Kayalvizhi Madhivanan

Author

Purdue University West Lafayette ORCID

Also Known As

K Madhivanan, K. Madhivanan, Kayalvizhi Madhivanan

Publications

524

Citations

H-Index

Concepts

All Affiliations

Purdue University West Lafayette Center for Cancer Research Research Network (United States)Indiana University – Purdue University Indianapolis University of California San Diego

About

Kayalvizhi Madhivanan is an author at Purdue University West Lafayette specializing in medicine, developmental biology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	199
2	Cell Biology	4	4	199
3	Cellular Physiology	2	2	90
4	Natural Sciences	1	1	96
5	Molecular Biology	1	1	96

Kayalvizhi Madhivanan

Publications

403

Citations

H-Index

Page 1

	Year	Citations
Serine-129 phosphorylation of α-synuclein is an activity-dependent trigger for physiologic protein-protein interactions and synaptic function Leonardo A Parra‐Rivas, Kayalvizhi Madhivanan, Brent Aulston, Neuron	2023	114
The Lowe syndrome protein OCRL1 is involved in primary cilia assembly Brian G. Coon, Víctor Hernández-Hernández, Kayalvizhi Madhivanan, Human Molecular Genetics Developmental BiologyGenetic DisorderNatural SciencesGeneticsPrimary Cilia Assembly	2012	96
The epsin protein family: coordinators of endocytosis and signaling Arpita Sen, Kayalvizhi Madhivanan, Debarati Mukherjee, BioMolecular Concepts Signal TransductionDevelopmental BiologyConserved FamilyMembrane BendingSignaling Pathway	2012	68
Cellular clearance of circulating transthyretin decreases cell-nonautonomous proteotoxicity in <i>Caenorhabditis elegans</i> Kayalvizhi Madhivanan, Erin R. Greiner, Miguel Alves‐Ferreira, Proceedings of the National Academy of Sciences	2018	33
A novel, safe, fast and efficient treatment for Her2‐positive and negative bladder cancer utilizing an EGF‐anthrax toxin chimera Sherwin Jack, Kayalvizhi Madhivanan, Swetha Ramadesikan, International Journal of Cancer	2019	29
Lowe syndrome Kayalvizhi Madhivanan, Debarati Mukherjee, R. Claudio Aguilar Communicative & Integrative Biology Functional DeficienciesOcrl1 FunctionSignal TransductionDevelopmental BiologySignaling Pathway	2012	22
Genotype & phenotype in Lowe Syndrome: specific <i>OCRL1</i> patient mutations differentially impact cellular phenotypes Swetha Ramadesikan, Lisette Skiba, Jennifer Lee, Human Molecular Genetics	2021	18
Lowe syndrome patient cells display mTOR- and RhoGTPase-dependent phenotypes alleviated by rapamycin and statins Kayalvizhi Madhivanan, Swetha Ramadesikan, W.‐C. Hsieh, Human Molecular Genetics PathologyCytoskeletonInflammationSignaling PathwayNutrient Signalling	2020	13
Synapsin E-domain is essential for α-synuclein function Alexandra Stavsky, Leonardo A Parra‐Rivas, Shani Tal, eLife	2024	10

Page 1