Partha S. Sarkar

2.9k total citations
40 papers, 2.2k citations indexed

About

Partha S. Sarkar is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Partha S. Sarkar has authored 40 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Partha S. Sarkar's work include Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (16 papers) and DNA Repair Mechanisms (14 papers). Partha S. Sarkar is often cited by papers focused on Genetic Neurodegenerative Diseases (24 papers), Mitochondrial Function and Pathology (16 papers) and DNA Repair Mechanisms (14 papers). Partha S. Sarkar collaborates with scholars based in United States, India and Germany. Partha S. Sarkar's co-authors include Tetsuo Ashizawa, Tapas K. Hazra, Sita Reddy, Rui Gao, Sanjeev Choudhary, Ronald G. Tilton, Benedikt Schoser, Anirban Chakraborty, István Boldogh and Santi M. Mandal and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Partha S. Sarkar

38 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Partha S. Sarkar United States 31 1.8k 893 258 198 172 40 2.2k
Thomas Floß Germany 25 1.8k 1.0× 209 0.2× 457 1.8× 206 1.0× 92 0.5× 44 2.4k
Pieter Faber United States 15 1.0k 0.6× 435 0.5× 190 0.7× 122 0.6× 59 0.3× 22 1.6k
Masato Hoshi Japan 21 876 0.5× 141 0.2× 184 0.7× 76 0.4× 118 0.7× 43 1.6k
Helen Griffin United Kingdom 23 1.0k 0.6× 374 0.4× 247 1.0× 174 0.9× 13 0.1× 49 1.5k
Annachiara De Sandre‐Giovannoli France 26 3.2k 1.8× 255 0.3× 183 0.7× 69 0.3× 15 0.1× 58 3.6k
Josef G. Heuer United States 20 818 0.5× 302 0.3× 137 0.5× 25 0.1× 84 0.5× 34 1.7k
Makoto Matsuyama Japan 22 1.2k 0.7× 151 0.2× 481 1.9× 36 0.2× 46 0.3× 58 1.8k
Timothy A. Fields United States 25 1.6k 0.9× 274 0.3× 434 1.7× 11 0.1× 272 1.6× 40 2.2k
Michiko Hayasaka Japan 14 1.6k 0.9× 91 0.1× 421 1.6× 38 0.2× 77 0.4× 22 2.0k
Thomas F. Wienker Germany 20 658 0.4× 171 0.2× 382 1.5× 58 0.3× 33 0.2× 59 1.3k

Countries citing papers authored by Partha S. Sarkar

Since Specialization
Citations

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

Fields of papers citing papers by Partha S. Sarkar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Partha S. Sarkar. 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 Partha S. Sarkar. The network helps show where Partha S. Sarkar may publish in the future.

Co-authorship network of co-authors of Partha S. Sarkar

This figure shows the co-authorship network connecting the top 25 collaborators of Partha S. Sarkar. A scholar is included among the top collaborators of Partha S. Sarkar 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 Partha S. Sarkar. Partha S. Sarkar 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.
Sarkar, Partha S., et al.. (2024). Dissecting sequence-structure-function-diversity in plant cryptochromes. Plant Science. 352. 112381–112381.
2.
Pradhan, Subrata, et al.. (2022). Polyglutamine Expansion in Huntingtin and Mechanism of DNA Damage Repair Defects in Huntington’s Disease. Frontiers in Cellular Neuroscience. 16. 837576–837576. 20 indexed citations
3.
Sellier, Chantal, Estefanía Cerro-Herreros, Markus Blatter, et al.. (2018). rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences. Nature Communications. 9(1). 2009–2009. 57 indexed citations
4.
Fry, Christopher S., E. Lichar Dillon, Partha S. Sarkar, et al.. (2016). Glucocorticoids increase skeletal muscle NF‐κB inducing kinase (NIK): links to muscle atrophy. Physiological Reports. 4(21). 33 indexed citations
5.
Chakraborty, Anirban, Nisha Tapryal, Nobuo Horikoshi, et al.. (2016). Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes. Nature Communications. 7(1). 13049–13049. 129 indexed citations
6.
Chatterjee, Arpita, Saikat Saha, Anirban Chakraborty, et al.. (2015). The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3’-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis. PLoS Genetics. 11(1). e1004749–e1004749. 73 indexed citations
7.
Childs‐Disney, Jessica L., Ilyas Yildirim, HaJeung Park, et al.. (2013). Structure of the Myotonic Dystrophy Type 2 RNA and Designed Small Molecules That Reduce Toxicity. ACS Chemical Biology. 9(2). 538–550. 59 indexed citations
8.
McFarland, Karen N., Jilin Liu, Rui Gao, et al.. (2013). Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability. European Journal of Human Genetics. 21(11). 1272–1276. 34 indexed citations
9.
Dey, Sanjib, Amit K. Maiti, Muralidhar L. Hegde, et al.. (2012). Increased risk of lung cancer associated with a functionally impaired polymorphic variant of the human DNA glycosylase NEIL2. DNA repair. 11(6). 570–578. 36 indexed citations
10.
Jones, Karlie, Bingwen Jin, Polina Iakova, et al.. (2011). RNA Foci, CUGBP1, and ZNF9 Are the Primary Targets of the Mutant CUG and CCUG Repeats Expanded in Myotonic Dystrophies Type 1 and Type 2. American Journal Of Pathology. 179(5). 2475–2489. 31 indexed citations
11.
Shishkin, A.A., et al.. (2011). Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast. Proceedings of the National Academy of Sciences. 108(7). 2843–2848. 42 indexed citations
12.
Mandal, Santi M., Muralidhar L. Hegde, Arpita Chatterjee, et al.. (2011). Role of Human DNA Glycosylase Nei-like 2 (NEIL2) and Single Strand Break Repair Protein Polynucleotide Kinase 3′-Phosphatase in Maintenance of Mitochondrial Genome. Journal of Biological Chemistry. 287(4). 2819–2829. 77 indexed citations
13.
White, Misti C., Guangbin Xia, Rui Gao, et al.. (2011). Transgenic mice with SCA10 pentanucleotide repeats show motor phenotype and susceptibility to seizure: A toxic RNA gain‐of‐function model. Journal of Neuroscience Research. 90(3). 706–714. 40 indexed citations
14.
White, Misti C., Rui Gao, Weidong Xu, et al.. (2010). Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10. PLoS Genetics. 6(6). e1000984–e1000984. 89 indexed citations
15.
Salisbury, Elizabeth, Benedikt Schoser, Christiane Schneider‐Gold, et al.. (2009). Expression of RNA CCUG Repeats Dysregulates Translation and Degradation of Proteins in Myotonic Dystrophy 2 Patients. American Journal Of Pathology. 175(2). 748–762. 70 indexed citations
16.
Sarkar, Partha S.. (2004). Six5 is required for spermatogenic cell survival and spermiogenesis. Human Molecular Genetics. 13(14). 1421–1431. 41 indexed citations
17.
Ito, Yoshihiro, Partha S. Sarkar, Nancy Wu, et al.. (2001). Overexpression of Smad2 Reveals Its Concerted Action with Smad4 in Regulating TGF- β-Mediated Epidermal Homeostasis. Developmental Biology. 236(1). 181–194. 56 indexed citations
18.
Sarkar, Partha S., et al.. (1998). CTG Repeats Show Bimodal Amplification in E. coli. Cell. 95(4). 531–540. 59 indexed citations
19.
Brahmachari, Samir K., et al.. (1995). Simple repetitive sequences in the genome: Structure and functional significance. Electrophoresis. 16(1). 1705–1714. 78 indexed citations
20.
Brahmachari, Samir K., et al.. (1991). Synthetic gene design to investigate the role of cis-acting DNA structural elements in regulation of gene expression in vivo.. PubMed. 163–6. 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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