Anja Steyls

514 total citations
13 papers, 390 citations indexed

About

Anja Steyls is a scholar working on Pathology and Forensic Medicine, Oncology and Molecular Biology. According to data from OpenAlex, Anja Steyls has authored 13 papers receiving a total of 390 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pathology and Forensic Medicine, 6 papers in Oncology and 5 papers in Molecular Biology. Recurrent topics in Anja Steyls's work include Lymphoma Diagnosis and Treatment (6 papers), Viral-associated cancers and disorders (3 papers) and Chronic Lymphocytic Leukemia Research (3 papers). Anja Steyls is often cited by papers focused on Lymphoma Diagnosis and Treatment (6 papers), Viral-associated cancers and disorders (3 papers) and Chronic Lymphocytic Leukemia Research (3 papers). Anja Steyls collaborates with scholars based in Netherlands, Belgium and United Kingdom. Anja Steyls's co-authors include Peter Marynen, Brigitte Maes, Christiane De Wolf‐Peeters, Karel Geboes, Mathijs Baens, Judith Dierlamm, Chris De Wolf‐Peeters, Aimée Paulussen, Anne Hagemeijer and Kristina Hinz and has published in prestigious journals such as Blood, American Journal Of Pathology and International Journal of Obesity.

In The Last Decade

Anja Steyls

12 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anja Steyls Netherlands	9	232	113	92	75	71	13	390
L Pan United Kingdom	6	246 1.1×	149 1.3×	78 0.8×	79 1.1×	82 1.2×	8	371
Philip Paul United States	8	193 0.8×	165 1.5×	69 0.8×	34 0.5×	25 0.4×	16	379
Carolina Moreno Brazil	8	98 0.4×	78 0.7×	123 1.3×	115 1.5×	46 0.6×	12	331
Kimberly F. Kerstann United States	5	82 0.4×	137 1.2×	174 1.9×	69 0.9×	41 0.6×	9	400
P Cavazzini Italy	11	146 0.6×	98 0.9×	71 0.8×	120 1.6×	58 0.8×	13	365
Sophie Kaltenbach France	10	75 0.3×	71 0.6×	237 2.6×	75 1.0×	80 1.1×	21	421
Motohiko Tanino Japan	9	119 0.5×	125 1.1×	151 1.6×	20 0.3×	31 0.4×	12	342
Rosa M Martín Orozco Spain	6	207 0.9×	121 1.1×	80 0.9×	23 0.3×	105 1.5×	6	459
Ulrike Naumann Switzerland	11	122 0.5×	121 1.1×	124 1.3×	14 0.2×	81 1.1×	20	457
Yoshifumi Abe Japan	11	152 0.7×	53 0.5×	116 1.3×	24 0.3×	43 0.6×	17	432

Countries citing papers authored by Anja Steyls

Since Specialization

Citations

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

Fields of papers citing papers by Anja Steyls

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anja Steyls

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

All Works

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13 of 13 papers shown

1.

Roemen, Guido M.J.M., Tom E. J. Theunissen, Anja Steyls, et al.. (2024). Detection of PTCH1 Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome. Biomedicines. 12(2). 330–330.

2.

Sallevelt, Suzanne C.E.H., Alexander P.A. Stegmann, Bart de Koning, et al.. (2021). Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice. Genetics in Medicine. 23(6). 1125–1136. 26 indexed citations

3.

Coenen, Marieke J. H., Aimée Paulussen, Martijn Lindhout, et al.. (2018). Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time. Current Therapeutic Research. 90. 1–7. 10 indexed citations

4.

Paulussen, Aimée, Anja Steyls, Jo Vanoevelen, et al.. (2016). Rare novel variants in the ZIC3 gene cause X-linked heterotaxy. European Journal of Human Genetics. 24(12). 1783–1791. 16 indexed citations

5.

Souren, Nicole Y., Aimée Paulussen, Anja Steyls, et al.. (2009). Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors. International Journal of Obesity. 33(9). 962–970. 11 indexed citations

6.

Souren, Nicole Y., Aimée Paulussen, Anja Steyls, et al.. (2008). Common SNPs in LEP and LEPR associated with birth weight and type 2 diabetes-related metabolic risk factors in twins. International Journal of Obesity. 32(8). 1233–1239. 36 indexed citations

7.

Souren, Nicole Y., Maurice P. Zeegers, Rob Janssen, et al.. (2008). Anthropometry, Carbohydrate and Lipid Metabolism in the East Flanders Prospective Twin Survey: Linkage of Candidate Genes Using Two Sib-Pair Based Variance Components Analyses. Twin Research and Human Genetics. 11(5). 505–516. 8 indexed citations

8.

Baens, Mathijs, Anja Steyls, Judith Dierlamm, Chris De Wolf‐Peeters, & Peter Marynen. (2000). Structure of theMLT gene and molecular characterization of the genomic breakpoint junctions in the t(11;18)(q21;q21) of marginal zone B-cell lymphomas of MALT type. Genes Chromosomes and Cancer. 29(4). 281–291. 37 indexed citations

9.

Maes, Brigitte, et al.. (2000). The Product of the t(11;18), an API2-MLT Fusion, Marks Nearly Half of Gastric MALT Type Lymphomas without Large Cell Proliferation. American Journal Of Pathology. 156(4). 1433–1439. 153 indexed citations

10.

Dierlamm, Judith, Mathijs Baens, Kristina Hinz, et al.. (2000). Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLTspecific probes. Blood. 96(6). 2215–2218. 15 indexed citations

11.

Dierlamm, Judith, Mathijs Baens, Kristina Hinz, et al.. (2000). Detection of t(11;18)(q21;q21) by interphase fluorescence in situ hybridization using API2 and MLTspecific probes. Blood. 96(6). 2215–2218. 73 indexed citations

12.

Maes, Brigitte, et al.. (1999). Fusion between the apoptosis inhibitor gene AP12 and a novel 18q gene MLT , rearranged in the t(11,18)(q21;q21), marks half of the gastro-intestinal MALT type lymphomas without large cell proliferation. Blood. 4 indexed citations

13.

Dierlamm, Judith, M Stefanova, Kristina Hinz, et al.. (1999). The t(11;18)(q21;q21) characterizes a subgroup of extranodal MALT lymphomas: a two-color fluor-escence in situ hybridization study using AP12 and MLT specific probes. Blood. 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.

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