C. S. Paththinige

749 total citations
12 papers, 198 citations indexed

About

C. S. Paththinige is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, C. S. Paththinige has authored 12 papers receiving a total of 198 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pediatrics, Perinatology and Child Health, 5 papers in Genetics and 4 papers in Surgery. Recurrent topics in C. S. Paththinige's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (2 papers). C. S. Paththinige is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (2 papers). C. S. Paththinige collaborates with scholars based in Sri Lanka, United States and Singapore. C. S. Paththinige's co-authors include Vajira H. W. Dissanayake, Nirmala D. Sirisena, Priyadarshani Galappatthy, Rezvi Sheriff, GR Constantine, Rohan W. Jayasekara, Roshni R. Singaraja, Florence Petit, Sylvie Manouvrier and Maximilian Muenke and has published in prestigious journals such as SHILAP Revista de lepidopterología, BioMed Research International and Annual Review of Genomics and Human Genetics.

In The Last Decade

C. S. Paththinige

11 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
C. S. Paththinige Sri Lanka 7 53 50 44 44 42 12 198
Sylwia Szymańska Poland 9 70 1.3× 88 1.8× 6 0.1× 16 0.4× 49 1.2× 40 262
Kyoko Ban Japan 8 57 1.1× 23 0.5× 17 0.4× 30 0.7× 61 1.5× 19 191
Ruken Yıldırım Türkiye 9 26 0.5× 68 1.4× 9 0.2× 15 0.3× 98 2.3× 29 197
Sarah M. Nordstrom United States 6 24 0.5× 23 0.5× 12 0.3× 11 0.3× 79 1.9× 11 282
Namiko Kobayashi Japan 8 36 0.7× 22 0.4× 8 0.2× 15 0.3× 74 1.8× 14 228
Mesut Öktem Türkiye 12 37 0.7× 98 2.0× 19 0.4× 72 1.6× 41 1.0× 33 589
Giuseppina Casu Italy 8 16 0.3× 192 3.8× 7 0.2× 38 0.9× 96 2.3× 13 325
Jyrki Taurio Finland 5 37 0.7× 27 0.5× 36 0.8× 3 0.1× 18 0.4× 9 174
Jeanne E. O’Brien United States 10 24 0.5× 142 2.8× 10 0.2× 70 1.6× 44 1.0× 26 332

Countries citing papers authored by C. S. Paththinige

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of C. S. Paththinige

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

All Works

12 of 12 papers shown
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Sirisena, Nirmala D., Osório Lopes Abath Neto, A. Reghan Foley, et al.. (2021). A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report. BMC Neurology. 21(1). 105–105. 1 indexed citations
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Paththinige, C. S., Nirmala D. Sirisena, Fabienne Escande, et al.. (2019). Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature. BMC Medical Genetics. 20(1). 108–108. 8 indexed citations
5.
Paththinige, C. S., et al.. (2019). The Frequency and Spectrum of Chromosomal Translocations in a Cohort of Sri Lankans. BioMed Research International. 2019. 1–11. 7 indexed citations
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Paththinige, C. S., et al.. (2018). Spectrum of low-density lipoprotein receptor (LDLR) mutations in a cohort of Sri Lankan patients with familial hypercholesterolemia – a preliminary report. Lipids in Health and Disease. 17(1). 100–100. 14 indexed citations
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Paththinige, C. S., et al.. (2018). Population Screening for Hemoglobinopathies. Annual Review of Genomics and Human Genetics. 19(1). 355–380. 53 indexed citations
10.
Paththinige, C. S., Nirmala D. Sirisena, & Vajira H. W. Dissanayake. (2017). Genetic determinants of inherited susceptibility to hypercholesterolemia – a comprehensive literature review. Lipids in Health and Disease. 16(1). 103–103. 81 indexed citations
11.
Galappatthy, Priyadarshani, et al.. (2017). Pregnancy outcomes and contraceptive use in patients with systemic lupus Erythematosus, rheumatoid arthritis and women without a chronic illness: a comparative study. International Journal of Rheumatic Diseases. 20(6). 746–754. 16 indexed citations
12.
Paththinige, C. S., et al.. (2016). Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature. SHILAP Revista de lepidopterología. 2016. 1–7. 3 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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