Annet Simons

2.8k citations

42 papers · 2.2k · 1 hit paper · h-index 19

Impact in

Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
Infectious Diseases top 5%
- SARS-CoV-2 and COVID-19 Research
- COVID-19 Clinical Research Studies

Papers in

Hematology 11
- Acute Myeloid Leukemia Research 4
- Platelet Disorders and Treatments 4
Immunology 12
- Immunodeficiency and Autoimmune Disorders 9

Co-authors: Ad Geurts van Kessel (9 shared papers)Marian Stevens‐Kroef (7 shared papers)Caspar I. van der Made (5 shared papers)Alexander Hoischen (6 shared papers)Frank L. van de Veerdonk (4 shared papers)Paul Brons (3 shared papers)Geneviève Laureys (1 shared paper)Peter Vandenberghe (1 shared paper)
Journals: Blood (4 papers)Genes Chromosomes and Cancer (4 papers)European Journal of Human Genetics (3 papers)Journal of Thrombosis and Haemostasis (2 papers)Frontiers in Immunology (2 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Annet Simons

41 papers receiving 2.1k citations

Annet Simons's Hit Papers

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Presence of Genetic Variants Among Young Men With Severe COVID-19 2020 · 624 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2020 JAMA

Peers

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-authors

The 25 scholars most cited alongside Annet Simons, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Annet Simons Line = papers co-authored together Annet Simons links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Presence of Genetic Variants Among Young Men With Severe COVID-19 JAMA ·Caspar I. van der Made, Annet Simons, Janneke H. M. Schuurs-Hoeijmakers, Guus van den Heuvel, Tuomo Mantere, Simone Kersten, Rosanne C. van Deuren, Marloes Steehouwer Hit paper breakdown →	2020	624
2	A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia Nature Genetics ·Sohela Shah, Kasmintan A. Schrader, Esmé Waanders, Andrew E. Timms, Joseph Vijai, Cornelius Miething, Jeremy Wechsler, Jun J.J. Yang	2013	261
3	Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS Journal of Allergy and Clinical Immunology ·Caspar I. van der Made, Judith Potjewijd, Annemiek Hoogstins, Huub P J Willems, Arjan J. Kwakernaak, Ruud G.L. de Sévaux, Paul L. A. van Daele, Annet Simons	2021	171
4	ALK activation by the CLTC-ALK fusion is a recurrent event in large B-cell lymphoma Blood ·Pascale De Paepe, Mathijs Baens, J. Han van Krieken, Bruno Verhasselt, Michel S. Stul, Annet Simons, Bruce Graham Poppe, Geneviève Laureys	2003	159
5	Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders Genetics in Medicine ·Rolph Pfundt, Marisol del Rosario, Lisenka E.L.M. Vissers, Michael P. Kwint, Irene M. Janssen, Nicole de Leeuw, Helger G. Yntema, Marcel R. Nelen	2016	153
6	Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype American Journal of Medical Genetics Part A ·Mariëlle E.M. Swinkels, Annet Simons, Dominique Smeets, Lisenka E.L.M. Vissers, Joris Andre Veltman, Rolph Pfundt, de Vries Bj, B. H. W. Faas	2008	112
7	Genetic Screening for TLR7 Variants in Young and Previously Healthy Men With Severe COVID-19 Frontiers in Immunology ·Xavier Solanich, Gardenia Vargas‐Parra, Caspar I. van der Made, Annet Simons, Janneke H. M. Schuurs-Hoeijmakers, Arnau Antolí, Jesús Del Valle, Gemma Rocamora-Blanch	2021	93
8	Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies Genome Medicine ·Peer Arts, Annet Simons, Mofareh AlZahrani, Elanur Yılmaz, Eman AlIdrissi, Koen van Aerde, Njood Alenezi, Hamza Ali Alghamdi	2019	61
9	Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma Cancer Genetics and Cytogenetics ·Annet Simons, Marga T. Schepens, Judith W. M. Jeuken, Sandra H. E. Sprenger, Guillaume van de Zande, Bodil Bjerkehagen, Anne Forus, Vines Weibolt	2000	59
10	Genome-wide arrays in routine diagnostics of hematological malignancies Human Mutation ·Annet Simons, Birgit Sikkema‐Raddatz, Nicole de Leeuw, Nicole Claudia Konrad, Rosalind J. Hastings, Jacqueline Schoumans	2012	46
11	Cytogenetic Nomenclature and Reporting Methods in molecular biology ·Marian Stevens‐Kroef, Annet Simons, Katrina A. Rack, Rosalind J. Hastings	2016	38
12	Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB‐MYH11 gene fusion British Journal of Haematology ·Bert A. van der Reijden, Annet Simons, Erna B Luiten, Sonja C.P.A.M. van der Poel, Pauline Hogenbirk, Evelyn Tönnissen, Peter J.M. Valk, Bob Löwenberg	2002	32
13	Platelet CD34 expression and α/δ-granule abnormalities in GFI1B- and RUNX1-related familial bleeding disorders Blood ·Anna E. Marneth, Waander L. van Heerde, Konnie M. Hebeda, Britta A. P. Laros‐van Gorkom, Wideke Barteling, Brigith K. Willemsen, Aniek O. de Graaf, Annet Simons	2017	30
14	Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity: A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers Frontiers in Immunology ·Kim Elsink, Manon M. H. Huibers, Iris H.I.M. Hollink, Annet Simons, Evelien Zonneveld‐Huijssoon, Lars T. van der Veken, Helen Louisa Leavis, Stefanie Henriet	2021	27
15	Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification Cancer Genetics and Cytogenetics ·Marian Stevens‐Kroef, Annet Simons, Hanneke Gorissen, Ton B. Feuth, Daniël Olde Weghuis, Arjan Buijs, Reinier A P Raymakers, Ad Geurts van Kessel	2009	24
16	The phenotypic spectrum of germline YARS2 variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2 Haematologica ·Lisa G. Riley, Matthew M. Heeney, Joëlle Rudinger‐Thirion, Magali Frugier, Dean R. Campagna, Ronghao Zhou, Gregory A. Hale, Lee Hilliard	2018	24
17	Guidelines for cytogenetic investigations in tumours European Journal of Human Genetics ·Rosalind J. Hastings, Nick P. Bown, Maria Grazia Tibiletti, Maria Dêbiec‐Rychter, Roberta Vanni, Blanca Espinet, Nadine Van Roy, Paul Roberts	2015	23
18	High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma Genes Chromosomes and Cancer ·Marian Stevens‐Kroef, Daniël Olde Weghuis, Sandra Croockewit, Leo Derksen, Jeroen D Hooijer, Najat El Idrissi‐Zaynoun, Angélique Siepman, Annet Simons	2012	22
19	Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis Haemophilia ·Joline L. Saes, Annet Simons, Sonja A. de Munnik, Marten R. Nijziel, Nicole Blijlevens, Marjolijn C.J. Jongmans, Bert A. van der Reijden, Yolba Smit	2018	22
20	Identification of prognostic relevant chromosomal abnormalities in chronic lymphocytic leukemia using microarray-based genomic profiling Molecular Cytogenetics ·Marian Stevens‐Kroef, Eva van den Berg, Daniël Olde Weghuis, Ad Geurts van Kessel, Rolph Pfundt, Matty Linssen-Wiersma, Marloes Benjamins, Trijnie Dijkhuizen	2014	19

About Annet Simons

Annet Simons is a scholar working on Hematology, Immunology, Genetics, Genetics and Pulmonary and Respiratory Medicine, having authored 42 papers that have together received 2.2k indexed citations. Recurring topics across this work include Immunodeficiency and Autoimmune Disorders (9 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Acute Myeloid Leukemia Research (4 papers), Platelet Disorders and Treatments (4 papers), Sarcoma Diagnosis and Treatment (3 papers), Inflammasome and immune disorders (3 papers) and Chronic Lymphocytic Leukemia Research (2 papers). The work is most often cited by research in Immunology (491 citations), Infectious Diseases (459 citations), Hematology (289 citations), Genetics (538 citations) and Public Health, Environmental and Occupational Health (237 citations). Annet Simons has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Ad Geurts van Kessel, Marian Stevens‐Kroef, Caspar I. van der Made, Alexander Hoischen, Frank L. van de Veerdonk, Paul Brons, Geneviève Laureys, Peter Vandenberghe, Peter Marynen and Bruno Verhasselt. Their work appears in journals such as Blood, Genes Chromosomes and Cancer, European Journal of Human Genetics, Journal of Thrombosis and Haemostasis and Frontiers in Immunology.

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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Annet Simons

Annet Simons's Hit Papers

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About Annet Simons

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