Konstantinos Nikopoulos

1.5k total citations
20 papers, 802 citations indexed

About

Konstantinos Nikopoulos is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Konstantinos Nikopoulos has authored 20 papers receiving a total of 802 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 6 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Konstantinos Nikopoulos's work include Retinal Development and Disorders (6 papers), Ocular Disorders and Treatments (4 papers) and Retinal and Macular Surgery (4 papers). Konstantinos Nikopoulos is often cited by papers focused on Retinal Development and Disorders (6 papers), Ocular Disorders and Treatments (4 papers) and Retinal and Macular Surgery (4 papers). Konstantinos Nikopoulos collaborates with scholars based in Switzerland, Netherlands and Greece. Konstantinos Nikopoulos's co-authors include Frans P.M. Cremers, Arijit Mukhopadhyay, Lies H. Hoefsloot, Carmen Ayuso, Ilse J. de Wijs, F. Nienke Boonstra, M. A. D. Tilanus, Rob W.J. Collin, Carlo Rivolta and Hans Scheffer and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Konstantinos Nikopoulos

20 papers receiving 780 citations

Peers

Konstantinos Nikopoulos

MB

GENET

OPHTH

PS

RNMI

V. Ventruto Italy

Nizar Smaoui United States

William Bromley United States

Kinga M. Bujakowska United States

Arif O. Khan Saudi Arabia

Franziska Krämer Germany

Gail Billingsley Canada

Neil G. Della Australia

Anneke I. den Hollander Netherlands

V. Ventruto Italy

Konstantinos Nikopoulos

479 ×0.8

MB

288 ×1.3

GENET

54 ×0.4

OPHTH

38 ×0.3

PS

52 ×0.4

RNMI

Citations per year, relative to Konstantinos Nikopoulos Konstantinos Nikopoulos (= 1×) peers V. Ventruto

Countries citing papers authored by Konstantinos Nikopoulos

Since Specialization

Citations

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

Fields of papers citing papers by Konstantinos Nikopoulos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konstantinos Nikopoulos

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

All Works

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20 of 20 papers shown

1.

Patzke, Sebastian, Pernille Martens, Mathieu Quinodoz, et al.. (2021). CEP78 functions downstream of CEP350 to control biogenesis of primary cilia by negatively regulating CP110 levels. eLife. 10. 23 indexed citations

2.

Nikopoulos, Konstantinos, et al.. (2020). Management of Full-Thickness Macular Hole in A Genetically Confirmed Case with Usher Syndrome. Ophthalmology and Therapy. 9(3). 677–684. 4 indexed citations

3.

Peter, Virginie G., Konstantinos Nikopoulos, Mathieu Quinodoz, et al.. (2019). A novel missense variant in IDH3A causes autosomal recessive retinitis pigmentosa. Ophthalmic Genetics. 40(2). 177–181. 12 indexed citations

4.

Verbakel, Sanne K., Ramon A. C. van Huet, Anneke I. den Hollander, et al.. (2019). Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in theRP1Gene: Extending theRP1Disease Spectrum. Investigative Ophthalmology & Visual Science. 60(4). 1192–1192. 25 indexed citations

5.

Nikopoulos, Konstantinos, Pietro Farinelli, Béryl Royer‐Bertrand, et al.. (2016). Whole exome sequencing reveals CEP78 as a novel disease gene for cone-rod dystrophy. Investigative Ophthalmology & Visual Science. 57(12). 1 indexed citations

6.

Nikopoulos, Konstantinos, Almudena Ávila‐Fernández, Marta Cortón, et al.. (2015). Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy. Scientific Reports. 5(1). 13902–13902. 23 indexed citations

7.

Saqib, Muhammad Arif Nadeem, Konstantinos Nikopoulos, Ehsan Ullah, et al.. (2015). Homozygosity mapping reveals novel and known mutations in Pakistani families with inherited retinal dystrophies. Scientific Reports. 5(1). 9965–9965. 26 indexed citations

8.

Nikopoulos, Konstantinos, Almudena Ávila‐Fernández, Marta Cortón, et al.. (2015). Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy. edoc (University of Basel). 56(7). 1098–1098. 1 indexed citations

9.

Saqib, Muhammad Arif Nadeem, Ehsan Ullah, Falak Sher Khan, et al.. (2014). Homozygosity Mapping and Disease Genes Screening in Pakistani Families with Inherited Retinal Dystrophies. Investigative Ophthalmology & Visual Science. 55(13). 3292–3292. 1 indexed citations

10.

Cortón, Marta, Koji M. Nishiguchi, Almudena Ávila‐Fernández, et al.. (2013). Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis. PLoS ONE. 8(6). e65574–e65574. 62 indexed citations

11.

Vasiliadis, Konstantinos, et al.. (2013). Acute Pancreatitis as the Initial Manifestation of an Adenocarcinoma of the Major Duodenal Papilla in a Patient with Familial Adenomatous Polyposis Syndrome. Acta chirurgica Belgica. 113(6). 463–467. 3 indexed citations

12.

Nikopoulos, Konstantinos, Isabelle Schrauwen, Marleen Simon, et al.. (2011). Autosomal Recessive Stickler Syndrome in Two Families Is Caused by Mutations in theCOL9A1Gene. Investigative Ophthalmology & Visual Science. 52(7). 4774–4774. 37 indexed citations

13.

Nikopoulos, Konstantinos, Christian Gilissen, Alexander Hoischen, et al.. (2010). Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy. The American Journal of Human Genetics. 86(2). 240–247. 168 indexed citations

14.

Nikopoulos, Konstantinos, Hanka Venselaar, Rob W.J. Collin, et al.. (2010). Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP. Human Mutation. 31(6). 656–666. 121 indexed citations

15.

Boonstra, F. Nienke, C. E. van Nouhuys, J. Schuil, et al.. (2009). Clinical and Molecular Evaluation of Probands and Family Members with Familial Exudative Vitreoretinopathy. Investigative Ophthalmology & Visual Science. 50(9). 4379–4379. 64 indexed citations

16.

Hurk, José A. J. M. van den, Iwan C. Meij, Hiroki Kano, et al.. (2007). L1 retrotransposition can occur early in human embryonic development. Human Molecular Genetics. 16(13). 1587–1592. 148 indexed citations

17.

Dionyssopoulos, Alexander, et al.. (2006). T- and B-Cutaneous Pseudolymphomas Treated by Surgical Excision and Immediate Reconstruction. Dermatologic Surgery. 32(12). 1526–1529. 7 indexed citations

18.

Mukhopadhyay, Arijit, Konstantinos Nikopoulos, Alessandra Maugeri, et al.. (2006). Erosive Vitreoretinopathy and Wagner Disease Are Caused by Intronic Mutations inCSPG2/VersicanThat Result in an Imbalance of Splice Variants. Investigative Ophthalmology & Visual Science. 47(8). 3565–3565. 61 indexed citations

19.

Dionyssopoulos, Alexander, et al.. (2006). T- and B-Cutaneous Pseudolymphomas Treated by Surgical Excision and Immediate Reconstruction. Dermatologic Surgery. 32(12). 1526–1529. 6 indexed citations

20.

Griveas, Ioannis, et al.. (2004). Lymphocytes Subsets in the Course of Continuous Ambulatory Peritoneal Dialysis (CAPD). Renal Failure. 26(6). 641–646. 9 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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