Bindhu Paul‐Prasanth

2.8k total citations
31 papers, 2.2k citations indexed

About

Bindhu Paul‐Prasanth is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Bindhu Paul‐Prasanth has authored 31 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Physiology and 8 papers in Molecular Biology. Recurrent topics in Bindhu Paul‐Prasanth's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers), Reproductive biology and impacts on aquatic species (13 papers) and Sperm and Testicular Function (6 papers). Bindhu Paul‐Prasanth is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers), Reproductive biology and impacts on aquatic species (13 papers) and Sperm and Testicular Function (6 papers). Bindhu Paul‐Prasanth collaborates with scholars based in India, Japan and China. Bindhu Paul‐Prasanth's co-authors include Yoshitaka Nagahama, Tohru Kobayashi, Fumie Sakai, Shigeho Ijiri, Aya Suzuki, Deshou Wang, Yasushi Shibata, Kataaki Okubo, Ken-ichirou Morohashi and Masaru Matsuda and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Physiological Reviews and SHILAP Revista de lepidopterología.

In The Last Decade

Bindhu Paul‐Prasanth

30 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Bindhu Paul‐Prasanth India	19	1.6k	1.1k	547	460	257	31	2.2k
Yunhan Hong Singapore	33	2.2k 1.4×	859 0.8×	1.8k 3.3×	395 0.9×	190 0.7×	106	3.6k
Dongneng Jiang China	28	1.3k 0.8×	796 0.7×	1.2k 2.2×	288 0.6×	382 1.5×	107	2.8k
Huiping Yang United States	22	389 0.2×	769 0.7×	181 0.3×	451 1.0×	387 1.5×	101	1.6k
Mingyou Li China	22	995 0.6×	564 0.5×	523 1.0×	232 0.5×	114 0.4×	93	1.5k
Alfonsa García‐Ayala Spain	26	463 0.3×	747 0.7×	231 0.4×	146 0.3×	601 2.3×	75	2.0k
Lina Sun China	24	1.4k 0.9×	845 0.8×	746 1.4×	337 0.7×	256 1.0×	72	2.1k
Elena Chaves-Pozo Spain	32	434 0.3×	698 0.6×	338 0.6×	134 0.3×	824 3.2×	98	2.7k
Wenxian Zeng China	37	897 0.6×	256 0.2×	1.4k 2.5×	2.1k 4.6×	40 0.2×	148	3.7k
Kaikun Luo China	22	727 0.5×	358 0.3×	300 0.5×	61 0.1×	397 1.5×	88	1.4k
Núria Saperas Spain	16	258 0.2×	138 0.1×	414 0.8×	141 0.3×	41 0.2×	34	724

Countries citing papers authored by Bindhu Paul‐Prasanth

Since Specialization

Citations

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

Fields of papers citing papers by Bindhu Paul‐Prasanth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bindhu Paul‐Prasanth. 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 Bindhu Paul‐Prasanth. The network helps show where Bindhu Paul‐Prasanth may publish in the future.

Co-authorship network of co-authors of Bindhu Paul‐Prasanth

This figure shows the co-authorship network connecting the top 25 collaborators of Bindhu Paul‐Prasanth. A scholar is included among the top collaborators of Bindhu Paul‐Prasanth 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 Bindhu Paul‐Prasanth. Bindhu Paul‐Prasanth 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

Harris, M., et al.. (2025). Biomarkers in orofacial pain conditions: A narrative review. Journal of Oral Biology and Craniofacial Research. 15(2). 365–382.

Nair, Shantikumar V., et al.. (2024). Nano-graphene oxide particles induce inheritable anomalies through altered gene expressions involved in oocyte maturation. Nanotoxicology. 18(2). 160–180. 2 indexed citations

Amirthalingam, Sivashanmugam, et al.. (2021). Effects of Whitlockite Nanoparticles on Germ Cell Development and Spermatogenesis in Japanese Medaka. SHILAP Revista de lepidopterología. 4(4). 4 indexed citations

Paul‐Prasanth, Bindhu, et al.. (2021). Differentiation Potential of Cultured Extracellular DEAD-Box Helicase 4<sup>+</sup> Oogonial Stem Cells from Adult Human Ovaries into Somatic Lineages. Cells Tissues Organs. 211(5). 577–588. 3 indexed citations

Nagahama, Yoshitaka, Tapas Chakraborty, Bindhu Paul‐Prasanth, Kohei Ohta, & Masaru Nakamura. (2020). Sex determination, gonadal sex differentiation, and plasticity in vertebrate species. Physiological Reviews. 101(3). 1237–1308. 187 indexed citations

Padmakumar, Smrithi, Bindhu Paul‐Prasanth, K Pavithran, et al.. (2018). Long-term drug delivery using implantable electrospun woven polymeric nanotextiles. Nanomedicine Nanotechnology Biology and Medicine. 15(1). 274–284. 38 indexed citations

Chatterjee, Maitrayee, Vinod Paul, Anil Vasudevan, et al.. (2017). Mechanistic understanding of Phenyllactic acid mediated inhibition of quorum sensing and biofilm development in Pseudomonas aeruginosa. Applied Microbiology and Biotechnology. 101(22). 8223–8236. 85 indexed citations

Paul, Vinod, et al.. (2017). Effects of N-Nitrosodiethylamine, a Potent Carcinogen, on Sexual Development, Gametogenesis, and Oocyte Maturation. Sexual Development. 11(3). 161–167. 5 indexed citations

Paul‐Prasanth, Bindhu, et al.. (2016). Influence of surface passivation of 2-Methoxyestradiol loaded PLGA nanoparticles on cellular interactions, pharmacokinetics and tumour accumulation. Colloids and Surfaces B Biointerfaces. 150. 242–249. 18 indexed citations

10.

Narayanan, Sreeja, Ullas Mony, D. K. Vijaykumar, et al.. (2015). Sequential release of epigallocatechin gallate and paclitaxel from PLGA-casein core/shell nanoparticles sensitizes drug-resistant breast cancer cells. Nanomedicine Nanotechnology Biology and Medicine. 11(6). 1399–1406. 87 indexed citations

11.

Takeuchi, Akio, Junpei Yamashita, Takeshi Usami, et al.. (2014). Sexually dimorphic expression of the sex chromosome-linked genes cntfa and pdlim3a in the medaka brain. Biochemical and Biophysical Research Communications. 445(1). 113–119. 8 indexed citations

12.

Shalumon, K.T., Liming Milbauer, R. Jayakumar, et al.. (2013). Poly (lactic acid)–chitosan–collagen composite nanofibers as substrates for blood outgrowth endothelial cells. International Journal of Biological Macromolecules. 58. 220–224. 23 indexed citations

13.

Paul‐Prasanth, Bindhu, Ramji Kumar Bhandari, Tohru Kobayashi, et al.. (2013). Estrogen oversees the maintenance of the female genetic program in terminally differentiated gonochorists. Scientific Reports. 3(1). 2862–2862. 86 indexed citations

14.

Fernandino, Juan I., Jason T. Popesku, Bindhu Paul‐Prasanth, et al.. (2011). Analysis of Sexually Dimorphic Expression of Genes at Early Gonadogenesis of Pejerrey <i>Odontesthes bonariensis</i> Using a Heterologous Microarray. Sexual Development. 5(2). 89–101. 25 indexed citations

15.

Okubo, Kataaki, Akio Takeuchi, Radha Chaube, et al.. (2011). Sex Differences in Aromatase Gene Expression in the Medaka Brain. Journal of Neuroendocrinology. 23(5). 412–423. 53 indexed citations

16.

Matsuda, Masaru, Ai Shinomiya, Masato Kinoshita, et al.. (2007). DMY gene induces male development in genetically female (XX) medaka fish. Proceedings of the National Academy of Sciences. 104(10). 3865–3870. 152 indexed citations

17.

Ijiri, Shigeho, Tohru Kobayashi, Deshou Wang, et al.. (2007). Sexual Dimorphic Expression of Genes in Gonads During Early Differentiation of a Teleost Fish, the Nile Tilapia Oreochromis niloticus1. Biology of Reproduction. 78(2). 333–341. 338 indexed citations

18.

Zhou, Linyan, Deshou Wang, Yasushi Shibata, et al.. (2007). Characterization, expression and transcriptional regulation of P450c17-I and -II in the medaka, Oryzias latipes. Biochemical and Biophysical Research Communications. 362(3). 619–625. 92 indexed citations

19.

Zhou, Linyan, Deshou Wang, Tohru Kobayashi, et al.. (2007). A Novel Type of P450c17 Lacking the Lyase Activity Is Responsible for C21-Steroid Biosynthesis in the Fish Ovary and Head Kidney. Endocrinology. 148(9). 4282–4291. 126 indexed citations

20.

Paul‐Prasanth, Bindhu, Masaru Matsuda, En‐Lieng Lau, et al.. (2006). Knock-down of DMY initiates female pathway in the genetic male medaka, Oryzias latipes. Biochemical and Biophysical Research Communications. 351(4). 815–819. 41 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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