Ronny Derks

1.2k total citations
15 papers, 326 citations indexed

About

Ronny Derks is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Ronny Derks has authored 15 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Ronny Derks's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Retinal Development and Disorders (3 papers). Ronny Derks is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Retinal Development and Disorders (3 papers). Ronny Derks collaborates with scholars based in Netherlands, United States and Germany. Ronny Derks's co-authors include Lisenka E.L.M. Vissers, Christian Gilissen, Han G. Brunner, Lies H. Hoefsloot, Marcel Nelen, Kornelia Neveling, William Reardon, Charu Deshpande, Michael A. Simpson and Ernie M.H.F. Bongers and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Clinical Chemistry.

In The Last Decade

Ronny Derks

14 papers receiving 323 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ronny Derks Netherlands	10	221	130	40	35	33	15	326
Pietro Sirleto Italy	12	221 1.0×	137 1.1×	31 0.8×	31 0.9×	13 0.4×	25	399
Anthony Raizis New Zealand	9	434 2.0×	136 1.0×	53 1.3×	67 1.9×	50 1.5×	18	550
Filippo Beleggia Germany	12	243 1.1×	111 0.9×	38 0.9×	33 0.9×	13 0.4×	16	382
Gökhan Yigit Germany	11	207 0.9×	132 1.0×	25 0.6×	65 1.9×	57 1.7×	24	355
Ola Khalifa Saudi Arabia	9	146 0.7×	80 0.6×	16 0.4×	16 0.5×	14 0.4×	18	255
Simon A. Ramsbottom United Kingdom	13	360 1.6×	209 1.6×	22 0.6×	23 0.7×	21 0.6×	16	432
Nicholas Stong United States	11	330 1.5×	95 0.7×	34 0.8×	9 0.3×	17 0.5×	28	471
Elodie Sanchez France	9	159 0.7×	95 0.7×	21 0.5×	16 0.5×	6 0.2×	15	272
T. Holm United States	10	175 0.8×	158 1.2×	43 1.1×	37 1.1×	29 0.9×	23	382
Natália D. Linhares Brazil	10	168 0.8×	102 0.8×	16 0.4×	27 0.8×	34 1.0×	21	350

Countries citing papers authored by Ronny Derks

Since Specialization

Citations

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

Fields of papers citing papers by Ronny Derks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ronny Derks

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Bruijn, Suzanne E. de, L. Ingeborgh van den Born, Ronny Derks, et al.. (2025). Long-read technologies identify a hidden LINE-1/ERV1 insertion in IQCB1 as causative variant for Senior-Løken syndrome. npj Genomic Medicine. 10(1). 33–33.

Höps, Wolfram, Marjan M. Weiss, Ronny Derks, et al.. (2025). HiFi long-read genomes for difficult-to-detect, clinically relevant variants. The American Journal of Human Genetics. 112(2). 450–456. 6 indexed citations

Westra, Dineke, Eddy N. de Boer, Tom Hofste, et al.. (2024). Future of Dutch NGS-Based Newborn Screening: Exploring the Technical Possibilities and Assessment of a Variant Classification Strategy. International Journal of Neonatal Screening. 10(1). 20–20. 6 indexed citations

Kwint, Michael, Ronny Derks, Aaron M. Wenger, et al.. (2023). Comprehensive de novo mutation discovery with HiFi long-read sequencing. Genome Medicine. 15(1). 34–34. 18 indexed citations

Schieving, Jolanda, Helger G. Yntema, Maartje Pennings, et al.. (2022). Reanalysis of exome negative patients with rare disease: a pragmatic workflow for diagnostic applications. Genome Medicine. 14(1). 66–66. 25 indexed citations

Haer‐Wigman, Lonneke, Maria M. van Genderen, Hester Y. Kroes, et al.. (2022). Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA. npj Genomic Medicine. 7(1). 65–65. 7 indexed citations

Neveling, Kornelia, Tuomo Mantere, Ronny Derks, et al.. (2021). Long-read technologies identify a hidden inverted duplication in a family with choroideremia. SHILAP Revista de lepidopterología. 2(4). 100046–100046. 13 indexed citations

Pauper, Marc, Aaron M. Wenger, Shreyasee Chakraborty, et al.. (2021). Correction: Long-read trio sequencing of individuals with unsolved intellectual disability. European Journal of Human Genetics. 29(4). 720–720. 5 indexed citations

Pauper, Marc, Aaron M. Wenger, Shreyasee Chakraborty, et al.. (2020). Long-read trio sequencing of individuals with unsolved intellectual disability. European Journal of Human Genetics. 29(4). 637–648. 24 indexed citations

10.

Khan, Mubeen, Stéphanie S. Cornelis, Muhammad Imran Khan, et al.. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human Mutation. 40(10). 1749–1759. 37 indexed citations

11.

Voer, Richarda M. de, Robbert D.A. Weren, Arjen R. Mensenkamp, et al.. (2016). Identification of Novel Candidate Genes for Early-Onset Colorectal Cancer Susceptibility. PLoS Genetics. 12(2). e1005880–e1005880. 44 indexed citations

12.

Bosgoed, Ermanno, Bart van Lier, Erik‐Jan Kamsteeg, et al.. (2014). Translating Sanger-Based Routine DNA Diagnostics into Generic Massive Parallel Ion Semiconductor Sequencing. Clinical Chemistry. 61(1). 154–162. 22 indexed citations

13.

Corsten‐Janssen, Nicole, Sulagna C. Saitta, Lies H. Hoefsloot, et al.. (2013). More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated. Molecular Syndromology. 4(5). 235–245. 36 indexed citations

14.

Overheul, Gijs J., et al.. (2012). Gene duplication and conversion events shaped three homologous, differentially expressed myosin regulatory light chain (MLC2) genes. European Journal of Cell Biology. 91(8). 629–639. 11 indexed citations

15.

Simpson, Michael A., Charu Deshpande, Dimitra Dafou, et al.. (2012). De Novo Mutations of the Gene Encoding the Histone Acetyltransferase KAT6B Cause Genitopatellar Syndrome. The American Journal of Human Genetics. 90(2). 290–294. 72 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.

Explore authors with similar magnitude of impact