Harendra Guturu

4.5k total citations · 1 hit paper
24 papers, 1.3k citations indexed

About

Harendra Guturu is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Harendra Guturu has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Genetics and 2 papers in Infectious Diseases. Recurrent topics in Harendra Guturu's work include Genomics and Rare Diseases (7 papers), Genomics and Chromatin Dynamics (6 papers) and Genetic Associations and Epidemiology (5 papers). Harendra Guturu is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomics and Chromatin Dynamics (6 papers) and Genetic Associations and Epidemiology (5 papers). Harendra Guturu collaborates with scholars based in United States, United Kingdom and Qatar. Harendra Guturu's co-authors include Gill Bejerano, Aaron M. Wenger, Jonathan A. Bernstein, Karthik A. Jagadeesh, Peter D. Stenson, D.N. Cooper, Mark J. Berger, Jenny Chen, Preslav Nakov and Anna Divoli and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Nature Genetics.

In The Last Decade

Harendra Guturu

22 papers receiving 1.3k citations

Hit Papers

align trajectories

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.

M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

2016 512 citations Karthik A. Jagadeesh, Aaron M. Wenger et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Harendra Guturu United States	15	766	663	157	69	59	24	1.3k
Jorge Amigo Spain	21	797 1.0×	662 1.0×	159 1.0×	50 0.7×	46 0.8×	51	1.4k
Manuel Corpas United Kingdom	13	893 1.2×	1.1k 1.6×	151 1.0×	26 0.4×	59 1.0×	41	1.6k
Rebecca Truty United States	18	1.3k 1.7×	664 1.0×	250 1.6×	28 0.4×	89 1.5×	32	1.8k
Kristian Gray United Kingdom	9	1.1k 1.5×	280 0.4×	292 1.9×	38 0.6×	43 0.7×	11	1.5k
María Cerezo Spain	13	917 1.2×	1.1k 1.6×	152 1.0×	26 0.4×	71 1.2×	19	1.8k
Charles E. Chapple France	10	859 1.1×	494 0.7×	140 0.9×	22 0.3×	88 1.5×	11	1.6k
Wenwu Cui United States	11	1.4k 1.8×	567 0.9×	226 1.4×	40 0.6×	86 1.5×	16	2.0k
Lifeng Tian United States	15	474 0.6×	366 0.6×	146 0.9×	14 0.2×	45 0.8×	47	900
Giovanna Ambrosini Switzerland	22	1.3k 1.7×	268 0.4×	276 1.8×	24 0.3×	58 1.0×	37	1.8k

Countries citing papers authored by Harendra Guturu

Since Specialization

Citations

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

Fields of papers citing papers by Harendra Guturu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harendra Guturu

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

All Works

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20 of 20 papers shown

Suhre, Karsten, Qingwen Chen, Anna Halama, et al.. (2025). A genome-wide association study of mass spectrometry proteomics using a nanoparticle enrichment platform. Nature Genetics. 57(12). 2987–2996.

Guturu, Harendra, Andrew Nichols, Seth Just, et al.. (2025). Cloud-Enabled Scalable Analysis of Large Proteomics Cohorts. Journal of Proteome Research. 24(3). 1462–1469.

Suhre, Karsten, Guhan Venkataraman, Harendra Guturu, et al.. (2024). Nanoparticle enrichment mass-spectrometry proteomics identifies protein-altering variants for precise pQTL mapping. Nature Communications. 15(1). 989–989. 19 indexed citations

Roberts, Genevieve H. L., Raghavendran Partha, Brooke Rhead, et al.. (2022). Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. Nature Genetics. 54(4). 374–381. 42 indexed citations

Knight, Spencer C., Shannon McCurdy, Brooke Rhead, et al.. (2022). COVID-19 susceptibility and severity risks in a cross-sectional survey of over 500 000 US adults. BMJ Open. 12(10). e049657–e049657. 5 indexed citations

Birgmeier, Johannes, Maximilian Haeussler, Cole A. Deisseroth, et al.. (2020). AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literature. Science Translational Medicine. 12(544). 56 indexed citations

Madelaine, Romain, Marion Aguirrebengoa, Harendra Guturu, et al.. (2020). Morphogenesis is transcriptionally coupled to neurogenesis during peripheral olfactory organ development. Development. 147(24). 6 indexed citations

Chen, Heidi I., Karthik A. Jagadeesh, Johannes Birgmeier, et al.. (2018). An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease. European Journal of Human Genetics. 26(12). 1810–1818. 16 indexed citations

Jagadeesh, Karthik A., Johannes Birgmeier, Harendra Guturu, et al.. (2018). Phrank measures phenotype sets similarity to greatly improve Mendelian diagnostic disease prioritization. Genetics in Medicine. 21(2). 464–470. 28 indexed citations

10.

Han, Eunjung, Peter Carbonetto, Yong Wang, et al.. (2017). Clustering of 770,000 genomes reveals post-colonial population structure of North America. Nature Communications. 8(1). 14238–14238. 61 indexed citations

11.

Guturu, Harendra, Sandeep Chinchali, Shoa L. Clarke, & Gill Bejerano. (2016). Erosion of Conserved Binding Sites in Personal Genomes Points to Medical Histories. PLoS Computational Biology. 12(2). e1004711–e1004711. 5 indexed citations

12.

Wenger, Aaron M., Harendra Guturu, Jonathan A. Bernstein, & Gill Bejerano. (2016). Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers. Genetics in Medicine. 19(2). 209–214. 190 indexed citations

13.

Jagadeesh, Karthik A., Aaron M. Wenger, Mark J. Berger, et al.. (2016). M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity. Nature Genetics. 48(12). 1581–1586. 512 indexed citations breakdown →

14.

Balasubramanian, Meena, Helen Lord, Sébastien Levesque, et al.. (2016). Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene. Journal of Medical Genetics. 54(3). 157–165. 15 indexed citations

15.

Karr, Jonathan R., Harendra Guturu, Edward Y. Chen, et al.. (2015). NetworkPainter: dynamic intracellular pathway animation in Cytobank. BMC Bioinformatics. 16(1). 172–172. 3 indexed citations

16.

Camp, J. Gray, Christopher L. Frank, Colin R. Lickwar, et al.. (2014). Microbiota modulate transcription in the intestinal epithelium without remodeling the accessible chromatin landscape. Genome Research. 24(9). 1504–1516. 102 indexed citations

17.

Wenger, Aaron M., Shoa L. Clarke, Harendra Guturu, et al.. (2013). PRISM offers a comprehensive genomic approach to transcription factor function prediction. Genome Research. 23(5). 889–904. 22 indexed citations

18.

Wenger, Aaron M., Shoa L. Clarke, James H. Notwell, et al.. (2013). The Enhancer Landscape during Early Neocortical Development Reveals Patterns of Dense Regulation and Co-option. PLoS Genetics. 9(8). e1003728–e1003728. 22 indexed citations

19.

Hiller, Michael, James H. Notwell, Ravi Parikh, et al.. (2013). Computational methods to detect conserved non-genic elements in phylogenetically isolated genomes: application to zebrafish. Nucleic Acids Research. 41(15). e151–e151. 55 indexed citations

20.

Guturu, Harendra, Andrew C. Doxey, Aaron M. Wenger, & Gill Bejerano. (2013). Structure-aided prediction of mammalian transcription factor complexes in conserved non-coding elements. Philosophical Transactions of the Royal Society B Biological Sciences. 368(1632). 20130029–20130029. 31 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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