Marloes Steehouwer

5.1k citations

18 papers · 1.4k indexed · 1 hit paper · h-index 13

Genetics top 2%
Molecular Biology top 10%
Cancer Research top 10%
Hematology top 10%
Genetics top 10%

Co-authors: Alexander Hoischen Christian Gilissen Joris A. Veltman Han G. Brunner Peer Arts Bart van Lier Lisenka E.L.M. Vissers Petra de Vries
Topics: Genomics and Rare Diseases (5 papers)Acute Myeloid Leukemia Research (4 papers)Genomics and Phylogenetic Studies (3 papers)
Cited by: Genetics Cancer Research Hematology
Journals: Nature Communications Nature Genetics The Journal of Infectious Diseases
Partner nations: Netherlands United States Germany

In The Last Decade

Marloes Steehouwer

18 papers receiving 1.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A de novo paradigm for mental retardation

2010 526 citations Lisenka E.L.M. Vissers, Joep de Ligt et al. Nature Genetics profile →

Peers

Countries citing papers authored by Marloes Steehouwer

Since Specialization

Citations

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

Fields of papers citing papers by Marloes Steehouwer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marloes Steehouwer

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation 2023 ·Nature Communications ·Wouter Steyaert,Lonneke Haer‐Wigman,Rolph Pfundt,Debby M.E.I. Hellebrekers,Marloes Steehouwer,(unknown),Elke de Boer,Alexander P.A. Stegmann,Helger G. Yntema,Erik‐Jan Kamsteeg,Han G. Brunner,Alexander Hoischen,Christian Gilissen	5
2	Evolution of age-related mutation-driven clonal haematopoiesis over 20 years is associated with metabolic dysfunction in obesity 2023 ·EBioMedicine ·Johanna C. Andersson‐Assarsson,Rosanne C. van Deuren,(unknown),Marloes Steehouwer,Kajsa Sjöholm,Per‐Arne Svensson,(unknown),Christian Gilissen,Magdalena Taube,Peter Jacobson,Rosie Perkins,Han G. Brunner,Mihai G. Netea,Markku Peltonen,Björn Carlsson,Alexander Hoischen,Lena Carlsson	17
3	Clonal hematopoiesis has prognostic value in dilated cardiomyopathy independent of age and clone size 2023 ·European Heart Journal ·(unknown),(unknown),Michiel T.H.M. Henkens,Anne G. Raafs,(unknown),(unknown),Marloes Steehouwer,Niels P. Riksen,Arthur van den Wijngaard,Han G. Brunner,Alexander Hoischen,Job A.J. Verdonschot,Stéphane Heymans	2
4	Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics 2021 ·Journal of Molecular Diagnostics ·Paul Roepman,Ewart de Bruijn,Stef van Lieshout,(unknown),Mirjam C. Boelens,Hendrikus J. Dubbink,Willemina R.R. Geurts-Giele,Floris H. Groenendijk,Manon M. H. Huibers,Mariëtte E.G. Kranendonk,Margaretha G.M. Roemer,Kris G. Samsom,Marloes Steehouwer,Wendy W.J. de Leng,Alexander Hoischen,Bauke Ylstra,Kim Monkhorst,Jacobus J. M. van der Hoeven,Edwin Cuppen	39
5	Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses 2021 ·Genome Medicine ·Rosanne C. van Deuren,Peer Arts,Giulio Cavalli,Martin Jaeger,Marloes Steehouwer,Maartje van de Vorst,Christian Gilissen,Leo A. B. Joosten,Charles A. Dinarello,Musa M. Mhlanga,Vinod Kumar,Mihai G. Netea,Frank L. van de Veerdonk,Alexander Hoischen	7
6	Clonal Hematopoiesis Is Associated With Low CD4 Nadir and Increased Residual HIV Transcriptional Activity in Virally Suppressed Individuals With HIV 2021 ·The Journal of Infectious Diseases ·Wouter A. van der Heijden,Rosanne C. van Deuren,Lisa Van de Wijer,Inge van den Munckhof,Marloes Steehouwer,Niels P. Riksen,Mihai G. Netea,Quirijn de Mast,Linos Vandekerckhove,Richarda M. de Voer,André van der Ven,Alexander Hoischen	23
7	P105 Identification of rare coding variants in IL-1-related pathways in patients with adult-onset still's disease 2019 ·Annals of the Rheumatic Diseases ·Giulio Cavalli,(unknown),Peer Arts,Marloes Steehouwer,Paolo Sfriso,Serena Colafrancesco,Roberta Priori,Luca Cantarini,Elena Baldissera,Frank L. van de Veerdonk,Lorenzo Dagna,Alexander Hoischen,CA Dinarello	2
8	Quantification of differential gene expression by multiplexed targeted resequencing of cDNA 2017 ·Nature Communications ·Peer Arts,(unknown),(unknown),Marloes Steehouwer,Jay Shendure,Alexander Hoischen,Cornelis A. Albers	18
9	Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life 2017 ·The American Journal of Human Genetics ·Rocío Acuña‐Hidalgo,Hilal Sengül,Marloes Steehouwer,Maartje van de Vorst,Sita H. Vermeulen,Lambertus A. Kiemeney,Joris A. Veltman,Christian Gilissen,Alexander Hoischen	172
10	DVL3 Alleles Resulting in a −1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome 2016 ·The American Journal of Human Genetics ·Janson J. White,Juliana F. Mazzeu,Alexander Hoischen,Yavuz Bayram,Marjorie Withers,Alper Gezdirici,Virginia Kimonis,Marloes Steehouwer,Shalini N. Jhangiani,Donna M. Muzny,Richard A. Gibbs,Bregje W.M. van Bon,V. Reid Sutton,James R. Lupski,Han G. Brunner,Claudia M.B. Carvalho	69
11	Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes 2016 ·European Journal of Human Genetics ·(unknown),Wybrich R Cnossen,Joris A. Veltman,Rob Woestenenk,Marloes Steehouwer,(unknown),René H. M. te Morsche,Meritxell Huch,Jayne Y. Hehir‐Kwa,(unknown),Rolph Pfundt,Ronald Roepman,Alexander Hoischen,Joost P.H. Drenth	14
12	Thyroid hormone resistance syndrome due to mutations in the thyroid hormone receptor α gene (THRA) 2015 ·Journal of Medical Genetics ·Anna Tylki‐Szymańska,Rocío Acuña‐Hidalgo,Małgorzata Krajewska‐Walasek,(unknown),Marloes Steehouwer,Christian Gilissen,Han G. Brunner,Agnieszka Jurecka,Agnieszka Różdżyńska‐Świątkowska,Alexander Hoischen,Krystyńa Chrzańowska	65
13	Mobster: accurate detection of mobile element insertions in next generation sequencing data 2014 ·Genome biology ·Djie Tjwan Thung,Joep de Ligt,Lisenka E.L.M. Vissers,Marloes Steehouwer,(unknown),Petra de Vries,P. Eline Slagboom,Kai Ye,Joris A. Veltman,Jayne Y. Hehir‐Kwa	64
14	Mobster: accurate detection of mobile element insertions in next generation sequencing data 2014 ·Genome Biology ·Djie Tjwan Thung,Joep de Ligt,Lisenka E.L.M. Vissers,Marloes Steehouwer,(unknown),Petra de Vries,P. Eline Slagboom,Kai Ye,Joris A. Veltman,Jayne Y. Hehir‐Kwa	2
15	Recurrent De Novo Mutations in PACS1 Cause Defective Cranial-Neural-Crest Migration and Define a Recognizable Intellectual-Disability Syndrome 2012 ·The American Journal of Human Genetics ·Janneke Schuurs-Hoeijmakers,Edwin C. Oh,Lisenka E.L.M. Vissers,Mariëlle E.M. Swinkels,Christian Gilissen,Michèl A.A.P. Willemsen,Maureen Holvoet,Marloes Steehouwer,Joris A. Veltman,Bert B.A. de Vries,Hans van Bokhoven,Arjan P.M. de Brouwer,Nicholas Katsanis,Koenraad Devriendt,Han G. Brunner	78
16	Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome 2010 ·The American Journal of Human Genetics ·Christian Gilissen,Heleen H. Arts,Alexander Hoischen,Liesbeth Spruijt,Dorus A. Mans,Peer Arts,Bart van Lier,Marloes Steehouwer,Jeroen van Reeuwijk,Sarina G. Kant,Ronald Roepman,Nine V.A.M. Knoers,Joris A. Veltman,Han G. Brunner	197
17	A de novo paradigm for mental retardationbreakdown → 2010 ·Nature Genetics ·Lisenka E.L.M. Vissers,Joep de Ligt,Christian Gilissen,Irene M. Janssen,Marloes Steehouwer,Petra de Vries,Bart van Lier,Peer Arts,Nienke Wieskamp,Marisol del Rosario,Bregje W.M. van Bon,Alexander Hoischen,Bert B.A. de Vries,Han G. Brunner,Joris A. Veltman	526
18	Massively parallel sequencing of ataxia genes after array-based enrichment 2010 ·Human Mutation ·Alexander Hoischen,Christian Gilissen,Peer Arts,Nienke Wieskamp,Walter van der Vliet,Sascha Vermeer,Marloes Steehouwer,Petra de Vries,Rowdy Meijer,(unknown),Nine V.A.M. Knoers,Michael F. Buckley,Hans Scheffer,Joris A. Veltman	63

About Marloes Steehouwer

Marloes Steehouwer is a scholar working on Hematology, Cancer Research and Genetics, having authored 18 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Acute Myeloid Leukemia Research (4 papers) and Genomics and Phylogenetic Studies (3 papers). The work is most often cited by research in Genetics (740 citations), Cancer Research (217 citations) and Hematology (138 citations). Marloes Steehouwer has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Alexander Hoischen, Christian Gilissen, Joris A. Veltman, Han G. Brunner, Peer Arts, Bart van Lier, Lisenka E.L.M. Vissers, Petra de Vries, Joep de Ligt and Nienke Wieskamp. Their work appears in journals such as Nature Communications, Nature Genetics and The Journal of Infectious Diseases.

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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