Lee Darwent

1.2k total citations
13 papers, 279 citations indexed

About

Lee Darwent is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Lee Darwent has authored 13 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Neurology and 4 papers in Physiology. Recurrent topics in Lee Darwent's work include Prion Diseases and Protein Misfolding (6 papers), Neurological diseases and metabolism (5 papers) and Trace Elements in Health (3 papers). Lee Darwent is often cited by papers focused on Prion Diseases and Protein Misfolding (6 papers), Neurological diseases and metabolism (5 papers) and Trace Elements in Health (3 papers). Lee Darwent collaborates with scholars based in United Kingdom, United States and Portugal. Lee Darwent's co-authors include Rita Guerreiro, José Brás, John Hardy, Paula Coutinho, Isabel Alonso, Clara Barbot, Jorge Sequeiros, Maria Manuela Costa, Tatiana Orme and Suzanne Lesage and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Lee Darwent

11 papers receiving 278 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lee Darwent United Kingdom	7	170	83	70	66	61	13	279
Julian Curiel United States	7	202 1.2×	34 0.4×	46 0.7×	96 1.5×	38 0.6×	9	305
Estelle Arnaud Switzerland	7	227 1.3×	58 0.7×	194 2.8×	73 1.1×	34 0.6×	7	381
Keith Crosby United States	8	160 0.9×	104 1.3×	75 1.1×	28 0.4×	63 1.0×	10	292
Dorothée Bleckmann Switzerland	8	228 1.3×	81 1.0×	172 2.5×	38 0.6×	38 0.6×	9	334
Lauren M. Gittings United States	9	299 1.8×	184 2.2×	54 0.8×	51 0.8×	51 0.8×	11	404
Tamal Sadhukhan United States	9	165 1.0×	69 0.8×	38 0.5×	72 1.1×	107 1.8×	20	315
Pontus Klein Germany	8	154 0.9×	83 1.0×	139 2.0×	35 0.5×	41 0.7×	15	337
Philippe Couarch France	7	77 0.5×	66 0.8×	32 0.5×	49 0.7×	57 0.9×	7	253
Eric Dec United States	5	134 0.8×	159 1.9×	50 0.7×	97 1.5×	37 0.6×	5	300
Kyriaki Markoullis Cyprus	9	219 1.3×	54 0.7×	119 1.7×	23 0.3×	53 0.9×	11	375

Countries citing papers authored by Lee Darwent

Since Specialization

Citations

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

Fields of papers citing papers by Lee Darwent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lee Darwent

This figure shows the co-authorship network connecting the top 25 collaborators of Lee Darwent. A scholar is included among the top collaborators of Lee Darwent 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 Lee Darwent. Lee Darwent is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Jaunmuktane, Zane, Laszlo L. P. Hosszu, Nour K. Majbour, et al.. (2025). PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features. Journal of Neurology. 272(4). 299–299.

Mok, Tze How, Peter Rudge, Hawraman Ramadan, et al.. (2025). Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157. Journal of Alzheimer s Disease. 106(3). 1087–1096.

Campbell, Tracy, et al.. (2022). Estimation of the number of inherited prion disease mutation carriers in the UK. European Journal of Human Genetics. 30(10). 1167–1170. 3 indexed citations

Kroll, François, Athanasios Dimitriadis, Tracy Campbell, et al.. (2022). Prion protein gene mutation detection using long-read Nanopore sequencing. Scientific Reports. 12(1). 8284–8284. 6 indexed citations

Viré, Emmanuelle, Lee Darwent, Holger Hummerich, et al.. (2022). DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease. Acta Neuropathologica. 144(4). 785–787. 2 indexed citations

Hassan, Ahamad, Tracy Campbell, Lee Darwent, et al.. (2021). Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease. BMC Neurology. 21(1). 248–248. 6 indexed citations

Darwent, Lee, Susana Carmona, Ebba Lohmann, et al.. (2017). Mutations in TYROBP are not a common cause of dementia in a Turkish cohort. Neurobiology of Aging. 58. 240.e1–240.e3. 9 indexed citations

Brás, José, Ruth Djaldetti, Simon Mead, et al.. (2016). Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation. Neurobiology of Aging. 46. 236.e1–236.e6. 18 indexed citations

Faller, Kiterie M. E., José Brás, Glenn Anderson, et al.. (2016). The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease?. Journal of Neuroscience Research. 94(4). 339–347. 29 indexed citations

10.

Brás, José, Isabel Alonso, Clara Barbot, et al.. (2015). Mutations in PNKP Cause Recessive Ataxia with Oculomotor Apraxia Type 4. The American Journal of Human Genetics. 96(3). 474–479. 93 indexed citations

11.

Lesage, Suzanne, José Brás, Florence Cormier‐Dequaire, et al.. (2015). Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology Genetics. 1(1). e9–e9. 70 indexed citations

12.

Kun‐Rodrigues, Célia, Christos Ganos, Rita Guerreiro, et al.. (2015). A systematic screening to identifyde novomutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics. 24(23). 6711–6720. 35 indexed citations

13.

Brás, José, Rita Guerreiro, James Teo, et al.. (2014). Atypical Parkinsonism‐Dystonia Syndrome Caused by a Novel DJ1 Mutation. Movement Disorders Clinical Practice. 1(1). 45–49. 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.

Explore authors with similar magnitude of impact