Vijayaraghavan Rangachari

2.2k total citations · 1 hit paper
35 papers, 1.6k citations indexed

About

Vijayaraghavan Rangachari is a scholar working on Molecular Biology, Physiology and Biomaterials. According to data from OpenAlex, Vijayaraghavan Rangachari has authored 35 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Physiology and 5 papers in Biomaterials. Recurrent topics in Vijayaraghavan Rangachari's work include Alzheimer's disease research and treatments (17 papers), Chemical Synthesis and Analysis (7 papers) and Prion Diseases and Protein Misfolding (5 papers). Vijayaraghavan Rangachari is often cited by papers focused on Alzheimer's disease research and treatments (17 papers), Chemical Synthesis and Analysis (7 papers) and Prion Diseases and Protein Misfolding (5 papers). Vijayaraghavan Rangachari collaborates with scholars based in United States, India and Switzerland. Vijayaraghavan Rangachari's co-authors include Terrone L. Rosenberry, Dennis W. Dickson, Brenda D. Moore, Dana Kim Reed, Todd E. Golde, Leonard Petrucelli, Jennifer Gass, Emanuele Buratti, Tania F. Gendron and Christopher D. Link and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Neuroscience and Biochemistry.

In The Last Decade

Vijayaraghavan Rangachari

34 papers receiving 1.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity

2009 484 citations Vijayaraghavan Rangachari, Todd E. Golde et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vijayaraghavan Rangachari United States	15	860	770	519	256	204	35	1.6k
David R. Boyer United States	19	1.2k 1.4×	1.7k 2.2×	766 1.5×	191 0.7×	111 0.5×	32	2.6k
Andreas Muhs Switzerland	21	939 1.1×	625 0.8×	115 0.2×	201 0.8×	334 1.6×	43	1.8k
Leila M. Luheshi United Kingdom	19	2.0k 2.3×	2.0k 2.6×	519 1.0×	286 1.1×	299 1.5×	26	3.1k
Mathew H. Horrocks United Kingdom	27	997 1.2×	1.5k 1.9×	847 1.6×	457 1.8×	90 0.4×	68	3.0k
Dag Sehlin Sweden	33	1.6k 1.9×	1.3k 1.7×	301 0.6×	418 1.6×	340 1.7×	85	3.0k
Yue‐De Yang China	15	882 1.0×	777 1.0×	650 1.3×	258 1.0×	63 0.3×	33	1.8k
Michele Perni United Kingdom	17	923 1.1×	907 1.2×	416 0.8×	164 0.6×	122 0.6×	29	1.6k
Katharina Tepper Germany	14	1.3k 1.5×	1.7k 2.3×	227 0.4×	408 1.6×	200 1.0×	14	2.6k
Marten Beeg Italy	23	949 1.1×	1.0k 1.3×	120 0.2×	183 0.7×	198 1.0×	47	1.8k
Michael P. Hughes United States	13	456 0.5×	1.0k 1.3×	356 0.7×	85 0.3×	32 0.2×	20	1.4k

Countries citing papers authored by Vijayaraghavan Rangachari

Since Specialization

Citations

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

Fields of papers citing papers by Vijayaraghavan Rangachari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vijayaraghavan Rangachari

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Mukund, Amar, Vijayaraghavan Rangachari, Yashwant Patıdar, et al.. (2021). Response evaluation of locoregional therapies in combined hepatocellular–cholangiocarcinoma and intrahepatic cholangiocarcinoma versus hepatocellular carcinoma: a propensity score matched study. Clinical Radiology. 77(2). 121–129. 8 indexed citations

Dean, Dexter N., et al.. (2021). Biophysical characteristics of lipid‐induced Aβ oligomers correlate to distinctive phenotypes in transgenic mice. The FASEB Journal. 35(2). e21318–e21318. 10 indexed citations

Ghosh, Preetam, et al.. (2020). A game-theoretic approach to deciphering the dynamics of amyloid- β aggregation along competing pathways. Royal Society Open Science. 7(4). 191814–191814. 3 indexed citations

Ghosh, Preetam, et al.. (2020). A network thermodynamic analysis of amyloid aggregation along competing pathways. Applied Mathematics and Computation. 393. 125778–125778. 4 indexed citations

Rangachari, Vijayaraghavan, Dexter N. Dean, Pratip Rana, Ashwin Vaidya, & Preetam Ghosh. (2018). Cause and consequence of Aβ – Lipid interactions in Alzheimer disease pathogenesis. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1860(9). 1652–1662. 40 indexed citations

Dean, Dexter N., Pradipta Das, Pratip Rana, et al.. (2017). Strain-Specific Propagation by an Amyloid-Beta Dodecamer. Biophysical Journal. 112(3). 362a–362a. 1 indexed citations

Morgan, Sarah E., et al.. (2014). Dopamine‐induced α‐synuclein oligomers show self‐ and cross‐propagation properties. Protein Science. 23(10). 1369–1379. 31 indexed citations

Kumar, Amit, et al.. (2010). Inhibition of Aβ42 Peptide Aggregation by a Binuclear Ruthenium(II)−Platinum(II) Complex: Potential for Multimetal Organometallics as Anti-amyloid Agents. ACS Chemical Neuroscience. 1(10). 691–701. 58 indexed citations

Rangachari, Vijayaraghavan, Brenda D. Moore, Bernadette Cusack, et al.. (2009). Rationally designed dehydroalanine (ΔAla)‐containing peptides inhibit amyloid‐β (Aβ) peptide aggregation. Biopolymers. 91(6). 456–465. 22 indexed citations

10.

Kim, Jungsu, Virginia M. Miller, Yona Levites, et al.. (2008). BRI2 (ITM2b) Inhibits A Deposition In Vivo. Journal of Neuroscience. 28(23). 6030–6036. 94 indexed citations

11.

Berger, Zdenek, Hanno M. Roder, Amanda Hanna, et al.. (2007). Accumulation of Pathological Tau Species and Memory Loss in a Conditional Model of Tauopathy. Journal of Neuroscience. 27(14). 3650–3662. 387 indexed citations

12.

Rangachari, Vijayaraghavan, Brenda D. Moore, Dana Kim Reed, et al.. (2007). Amyloid-β(1−42) Rapidly Forms Protofibrils and Oligomers by Distinct Pathways in Low Concentrations of Sodium Dodecylsulfate. Biochemistry. 46(43). 12451–12462. 133 indexed citations

13.

Rangachari, Vijayaraghavan, Dana Kim Reed, Brenda D. Moore, & Terrone L. Rosenberry. (2006). Secondary Structure and Interfacial Aggregation of Amyloid-β(1−40) on Sodium Dodecyl Sulfate Micelles. Biochemistry. 45(28). 8639–8648. 70 indexed citations

14.

Rangachari, Vijayaraghavan, et al.. (2005). Design of Peptides with α,β-Dehydro Residues: Synthesis, Crystal Structure and Molecular Conformation of a Peptide N-Boc-Phe-ΔPhe-Ile-OCH3. Structural Chemistry. 16(4). 445–452. 4 indexed citations

15.

Dey, Sharmistha, Vijayaraghavan Rangachari, Vivek Goel, et al.. (2004). Design rules for peptides with α, β-dehydro-residues: synthesis of a model peptide Boc-Ile-ΔAla-OCH3 and its crystal structures obtained from two different solvents. Journal of Molecular Structure. 737(2-3). 109–116. 7 indexed citations

16.

Rangachari, Vijayaraghavan, Ewa A. Bienkiewicz, Nilakshee Bhattacharya, et al.. (2004). Prolylpeptide Binding by the Prokaryotic SH3-like Domain of the Diphtheria Toxin Repressor: A Regulatory Switch^,. Biochemistry. 44(1). 40–51. 30 indexed citations

17.

Rangachari, Vijayaraghavan, Pravindra Kumar, Sharmistha Dey, & T.P. Singh. (2003). Design of peptides with branched β‐carbon dehydro‐residues: syntheses, crystal structures and molecular conformations of two peptides, (I) N‐Carbobenzoxy‐ΔVal‐Ala‐Leu‐OCH₃ and (II) N‐Carbobenzoxy‐ΔIle‐Ala‐Leu‐OCH₃. Journal of Peptide Research. 62(2). 63–69. 10 indexed citations

18.

Rangachari, Vijayaraghavan, Pravindra Kumar, Sharmistha Dey, & T.P. Singh. (2001). Design of peptides with α,β-dehydro residues: a dipeptide with a branched β-carbon dehydro residue at the (i+1) position, methylN-(benzyloxycarbonyl)-α,β-didehydrovalyl-L-tryptophanate. Acta Crystallographica Section C Crystal Structure Communications. 57(10). 1220–1221. 8 indexed citations

19.

Rangachari, Vijayaraghavan, Pravindra Kumar, Sharmistha Dey, & T.P. Singh. (1998). Design of peptides with αβ‐dehydro residues: Synthesis, crystal structure and molecular conformation of N‐Boc‐L‐Ile‐ΔPhe‐L‐Trp‐OCH₃. Journal of Peptide Research. 52(2). 89–94. 10 indexed citations

20.

Gopalakrishnan, J., et al.. (1997). A new charge density wave oxide, LiVMoO5, and its tungsten analogue obtained by topotactic reduction of LiVMO6 (M=Mo, W) brannerites. Journal of Materials Chemistry. 7(2). 307–310. 14 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.

Explore authors with similar magnitude of impact