Bhaven K. Mehta

1.7k total citations
10 papers, 801 citations indexed

About

Bhaven K. Mehta is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Bhaven K. Mehta has authored 10 papers receiving a total of 801 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Pathology and Forensic Medicine and 3 papers in Genetics. Recurrent topics in Bhaven K. Mehta's work include Systemic Sclerosis and Related Diseases (4 papers), Genomics and Rare Diseases (2 papers) and Single-cell and spatial transcriptomics (2 papers). Bhaven K. Mehta is often cited by papers focused on Systemic Sclerosis and Related Diseases (4 papers), Genomics and Rare Diseases (2 papers) and Single-cell and spatial transcriptomics (2 papers). Bhaven K. Mehta collaborates with scholars based in United States and United Kingdom. Bhaven K. Mehta's co-authors include Christopher A. Walsh, Xuyu Cai, Gilad D. Evrony, Hillel S. Lehmann, Peter J. Park, Annapurna Poduri, Princess C. Elhosary, Alissa M. D’Gama, Amir Karger and Soohyun Lee and has published in prestigious journals such as Science, Neuron and SHILAP Revista de lepidopterología.

In The Last Decade

Bhaven K. Mehta

10 papers receiving 797 citations

Peers

Bhaven K. Mehta
Hillel S. Lehmann United States
L. Benjamin Hills United States
Princess C. Elhosary United States
Craig L. Bohrson United States
Rongxin Fang United States
Rebecca Petri Sweden
Nicole E. Hatem United States
Sahar Gelfman United States
Jill E. Moore United States
Tahsin Stefan Barakat Netherlands
Hillel S. Lehmann United States
Bhaven K. Mehta
Citations per year, relative to Bhaven K. Mehta Bhaven K. Mehta (= 1×) peers Hillel S. Lehmann

Countries citing papers authored by Bhaven K. Mehta

Since Specialization
Citations

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

Fields of papers citing papers by Bhaven K. Mehta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bhaven K. Mehta. 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 Bhaven K. Mehta. The network helps show where Bhaven K. Mehta may publish in the future.

Co-authorship network of co-authors of Bhaven K. Mehta

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

All Works

10 of 10 papers shown
1.
Mehta, Bhaven K., Jennifer M. Franks, Yue Wang, et al.. (2022). Machine-learning classification identifies patients with early systemic sclerosis as abatacept responders via CD28 pathway modulation. JCI Insight. 7(24). 4 indexed citations
2.
Mehta, Bhaven K., Kathleen Aren, Mary Carns, et al.. (2020). Mast cell activation in the systemic sclerosis esophagus. Journal of Scleroderma and Related Disorders. 6(1). 77–86. 2 indexed citations
3.
Schmitz‐Abe, Klaus, Guzman Sánchez‐Schmitz, Ryan N. Doan, et al.. (2020). Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder. Scientific Reports. 10(1). 14045–14045. 13 indexed citations
4.
Mehta, Bhaven K., et al.. (2020). Molecular “omic” signatures in systemic sclerosis. SHILAP Revista de lepidopterología. 7(3). S173–S180. 8 indexed citations
5.
Johnson, Michael E., Jennifer M. Franks, Guoshuai Cai, et al.. (2019). Microbiome dysbiosis is associated with disease duration and increased inflammatory gene expression in systemic sclerosis skin. Arthritis Research & Therapy. 21(1). 49–49. 27 indexed citations
6.
Franks, Jennifer M., Bhaven K. Mehta, Veronica J. Berrocal, et al.. (2019). THU0354 MACHINE LEARNING CLASSIFICATION OF SKIN GENE EXPRESSION IDENTIFIES A SUBSET OF SYSTEMIC SCLEROSIS PATIENTS MOST LIKELY TO SHOW CLINICAL IMPROVEMENT IN RESPONSE TO ABATACEPT. Annals of the Rheumatic Diseases. 78. 458–459. 2 indexed citations
7.
Evrony, Gilad D., Eun‐Jung Lee, Bhaven K. Mehta, et al.. (2015). Cell Lineage Analysis in Human Brain Using Endogenous Retroelements. Neuron. 85(1). 49–59. 184 indexed citations
8.
Lodato, Michael A., Mollie B. Woodworth, Semin Lee, et al.. (2015). Somatic mutation in single human neurons tracks developmental and transcriptional history. Science. 350(6256). 94–98. 359 indexed citations
9.
Cai, Xuyu, Gilad D. Evrony, Hillel S. Lehmann, et al.. (2014). Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain. Cell Reports. 8(5). 1280–1289. 201 indexed citations
10.
Mehta, Bhaven K., Zhenyu Li, & Mona Zaghloul. (2011). Optical bio sensor using Graphene Nano Ribbons. 1 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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