Annet Simons

2.8k total citations
29 papers, 800 citations indexed

About

Annet Simons is a scholar working on Genetics, Cancer Research and Hematology. According to data from OpenAlex, Annet Simons has authored 29 papers receiving a total of 800 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Cancer Research and 8 papers in Hematology. Recurrent topics in Annet Simons's work include Genomic variations and chromosomal abnormalities (9 papers), Cancer Genomics and Diagnostics (8 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Annet Simons is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Cancer Genomics and Diagnostics (8 papers) and Immunodeficiency and Autoimmune Disorders (6 papers). Annet Simons collaborates with scholars based in Netherlands, United Kingdom and United States. Annet Simons's co-authors include Ad Geurts van Kessel, Marian Stevens‐Kroef, Paul Brons, Caspar I. van der Made, Alexander Hoischen, Frank L. van de Veerdonk, Michel Stul, Geneviève Laureys, Iwona Włodarska and Chris De Wolf‐Peeters and has published in prestigious journals such as Blood, Scientific Reports and Journal of Allergy and Clinical Immunology.

In The Last Decade

Annet Simons

29 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annet Simons Netherlands	17	239	198	181	154	153	29	800
Barbara Crescenzi Italy	18	344 1.4×	235 1.2×	134 0.7×	161 1.0×	476 3.1×	55	1.0k
Rizwan Naeem United States	15	194 0.8×	71 0.4×	110 0.6×	133 0.9×	142 0.9×	31	700
Rosamma DeCastro United States	11	246 1.0×	98 0.5×	200 1.1×	82 0.5×	67 0.4×	15	1.2k
Jennifer Willert United States	13	485 2.0×	93 0.5×	129 0.7×	70 0.5×	69 0.5×	37	926
Pierre Heimann Belgium	16	543 2.3×	120 0.6×	117 0.6×	180 1.2×	91 0.6×	49	1.2k
Beata Grygalewicz Poland	14	243 1.0×	143 0.7×	119 0.7×	210 1.4×	45 0.3×	40	659
Klaus Fenchel Germany	14	258 1.1×	154 0.8×	52 0.3×	109 0.7×	133 0.9×	31	855
Nicola Foot United Kingdom	14	402 1.7×	213 1.1×	120 0.7×	157 1.0×	481 3.1×	25	837
C Mecucci Italy	16	293 1.2×	272 1.4×	51 0.3×	176 1.1×	392 2.6×	35	765
Diane L. Pickering United States	16	271 1.1×	235 1.2×	134 0.7×	490 3.2×	60 0.4×	29	1.3k

Countries citing papers authored by Annet Simons

Since Specialization

Citations

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

Fields of papers citing papers by Annet Simons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annet Simons

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

Willems, Sara M., Marjon H. Cnossen, Nick van Es, et al.. (2025). Bleeding symptoms in persons with rare bleeding disorders and a heterozygous genotype: data from the Rare Bleeding Disorders in the Netherlands study. Journal of Thrombosis and Haemostasis. 23(6). 1787–1799. 1 indexed citations

Simons, Annet, Marjan M. Weiss, Sanna R. Rijpma, et al.. (2024). Targeted exome analysis in patients with rare bleeding disorders: data from the Rare Bleeding Disorders in the Netherlands study. Research and Practice in Thrombosis and Haemostasis. 8(4). 102477–102477. 4 indexed citations

Arts, Rob J.W., Caspar I. van der Made, M. Hendriks, et al.. (2023). OTULIN Haploinsufficiency-Related Fasciitis and Skin Necrosis Treated by TNF Inhibition. Journal of Clinical Immunology. 44(1). 10–10. 4 indexed citations

Simons, Annet, Janneke Schuurs-Hoeijmakers, Evelien Zonneveld‐Huijssoon, et al.. (2022). Trio-based whole exome sequencing in patients with suspected sporadic inborn errors of immunity: A retrospective cohort study. eLife. 11. 4 indexed citations

Made, Caspar I. van der, Viola Klück, Annet Simons, et al.. (2022). Effect of exogenous IL-37 on immune cells from a patient carrying a potential IL37 loss-of-function variant: A case study. Cytokine. 162. 156102–156102. 1 indexed citations

Made, Caspar I. van der, Judith Potjewijd, Huub P J Willems, et al.. (2021). Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS. Journal of Allergy and Clinical Immunology. 149(1). 432–439.e4. 128 indexed citations

Atiq, Ferdows, Nicole M. A. Blijlevens, Paul Brons, et al.. (2021). Von Willebrand disease type 2M: Correlation between genotype and phenotype. Journal of Thrombosis and Haemostasis. 20(2). 316–327. 7 indexed citations

Solanich, Xavier, Gardenia Vargas‐Parra, Caspar I. van der Made, et al.. (2021). Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19. Frontiers in Immunology. 12. 719115–719115. 74 indexed citations

Huibers, Manon M. H., Iris H.I.M. Hollink, Lars T. van der Veken, et al.. (2020). National external quality assessment for next-generation sequencing-based diagnostics of primary immunodeficiencies. European Journal of Human Genetics. 29(1). 20–28. 5 indexed citations

10.

Halilović, Altuna, Annet Simons, Marian Stevens‐Kroef, et al.. (2019). HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study. Scientific Reports. 9(1). 11679–11679. 10 indexed citations

11.

Simons, Annet, Sonja A. de Munnik, Marten R. Nijziel, et al.. (2018). Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis. Haemophilia. 25(1). 127–135. 19 indexed citations

12.

Schatorjé, Ellen, Michiel van der Flier, Mikko Seppänen, et al.. (2016). Primary immunodeficiency associated with chromosomal aberration – an ESID survey. Orphanet Journal of Rare Diseases. 11(1). 110–110. 16 indexed citations

13.

Stevens‐Kroef, Marian, Eva van den Berg, Daniël Olde Weghuis, et al.. (2014). Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling. Molecular Cytogenetics. 7(1). 3–3. 17 indexed citations

14.

Simons, Annet, et al.. (2012). Genome-wide arrays in routine diagnostics of hematological malignancies. Human Mutation. 33(6). 941–948. 44 indexed citations

15.

Stevens‐Kroef, Marian, et al.. (2012). High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma. Genes Chromosomes and Cancer. 51(11). 997–1006. 20 indexed citations

16.

Simons, Annet, Marian Stevens‐Kroef, Daniël Olde Weghuis, et al.. (2011). Microarray‐based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia. Genes Chromosomes and Cancer. 50(12). 969–981. 16 indexed citations

17.

Stevens‐Kroef, Marian, Annet Simons, Ton Feuth, et al.. (2009). Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification. Cancer Genetics and Cytogenetics. 195(2). 97–104. 22 indexed citations

18.

Reijden, Bert A. van der, Annet Simons, Evelyn Tönnissen, et al.. (2002). Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB‐MYH11 gene fusion. British Journal of Haematology. 118(2). 411–418. 27 indexed citations

19.

Simons, Annet, Marga Schepens, Judith W. M. Jeuken, et al.. (2000). Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma. Cancer Genetics and Cytogenetics. 118(2). 89–98. 49 indexed citations

20.

Simons, Annet, Judith W. M. Jeuken, Marc J. Eleveld, Rudolf H. Boerman, & Ad Geurts van Kessel. (1999). Isolation and characterization of glioblastoma-associated homozygously deleted DNA fragments from chromosomal region 9p21 suggests involvement of multiple tumour suppressor genes. The Journal of Pathology. 189(3). 402–409. 5 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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