Elena Lorenzo

1.3k total citations
20 papers, 741 citations indexed

About

Elena Lorenzo is a scholar working on Neurology, Neurology and Genetics. According to data from OpenAlex, Elena Lorenzo has authored 20 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 7 papers in Neurology and 7 papers in Genetics. Recurrent topics in Elena Lorenzo's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Alzheimer's disease research and treatments (5 papers) and Neurological diseases and metabolism (4 papers). Elena Lorenzo is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Alzheimer's disease research and treatments (5 papers) and Neurological diseases and metabolism (4 papers). Elena Lorenzo collaborates with scholars based in Spain, United States and France. Elena Lorenzo's co-authors include Pau Pástor, Jaione Irigoyen, María A. Pastor, Oswaldo Lorenzo‐Betancor, Lluı́s Samaranch, Carlos Cruchaga, Sebastián Cervantes, Bruno A. Benítez, José Matías Arbelo and Sara Ortega‐Cubero and has published in prestigious journals such as PLoS ONE, Brain and International Journal of Molecular Sciences.

In The Last Decade

Elena Lorenzo

19 papers receiving 736 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elena Lorenzo Spain 13 403 237 234 185 179 20 741
Yi Jayne Tan Singapore 15 221 0.5× 104 0.4× 150 0.6× 97 0.5× 165 0.9× 43 536
Melanie B. Watson United States 8 427 1.1× 309 1.3× 150 0.6× 227 1.2× 255 1.4× 8 786
H. Kondo Japan 12 229 0.6× 148 0.6× 297 1.3× 278 1.5× 167 0.9× 23 670
Yi‐Min Sun China 18 477 1.2× 127 0.5× 246 1.1× 307 1.7× 225 1.3× 73 919
Atsuko Katsumoto Japan 12 186 0.5× 275 1.2× 295 1.3× 136 0.7× 136 0.8× 20 733
Mohamad Saad Egypt 5 477 1.2× 216 0.9× 247 1.1× 155 0.8× 212 1.2× 7 706
Carolina Cebrián Spain 9 277 0.7× 210 0.9× 199 0.9× 130 0.7× 325 1.8× 13 787
Inés García‐Gorostiaga Spain 15 324 0.8× 114 0.5× 192 0.8× 185 1.0× 143 0.8× 20 692
Tara M. Caffrey United Kingdom 12 203 0.5× 195 0.8× 349 1.5× 258 1.4× 185 1.0× 16 699
Lilach Soreq Israel 16 195 0.5× 496 2.1× 580 2.5× 238 1.3× 219 1.2× 23 1.2k

Countries citing papers authored by Elena Lorenzo

Since Specialization
Citations

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

Fields of papers citing papers by Elena Lorenzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elena Lorenzo

This figure shows the co-authorship network connecting the top 25 collaborators of Elena Lorenzo. A scholar is included among the top collaborators of Elena Lorenzo 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 Elena Lorenzo. Elena Lorenzo 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.
2.
Pourchet, Léa, Yvonne Richaud‐Patín, Elena Lorenzo, et al.. (2025). 3D bioprinting of human iPSC-derived cardiac constructs with microvascular network support for improved graft survival in vivo. Biofabrication. 17(3). 35010–35010. 5 indexed citations
3.
Pérez-González, Marta, Elena Lorenzo, Elizabeth Guruceaga, et al.. (2021). Identifying the Main Functional Pathways Associated with Cognitive Resilience to Alzheimer’s Disease. International Journal of Molecular Sciences. 22(17). 9120–9120. 16 indexed citations
4.
Díez-Fairén, Mónica, Bruno A. Benítez, Sara Ortega‐Cubero, et al.. (2018). Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish population. Neurobiology of Aging. 70. 325.e1–325.e5. 3 indexed citations
5.
Razquín, Cristina, Sara Ortega‐Cubero, Mónica Díez-Fairén, et al.. (2018). Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants. Neurobiology of Aging. 66. 177.e7–177.e10. 1 indexed citations
6.
Castellanos, Gabriel, María A. Fernández‐Seara, Oswaldo Lorenzo‐Betancor, et al.. (2015). Automated Neuromelanin Imaging as a Diagnostic Biomarker for Parkinson's Disease. Movement Disorders. 30(7). 945–952. 131 indexed citations
7.
Fachal, Laura, Ana Mosquera‐Miguel, Pau Pástor, et al.. (2014). No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(1). 54–65. 39 indexed citations
8.
Lorenzo‐Betancor, Oswaldo, Kotaro Ogaki, Alexandra I. Soto‐Ortolaza, et al.. (2014). Analysis of Nuclear Export Sequence Regions of FUS-Related RNA-Binding Proteins in Essential Tremor. PLoS ONE. 9(11). e111989–e111989. 10 indexed citations
9.
Luís, Elkin O., Sara Ortega‐Cubero, Isabel Lamet, et al.. (2014). Frontobasal gray matter loss is associated with the TREM2 p.R47H variant. Neurobiology of Aging. 35(12). 2681–2690. 40 indexed citations
10.
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
11.
Benítez, Bruno A., Breanna Cooper, Pau Pástor, et al.. (2013). TREM2 is associated with the risk of Alzheimer's disease in Spanish population. Neurobiology of Aging. 34(6). 1711.e15–1711.e17. 118 indexed citations
12.
Garcı́a-Martı́n, Elena, Carmen Martínez, Hortensia Alonso‐Navarro, et al.. (2012). H1-MAPT and the Risk for Familial Essential Tremor. PLoS ONE. 7(7). e41581–e41581. 18 indexed citations
13.
Mena, Lorena de, Lluı́s Samaranch, Eliécer Coto, et al.. (2012). Mutational Screening of PARKIN Identified a 3′ UTR Variant (rs62637702) Associated with Parkinson’s Disease. Journal of Molecular Neuroscience. 50(2). 264–269. 10 indexed citations
14.
Lorenzo‐Betancor, Oswaldo, Lluı́s Samaranch, Mario Ezquerra, et al.. (2011). LRRK2 haplotype‐sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation. Movement Disorders. 27(1). 146–150. 15 indexed citations
15.
Lorenzo‐Betancor, Oswaldo, Lluı́s Samaranch, Elena Garcı́a-Martı́n, et al.. (2011). LINGO1 gene analysis in Parkinson's disease phenotypes. Movement Disorders. 26(4). 722–727. 15 indexed citations
16.
Cervantes, Sebastián, Lluı́s Samaranch, José Vidal, et al.. (2011). Genetic variation in APOE cluster region and Alzheimer's disease risk. Neurobiology of Aging. 32(11). 2107.e7–2107.e17. 48 indexed citations
17.
Samaranch, Lluı́s, Sebastián Cervantes, Ana Barabash, et al.. (2011). The Effect of MAPT H1 and APOE ε4 on Transition from Mild Cognitive Impairment to Dementia. Journal of Alzheimer s Disease. 22(4). 1065–1071. 19 indexed citations
18.
Samaranch, Lluı́s, Oswaldo Lorenzo‐Betancor, José Matías Arbelo, et al.. (2010). PINK1-linked parkinsonism is associated with Lewy body pathology. Brain. 133(4). 1128–1142. 187 indexed citations
19.
Cruchaga, Carlos, María A. Fernández‐Seara, Manuel Seijo‐Martínez, et al.. (2008). Cortical Atrophy and Language Network Reorganization Associated with a Novel Progranulin Mutation. Cerebral Cortex. 19(8). 1751–1760. 36 indexed citations
20.
Cruchaga, Carlos, José Vidal, Mario Ezquerra, et al.. (2008). 5′-upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration. Neurobiology of Disease. 33(2). 164–170. 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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