Devika Ganesamoorthy
Impact in
- Molecular Medicine top 5%
- Antibiotic Resistance in Bacteria
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
-
- Genomics and Phylogenetic Studies 9
- Congenital heart defects research 3
- Genetics 13
- Genomic variations and chromosomal abnormalities 10
- Genomics and Rare Diseases 3
- Co-authors
- Lachlan Coin (14 shared papers)Minh Duc Cao (11 shared papers)Matthew A. Cooper (8 shared papers)Alysha G. Elliott (6 shared papers)Howard R. Slater (9 shared papers)Damien L. Bruno (7 shared papers)Trent Burgess (5 shared papers)Son Hoang Nguyen (3 shared papers)
- Journals
- Bioinformatics (2 papers)Clinical Chemistry (2 papers)PLoS ONE (2 papers)Human Molecular Genetics (1 paper)Nature Communications (1 paper)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Devika Ganesamoorthy
25 papers receiving 684 citations
Peers
Comparison fields: 5 of 86
- Molecular Medicine 112
- Genetics 323
- Clinical Biochemistry 51
- Pediatrics, Perinatology and Child Health 114
- Molecular Biology 390
Countries citing papers authored by Devika Ganesamoorthy
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
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-authors
The 25 scholars most cited alongside Devika Ganesamoorthy, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 85 | |
| 2 | 2017 | 76 | |
| 3 | 2011 | 64 | |
| 4 | 2016 | 63 | |
| 5 | 2018 | 54 | |
| 6 | 2011 | 54 | |
| 7 | 2016 | 34 | |
| 8 | 2009 | 33 | |
| 9 | 2011 | 32 | |
| 10 | 2018 | 31 | |
| 11 | 2013 | 29 | |
| 12 | 2014 | 21 | |
| 13 | 2010 | 21 | |
| 14 | 2022 | 18 | |
| 15 | 2014 | 18 | |
| 16 | 2015 | 18 | |
| 17 | 2012 | 15 | |
| 18 | 2018 | 14 | |
| 19 | 2014 | 13 | |
| 20 | 2017 | 9 |
About Devika Ganesamoorthy
Devika Ganesamoorthy is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Molecular Medicine and Cancer Research, having authored 25 papers that have together received 719 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Phylogenetic Studies (9 papers), Prenatal Screening and Diagnostics (6 papers), Fetal and Pediatric Neurological Disorders (4 papers), Antibiotic Resistance in Bacteria (3 papers), Cancer Genomics and Diagnostics (3 papers), Congenital heart defects research (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Molecular Medicine (112 citations), Genetics (323 citations), Clinical Biochemistry (51 citations), Pediatrics, Perinatology and Child Health (114 citations) and Molecular Biology (390 citations). Devika Ganesamoorthy has collaborated with scholars based in Australia, United Kingdom and United States. Frequent 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. Their work appears in journals such as Bioinformatics, Clinical Chemistry, PLoS ONE, Human Molecular Genetics and Nature Communications.
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.