Annet Simons

2.8k citations

29 papers · 800 indexed · h-index 17

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Vascular Anomalies and Treatments
- Chronic Lymphocytic Leukemia Research
Hematology top 5%
- Acute Myeloid Leukemia Research

Papers in ⓘ

Hematology 8
- Hemophilia Treatment and Research 3
- Platelet Disorders and Treatments 3
Genetics 7
- Genomic variations and chromosomal abnormalities 9
- Chronic Lymphocytic Leukemia Research 3
- Myeloproliferative Neoplasms: Diagnosis and Treatment 2

Co-authors: Ad Geurts van Kessel (8 shared papers)Marian Stevens‐Kroef (7 shared papers)Paul Brons (3 shared papers)Alexander Hoischen (5 shared papers)Caspar I. van der Made (5 shared papers)Frank L. van de Veerdonk (4 shared papers)Jacqueline Schoumans (3 shared papers)Chris De Wolf‐Peeters (1 shared paper)
Journals: Genes Chromosomes and Cancer (5 papers)Journal of Thrombosis and Haemostasis (2 papers)European Journal of Human Genetics (2 papers)Scientific Reports (1 paper)British Journal of Haematology (1 paper)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Annet Simons

29 papers receiving 774 citations

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 29 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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 Stul, Annet Simons, Bruce Poppe, Geneviève Laureys, Paul Brons, Peter Vandenberghe, Frank Speleman, Marleen Praet, Chris De Wolf‐Peeters, Peter Marynen, Iwona Włodarska	2003	139
2	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 Van Daele, Annet Simons, Marloes W Heijstek, David B. Beck, Mihai G. Netea, Pieter van Paassen, A. Elizabeth Hak, Lars T. van der Veken, Mariëlle van Gijn, Alexander Hoischen, Frank L. van de Veerdonk, Helen L. Leavis, Abraham Rutgers	2021	128
3	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 A. Veltman, Rolph Pfundt, Bert B.A. de Vries, Brigitte H. W. Faas, Connie T.R.M. Schrander‐Stumpel, Emma McCann, Elizabeth Sweeney, Paul May, Jos Draaisma, Nine V.A.M. Knoers, Ad Geurts van Kessel, Conny M.A. van Ravenswaaij‐Arts	2008	89
4	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 Schuurs-Hoeijmakers, Arnau Antolí, Jesús Del Valle, Gemma Rocamora-Blanch, Fernando Setién, Manel Esteller, Simon V. van Reijmersdal, Antoni Riera‐Mestre, Joan Sabater‐Riera, Gabriel Capellá, Frank L. van de Veerdonk, Ben van der Hoven, Xavier Corbella, Alexander Hoischen, Conxi Lázaro	2021	74
5	Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous Histiocytoma Cancer Genetics and Cytogenetics ·Annet Simons, Marga Schepens, Judith W. M. Jeuken, Sandra H. E. Sprenger, Guillaume van de Zande, Bodil Bjerkehagen, Anne Forus, Vines Weibolt, Ineke Molenaar, Eva van den Berg, Ola Myklebost, Julia A. Bridge, Ad Geurts van Kessel, Ron F. Suijkerbuijk	2000	49
6	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	44
7	Cytogenetic Nomenclature and Reporting Methods in molecular biology ·Marian Stevens‐Kroef, Annet Simons, Katrina Rack, Rosalind J. Hastings	2016	35
8	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. Van Der Poel, Pauline Hogenbirk, Evelyn Tönnissen, Peter J.M. Valk, Bob Löwenberg, Georgine E. de Greef, Martijn H. Breuning, Joop H. Jansen	2002	27
9	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 Feuth, Daniël Olde Weghuis, Arjan Buijs, Reinier Raymakers, Ad Geurts van Kessel	2009	22
10	Guidelines for cytogenetic investigations in tumours European Journal of Human Genetics ·Rosalind J. Hastings, Nick Bown, Maria Grazia Tibiletti, Maria Dêbiec‐Rychter, Roberta Vanni, Blanca Espinet, Nadine Van Roy, Paul Roberts, Eva van den Berg-de-Ruiter, Alain Bernheim, Jacqueline Schoumans, Steve Chatters, Zuzana Zemanová, Marian Stevens‐Kroef, Annet Simons, Sverre Heim, Marta Salido, Bauke Ylstra, David R. Betts	2015	21
11	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 ElIdrissi‐Zaynoun, Angélique Siepman, Annet Simons, Ad Geurts van Kessel	2012	20
12	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 M. A. Blijlevens, Marjolijn C.J. Jongmans, Bert A. van der Reijden, Yolba Smit, Paul Brons, Waander L. van Heerde, Saskia E.M. Schols	2018	19
13	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, Patricia J.T.A. Groenen, Annet Simons	2014	17
14	A novel chromosomal region of allelic loss, 4q32-q34, in human osteosarcomas revealed by representational difference analysis Genes Chromosomes and Cancer ·Annet Simons, Marga Schepens, Anne Forus, Linda H. Godager, Martien van Asseldonk, Ola Myklebost, Ad Geurts van Kessel	1999	17
15	Microarray‐based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia Genes Chromosomes and Cancer ·Annet Simons, Marian Stevens‐Kroef, Najat El Idrissi‐Zaynoun, Sabine van Gessel, Daniël Olde Weghuis, Eva van den Berg, Esmé Waanders, Peter M. Hoogerbrugge, Roland P. Kuiper, Ad Geurts van Kessel	2011	16
16	Primary immunodeficiency associated with chromosomal aberration – an ESID survey Orphanet Journal of Rare Diseases ·Ellen Schatorjé, Michiel van der Flier, Mikko Seppänen, Michael J. Browning, Megan Morsheimer, Stefanie Henriet, João Farela Neves, Donald C. Vinh, Laia Alsina, Anete Sevciovic Grumach, Pere Soler‐Palacín, Thomas G. Boyce, Fatih Çelmeli, Ekaterini Goudouris, Grant Hayman, Richard Herriot, Elisabeth Förster‐Waldl, Markus G. Seidel, Annet Simons, Esther de Vries	2016	16
17	Isolation of osteosarcoma-associated amplified DNA sequences using representational difference analysis Genes Chromosomes and Cancer ·Annet Simons, Irene M. Janssen, Ron F. Suijkerbuijk, R.P.H. Veth, M Pruszczyński, Christina A. Hulsbergen‐van de Kaa, Stanislas du Manoir, Ad Geurts van Kessel	1997	16
18	HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study Scientific Reports ·Altuna Halilović, Dagmar I. Verweij, Annet Simons, Marian Stevens‐Kroef, Susan Vermeulen, Janet Elsink, Bastiaan B.J. Tops, Irene Otte‐Höller, Jeroen van der Laak, Carlijn van de Water, Oliver B. Boelens, Margrethe Schlooz-Vries, Jeroen R. Dijkstra, Irıs D. Nagtegaal, Jolien Tol, Patricia H. J. van Cleef, Paul N. Span, Peter Bult	2019	10
19	Von Willebrand disease type 2M: Correlation between genotype and phenotype Journal of Thrombosis and Haemostasis ·Dominique P.M.S.M. Maas, Ferdows Atiq, Nicole M. A. Blijlevens, Paul Brons, Sandy Krouwel, Britta A. P. Laros‐van Gorkom, Frank W.G. Leebeek, Laurens Nieuwenhuizen, Selene C. M. Schoormans, Annet Simons, Daniëlle Meijer, Waander L. van Heerde, Saskia E.M. Schols	2021	7
20	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 ·Annet Simons, Judith W. M. Jeuken, Marc J. Eleveld, Rudolf H. Boerman, Ad Geurts van Kessel	1999	5

About Annet Simons

Annet Simons is a scholar working on Hematology, Genetics, Cancer Research, Genetics and Immunology, having authored 29 papers that have together received 800 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Cancer Genomics and Diagnostics (8 papers), Immunodeficiency and Autoimmune Disorders (6 papers), Prenatal Screening and Diagnostics (4 papers), Hemophilia Treatment and Research (3 papers), Chronic Lymphocytic Leukemia Research (3 papers), Platelet Disorders and Treatments (3 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (2 papers). The work is most often cited by research in Genetics (198 citations), Hematology (153 citations), Rheumatology (149 citations), Pathology and Forensic Medicine (154 citations) and Genetics (181 citations). Annet Simons has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Ad Geurts van Kessel, Marian Stevens‐Kroef, Paul Brons, Alexander Hoischen, Caspar I. van der Made, Frank L. van de Veerdonk, Jacqueline Schoumans, Chris De Wolf‐Peeters, Mathijs Baens and Bruce Poppe. Their work appears in journals such as Genes Chromosomes and Cancer, Journal of Thrombosis and Haemostasis, European Journal of Human Genetics, Scientific Reports and British Journal of Haematology.

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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