Devika Ganesamoorthy

1.5k total citations
25 papers, 719 citations indexed

About

Devika Ganesamoorthy is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Devika Ganesamoorthy has authored 25 papers receiving a total of 719 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Devika Ganesamoorthy's work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Phylogenetic Studies (9 papers) and Prenatal Screening and Diagnostics (6 papers). Devika Ganesamoorthy is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genomics and Phylogenetic Studies (9 papers) and Prenatal Screening and Diagnostics (6 papers). Devika Ganesamoorthy collaborates with scholars based in Australia, United Kingdom and United States. Devika Ganesamoorthy's co-authors include Lachlan Coin, Minh Duc Cao, Matthew A. Cooper, Alysha G. Elliott, Howard R. Slater, Damien L. Bruno, Trent Burgess, Son Hoang Nguyen, David J. Amor and Huihui Zhang and has published in prestigious journals such as Nucleic Acids Research, Nature Communications and Bioinformatics.

In The Last Decade

Devika Ganesamoorthy

25 papers receiving 684 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Devika Ganesamoorthy Australia 16 390 323 114 112 70 25 719
Jocelyn M. Bischof Canada 11 350 0.9× 309 1.0× 43 0.4× 35 0.3× 20 0.3× 11 818
Takashi Hirano Japan 15 424 1.1× 295 0.9× 11 0.1× 20 0.2× 21 0.3× 31 875
Paweł Parniewski Poland 15 625 1.6× 132 0.4× 8 0.1× 93 0.8× 43 0.6× 39 861
C Laurent France 16 398 1.0× 407 1.3× 116 1.0× 77 0.7× 6 0.1× 50 813
Tian Wang China 9 280 0.7× 59 0.2× 37 0.3× 9 0.1× 27 0.4× 27 510
Anne‐Marie Brun‐Zinkernagel United States 10 408 1.0× 235 0.7× 11 0.1× 33 0.3× 74 1.1× 11 652
Jingchu Hu China 9 292 0.7× 244 0.8× 6 0.1× 16 0.1× 29 0.4× 17 575
Christine Lambert United States 8 241 0.6× 171 0.5× 11 0.1× 18 0.2× 24 0.3× 11 411
Jeroen van Reeuwijk Netherlands 6 434 1.1× 155 0.5× 37 0.3× 19 0.2× 52 0.7× 6 548
Warren Emmett United Kingdom 12 485 1.2× 104 0.3× 6 0.1× 13 0.1× 57 0.8× 12 747

Countries citing papers authored by Devika Ganesamoorthy

Since Specialization
Citations

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

Fields of papers citing papers by Devika Ganesamoorthy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Devika Ganesamoorthy

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

All Works

20 of 20 papers shown
1.
Ganesamoorthy, Devika, Jessie J.‐Y. Chang, Jianshu Zhang, et al.. (2025). Utilizing Nanopore direct RNA sequencing of blood from patients with sepsis for discovery of co- and post-transcriptional disease biomarkers. BMC Infectious Diseases. 25(1). 692–692. 2 indexed citations
2.
Ganesamoorthy, Devika, Alan J. Robertson, Wenhan Chen, et al.. (2022). Whole genome deep sequencing analysis of cell-free DNA in samples with low tumour content. BMC Cancer. 22(1). 85–85. 18 indexed citations
3.
Zhang, Ping, et al.. (2020). Nanopore sequencing as a scalable, cost-effective platform for analyzing polyclonal vector integration sites following clinical T cell therapy. Journal for ImmunoTherapy of Cancer. 8(1). e000299–e000299. 9 indexed citations
4.
Pitt, Miranda E., Alysha G. Elliott, Minh Duc Cao, et al.. (2018). Multifactorial chromosomal variants regulate polymyxin resistance in extensively drug-resistant Klebsiella pneumoniae. Microbial Genomics. 4(3). 54 indexed citations
5.
Pitt, Miranda E., Minh Duc Cao, Mark S. Butler, et al.. (2018). Octapeptin C4 and polymyxin resistance occur via distinct pathways in an epidemic XDR Klebsiella pneumoniae ST258 isolate. Journal of Antimicrobial Chemotherapy. 74(3). 582–593. 14 indexed citations
6.
Shao, Haojing, Devika Ganesamoorthy, Tânia Duarte, et al.. (2018). npInv: accurate detection and genotyping of inversions using long read sub-alignment. BMC Bioinformatics. 19(1). 261–261. 31 indexed citations
7.
Cao, Minh Duc, Devika Ganesamoorthy, Chenxi Zhou, & Lachlan Coin. (2017). Simulating the dynamics of targeted capture sequencing with CapSim. Bioinformatics. 34(5). 873–874. 9 indexed citations
8.
Cao, Minh Duc, Son Hoang Nguyen, Devika Ganesamoorthy, et al.. (2017). Scaffolding and completing genome assemblies in real-time with nanopore sequencing. Nature Communications. 8(1). 14515–14515. 76 indexed citations
9.
Cao, Minh Duc, Devika Ganesamoorthy, Alysha G. Elliott, et al.. (2016). Streaming algorithms for identification pathogens and antibiotic resistance potential from real-time MinION™ sequencing. GigaScience. 5(1). 32–32. 63 indexed citations
10.
Chen, Wenhan, Alan J. Robertson, Devika Ganesamoorthy, & Lachlan Coin. (2016). sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors. Nucleic Acids Research. 45(5). e34–e34. 4 indexed citations
11.
Nguyen, Son Hoang, Minh Duc Cao, Devika Ganesamoorthy, et al.. (2016). Scaffolding and completing genome assemblies in real-time using nanopore sequencing. Faculty of 1000 Research Ltd. 5. 1 indexed citations
12.
Cao, Minh Duc, Devika Ganesamoorthy, Alysha G. Elliott, et al.. (2015). Real-time identification of pathogens and antibiotic resistance using Oxford Nanopore MinION sequencing. Faculty of 1000 Research Ltd. 4. 1 indexed citations
13.
Chandrananda, Dineika, Natalie Thorne, Devika Ganesamoorthy, et al.. (2014). Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery. PLoS ONE. 9(1). e86993–e86993. 21 indexed citations
14.
Walker, Susan, et al.. (2014). High‐resolution microarray in the assessment of fetal anomalies detected by ultrasound. Australian and New Zealand Journal of Obstetrics and Gynaecology. 54(1). 46–52. 13 indexed citations
15.
Grati, Francesca Romana, D. Molina Gomes, Devika Ganesamoorthy, et al.. (2012). Application of a new molecular technique for the genetic evaluation of products of conception. Prenatal Diagnosis. 33(1). 32–41. 15 indexed citations
16.
Tan, Tiong Yang, Amanda Collins, Paul A. James, et al.. (2011). Phenotypic variability of distal 22q11.2 copy number abnormalities. American Journal of Medical Genetics Part A. 155(7). 1623–1633. 54 indexed citations
17.
Bruno, Damien L., Stuart White, Devika Ganesamoorthy, et al.. (2011). Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping. Journal of Medical Genetics. 48(12). 831–839. 64 indexed citations
18.
Bruno, Damien L., Zornitza Stark, David J. Amor, et al.. (2011). Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high-resolution SNP microarrays. Human Mutation. 32(12). 1500–1506. 32 indexed citations
19.
Traylor, Ryan N., Damien L. Bruno, Trent Burgess, et al.. (2010). A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33. PLoS ONE. 5(8). e12462–e12462. 21 indexed citations
20.
Godler, David E., Flora Tassone, Danuta Z. Loesch, et al.. (2010). Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio. Human Molecular Genetics. 19(8). 1618–1632. 85 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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