Manu Sharma

21.5k total citations · 1 hit paper
41 papers, 1.6k citations indexed

About

Manu Sharma is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Manu Sharma has authored 41 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Neurology, 18 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Manu Sharma's work include Parkinson's Disease Mechanisms and Treatments (22 papers), Neurological diseases and metabolism (8 papers) and RNA regulation and disease (7 papers). Manu Sharma is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (22 papers), Neurological diseases and metabolism (8 papers) and RNA regulation and disease (7 papers). Manu Sharma collaborates with scholars based in Germany, India and United States. Manu Sharma's co-authors include Thomas Gasser, Claudia Schulte, John Hardy, Michael A. Nalls, Javier Simón‐Sánchez, Peter Heutink, Vincent Plagnol, Sigurlaug Sveinbjörnsdóttir, Andrew B. Singleton and Hreinn Stefánsson and has published in prestigious journals such as The Lancet, PLoS ONE and Neurology.

In The Last Decade

Manu Sharma

37 papers receiving 1.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

2011 660 citations Michael A. Nalls, Vincent Plagnol et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Manu Sharma Germany	17	1.0k	680	552	380	311	41	1.6k
Una‐Marie Sheerin United Kingdom	13	1.3k 1.2×	495 0.7×	567 1.0×	370 1.0×	296 1.0×	19	1.7k
Ikuko Mizuta Japan	26	891 0.9×	736 1.1×	762 1.4×	478 1.3×	334 1.1×	98	2.0k
Hiroyuki Tomiyama Japan	23	1.3k 1.3×	513 0.8×	614 1.1×	549 1.4×	430 1.4×	43	2.0k
Ingrid Goebel Germany	13	675 0.7×	619 0.9×	310 0.6×	307 0.8×	315 1.0×	18	1.4k
Rim Amouri Tunisia	24	541 0.5×	702 1.0×	667 1.2×	345 0.9×	236 0.8×	58	1.5k
Philip Seibler Germany	22	948 0.9×	1.1k 1.6×	629 1.1×	243 0.6×	365 1.2×	47	2.0k
Hiroyo Yoshino Japan	26	1.7k 1.7×	741 1.1×	985 1.8×	706 1.9×	478 1.5×	62	2.3k
Jason P. Covy United States	12	597 0.6×	1.0k 1.5×	608 1.1×	268 0.7×	378 1.2×	14	1.8k
Amber D. Van Laar United States	16	716 0.7×	445 0.7×	475 0.9×	158 0.4×	196 0.6×	21	1.2k
Rubén Fernández‐Santiago Spain	23	849 0.8×	643 0.9×	372 0.7×	202 0.5×	243 0.8×	46	1.5k

Countries citing papers authored by Manu Sharma

Since Specialization

Citations

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

Fields of papers citing papers by Manu Sharma

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manu Sharma

This figure shows the co-authorship network connecting the top 25 collaborators of Manu Sharma. A scholar is included among the top collaborators of Manu Sharma 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 Manu Sharma. Manu Sharma 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

Sharma, Manu, et al.. (2025). Imidazopyridine Based Fluorescent Turn-Off Sensor for Selective Recognition of Fe3+ Ions and its Application in Test Strips. Journal of Fluorescence. 35(11). 10961–10976. 1 indexed citations

Sharma, Manu, Kamal Kishor Thakur, Sunil Kumar, et al.. (2024). Rosuvastatin calcium electrochemical sensor based on a sulfur doped graphitic carbon nitride modified glassy carbon electrode: A metal free analysis approach. Microchemical Journal. 207. 112177–112177.

Kishore, Asha, Marc Sturm, Syam Krishnan, et al.. (2024). Resequencing the complete SNCA locus in Indian patients with Parkinson’s disease. npj Parkinson s Disease. 10(1). 85–85. 3 indexed citations

Cheng, Fubo, Chang Liu, Peter A. Barbuti, et al.. (2022). Intronic enhancers of the human SNCA gene predominantly regulate its expression in brain in vivo. Science Advances. 8(47). eabq6324–eabq6324. 6 indexed citations

Grover, Sandeep & Manu Sharma. (2022). Sleep, Pain, and Neurodegeneration: A Mendelian Randomization Study. Frontiers in Neurology. 13. 765321–765321. 14 indexed citations

Blauwendraat, Cornelis, Mary B. Makarious, Hampton L. Leonard, et al.. (2022). Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors. Annals of Neurology. 92(2). 270–278. 13 indexed citations

Yu, Eric, Aditya Ambati, Lynne Krohn, et al.. (2021). Fine mapping of the HLA locus in Parkinson’s disease in Europeans. npj Parkinson s Disease. 7(1). 84–84. 34 indexed citations

Grover, Sandeep, Dheeraj Reddy Bobbili, Patrick May, et al.. (2021). Replication of a Novel Parkinson's Locus in a European Ancestry Population. Movement Disorders. 36(7). 1689–1695. 7 indexed citations

Großmann, Dajana, David Scheibner, François Massart, et al.. (2019). Mutations in RHOT1 Disrupt Endoplasmic Reticulum–Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's Disease. Antioxidants and Redox Signaling. 31(16). 1213–1234. 66 indexed citations

10.

Paliwal, Sarvesh, et al.. (2018). Pharmacophore Modeling and Database Mining to Identify Novel Lead Compounds Active Against the Disease Stage of Trypanosomiasis in the Central Nervous System. International journal of Nutrition Pharmacology Neurological Diseases. 8(1). 16. 2 indexed citations

11.

Kishore, Asha, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.. (2018). Understanding the role of genetic variability in LRRK2 in Indian population. Movement Disorders. 34(4). 496–505. 8 indexed citations

12.

Jansen, Iris E., J. Raphael Gibbs, T. Ryan Price, et al.. (2017). Establishing the role of rare coding variants in known Parkinson's disease risk loci. Neurobiology of Aging. 59. 220.e11–220.e18. 11 indexed citations

13.

Martens, Gerard J.M., Manu Sharma, Marijn Bart Martens, et al.. (2017). Integrated molecular landscape of Parkinson’s disease. npj Parkinson s Disease. 3(1). 14–14. 100 indexed citations

14.

Maurer, Brigitte, et al.. (2015). Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's disease. Neurobiology of Aging. 39. 217.e13–217.e15. 20 indexed citations

15.

Nalls, Michael A., Vincent Plagnol, Manu Sharma, et al.. (2011). Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet. 377(9766). 641–649. 660 indexed citations breakdown →

16.

Rothfuss, Oliver C., Heike Fischer, Takafumi Hasegawa, et al.. (2009). Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair. Human Molecular Genetics. 18(20). 3832–3850. 143 indexed citations

17.

Kamm, Christoph, Petra Mayer, Manu Sharma, G. Niemann, & Thomas Gasser. (2007). New family with paroxysmal exercise‐induced dystonia and epilepsy. Movement Disorders. 22(6). 873–877. 15 indexed citations

18.

Fuchs, Julia, Jakob C. Mueller, Peter Lichtner, et al.. (2007). The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiology of Aging. 30(5). 731–738. 91 indexed citations

19.

Sharma, Manu, et al.. (2006). The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson’s disease in European populations. Journal of Medical Genetics. 43(7). 557–562. 29 indexed citations

20.

Berg, Daniela, Friedrich Asmus, Gerhard Ransmayr, et al.. (2004). The role of α-synuclein gene multiplications in early-onset Parkinson’s disease and dementia with Lewy bodies. Journal of Neural Transmission. 112(9). 1249–1254. 22 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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