Merel A.W. Oortveld

1.3k total citations
10 papers, 769 citations indexed

About

Merel A.W. Oortveld is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Merel A.W. Oortveld has authored 10 papers receiving a total of 769 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Immunology. Recurrent topics in Merel A.W. Oortveld's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Chromatin Dynamics (3 papers) and Chromosomal and Genetic Variations (2 papers). Merel A.W. Oortveld is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Chromatin Dynamics (3 papers) and Chromosomal and Genetic Variations (2 papers). Merel A.W. Oortveld collaborates with scholars based in Netherlands, Germany and United Kingdom. Merel A.W. Oortveld's co-authors include Annette Schenck, Christiane Zweier, Eiko K. de Jong, Bonnie Nijhof, Jamie M. Kramer, Markus Zweier, Arif B. Ekici, André Reis, Emilia K. Bijlsma and Lilian Bomme Ousager and has published in prestigious journals such as The FASEB Journal, Neuroscience & Biobehavioral Reviews and PLoS Biology.

In The Last Decade

Merel A.W. Oortveld

10 papers receiving 761 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Merel A.W. Oortveld Netherlands	9	458	427	148	118	65	10	769
Aparna Prasad United States	18	400 0.9×	493 1.2×	111 0.8×	75 0.6×	79 1.2×	44	1.0k
Lauren Provini United States	7	614 1.3×	186 0.4×	154 1.0×	141 1.2×	49 0.8×	9	849
Zhigao Long China	14	358 0.8×	206 0.5×	58 0.4×	174 1.5×	68 1.0×	42	673
Ashwin S. Shetty India	13	742 1.6×	267 0.6×	171 1.2×	203 1.7×	73 1.1×	25	1.0k
Naomi B. Zak Israel	13	605 1.3×	128 0.3×	39 0.3×	136 1.2×	83 1.3×	22	853
Showming Kwok United States	8	615 1.3×	451 1.1×	227 1.5×	103 0.9×	36 0.6×	9	827
Bruno Delobel France	19	366 0.8×	481 1.1×	92 0.6×	28 0.2×	93 1.4×	37	804
Marco Benevento Netherlands	20	722 1.6×	323 0.8×	91 0.6×	102 0.9×	50 0.8×	30	1.1k
Edwin Mientjes Netherlands	23	1.4k 3.1×	1.1k 2.5×	387 2.6×	180 1.5×	109 1.7×	37	1.9k
Yael Zilberstein Israel	14	148 0.3×	101 0.2×	96 0.6×	179 1.5×	54 0.8×	21	579

Countries citing papers authored by Merel A.W. Oortveld

Since Specialization

Citations

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

Fields of papers citing papers by Merel A.W. Oortveld

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Merel A.W. Oortveld. 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 Merel A.W. Oortveld. The network helps show where Merel A.W. Oortveld may publish in the future.

Co-authorship network of co-authors of Merel A.W. Oortveld

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

All Works

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10 of 10 papers shown

Smits, Jos P.H., René A. M. Dirks, Jieqiong Qu, et al.. (2020). Terminal keratinocyte differentiation in vitro is associated with a stable DNA methylome. Experimental Dermatology. 30(8). 1023–1032. 9 indexed citations

Oortveld, Merel A.W., Ivonne M.J.J. van Vlijmen‐Willems, Ferry F.J. Kersten, et al.. (2017). Cathepsin B as a potential cystatin M/E target in the mouse hair follicle. The FASEB Journal. 31(10). 4286–4294. 5 indexed citations

Niehues, Hanna, Lam C. Tsoi, Patrick A.M. Jansen, et al.. (2017). Psoriasis-Associated Late Cornified Envelope (LCE) Proteins Have Antibacterial Activity. Journal of Investigative Dermatology. 137(11). 2380–2388. 51 indexed citations

Zweier, Christiane, Bonnie Nijhof, Michaela Fencková, et al.. (2016). Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules. The American Journal of Human Genetics. 98(1). 149–164. 189 indexed citations

Voet, Monique van der, Bonnie Nijhof, Merel A.W. Oortveld, & Annette Schenck. (2014). Drosophila models of early onset cognitive disorders and their clinical applications. Neuroscience & Biobehavioral Reviews. 46. 326–342. 49 indexed citations

Oortveld, Merel A.W., Shivakumar Keerthikumar, Martin Oti, et al.. (2013). Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila. PLoS Genetics. 9(10). e1003911–e1003911. 28 indexed citations

Kramer, Jamie M., Merel A.W. Oortveld, Hendrik Marks, et al.. (2011). Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a. PLoS Biology. 9(1). e1000569–e1000569. 141 indexed citations

Mukhopadhyay, Arijit, Jamie M. Kramer, Gerard Merkx, et al.. (2010). CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation. Human Genetics. 128(3). 281–291. 37 indexed citations

Joerink, Maaike, et al.. (2010). Lifestyle and parental allergen sensitization are reflected in the intrauterine environment at gene expression level. Allergy. 65(10). 1282–1289. 16 indexed citations

10.

Zweier, Christiane, Eiko K. de Jong, Markus Zweier, et al.. (2009). CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. The American Journal of Human Genetics. 85(5). 655–666. 244 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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