Seetha Mannepalli

988 total citations
16 papers, 576 citations indexed

About

Seetha Mannepalli is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Cell Biology. According to data from OpenAlex, Seetha Mannepalli has authored 16 papers receiving a total of 576 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 10 papers in Molecular Biology and 5 papers in Cell Biology. Recurrent topics in Seetha Mannepalli's work include Axon Guidance and Neuronal Signaling (7 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Protein Structure and Dynamics (3 papers). Seetha Mannepalli is often cited by papers focused on Axon Guidance and Neuronal Signaling (7 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Protein Structure and Dynamics (3 papers). Seetha Mannepalli collaborates with scholars based in United States, Belgium and Denmark. Seetha Mannepalli's co-authors include Lawrence Shapiro, Barry Honig, Fabiana Bahna, Göran Ahlsén, K.M. Goodman, Tom Maniatis, Rotem Rubinstein, Chan Aye Thu, Phinikoula S. Katsamba and Chelsea Rittenhouse and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Seetha Mannepalli

16 papers receiving 573 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Seetha Mannepalli United States	12	417	218	145	41	40	16	576
Callista B. Harper Australia	14	350 0.8×	252 1.2×	300 2.1×	24 0.6×	57 1.4×	19	734
Torsten Schulz Germany	11	507 1.2×	429 2.0×	104 0.7×	22 0.5×	79 2.0×	23	898
Margaret M. Stratton United States	14	528 1.3×	275 1.3×	80 0.6×	12 0.3×	56 1.4×	23	692
Daichi Kamiyama United States	8	479 1.1×	126 0.6×	179 1.2×	15 0.4×	66 1.6×	16	648
C. Kimberly Tsui United States	12	632 1.5×	337 1.5×	189 1.3×	17 0.4×	80 2.0×	18	1.1k
C. Jacobs United States	6	408 1.0×	101 0.5×	86 0.6×	14 0.3×	49 1.2×	6	562
Robert P. Kruger United States	10	466 1.1×	405 1.9×	226 1.6×	24 0.6×	56 1.4×	28	949
Michael C. Lanz United States	16	543 1.3×	82 0.4×	149 1.0×	7 0.2×	39 1.0×	36	884
Christopher T. Burket United States	8	524 1.3×	106 0.5×	286 2.0×	32 0.8×	68 1.7×	10	648
Elissa D. Pastuzyn United States	9	507 1.2×	205 0.9×	37 0.3×	24 0.6×	106 2.6×	12	763

Countries citing papers authored by Seetha Mannepalli

Since Specialization

Citations

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

Fields of papers citing papers by Seetha Mannepalli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seetha Mannepalli

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

All Works

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16 of 16 papers shown

Sergeeva, Alina P., Göran Ahlsén, Seetha Mannepalli, et al.. (2025). Astrocyte morphogenesis requires self-recognition. Nature. 644(8075). 164–172. 3 indexed citations

Cerutti, Gabriele, Fabiana Bahna, Seetha Mannepalli, et al.. (2024). Structures and pH-dependent dimerization of the sevenless receptor tyrosine kinase. Molecular Cell. 84(23). 4677–4690.e6. 1 indexed citations

Sergeeva, Alina P., Phinikoula S. Katsamba, Jared M. Sampson, et al.. (2023). Free Energy Perturbation Calculations of Mutation Effects on SARS-CoV-2 RBD::ACE2 Binding Affinity. Journal of Molecular Biology. 435(15). 168187–168187. 16 indexed citations

Xu, Shuwa, Alina P. Sergeeva, Phinikoula S. Katsamba, et al.. (2022). Affinity requirements for control of synaptic targeting and neuronal cell survival by heterophilic IgSF cell adhesion molecules. Cell Reports. 39(1). 110618–110618. 10 indexed citations

Goodman, K.M., Phinikoula S. Katsamba, Rotem Rubinstein, et al.. (2022). How clustered protocadherin binding specificity is tuned for neuronal self-/nonself-recognition. eLife. 11. 20 indexed citations

Rapp, Micah, Yicheng Guo, Eswar R. Reddem, et al.. (2021). Modular basis for potent SARS-CoV-2 neutralization by a prevalent VH1-2-derived antibody class. Cell Reports. 35(1). 108950–108950. 36 indexed citations

Blockus, Heike, Sebi V. Rolotti, Miklos Szoboszlay, et al.. (2021). Synaptogenic activity of the axon guidance molecule Robo2 underlies hippocampal circuit function. Cell Reports. 37(3). 109828–109828. 22 indexed citations

Sergeeva, Alina P., Phinikoula S. Katsamba, Göran Ahlsén, et al.. (2020). DIP/Dpr interactions and the evolutionary design of specificity in protein families. Nature Communications. 11(1). 2125–2125. 24 indexed citations

Brasch, Julia, K.M. Goodman, Alex J. Noble, et al.. (2019). Visualization of clustered protocadherin neuronal self-recognition complexes. Nature. 569(7755). 280–283. 72 indexed citations

10.

Goodman, K.M., Rotem Rubinstein, Hanbin Dan, et al.. (2017). Protocadherin cis -dimer architecture and recognition unit diversity. Proceedings of the National Academy of Sciences. 114(46). E9829–E9837. 46 indexed citations

11.

Goodman, K.M., Rotem Rubinstein, Chan Aye Thu, et al.. (2016). Structural Basis of Diverse Homophilic Recognition by Clustered α- and β-Protocadherins. Neuron. 90(4). 709–723. 76 indexed citations

12.

Goodman, K.M., Rotem Rubinstein, Chan Aye Thu, et al.. (2016). γ-Protocadherin structural diversity and functional implications. eLife. 5. 48 indexed citations

13.

Goodman, K.M., Masahito Yamagata, Xiangshu Jin, et al.. (2016). Molecular basis of sidekick-mediated cell-cell adhesion and specificity. eLife. 5. 39 indexed citations

14.

Rubinstein, Rotem, Chan Aye Thu, K.M. Goodman, et al.. (2015). Molecular Logic of Neuronal Self-Recognition through Protocadherin Domain Interactions. Cell. 163(3). 629–642. 122 indexed citations

15.

Jin, Xiangshu, Melissa Walker, Klára Felsövályi, et al.. (2011). Crystal structures of Drosophila N-cadherin ectodomain regions reveal a widely used class of Ca ²⁺ -free interdomain linkers. Proceedings of the National Academy of Sciences. 109(3). E127–34. 33 indexed citations

16.

Mannepalli, Seetha, Ashish Dutta, & Ashutosh Saxena. (2010). A MULTI-OBJECTIVE GA BASED ALGORITHM FOR 2D FORM AND FORCE CLOSURE GRASP OF PRISMATIC OBJECTS. International Journal of Robotics and Automation. 25(2). 8 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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