Dinu Antony

4.3k total citations
12 papers, 258 citations indexed

About

Dinu Antony is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Dinu Antony has authored 12 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Dinu Antony's work include Genetic and Kidney Cyst Diseases (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Associations and Epidemiology (2 papers). Dinu Antony is often cited by papers focused on Genetic and Kidney Cyst Diseases (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Associations and Epidemiology (2 papers). Dinu Antony collaborates with scholars based in Kuwait, Netherlands and Germany. Dinu Antony's co-authors include Miriam Schmidts, Osama Alsmadi, Alexandros Onoufriadis, Gerard Pals, Amelia Shoemark, Hannah M. Mitchison, Stavroula Petridi, Johannes M. A. Daniels, Eric G. Haarman and Dimitra Micha and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Dinu Antony

12 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dinu Antony Kuwait 7 155 111 81 31 26 12 258
Rocío Mena Spain 7 75 0.5× 65 0.6× 48 0.6× 8 0.3× 32 1.2× 16 182
Juan Alberto Piñero‐Fernández Spain 7 125 0.8× 132 1.2× 22 0.3× 9 0.3× 36 1.4× 13 271
Lindsay R. Stolzenburg United States 8 45 0.3× 190 1.7× 78 1.0× 14 0.5× 7 0.3× 10 324
Hotaka Kamasaki Japan 9 59 0.4× 162 1.5× 29 0.4× 11 0.4× 10 0.4× 24 282
Keiichi Hara Japan 13 56 0.4× 146 1.3× 56 0.7× 4 0.1× 39 1.5× 37 349
Simone Salemink Netherlands 5 97 0.6× 42 0.4× 75 0.9× 29 0.9× 6 0.2× 5 171
Fernanda Caroline Soardi Brazil 13 171 1.1× 324 2.9× 13 0.2× 14 0.5× 27 1.0× 28 421
Victoria Arthur United States 4 43 0.3× 62 0.6× 109 1.3× 8 0.3× 6 0.2× 8 201
Vincenzo Rocco Italy 8 36 0.2× 229 2.1× 15 0.2× 24 0.8× 8 0.3× 24 338
Verena Wagner Germany 6 26 0.2× 70 0.6× 45 0.6× 10 0.3× 6 0.2× 12 199

Countries citing papers authored by Dinu Antony

Since Specialization
Citations

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

Fields of papers citing papers by Dinu Antony

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dinu Antony

This figure shows the co-authorship network connecting the top 25 collaborators of Dinu Antony. A scholar is included among the top collaborators of Dinu Antony 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 Dinu Antony. Dinu Antony 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
1.
Hebbar, Prashantha, Rasheeba Nizam, Sumi Elsa John, et al.. (2023). Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families. Scientific Reports. 13(1). 14978–14978. 4 indexed citations
2.
Antony, Dinu, Elif Yılmaz Güleç, Alper Gezdirici, et al.. (2022). Spectrum of Genetic Variants in a Cohort of 37 Laterality Defect Cases. Frontiers in Genetics. 13. 861236–861236. 3 indexed citations
3.
Antony, Dinu, Han G. Brunner, & Miriam Schmidts. (2021). Ciliary Dyneins and Dynein Related Ciliopathies. Cells. 10(8). 1885–1885. 20 indexed citations
4.
Najafi, Maryam, Dor Mohammad Kordi-Tamandani, Zeineb Bakey, et al.. (2019). A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East. Frontiers in Pediatrics. 7. 89–89. 4 indexed citations
5.
Maroofian, Reza, Maryam Najafi, Zeineb Bakey, et al.. (2018). Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an NEU1 Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child. Kidney International Reports. 3(6). 1454–1463. 9 indexed citations
6.
John, Sumi Elsa, Dinu Antony, Muthukrishnan Eaaswarkhanth, et al.. (2018). Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics. Scientific Reports. 8(1). 20 indexed citations
7.
Antony, Dinu, Narayanan Nampoory, Chiara Bacchelli, et al.. (2017). Exome sequencing for the differential diagnosis of ciliary chondrodysplasias: Example of a WDR35 mutation case and review of the literature. European Journal of Medical Genetics. 60(12). 658–666. 10 indexed citations
8.
John, Sumi Elsa, Dinu Antony, Muthukrishnan Eaaswarkhanth, et al.. (2017). Genetic Variants Associated with Warfarin Dosage in Kuwaiti Population. Pharmacogenomics. 18(8). 757–764. 5 indexed citations
9.
Melhem, Motasem, Mohamed Abu‐Farha, Dinu Antony, et al.. (2016). Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia. European Journal Of Haematology. 98(3). 218–227. 15 indexed citations
10.
Bulbanat, Bassam, et al.. (2014). Sudden cardiac death diagnosed with dilated cardiomyopathy in a Kuwaiti family: a case report. BMC Research Notes. 7(1). 914–914. 1 indexed citations
11.
12.
Onoufriadis, Alexandros, Tamara Paff, Dinu Antony, et al.. (2012). Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 92(1). 88–98. 137 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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