Corinne Lendon

11.0k total citations
67 papers, 3.1k citations indexed

About

Corinne Lendon is a scholar working on Physiology, Molecular Biology and Genetics. According to data from OpenAlex, Corinne Lendon has authored 67 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Physiology, 19 papers in Molecular Biology and 19 papers in Genetics. Recurrent topics in Corinne Lendon's work include Alzheimer's disease research and treatments (39 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Dementia and Cognitive Impairment Research (8 papers). Corinne Lendon is often cited by papers focused on Alzheimer's disease research and treatments (39 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Dementia and Cognitive Impairment Research (8 papers). Corinne Lendon collaborates with scholars based in United Kingdom, United States and France. Corinne Lendon's co-authors include P. D. Richardson, G. V. R. Born, Melanie J. Davies, Alison Goate, John C. Morris, Antonia L. Pritchard, Jean‐Charles Lambert, Nick Craddock, Sang Woo Han and David M. A. Mann and has published in prestigious journals such as Cell, The Lancet and JAMA.

In The Last Decade

Corinne Lendon

66 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinne Lendon United Kingdom 31 1.6k 993 523 486 427 67 3.1k
Jonathan A. Prince Sweden 34 1.1k 0.7× 1.3k 1.3× 333 0.6× 340 0.7× 557 1.3× 77 3.1k
Arto Mannermaa Finland 29 1.1k 0.7× 898 0.9× 885 1.7× 264 0.5× 324 0.8× 74 3.1k
Zsuzsanna Nagy United Kingdom 38 1.6k 1.0× 1.3k 1.3× 748 1.4× 207 0.4× 213 0.5× 90 3.8k
Jacqueline Rimmler United States 14 1.2k 0.8× 709 0.7× 476 0.9× 139 0.3× 272 0.6× 17 2.3k
William S. Brooks Australia 31 1.4k 0.9× 727 0.7× 553 1.1× 247 0.5× 134 0.3× 61 2.7k
Mitsuru Shinohara Japan 29 2.0k 1.3× 1.0k 1.0× 337 0.6× 250 0.5× 125 0.3× 59 3.3k
P. A. Locke United States 9 1.3k 0.8× 665 0.7× 501 1.0× 160 0.3× 381 0.9× 11 1.9k
Matthias Brendel Germany 32 1.4k 0.9× 693 0.7× 781 1.5× 468 1.0× 256 0.6× 209 4.1k
Eric Yuen United States 29 523 0.3× 645 0.6× 888 1.7× 474 1.0× 169 0.4× 55 2.9k
Silvana Archetti Italy 33 1.1k 0.7× 532 0.5× 746 1.4× 182 0.4× 189 0.4× 106 3.2k

Countries citing papers authored by Corinne Lendon

Since Specialization
Citations

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

Fields of papers citing papers by Corinne Lendon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinne Lendon

This figure shows the co-authorship network connecting the top 25 collaborators of Corinne Lendon. A scholar is included among the top collaborators of Corinne Lendon 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 Corinne Lendon. Corinne Lendon 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.
Lendon, Corinne, et al.. (2018). Hyaluronic acid and TGF-β1 in dogs with hepatobiliary diseases. Acta Veterinaria Brno. 87(3). 231–240. 3 indexed citations
2.
Boyle, John P., Nishani T. Hettiarachchi, Hugh A. Pearson, et al.. (2012). Cellular consequences of the expression of Alzheimer's disease-causing presenilin 1 mutations in human neuroblastoma (SH-SY5Y) cells. Brain Research. 1443. 75–88. 8 indexed citations
3.
Goumidi, Louisa, Frédéric Flamant, Corinne Lendon, et al.. (2009). Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of Aging. 32(4). 624–630. 14 indexed citations
4.
Pritchard, Antonia L., Laura E. Ratcliffe, Sayeed Haque, et al.. (2009). Investigation of dopamine receptors in susceptibility to behavioural and psychological symptoms in Alzheimer's disease. International Journal of Geriatric Psychiatry. 24(9). 1020–1025. 18 indexed citations
5.
Laumet, Geoffroy, Franck Hansmannel, Julien Chapuis, et al.. (2009). A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience Letters. 468(1). 1–2. 12 indexed citations
6.
Campagne, Fabien, Jean‐Charles Lambert, Ute Dreses‐Werringloer, et al.. (2008). Response: CALHM1 Association with Alzheimer's Disease Risk. Cell. 135(6). 994–996. 4 indexed citations
7.
Chapuis, Julien, Didier Hannequin, Florence Pasquier, et al.. (2008). Association study of the GAB2 gene with the risk of developing Alzheimer's disease. Neurobiology of Disease. 30(1). 103–106. 27 indexed citations
8.
Hansmannel, Franck, Corinne Lendon, Florence Pasquier, et al.. (2008). Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer’s disease?. Neuroscience Letters. 449(1). 76–80. 10 indexed citations
9.
Snowden, Julie S., Cheryl Stopford, Camille Julien, et al.. (2007). Cognitive Phenotypes in Alzheimer's Disease and Genetic Risk. Cortex. 43(7). 835–845. 186 indexed citations
10.
Zhang, Yong, Yinhua Wang, Yunshan Wang, et al.. (2006). Platelet glycoprotein polymorphisms: Risk, in vivo expression and severity of atherothrombotic stroke in Chinese. Clinica Chimica Acta. 378(1-2). 99–104. 11 indexed citations
11.
Snider, B. Joy, Joanne Norton, Mary A. Coats, et al.. (2005). Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life. Archives of Neurology. 62(12). 1821–1821. 96 indexed citations
12.
Zhang, Yong, Antonia L. Pritchard, Sayeed Haque, et al.. (2004). Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease. Neuroscience Letters. 362(2). 99–102. 29 indexed citations
13.
Pritchard, Antonia L., David St Clair, Helen Lemmon, David M. A. Mann, & Corinne Lendon. (2004). No association between polymorphisms in the lectin-like oxidised low density lipoprotein receptor (ORL1) gene on chromosome 12 and Alzheimer’s disease in a UK cohort. Neuroscience Letters. 366(2). 126–129. 11 indexed citations
14.
Shi, Jiawei, Kathryn L. Bailey, Jessica Harris, et al.. (2003). A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease. Neuroscience Letters. 354(2). 103–106. 31 indexed citations
15.
Lambert, Jean‐Charles, et al.. (2001). Are the estrogen receptors involved in Alzheimer's disease?. Neuroscience Letters. 306(3). 193–197. 55 indexed citations
16.
Jones, Ian, Corinne Lendon, Natasha Coyle, et al.. (2001). Chapter 23 Molecular genetic approaches to puerperal psychosis. Progress in brain research. 133. 321–331. 23 indexed citations
17.
Lambert, Jean‐Charles, Louisa Goumidi, Fabienne Wavrant‐De Vrièze, et al.. (2000). The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease. Human Molecular Genetics. 9(15). 2275–2280. 62 indexed citations
18.
Craddock, Nick & Corinne Lendon. (1998). New susceptibility gene for Alzheimer's disease on chromosome 12?. The Lancet. 352(9142). 1720–1721. 6 indexed citations
19.
Artiga, María J., María J. Bullido, Ana Frank, et al.. (1998). Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene. Human Molecular Genetics. 7(12). 1887–1892. 123 indexed citations
20.
Bullido, María J., María J. Artiga, Marı́a Recuero, et al.. (1998). A polymorphism in the regulatory region of APOE associated with risk for Alzheimer's dementia. Nature Genetics. 18(1). 69–71. 241 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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