Mayur Madhavan

2.0k total citations
18 papers, 888 citations indexed

About

Mayur Madhavan is a scholar working on Molecular Biology, Radiology, Nuclear Medicine and Imaging and Developmental Neuroscience. According to data from OpenAlex, Mayur Madhavan has authored 18 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Radiology, Nuclear Medicine and Imaging and 7 papers in Developmental Neuroscience. Recurrent topics in Mayur Madhavan's work include Corneal Surgery and Treatments (7 papers), Neurogenesis and neuroplasticity mechanisms (6 papers) and Connexins and lens biology (4 papers). Mayur Madhavan is often cited by papers focused on Corneal Surgery and Treatments (7 papers), Neurogenesis and neuroplasticity mechanisms (6 papers) and Connexins and lens biology (4 papers). Mayur Madhavan collaborates with scholars based in United States, Italy and India. Mayur Madhavan's co-authors include Katia Del Rio‐Tsonis, Panagiotis A. Tsonis, Jason R. Spence, Mindy K. Call, Benjamin L.L. Clayton, Paul J. Tesar, Kevin Allan, H. Elizabeth Shick, Daniel C. Factor and Zachary S. Nevin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Journal of Neuroscience.

In The Last Decade

Mayur Madhavan

18 papers receiving 879 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mayur Madhavan United States	13	632	237	157	104	91	18	888
Travis J. Bailey United States	10	923 1.5×	183 0.8×	163 1.0×	55 0.5×	194 2.1×	12	1.3k
Xitiz Chamling United States	15	761 1.2×	86 0.4×	285 1.8×	110 1.1×	96 1.1×	23	973
Huaiyu Hu United States	17	816 1.3×	345 1.5×	490 3.1×	42 0.4×	110 1.2×	28	1.3k
Gervasio Martín‐Partido Spain	25	818 1.3×	137 0.6×	225 1.4×	102 1.0×	56 0.6×	57	1.2k
Kevin M. Wright United States	18	929 1.5×	119 0.5×	294 1.9×	42 0.4×	87 1.0×	43	1.3k
Rajesh Ramachandran India	12	1.0k 1.6×	312 1.3×	230 1.5×	89 0.9×	71 0.8×	22	1.2k
Kevin J. Kim United States	12	850 1.3×	173 0.7×	226 1.4×	72 0.7×	160 1.8×	16	1.2k
Denise Stenzel Germany	10	815 1.3×	569 2.4×	285 1.8×	48 0.5×	133 1.5×	13	1.3k
Panagiotis Douvaras United States	16	908 1.4×	505 2.1×	221 1.4×	143 1.4×	112 1.2×	21	1.5k
Joachim Berger Australia	22	1.2k 1.9×	110 0.5×	115 0.7×	47 0.5×	288 3.2×	44	1.7k

Countries citing papers authored by Mayur Madhavan

Since Specialization

Citations

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

Fields of papers citing papers by Mayur Madhavan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mayur Madhavan

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

All Works

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18 of 18 papers shown

Clayton, Benjamin L.L., Mayur Madhavan, Yuriy Fedorov, et al.. (2024). Pervasive environmental chemicals impair oligodendrocyte development. Nature Neuroscience. 27(5). 836–845. 24 indexed citations

Allan, Kevin, Marissa A. Scavuzzo, Andrew R. Morton, et al.. (2020). Non-canonical Targets of HIF1a Impair Oligodendrocyte Progenitor Cell Function. Cell stem cell. 28(2). 257–272.e11. 33 indexed citations

Madhavan, Mayur, et al.. (2020). Temporally Distinct Roles for the Zinc Finger Transcription Factor Sp8 in the Generation and Migration of Dorsal Lateral Ganglionic Eminence (dLGE)-Derived Neuronal Subtypes in the Mouse. Cerebral Cortex. 31(3). 1744–1762. 8 indexed citations

Madhavan, Mayur, Zachary S. Nevin, H. Elizabeth Shick, et al.. (2018). Induction of myelinating oligodendrocytes in human cortical spheroids. Nature Methods. 15(9). 700–706. 240 indexed citations

Lager, Angela M., Olivia Corradin, Jared M. Cregg, et al.. (2018). Rapid functional genetics of the oligodendrocyte lineage using pluripotent stem cells. Nature Communications. 9(1). 3708–3708. 17 indexed citations

Elitt, Matthew S., H. Elizabeth Shick, Mayur Madhavan, et al.. (2018). Chemical Screening Identifies Enhancers of Mutant Oligodendrocyte Survival and Unmasks a Distinct Pathological Phase in Pelizaeus-Merzbacher Disease. Stem Cell Reports. 11(3). 711–726. 27 indexed citations

Madhavan, Mayur, et al.. (2016). Characterization of a new Gsx2‐cre line in the developing mouse telencephalon. genesis. 54(10). 542–549. 10 indexed citations

Borello, Ugo, Mayur Madhavan, Ilya Vilinsky, et al.. (2013). Sp8 and COUP-TF1 Reciprocally Regulate Patterning and Fgf Signaling in Cortical Progenitors. Cerebral Cortex. 24(6). 1409–1421. 39 indexed citations

Li, Xiaomu, Chao Lin, Tao Ma, et al.. (2011). The Transcription Factor Sp8 Is Required for the Production of Parvalbumin-Expressing Interneurons in the Olfactory Bulb. Journal of Neuroscience. 31(23). 8450–8455. 43 indexed citations

10.

Spence, Jason R., et al.. (2007). Retina regeneration in the chick embryo is not induced by spontaneous Mitf downregulation but requires FGF/FGFR/MEK/Erk dependent upregulation of Pax6.. PubMed. 13. 57–65. 65 indexed citations

11.

Madhavan, Mayur, et al.. (2006). The role of Pax-6 in lens regeneration. Proceedings of the National Academy of Sciences. 103(40). 14848–14853. 46 indexed citations

12.

Tsonis, Panagiotis A., M. Natalia Vergara, Jason R. Spence, et al.. (2004). A novel role of the hedgehog pathway in lens regeneration. Developmental Biology. 267(2). 450–461. 46 indexed citations

13.

Tsonis, Panagiotis A., et al.. (2004). A newt's eye view of lens regeneration. The International Journal of Developmental Biology. 48(8-9). 975–980. 80 indexed citations

14.

Tsonis, Panagiotis A., et al.. (2004). Effects of a CDK inhibitor on lens regeneration. Wound Repair and Regeneration. 12(1). 24–29. 7 indexed citations

15.

Spence, Jason R., et al.. (2004). The hedgehog pathway is a modulator of retina regeneration. Development. 131(18). 4607–4621. 84 indexed citations

16.

Madhavan, Mayur, et al.. (2003). Do Complement Molecules Play a Role in Lens Regeneration. Investigative Ophthalmology & Visual Science. 44(13). 1241–1241. 1 indexed citations

17.

Kimura, Yuko, Mayur Madhavan, Mindy K. Call, et al.. (2003). Expression of Complement 3 and Complement 5 in Newt Limb and Lens Regeneration. The Journal of Immunology. 170(5). 2331–2339. 115 indexed citations

18.

Madhavan, Mayur, Revati Kumar, & K.S. Krishnan. (2000). Genetics of anesthetic response: autosomal mutations that render Drosophila resistant to halothane. Pharmacology Biochemistry and Behavior. 67(4). 749–757. 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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