K. Puvan

514 total citations
8 papers, 397 citations indexed

About

K. Puvan is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, K. Puvan has authored 8 papers receiving a total of 397 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Neurology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Molecular Biology. Recurrent topics in K. Puvan's work include Parkinson's Disease Mechanisms and Treatments (6 papers), Nuclear Receptors and Signaling (4 papers) and RNA regulation and disease (3 papers). K. Puvan is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (6 papers), Nuclear Receptors and Signaling (4 papers) and RNA regulation and disease (3 papers). K. Puvan collaborates with scholars based in Singapore, Australia and Hong Kong. K. Puvan's co-authors include Pavanni Ratnagopal, Hui Shen, Martin C. S. Wong, Kenneth Yew, Yi Zhao, Eng‐King Tan, Roland Dominic G. Jamora, Louis C.S. Tan, Yuen Yih and Matthew J. Farrer and has published in prestigious journals such as Neurology, Movement Disorders and Neuroscience Letters.

In The Last Decade

K. Puvan

8 papers receiving 384 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
K. Puvan Singapore	7	347	168	140	107	81	8	397
Joseph Wiley Canada	6	403 1.2×	142 0.8×	157 1.1×	127 1.2×	103 1.3×	7	460
Philippe Pals Belgium	11	376 1.1×	191 1.1×	188 1.3×	206 1.9×	140 1.7×	15	573
G. Volpe Italy	7	302 0.9×	183 1.1×	107 0.8×	87 0.8×	59 0.7×	9	373
Petra Leitner Germany	6	359 1.0×	145 0.9×	115 0.8×	161 1.5×	106 1.3×	7	459
Shyla T. Govindappa India	10	223 0.6×	79 0.5×	55 0.4×	70 0.7×	54 0.7×	14	286
Z.K. Wszolek United States	6	416 1.2×	207 1.2×	160 1.1×	62 0.6×	116 1.4×	7	455
Samia Ben Yahmed United Kingdom	5	211 0.6×	80 0.5×	69 0.5×	59 0.6×	74 0.9×	5	240
Christoph B. Lücking Germany	9	385 1.1×	286 1.7×	127 0.9×	155 1.4×	55 0.7×	11	502
Karin Wiegers Germany	9	330 1.0×	251 1.5×	66 0.5×	120 1.1×	31 0.4×	11	428
Magali Periquet France	7	591 1.7×	411 2.4×	165 1.2×	183 1.7×	97 1.2×	7	696

Countries citing papers authored by K. Puvan

Since Specialization

Citations

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

Fields of papers citing papers by K. Puvan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K. Puvan

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

All Works

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8 of 8 papers shown

1.

Tan, Eng‐King, Kenneth Yew, K. Puvan, et al.. (2006). PINK1 mutations in sporadic early‐onset Parkinson's disease. Movement Disorders. 21(6). 789–793. 74 indexed citations

2.

Tan, Eng‐King, Hui Shen, Louis C.S. Tan, et al.. (2005). The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neuroscience Letters. 384(3). 327–329. 120 indexed citations

3.

Tan, Eng‐King, Hui Shen, Jeanne M.M. Tan, et al.. (2005). Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease. Neurogenetics. 6(4). 179–184. 31 indexed citations

4.

Tan, Eng‐King, Daniel Kam Yin Chan, Kenneth Yew, et al.. (2005). Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association. Human Genetics. 118(3-4). 484–488. 23 indexed citations

5.

Skipper, Lisa, Hui Shen, E. Chua, et al.. (2005). Analysis of LRRK2 functional domains in nondominant Parkinson disease. Neurology. 65(8). 1319–1321. 57 indexed citations

6.

Tan, Eng‐King, Yik‐Ying Teo, Yanping Zhao, et al.. (2004). Alpha-synuclein haplotypes implicated in risk of Parkinson’s disease. Neurology. 62(1). 128–131. 72 indexed citations

7.

Tan, Eng‐King, Henry Chung, V. R. Chandran, et al.. (2004). Nurr1 mutational screen in Parkinson's disease. Movement Disorders. 19(12). 1503–1505. 17 indexed citations

8.

Puvan, K., et al.. (1989). A case of sarcoidosis presenting as cranial polyneuritis.. PubMed. 30(4). 400–3. 3 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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