C. S. Paththinige
Impact in
-
- Williams Syndrome Research
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Hemoglobinopathies and Related Disorders
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
-
- Down syndrome and intellectual disability research 1
- Innovations in Medical Education 1
- Co-authors
- Vajira H. W. Dissanayake (9 shared papers)Nirmala D. Sirisena (7 shared papers)Rezvi Sheriff (1 shared paper)Priyadarshani Galappatthy (1 shared paper)Fabienne Escande (1 shared paper)Sylvie Manouvrier‐Hanu (1 shared paper)Kai Ping Sem (1 shared paper)Roshni Rebecca Singaraja (1 shared paper)
- Journals
- Lipids in Health and Disease (2 papers)Annual Review of Genomics and Human Genetics (1 paper)BMC Pediatrics (1 paper)BMC Neurology (1 paper)BMC Medical Genomics (1 paper)
- Partner nations
- Sri LankaUnited StatesNigeria
In The Last Decade
C. S. Paththinige
17 papers receiving 533 citations
Peers
Comparison fields: 5 of 70
- Developmental Neuroscience 28
- Genetics 220
- Health Informatics 18
- Genetics 54
- Developmental Biology 12
Countries citing papers authored by C. S. Paththinige
This map shows the geographic impact of C. S. Paththinige'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 C. S. Paththinige with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C. S. Paththinige more than expected).
Fields of papers citing papers by C. S. Paththinige
This network shows the impact of papers produced by C. S. Paththinige. 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 C. S. Paththinige. The network helps show where C. S. Paththinige may publish in the future.
Co-authors
The 18 scholars most cited alongside C. S. Paththinige, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 118 | |
| 2 | 2017 | 97 | |
| 3 | 2016 | 72 | |
| 4 | 2017 | 71 | |
| 5 | 2018 | 64 | |
| 6 | 2018 | 56 | |
| 7 | 2019 | 21 | |
| 8 | 2017 | 18 | |
| 9 | 2018 | 15 | |
| 10 | 2019 | 10 | |
| 11 | 2018 | 8 | |
| 12 | 2019 | 7 | |
| 13 | 2018 | 6 | |
| 14 | 2016 | 3 | |
| 15 | 2019 | 2 | |
| 16 | 2021 | 1 | |
| 17 | 2023 | 1 |
About C. S. Paththinige
C. S. Paththinige is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Developmental Biology, Developmental Neuroscience and Physical Therapy, Sports Therapy and Rehabilitation, having authored 17 papers that have together received 570 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Lipoproteins and Cardiovascular Health (2 papers), Down syndrome and intellectual disability research (1 paper), Muscle Physiology and Disorders (1 paper), Protein Tyrosine Phosphatases (1 paper), Congenital limb and hand anomalies (1 paper), Innovations in Medical Education (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Developmental Neuroscience (28 citations), Genetics (220 citations), Health Informatics (18 citations), Genetics (54 citations) and Developmental Biology (12 citations). C. S. Paththinige has collaborated with scholars based in Sri Lanka, United States and Nigeria. Frequent co-authors include Vajira H. W. Dissanayake, Nirmala D. Sirisena, Rezvi Sheriff, Priyadarshani Galappatthy, Fabienne Escande, Sylvie Manouvrier‐Hanu, Kai Ping Sem, Roshni Rebecca Singaraja, Florence Petit and GR Constantine. Their work appears in journals such as Lipids in Health and Disease, Annual Review of Genomics and Human Genetics, BMC Pediatrics, BMC Neurology and BMC Medical Genomics.
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.