Megana Prasad

1.1k total citations
19 papers, 550 citations indexed

About

Megana Prasad is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Megana Prasad has authored 19 papers receiving a total of 550 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Megana Prasad's work include Bone and Dental Protein Studies (3 papers), dental development and anomalies (3 papers) and CRISPR and Genetic Engineering (3 papers). Megana Prasad is often cited by papers focused on Bone and Dental Protein Studies (3 papers), dental development and anomalies (3 papers) and CRISPR and Genetic Engineering (3 papers). Megana Prasad collaborates with scholars based in United States, France and United Kingdom. Megana Prasad's co-authors include John D. Gearhart, Evanthia Pashos, Hélène Dollfus, Rui Lopes, Corinne Stoetzel, Agnès Bloch‐Zupan, Andrew S. McCallion, Anthony Antonellis, Stacie K. Loftus and William J. Pavan and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Biochemical Journal.

In The Last Decade

Megana Prasad

19 papers receiving 542 citations

Peers

Megana Prasad
Jiangxia Li China
Francesca Ferrante Germany
Karine Sii-Felice France
Alexander S. Garrett United States
K. G. Guruharsha United States
Wouter Steyaert Belgium
Rosa Bartolomeo Italy
Toni U. Wagner Germany
Pamela Magini Italy
Nadine Jalkh Lebanon
Jiangxia Li China
Megana Prasad
Citations per year, relative to Megana Prasad Megana Prasad (= 1×) peers Jiangxia Li

Countries citing papers authored by Megana Prasad

Since Specialization
Citations

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

Fields of papers citing papers by Megana Prasad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Megana Prasad

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

All Works

19 of 19 papers shown
1.
Lopes, Rui & Megana Prasad. (2024). Beyond the promise: evaluating and mitigating off-target effects in CRISPR gene editing for safer therapeutics. Frontiers in Bioengineering and Biotechnology. 11. 1339189–1339189. 36 indexed citations
2.
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Paris, Iñaki, Martin Ebeling, Christophe Schweitzer, et al.. (2021). Alzheimer’s Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia. Frontiers in Immunology. 11. 617860–617860. 42 indexed citations
4.
Prasad, Megana, Avinash Sahu, Radhouane Aniba, et al.. (2019). Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism. PLoS ONE. 14(4). e0215911–e0215911. 3 indexed citations
5.
Tarabeux, Julien, Bénédicte Gérard, Antony Le Béchec, et al.. (2019). Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement. Methods in molecular biology. 1922. 407–452. 10 indexed citations
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Gasse, Barbara, Megana Prasad, Sidney Delgado, et al.. (2017). Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta. Frontiers in Physiology. 8. 398–398. 9 indexed citations
8.
Tardieu, C, Sophie Jung, Karen Niederreither, et al.. (2017). Dental and extra‐oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype–phenotype study. Clinical Genetics. 92(5). 477–486. 23 indexed citations
9.
Nevers, Yannis, Megana Prasad, Laetitia Poidevin, et al.. (2017). Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling. Molecular Biology and Evolution. 34(8). 2016–2034. 35 indexed citations
10.
Schaefer, Élise, Corinne Stoetzel, Sophie Scheidecker, et al.. (2016). Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome. Journal of Human Genetics. 61(5). 447–450. 57 indexed citations
11.
Prasad, Megana, et al.. (2016). Amelogenesis Imperfecta. Journal of Dental Research. 95(13). 1457–1463. 34 indexed citations
12.
Prasad, Megana, Kavita Bhalla, Jeffrey R. O’Connell, et al.. (2013). A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure. PLoS ONE. 8(10). e76290–e76290. 16 indexed citations
13.
Harden, Maegan, Mirana Ramialison, Joachim Wittbrodt, et al.. (2012). Close association of olfactory placode precursors and cranial neural crest cells does not predestine cell mixing. Developmental Dynamics. 241(7). 1143–1154. 17 indexed citations
14.
Hodonsky, Chani J., Erica L. Kleinbrink, Megana Prasad, et al.. (2011). SOX10 regulates expression of the SH3-domain kinase binding protein 1 (Sh3kbp1) locus in Schwann cells via an alternative promoter. Molecular and Cellular Neuroscience. 49(2). 85–96. 13 indexed citations
15.
Prasad, Megana, Xylena Reed, David U. Gorkin, et al.. (2011). SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer. BMC Developmental Biology. 11(1). 40–40. 48 indexed citations
16.
Addis, Russell C., Megana Prasad, Xiangcan Zhan, et al.. (2010). OCT3/4 regulates transcription of histone deacetylase 4 (Hdac4) in mouse embryonic stem cells. Journal of Cellular Biochemistry. 111(2). 391–401. 10 indexed citations
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Loftus, Stacie K., Anthony Antonellis, Ivana Matera, et al.. (2008). Gpnmb is a melanoblast‐expressed, MITF‐dependent gene. Pigment Cell & Melanoma Research. 22(1). 99–110. 59 indexed citations
19.
Gearhart, John D., Evanthia Pashos, & Megana Prasad. (2007). Pluripotency Redux — Advances in Stem-Cell Research. New England Journal of Medicine. 357(15). 1469–1472. 102 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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