0.3×	49 0.5×	94 1.0×	40	454
Belén Pilo‐de‐la‐Fuente Spain	11	171 1.2×	113 0.8×	22 0.2×	78 0.8×	13 0.1×	18	365
Peter A. Weisskopf United States	10	73 0.5×	80 0.6×	203 1.9×	79 0.8×	47 0.5×	22	498
Madison T. Gray Canada	9	254 1.8×	65 0.5×	197 1.8×	14 0.1×	21 0.2×	12	570
D. Facchetti Italy	8	266 1.9×	15 0.1×	113 1.1×	36 0.4×	113 1.2×	13	442
Francesco Comacchio Italy	11	73 0.5×	39 0.3×	91 0.9×	72 0.7×	38 0.4×	34	342
Naotoshi Tamura Japan	10	126 0.9×	28 0.2×	28 0.3×	32 0.3×	36 0.4×	65	342

Countries citing papers authored by Laura Turpín‐Fenoll

Since Specialization

Citations

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

Fields of papers citing papers by Laura Turpín‐Fenoll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Turpín‐Fenoll

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Turpín‐Fenoll. A scholar is included among the top collaborators of Laura Turpín‐Fenoll 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 Turpín‐Fenoll. Laura Turpín‐Fenoll 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

Garcı́a-Martı́n, Elena, Pedro Ayuso, Hortensia Alonso‐Navarro, et al.. (2023). Vitamin D receptor and binding protein genes variants in patients with migraine. Annals of Clinical and Translational Neurology. 10(10). 1824–1832. 3 indexed citations

Garcı́a-Martı́n, Elena, Pedro Ayuso, Hortensia Alonso‐Navarro, et al.. (2023). Lack of Association between Common LAG3/CD4 Variants and Risk of Migraine. International Journal of Molecular Sciences. 24(2). 1292–1292. 3 indexed citations

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, Laura Turpín‐Fenoll, et al.. (2022). LAG3/CD4 Genes Variants and the Risk for Restless Legs Syndrome. International Journal of Molecular Sciences. 23(23). 14795–14795. 1 indexed citations

Garcı́a-Martı́n, Elena, José A. G. Agúndez, Julián Benito‐León, et al.. (2022). Association between LAG3/CD4 Genes Variants and Risk for Multiple Sclerosis. International Journal of Molecular Sciences. 23(23). 15244–15244. 2 indexed citations

Garcı́a-Martı́n, Elena, Hortensia Alonso‐Navarro, Laura Turpín‐Fenoll, et al.. (2022). Increased serum diamine oxidase activity in nonallergic patients with migraine. European Journal of Clinical Investigation. 52(6). e13757–e13757. 9 indexed citations

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, Laura Turpín‐Fenoll, et al.. (2021). Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome. Frontiers in Pharmacology. 12. 618989–618989. 3 indexed citations

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, Mónica Díez-Fairén, et al.. (2020). Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome. Journal of Neurology. 268(4). 1461–1472. 12 indexed citations

Agúndez, José A. G., Elena Garcı́a-Martı́n, Julián Benito‐León, et al.. (2020). Endothelial nitric oxide synthase (NOS3) rs2070744 polymorphism and risk for multiple sclerosis. Journal of Neural Transmission. 127(8). 1167–1175. 6 indexed citations

Garcı́a-Martı́n, Elena, Hortensia Alonso‐Navarro, Laura Turpín‐Fenoll, et al.. (2019). Association between endothelial nitric oxide synthase (NOS3) rs2070744 and the risk for migraine. The Pharmacogenomics Journal. 20(3). 426–432. 13 indexed citations

10.

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, M. Zurdo, et al.. (2017). Association Between the rs1229984 Polymorphism in the Alcohol Dehydrogenase 1B Gene and Risk for Restless Legs Syndrome. SLEEP. 40(12). 13 indexed citations

11.

Jiménez‐Jiménez, Félix Javier, Elena Garcı́a-Martı́n, Hortensia Alonso‐Navarro, et al.. (2016). Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome. Journal of Neural Transmission. 124(3). 285–291. 10 indexed citations

12.

Agúndez, José A. G., Elena Garcı́a-Martı́n, Carmen Martı́nez, et al.. (2016). Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis. Scientific Reports. 6(1). 20830–20830. 29 indexed citations

13.

Garcı́a-Martı́n, Elena, Félix Javier Jiménez‐Jiménez, Hortensia Alonso‐Navarro, et al.. (2015). Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. Medicine. 94(34). e1448–e1448. 29 indexed citations

14.

Jiménez‐Jiménez, Félix Javier, Elena Garcı́a-Martı́n, Hortensia Alonso‐Navarro, et al.. (2015). Association Between Vitamin D Receptor rs731236 (Taq1) Polymorphism and Risk for Restless Legs Syndrome in the Spanish Caucasian Population. Medicine. 94(47). e2125–e2125. 22 indexed citations

15.

Agúndez, José A. G., Elena Garcı́a-Martı́n, Carmen Martı́nez, et al.. (2014). The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis. Cellular and Molecular Immunology. 12(6). 777–779. 6 indexed citations

16.

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, Carmen Martínez, et al.. (2014). Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome. Journal of Neural Transmission. 122(6). 819–823. 21 indexed citations

17.

Agúndez, José A. G., Elena Garcı́a-Martı́n, Carmen Martı́nez, et al.. (2014). NQO1gene rs1800566 variant is not associated with risk for multiple sclerosis. BMC Neurology. 14(1). 87–87. 13 indexed citations

18.

Jiménez‐Jiménez, Félix Javier, Hortensia Alonso‐Navarro, Carmen Martínez, et al.. (2013). The solute carrier family 1 (glial high affinity glutamate transporter), member 2 gene, SLC1A2, rs3794087 variant and assessment risk for restless legs syndrome. Sleep Medicine. 15(2). 266–268. 18 indexed citations

19.

Garcı́a-Martı́n, Elena, Oswaldo Lorenzo‐Betancor, Carmen Martı́nez, et al.. (2013). LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis. BMC Neurology. 13(1). 34–34. 9 indexed citations

20.

Roco, Ãngela, Félix Javier Jiménez‐Jiménez, Hortensia Alonso‐Navarro, et al.. (2012). MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome. Journal of Neural Transmission. 120(3). 463–467. 16 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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