Manuela Tan

6.1k total citations
17 papers, 337 citations indexed

About

Manuela Tan is a scholar working on Neurology, Genetics and Physiology. According to data from OpenAlex, Manuela Tan has authored 17 papers receiving a total of 337 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Neurology, 6 papers in Genetics and 5 papers in Physiology. Recurrent topics in Manuela Tan's work include Parkinson's Disease Mechanisms and Treatments (15 papers), Lysosomal Storage Disorders Research (5 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Manuela Tan is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (15 papers), Lysosomal Storage Disorders Research (5 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Manuela Tan collaborates with scholars based in United Kingdom, United States and Norway. Manuela Tan's co-authors include Huw R. Morris, Donald G. Grosset, John Hardy, Rimona S. Weil, Michael Lawton, Yoav Ben‐Shlomo, Nigel Williams, Thomas Foltynie, Nigel Williams and Katherine A. Grosset and has published in prestigious journals such as Brain, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Manuela Tan

16 papers receiving 329 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Manuela Tan United Kingdom	10	221	134	72	57	57	17	337
Diana A. Olszewska Ireland	8	148 0.7×	76 0.6×	40 0.6×	71 1.2×	60 1.1×	32	240
Edoardo Monfrini Italy	13	196 0.9×	90 0.7×	50 0.7×	141 2.5×	88 1.5×	46	393
Milena Janković Serbia	12	152 0.7×	79 0.6×	40 0.6×	106 1.9×	91 1.6×	37	337
Kimiko Inoue Japan	9	150 0.7×	79 0.6×	40 0.6×	110 1.9×	49 0.9×	22	309
Linda Rousseau United States	7	173 0.8×	155 1.2×	82 1.1×	105 1.8×	63 1.1×	7	325
Anneke J.A. Kievit Netherlands	10	108 0.5×	103 0.8×	54 0.8×	139 2.4×	51 0.9×	17	352
Niko-Petteri Nykänen United States	8	170 0.8×	215 1.6×	102 1.4×	185 3.2×	91 1.6×	14	436
Tarja Kauppinen Finland	10	289 1.3×	177 1.3×	88 1.2×	106 1.9×	104 1.8×	12	445
Carlos Lahoz Spain	8	201 0.9×	127 0.9×	94 1.3×	111 1.9×	73 1.3×	14	353
Hsiu-Chuan Wu Taiwan	10	167 0.8×	116 0.9×	46 0.6×	245 4.3×	67 1.2×	20	464

Countries citing papers authored by Manuela Tan

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Tan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Tan

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Tan. A scholar is included among the top collaborators of Manuela Tan 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 Manuela Tan. Manuela Tan 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:

17 of 17 papers shown

Udayar, Vinod, Julien Bryois, Xi Chen, et al.. (2025). Enzyme Activity-Based Genome-wide Screening for Modifiers of Lysosomal Glucocerebrosidase Uncovers Candidate Risk Factors for Parkinson’s Disease. ACS Central Science. 11(10). 1933–1945.

Faouzi, Johann, Manuela Tan, Suzanne Lesage, et al.. (2024). Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores. npj Parkinson s Disease. 10(1). 8–8. 5 indexed citations

Tunold, Jon‐Anders, Manuela Tan, Mathias Toft, et al.. (2023). Lysosomal Polygenic Burden Drives Cognitive Decline in Parkinson's Disease with Low Alzheimer Risk. Movement Disorders. 39(3). 596–601. 8 indexed citations

Martínez-Carrasco, Alejandro, Raquel Real, Michael Lawton, et al.. (2023). Genome-wide Analysis of Motor Progression in Parkinson Disease. Neurology Genetics. 9(5). e200092–e200092. 5 indexed citations

Martínez-Carrasco, Alejandro, Raquel Real, Michael Lawton, et al.. (2023). Genetic meta-analysis of levodopa induced dyskinesia in Parkinson’s disease. npj Parkinson s Disease. 9(1). 128–128. 6 indexed citations

Tunold, Jon‐Anders, Manuela Tan, Shunsuke Koga, et al.. (2023). Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease. Brain. 146(10). 4077–4087. 15 indexed citations

Real, Raquel, Alejandro Martínez-Carrasco, Regina H. Reynolds, et al.. (2022). Association between the LRP1B and APOE loci and the development of Parkinson’s disease dementia. Brain. 146(5). 1873–1887. 31 indexed citations

Lawton, Michael, Manuela Tan, Yoav Ben‐Shlomo, et al.. (2022). Genetics of validated Parkinson’s disease subtypes in the Oxford Discovery and Tracking Parkinson’s cohorts. Journal of Neurology Neurosurgery & Psychiatry. 93(9). 952–959. 10 indexed citations

Tan, Manuela, et al.. (2022). Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease. Annals of Clinical and Translational Neurology. 9(8). 1289–1295. 9 indexed citations

10.

Brolin, Kajsa, Sara Bandrés‐Ciga, Hampton L. Leonard, et al.. (2021). RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts. Neurobiology of Aging. 109. 264–268. 2 indexed citations

11.

Oxtoby, Neil P., Louise‐Ann Leyland, Leon Aksman, et al.. (2021). Sequence of clinical and neurodegeneration events in Parkinson’s disease progression. Brain. 144(3). 975–988. 60 indexed citations

12.

Pihlstrøm, Lasse, Chun Chieh Fan, Oleksandr Frei, et al.. (2021). Genetic Stratification of Age‐Dependent Parkinson's Disease Risk by Polygenic Hazard Score. Movement Disorders. 37(1). 62–69. 14 indexed citations

13.

Lubbe, Steven, Bernabé I. Bustos, Jing Hu, et al.. (2021). Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk. Human Molecular Genetics. 30(1). 78–86. 37 indexed citations

14.

Jabbari, Edwin, John Woodside, Manuela Tan, et al.. (2019). The genetic and clinico‐pathological profile of early‐onset progressive supranuclear palsy. Movement Disorders. 34(9). 1307–1314. 16 indexed citations

15.

Malek, Naveed, Rimona S. Weil, Michael Lawton, et al.. (2018). Features of GBA-associated Parkinson’s disease at presentation in the UK Tracking Parkinson’s study. Journal of Neurology Neurosurgery & Psychiatry. 89(7). 702–709. 90 indexed citations

16.

Norman, Brendan P., et al.. (2017). Early Onset Parkinson’s Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report. BMC Neurology. 17(1). 153–153. 5 indexed citations

17.

Johnston, Ian N., et al.. (2017). Ibudilast reduces oxaliplatin-induced tactile allodynia and cognitive impairments in rats. Behavioural Brain Research. 334. 109–118. 24 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