Astrid S. Plomp

4.8k total citations
51 papers, 2.1k citations indexed

About

Astrid S. Plomp is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Astrid S. Plomp has authored 51 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 29 papers in Molecular Biology and 18 papers in Cell Biology. Recurrent topics in Astrid S. Plomp's work include Dermatological and Skeletal Disorders (15 papers), Skin and Cellular Biology Research (11 papers) and Retinal Development and Disorders (10 papers). Astrid S. Plomp is often cited by papers focused on Dermatological and Skeletal Disorders (15 papers), Skin and Cellular Biology Research (11 papers) and Retinal Development and Disorders (10 papers). Astrid S. Plomp collaborates with scholars based in Netherlands, Belgium and Switzerland. Astrid S. Plomp's co-authors include Arthur A. Bergen, Paulus T.V.M. de Jong, Frank Baas, S. van Soest, Xiao Hu, Ruud A. Wolterman, Theo J.M. Hulsebos, Pieter Wesseling, Els C. Robanus-Maandag and Jacoline B. ten Brink and has published in prestigious journals such as Nature Genetics, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Astrid S. Plomp

44 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Astrid S. Plomp Netherlands 23 1.2k 1.1k 573 313 264 51 2.1k
Jill Urquhart United Kingdom 23 519 0.4× 1.3k 1.2× 195 0.3× 203 0.6× 107 0.4× 48 1.9k
Ariana Kariminejad Iran 21 715 0.6× 756 0.7× 284 0.5× 127 0.4× 75 0.3× 100 1.5k
Mary Shago Canada 21 613 0.5× 1.4k 1.2× 233 0.4× 112 0.4× 175 0.7× 57 2.3k
Eissa Faqeih Saudi Arabia 28 920 0.8× 1.5k 1.3× 238 0.4× 181 0.6× 57 0.2× 80 2.2k
Sigrid Swagemakers Netherlands 26 299 0.3× 1.9k 1.7× 160 0.3× 71 0.2× 136 0.5× 61 2.6k
Nursel Elçioğlu Türkiye 19 1.3k 1.1× 1.2k 1.1× 195 0.3× 145 0.5× 110 0.4× 70 2.0k
Jeffrey A. Spencer United States 14 305 0.3× 1.1k 1.0× 213 0.4× 125 0.4× 60 0.2× 15 1.6k
Arif O. Khan Saudi Arabia 24 610 0.5× 845 0.8× 145 0.3× 56 0.2× 165 0.6× 131 1.8k
Hanan E. Shamseldin Saudi Arabia 24 590 0.5× 981 0.9× 182 0.3× 46 0.1× 68 0.3× 55 1.5k
Pierre Bitoun France 17 818 0.7× 1.4k 1.2× 123 0.2× 73 0.2× 44 0.2× 39 1.9k

Countries citing papers authored by Astrid S. Plomp

Since Specialization
Citations

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

Fields of papers citing papers by Astrid S. Plomp

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Astrid S. Plomp. 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 Astrid S. Plomp. The network helps show where Astrid S. Plomp may publish in the future.

Co-authorship network of co-authors of Astrid S. Plomp

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

All Works

20 of 20 papers shown
1.
Schooneveld, Mary J. van, Roselie M.H. Diederen, Astrid S. Plomp, et al.. (2025). Pseudocolobomatous autosomal dominant atrophic maculopathy (PADAM). Ophthalmic Genetics. 46(5). 468–473.
2.
Haverkamp, Margje H., Jeannette Ossewaarde‐van Norel, Remko van Leeuwen, et al.. (2025). Pseudoxanthoma Elasticum: The Diagnostic Accuracy of Genetic Testing Compared with Clinical Criteria in a Large Cohort. Journal of Investigative Dermatology. 145(12). 3217–3219.e6. 1 indexed citations
3.
Fernández‐Quintero, Monica L., Marta Campiglio, Petronel Tuluc, et al.. (2025). Two pairs of CACNA1I (CaV3.3) variants with opposite effects on channel function cause neurodevelopmental disorders of varying severity. PLoS Genetics. 21(8). e1011828–e1011828.
4.
Born, L. Ingeborgh van den, Carel B. Hoyng, Jan Willem R. Pott, et al.. (2024). Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium. Investigative Ophthalmology & Visual Science. 65(10). 40–40.
5.
Plomp, Astrid S., Ronald J. A. Wanders, Carel B. Hoyng, et al.. (2024). Syndromic retinitis pigmentosa. Progress in Retinal and Eye Research. 107. 101324–101324. 7 indexed citations
6.
Haer‐Wigman, Lonneke, Ralph J. Florijn, Ronald van Beek, et al.. (2024). Utilization of automated cilia analysis to characterize novel INPP5E variants in patients with non-syndromic retinitis pigmentosa. European Journal of Human Genetics. 32(11). 1412–1418. 1 indexed citations
7.
Plomp, Astrid S., et al.. (2023). Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies. International Journal of Molecular Sciences. 24(8). 7481–7481. 57 indexed citations
8.
Tacke, Carline E., Suzanne W. J. Terheggen-Lagro, Annemieke M. Boot, et al.. (2021). Chondrodysplasia, enchondromas and a chest deformity causing severe pulmonary morbidity in a boy with a PTHLH duplication: A case report. Bone Reports. 14. 101067–101067. 1 indexed citations
9.
Runhart, Esmee H., Riccardo Sangermano, Stéphanie S. Cornelis, et al.. (2018). The CommonABCA4Variant p.Asn1868Ile Shows Nonpenetrance and Variable Expression of Stargardt Disease When Present intransWith Severe Variants. Investigative Ophthalmology & Visual Science. 59(8). 3220–3220. 65 indexed citations
10.
Chatzispyrou, Iliana A., Mariëlle Alders, Sergio Guerrero‐Castillo, et al.. (2017). A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome. Human Molecular Genetics. 26(13). 2541–2550. 56 indexed citations
11.
Mathijssen, Inge B., Ralph J. Florijn, L. Ingeborgh van den Born, et al.. (2016). LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS. Retina. 37(1). 161–172. 38 indexed citations
12.
Rijsingen, Ingrid A.W. van, Astrid S. Plomp, A. H. Zwinderman, et al.. (2013). A novel lamin A/C mutation in a Dutch family with premature atherosclerosis. Atherosclerosis. 229(1). 169–173. 6 indexed citations
13.
Dijk, Fleur S. van, Ariana Kariminejad, Carlo Marcelis, et al.. (2010). Complete COL1A1 allele deletions in osteogenesis imperfecta. Genetics in Medicine. 12(11). 736–741. 33 indexed citations
14.
Hulsebos, Theo J.M., Astrid S. Plomp, Ruud A. Wolterman, et al.. (2007). Germline Mutation of INI1/SMARCB1 in Familial Schwannomatosis. The American Journal of Human Genetics. 80(4). 805–810. 252 indexed citations
15.
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
16.
Hu, Xiao, Astrid S. Plomp, Theo G. M. F. Gorgels, et al.. (2004). Efficient Molecular Diagnostic Strategy for ABCC6 in Pseudoxanthoma Elasticum. Genetic Testing. 8(3). 292–300. 19 indexed citations
17.
Plomp, Astrid S., Xiao Hu, Paulus T.V.M. de Jong, & Arthur A. Bergen. (2003). Does autosomal dominant pseudoxanthoma elasticum exist?. American Journal of Medical Genetics Part A. 126A(4). 403–412. 43 indexed citations
18.
Hu, Xiao, Astrid S. Plomp, Jan Wijnholds, et al.. (2003). ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum. European Journal of Human Genetics. 11(3). 215–224. 43 indexed citations
19.
Lagendijk, Jaap H., et al.. (2002). Pseudoxanthoma elasticum, niet alleen een cosmetisch probleem. Data Archiving and Networked Services (DANS). 12.
20.
Plomp, Astrid S., M Baraitser, Sarah F. Slaney, & Robin M. Winter. (2000). Severe microcephaly, choreiform movements, cataracts and sensorineural deafness in two patients. Clinical Dysmorphology. 9(1). 11–14. 1 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

Breakdown of academic impact, for papers by Jill Urquhart Breakdown of academic impact, for papers by Ariana Kariminejad Breakdown of academic impact, for papers by Mary Shago Breakdown of academic impact, for papers by Eissa Faqeih Breakdown of academic impact, for papers by Sigrid Swagemakers Breakdown of academic impact, for papers by Nursel Elçioğlu Breakdown of academic impact, for papers by Jeffrey A. Spencer Breakdown of academic impact, for papers by Arif O. Khan Breakdown of academic impact, for papers by Hanan E. Shamseldin Breakdown of academic impact, for papers by Pierre Bitoun
Rankless by CCL
2026