Raymon Vijzelaar

1.8k total citations
29 papers, 652 citations indexed

About

Raymon Vijzelaar is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Raymon Vijzelaar has authored 29 papers receiving a total of 652 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Genetics and 7 papers in Epidemiology. Recurrent topics in Raymon Vijzelaar's work include Genomic variations and chromosomal abnormalities (8 papers), Biochemical and Molecular Research (4 papers) and Congenital heart defects research (3 papers). Raymon Vijzelaar is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Biochemical and Molecular Research (4 papers) and Congenital heart defects research (3 papers). Raymon Vijzelaar collaborates with scholars based in Netherlands, United States and United Kingdom. Raymon Vijzelaar's co-authors include Hanneke N. Monsuur, P. J. van Diest, Roel A. de Weger, Cathy B. Moelans, Jacob Vorstman, G R Jalali, Jaclyn A. Biegel, Tamim H. Shaikh, B S Emanuel and Suparna Martis and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Raymon Vijzelaar

29 papers receiving 642 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Raymon Vijzelaar Netherlands	13	389	193	138	88	81	29	652
Nadia Akawi United Arab Emirates	16	332 0.9×	159 0.8×	49 0.4×	34 0.4×	68 0.8×	41	637
Dijana Plaseska‐Karanfilska North Macedonia	14	311 0.8×	262 1.4×	38 0.3×	64 0.7×	55 0.7×	102	805
Caroline Clark United Kingdom	14	188 0.5×	106 0.5×	256 1.9×	60 0.7×	68 0.8×	30	668
Tianbo Jin China	15	301 0.8×	93 0.5×	77 0.6×	46 0.5×	30 0.4×	48	522
Amy L. Stark United States	14	237 0.6×	82 0.4×	86 0.6×	32 0.4×	23 0.3×	29	423
Jean‐Philippe Babeu Canada	11	304 0.8×	139 0.7×	152 1.1×	63 0.7×	217 2.7×	13	588
Cecilia G. Sánchez United States	15	440 1.1×	100 0.5×	63 0.5×	179 2.0×	40 0.5×	18	821
N. J. Philpott United Kingdom	10	339 0.9×	109 0.6×	119 0.9×	39 0.4×	18 0.2×	14	703
Vidalba Rocher-Ros United Kingdom	3	222 0.6×	54 0.3×	137 1.0×	54 0.6×	30 0.4×	4	674
Jiong Yang China	10	275 0.7×	58 0.3×	119 0.9×	146 1.7×	46 0.6×	20	674

Countries citing papers authored by Raymon Vijzelaar

Since Specialization

Citations

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

Fields of papers citing papers by Raymon Vijzelaar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raymon Vijzelaar

This figure shows the co-authorship network connecting the top 25 collaborators of Raymon Vijzelaar. A scholar is included among the top collaborators of Raymon Vijzelaar 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 Raymon Vijzelaar. Raymon Vijzelaar 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

Kuilenburg, André B. P., Angelique Sijben, Thijs H. Oude Munnink, et al.. (2024). Lethal Capecitabine Toxicity in Patients With Complete Dihydropyrimidine Dehydrogenase Deficiency Due to Ultra-Rare DPYD Variants. JCO Precision Oncology. 8(8). e2300599–e2300599. 1 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

Saarenheimo, Jatta, Natalja Eigėlienė, Gajja S. Salomons, et al.. (2021). Preemptive screening of DPYD as part of clinical practice: high prevalence of a novel exon 4 deletion in the Finnish population. Cancer Chemotherapy and Pharmacology. 87(5). 657–663. 12 indexed citations

Vijzelaar, Raymon, et al.. (2019). The frequency of SMN gene variants lacking exon 7 and 8 is highly population dependent. PLoS ONE. 14(7). e0220211–e0220211. 27 indexed citations

Vijzelaar, Raymon, Mariana Rodrigues Botton, Lisette Stolk, et al.. (2018). Multi-ethnic SULT1A1 cOpy Number Profiling with Multiplex Ligation-Dependent Probe Amplification. Pharmacogenomics. 19(9). 761–770. 8 indexed citations

Qiao, Wanqiong, Suparna Martis, Geetu Mendiratta, et al.. (2018). Integrated CYP2D6 Interrogation for Multiethnic Copy Number and Tandem Allele Detection. Pharmacogenomics. 20(1). 9–20. 10 indexed citations

Vijzelaar, Raymon, et al.. (2016). Rapid Detection of the Three Celiac Disease Risk Genotypes HLA-DQ2.2, HLA-DQ2.5, and HLA-DQ8 by Multiplex Ligation-Dependent Probe Amplification. Genetic Testing and Molecular Biomarkers. 20(3). 158–161. 2 indexed citations

Grossi, Serena, et al.. (2016). MLPA-based approach for initial and simultaneous detection of GBA deletions and recombinant alleles in patients affected by Gaucher Disease. Molecular Genetics and Metabolism. 119(4). 329–337. 4 indexed citations

Türkkahraman, Doğa, Tülay Güran, Hannah E Ivison, et al.. (2015). Identification of a Novel Large <b><i>CYP17A1 </i></b>Deletion by MLPA Analysis in a Family with Classic 17α-Hydroxylase Deficiency. Sexual Development. 9(2). 91–97. 11 indexed citations

10.

Idkowiak, Jan, Angela E. Taylor, Donna O’Neil, et al.. (2014). Steroid sulfatase contributes to systemic androgen activation in pre-pubertal boys: lessons from steroid sulfatase deficiency. Endocrine Abstracts. 1 indexed citations

11.

Vijzelaar, Raymon, Sarah Waller, Abdellatif Errami, et al.. (2013). Deletions within COL11A1in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA). BMC Medical Genetics. 14(1). 48–48. 18 indexed citations

12.

Avril, Stefanie, Michaela Aubele, Tibor Schuster, et al.. (2013). Somatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers. British Journal of Cancer. 109(9). 2347–2355. 10 indexed citations

13.

Martis, Suparna, Hao Mei, Raymon Vijzelaar, et al.. (2012). Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation. The Pharmacogenomics Journal. 13(6). 558–566. 43 indexed citations

14.

Spencer, Emily, Fady M. Mikhail, Chuanhua Fu, et al.. (2011). Identification of SPRED1 deletions using RT‐PCR, multiplex ligation‐dependent probe amplification and quantitative PCR. American Journal of Medical Genetics Part A. 155(6). 1352–1359. 11 indexed citations

15.

Mikhail, Fady M., et al.. (2010). Identification of PKHD1 Multiexon Deletions Using Multiplex Ligation-Dependent Probe Amplification and Quantitative Polymerase Chain Reaction. Genetic Testing and Molecular Biomarkers. 14(4). 505–510. 14 indexed citations

16.

Moelans, Cathy B., Roel A. de Weger, Hanneke N. Monsuur, Raymon Vijzelaar, & P. J. van Diest. (2010). Molecular profiling of invasive breast cancer by multiplex ligation-dependent probe amplification-based copy number analysis of tumor suppressor and oncogenes. Modern Pathology. 23(7). 1029–1039. 79 indexed citations

17.

Kuilenburg, André B. P., Judith Meijer, Adri N. Mul, et al.. (2009). Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3). Human Genetics. 125(5-6). 581–590. 39 indexed citations

18.

Desviat, Lourdes R., Rocío Sánchez-Alcudia, Belén Pérez, et al.. (2009). High frequency of large genomic deletions in the PCCA gene causing propionic acidemia. Molecular Genetics and Metabolism. 96(4). 171–176. 25 indexed citations

19.

Jalali, G R, Jacob Vorstman, Raymon Vijzelaar, et al.. (2007). Detailed analysis of 22q11.2 with a high density MLPA probe set. Human Mutation. 29(3). 433–440. 77 indexed citations

20.

Felbor, Ute, et al.. (2007). Large germline deletions and duplication in isolated cerebral cavernous malformation patients. Neurogenetics. 8(2). 149–153. 21 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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