Esmé Waanders

3.7k citations

45 papers · 1.5k · h-index 21

Impact in

Hematology top 2%
- Acute Myeloid Leukemia Research
- Chronic Myeloid Leukemia Treatments
Public Health, Environmental and Occupational Health top 2%
- Acute Lymphoblastic Leukemia research

Papers in

Molecular Biology 17
- Cancer-related gene regulation 7
- Epigenetics and DNA Methylation 4
Public Health, Environmental and Occupational Health 17
- Acute Lymphoblastic Leukemia research 17

Co-authors: Roland P. Kuiper (22 shared papers)Peter M. Hoogerbrugge (17 shared papers)Frank N. van Leeuwen (15 shared papers)Patrick J. Keeling (1 shared paper)James Harper (1 shared paper)Ad Geurts van Kessel (13 shared papers)Vincent H. J. van der Velden (7 shared papers)Edwin Sonneveld (14 shared papers)
Journals: Blood (13 papers)Journal of Clinical Oncology (3 papers)Leukemia (3 papers)Haematologica (2 papers)Journal of Hepatology (2 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Esmé Waanders

42 papers receiving 1.4k citations

Peers

Countries citing papers authored by Esmé Waanders

Since Specialization

Citations

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

Fields of papers citing papers by Esmé Waanders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Esmé Waanders, 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 Esmé Waanders Line = papers co-authored together Esmé Waanders 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 45 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	IKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL Leukemia ·Roland P. Kuiper, Esmé Waanders, Vincent H. J. van der Velden, S V van Reijmersdal, Ramprasath Venkatachalam, Blanca Scheijen, Edwin Sonneveld, Jacques J. M. van Dongen, (unknown), Frank N. van Leeuwen, Ad Geurts van Kessel, Peter M. Hoogerbrugge	2010	197
2	Independent prognostic value of BCR-ABL1-like signature and IKZF1 deletion, but not high CRLF2 expression, in children with B-cell precursor ALL Blood ·Arian van der Veer, Esmé Waanders, Rob Pieters, Marieke E. Willemse, Simon V. van Reijmersdal, Lisa J. Russell, Christine J. Harrison, William E. Evans, Vincent H. J. van der Velden, Peter M. Hoogerbrugge, Frank N. van Leeuwen, Gabriele Escherich, Martin A. Horstmann, Leila mohammadi Khankahdani, Dimitris Rizopoulos, Hester A. de Groot‐Kruseman, Edwin Sonneveld, Roland P. Kuiper, Monique L. den Boer	2013	191
3	On the monophyly of chromalveolates using a six-protein phylogeny of eukaryotes INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY ·James Harper, Esmé Waanders, Patrick J. Keeling	2005	136
4	Recognition of genetic predisposition in pediatric cancer patients: An easy-to-use selection tool European Journal of Medical Genetics ·Marjolijn C.J. Jongmans, Jan Loeffen, Esmé Waanders, Peter M. Hoogerbrugge, Marjolijn J. L. Ligtenberg, Roland P. Kuiper, (unknown)	2016	110
5	Integrated use of minimal residual disease classification and IKZF1 alteration status accurately predicts 79% of relapses in pediatric acute lymphoblastic leukemia Leukemia ·Esmé Waanders, Vincent H. J. van der Velden, C. Ellen van der Schoot, Frank N. van Leeuwen, Simon V. van Reijmersdal, Válerie de Haas, (unknown), Ad Geurts van Kessel, Peter M. Hoogerbrugge, Roland P. Kuiper, Jacques J. M. van Dongen	2010	91
6	Mammaglobin Is Associated With Low-Grade, Steroid Receptor-Positive Breast Tumors From Postmenopausal Patients, and Has Independent Prognostic Value for Relapse-Free Survival Time Journal of Clinical Oncology ·Paul N. Span, Esmé Waanders, Peggy Manders, J.J.T.M. Heuvel, John A. Foekens, Mark A. Watson, L.V.A.M. Beex, Fred C.G.J. Sweep	2004	65
7	BTG1 regulates glucocorticoid receptor autoinduction in acute lymphoblastic leukemia Blood ·Joost C. van Galen, Roland P. Kuiper, Liesbeth van Emst, Marloes Levers, Esther Tijchon, Blanca Scheijen, Esmé Waanders, Simon V. van Reijmersdal, Christian Gilissen, Ad Geurts van Kessel, Peter M. Hoogerbrugge, Frank N. van Leeuwen	2010	64
8	The Origin and Nature of Tightly Clustered BTG1 Deletions in Precursor B-Cell Acute Lymphoblastic Leukemia Support a Model of Multiclonal Evolution PLoS Genetics ·Esmé Waanders, Blanca Scheijen, Laurens T. van der Meer, Simon V. van Reijmersdal, Liesbeth van Emst, Yvet Kroeze, Edwin Sonneveld, Peter M. Hoogerbrugge, Ad Geurts van Kessel, Frank N. van Leeuwen, Roland P. Kuiper	2012	59
9	Carbohydrate antigen 19‐9 is extremely elevated in polycystic liver disease Liver International ·Esmé Waanders, Loes van Keimpema, Johannes T. Brouwer, Martijn G.H. van Oijen, Raymond Aerts, Fred C.G.J. Sweep, Frederik Nevens, Joost P.H. Drenth	2009	58
10	Late Recurrence of Childhood T-Cell Acute Lymphoblastic Leukemia Frequently Represents a Second Leukemia Rather Than a Relapse: First Evidence for Genetic Predisposition Journal of Clinical Oncology ·Tomasz Szczepański, Vincent H. J. van der Velden, Esmé Waanders, Roland P. Kuiper, Pieter Van Vlierberghe, Bernd Gruhn, Cornelia Eckert, Renate Panzer‐Grümayer, Giuseppe Basso, Hélène Cavé, Udo zur Stadt, Dario Campana, André Schrauder, Rosemary Sutton, Elisabeth van Wering, Jules P.P. Meijerink, Jacques J. M. van Dongen	2011	51
11	Extensive mutational analysis ofPRKCSH andSEC63 broadens the spectrum of polycystic liver disease Human Mutation ·Esmé Waanders, René H. M. te Morsche, Rob A. de Man, Jan B.�M.�J. Jansen, Joost P.H. Drenth	2006	42
12	Tumor suppressors BTG1 and IKZF1 cooperate during mouse leukemia development and increase relapse risk in B-cell precursor acute lymphoblastic leukemia patients Haematologica ·Blanca Scheijen, Judith M. Boer, René Marke, Esther Tijchon, Dorette van Ingen Schenau, Esmé Waanders, Liesbeth van Emst, Laurens T. van der Meer, Rob Pieters, Gabriele Escherich, Martin A. Horstmann, Edwin Sonneveld, Nicola C. Venn, Rosemary Sutton, Luciano Dalla‐Pozza, Roland P. Kuiper, Peter M. Hoogerbrugge, Monique L. den Boer, Frank N. van Leeuwen	2016	40
13	Germline activating TYK2 mutations in pediatric patients with two primary acute lymphoblastic leukemia occurrences Leukemia ·Esmé Waanders, Blanca Scheijen, Marjolijn C.J. Jongmans, Hanka Venselaar, Simon V. van Reijmersdal, Anke H.A. van Dijk, Agata Pastorczak, Robbert D.A. Weren, C. Ellen van der Schoot, Micha van de Vorst, Edwin Sonneveld, (unknown), Vincent H. J. van der Velden, Bernd Gruhn, Peter M. Hoogerbrugge, Jacques J. M. van Dongen, Ad Geurts van Kessel, Frank N. van Leeuwen, Roland P. Kuiper	2016	39
14	Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutations Human Mutation ·Petra H.L. Schuilenga‐Hut, Pieter van der Vlies, Marcel F. Jonkman, Esmé Waanders, Charles H.C.M. Buys, Hans Scheffer	2003	38
15	Congenital disorders of glycosylation in hepatology: The example of polycystic liver disease Journal of Hepatology ·Manoe J. Janssen, Esmé Waanders, Jannes Woudenberg, Dirk J. Lefeber, Joost P.H. Drenth	2009	37
16	Secondary, Somatic Mutations Might Promote Cyst Formation in Patients With Autosomal Dominant Polycystic Liver Disease Gastroenterology ·Manoe J. Janssen, Esmé Waanders, René H. M. te Morsche, Ruoyu Xing, Henry Dijkman, Jannes Woudenberg, Joost P.H. Drenth	2011	32
17	Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63 Clinical Genetics ·Esmé Waanders, Hanka Venselaar, (unknown), DB De Koning, Patrick S. Kamath, VE Torres, Stefan Somlo, (unknown)	2010	31
18	Optical genome mapping identifies a germline retrotransposon insertion in SMARCB1 in two siblings with atypical teratoid rhabdoid tumors The Journal of Pathology ·Mariangela Sabatella, Tuomo Mantere, Esmé Waanders, Kornelia Neveling, Arjen R. Mensenkamp, Freerk van Dijk, Jayne Y. Hehir‐Kwa, Ronnie Derks, Michael Kwint, Luke O’Gorman, Madalena Tropa Martins, Corrie Gidding, Maarten H. Lequin, Benno Küsters, Pieter Wesseling, Marcel Nelen, Jacklyn Biegel, Alexander Hoischen, Marjolijn C.J. Jongmans, Roland P. Kuiper	2021	29
19	Childhood neuroendocrine tumours: a descriptive study revealing clues for genetic predisposition British Journal of Cancer ·Illja J. Diets, Irıs D. Nagtegaal, Jan Loeffen, Ivo de Blaauw, Esmé Waanders, (unknown), Marjolijn C.J. Jongmans	2016	24
20	Disrupted cell adhesion but not proliferation mediates cyst formation in polycystic liver disease Modern Pathology ·Esmé Waanders, J. Han van Krieken, Anke L. Lameris, Joost P.H. Drenth	2008	22

About Esmé Waanders

Esmé Waanders is a scholar working on Molecular Biology, Public Health, Environmental and Occupational Health, Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 45 papers that have together received 1.5k indexed citations. Recurring topics across this work include Acute Lymphoblastic Leukemia research (17 papers), Genetic and Kidney Cyst Diseases (9 papers), Cancer-related gene regulation (7 papers), Chronic Myeloid Leukemia Treatments (5 papers), Childhood Cancer Survivors' Quality of Life (5 papers), Cancer Genomics and Diagnostics (4 papers), Pediatric Hepatobiliary Diseases and Treatments (4 papers) and Epigenetics and DNA Methylation (4 papers). The work is most often cited by research in Hematology (449 citations), Public Health, Environmental and Occupational Health (629 citations), Pediatrics, Perinatology and Child Health (333 citations), Genetics (302 citations) and Genetics (69 citations). Esmé Waanders has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Roland P. Kuiper, Peter M. Hoogerbrugge, Frank N. van Leeuwen, Patrick J. Keeling, James Harper, Ad Geurts van Kessel, Vincent H. J. van der Velden, Edwin Sonneveld, Joost P.H. Drenth and Simon V. van Reijmersdal. Their work appears in journals such as Blood, Journal of Clinical Oncology, Leukemia, Haematologica and Journal of Hepatology.

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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Esmé Waanders

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About Esmé Waanders

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