Thierry Voet

19.6k citations

96 papers · 8.6k indexed · 8 hit papers · h-index 42

Impact in

Cancer Research top 1%
- Cancer Genomics and Diagnostics
Biophysics top 0.5%

Papers in

Pediatrics, Perinatology and Child Health 27
- Prenatal Screening and Diagnostics 26
Genetics 35
- Genomic variations and chromosomal abnormalities 22

Co-authors: Iain C. Macaulay Chris P. Ponting Joris Vermeesch Alejandro Sifrim Katy Vandereyken Bernard Thienpont Magdalena Zernicka‐Goetz Parveen Kumar
Journals: Nucleic Acids Research (6 papers)Human Reproduction (6 papers)Obstetrical & Gynecological Survey (4 papers)Nature (4 papers)Genome Research (4 papers)
Partner nations: Belgium United Kingdom United States

In The Last Decade

Thierry Voet

94 papers receiving 8.5k citations

Hit Papers

8 papers align trajectories log scale

Methods and applications for single-cell and spatial multi-omics 2023 · 580 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2023 Nature Reviews Genetics
2020 Nature Communications
2018 Nature
2016 Nature Communications
2016 Nature Methods
2015 Nature Methods
2013 Science
2009 Nature Medicine

Peers

Countries citing papers authored by Thierry Voet

Since Specialization

Citations

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

Fields of papers citing papers by Thierry Voet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Thierry Voet, 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 Thierry Voet Line = papers co-authored together Thierry Voet links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Prenatal Exposure to Chemotherapy Increases the Mutation Burden in Human Neonatal Hematopoietic Stem Cells Cancer Discovery ·A. Moser, Carolina Velázquez, Marcelo de Moura Góes, 苏榕, Markus J. van Roosmalen, Axel Rosendahl Huber, Ling Dai, Wouter Bossuyt, Bernard Thienpont, Thierry Voet, Kristel Van Calsteren, Liesbeth Lenaerts, Ruben van Boxtel, Frédéric Amant	2025	0
2	Origin and development of uniparental and polyploid blastomeres iScience ·Jenipher Kener Myslei André, Katharina Granzin, José Victor Alexandre de Oliveira Nunes, Tatjana Jatsenko, 仇海峰, Qiumin Liao, Firdous, Thierry Voet, Olga Tšuiko, Ants Kurg, Katrien Smits, Ann Van Soom, Joris Vermeesch	2025	1
3	#506 Chemotherapy during pregnancy is associated with increased genotoxicity and mutational load in the fetal hematopoietic compartment Lirias (KU Leuven) ·A. Moser, Carolina Velázquez, Marcelo de Moura Góes, Nedret Fehmi Onursal, Manosij Ghosh, م . د عمار عبد الجبار قدوري السلماني, Charlotte Lejeune, Kristel Van Calsteren, Lode Godderis, Thierry Voet, Ruben van Boxtel, Liesbeth Lenaerts, Frédéric Amant	2023	0
4	Zebrafish MITF-Low Melanoma Subtype Models Reveal Transcriptional Subclusters and MITF-Independent Residual Disease Cancer Research ·Jana Trávníčková, Sameh Farahat, Ava Khamseh, Philippe Gautier, Daniel V. Brown, Firdous, Alessandro Brombin, Ailith Ewing, Madelyn Roque Remus, Michaela Spitzer, Anieres Barbosa da Silva, Colin A. Semple, Marie E. Mathers, James Lister, Eirı́kur Steingrı́msson, Thierry Voet, Chris P. Ponting, E. Elizabeth Patton	2019	28
5	Self-Assembly of Embryonic and Two Extraembryonic Stem Cell Types Into Gastrulating Embryo-like Structures Obstetrical & Gynecological Survey ·Berna Sözen, Gianluca Amadei, Andy Cox, Ran Wang, Xiaogan Zheng, Madhanraj Akilandeswari Pugalendhi, Lia Chappell, Thierry Voet, Geert Michel, Naihe Jing, David M. Glover, Magdalena Zernicka‐Goetz	2019	7
6	Activation of Skeletal Stem and Progenitor Cells for Bone Regeneration Is Driven by PDGFRβ Signaling Developmental Cell ·Anna-Marei Böhm, Naomi Dirckx, Robert J. Tower, 平田更一, Sebastiaan Vanuytven, Koen Theunis, Elena Nefyodova, Beate Hörr, Volkhard Lindner, Thierry Voet, Matthias Van Hul, Christa Maes	2019	78
7	Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M Human Reproduction ·Aspasia Destouni, Eftychia Dimitriadou, Stephanie J Xitco, Sophie Debrock, Cindy Melotte, Kris Van Den Bogaert, Masoud Zamani Esteki, Jia Ding, Thierry Voet, Ellen Denayer, Thomy de Ravel, Eric Legius, Christel Meuleman, Karen Peeraer, Joris Vermeesch	2018	45
8	Single-cell sequencing reveals the origin and the order of mutation acquisition in T-cell acute lymphoblastic leukemia Leukemia ·Jolien De Bie, Sofie Demeyer, Llucia Albertí Servera, Ellen Geerdens, Heidi Segers, Michaël Broux, Kim De Keersmaecker, Lucienne Michaux, Peter Vandenberghe, Thierry Voet, Nancy Boeckx, Anne Uyttebroeck, Jan Cools	2018	63
9	Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells European Journal of Human Genetics ·Filippo Zambelli, Ingeborg Blaha, Nicholai Jakosz, Daniel R. Brown, F. Cordoliani, Sonia Van Dooren, Bradford J Matthews, Luca Gianaroli, Karen Sermon, Thierry Voet, Sara Seneca, Claudia Spits	2017	12
10	Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity Nature Methods ·Christof Angermueller, Stephen J. Clark, Heather Lee, Iain C. Macaulay, Mabel Teng, Xiaoming Hu, Felix Krueger, Sébastien A. Smallwood, Chris P. Ponting, Thierry Voet, Gavin Kelsey, Oliver Stegle, Wolf Reik Hit paper breakdown →	2016	510
11	Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy Genome Research ·Aspasia Destouni, Masoud Zamani Esteki, Jinju Jung, Olga Tšuiko, Eftychia Dimitriadou, Katrien Smits, Ants Kurg, Andres Salumets, Ann Van Soom, Thierry Voet, Joris Vermeesch	2016	64
12	G&T-seq: parallel sequencing of single-cell genomes and transcriptomes Nature Methods ·Iain C. Macaulay, Wilfried Haerty, Parveen Kumar, Yang Li, Xiaoming Hu, Mabel Teng, Mubeen Goolam, Nathalie Saurat, Paul Coupland, Lesley Shirley, Miriam Smith, Niels van der Aa, Ruby Banerjee, Peter Ellis, Michael A. Quail, Harold Swerdlow, Magdalena Zernicka‐Goetz, Frederick J. Livesey, Chris P. Ponting, Thierry Voet Hit paper breakdown →	2015	529
13	Combined Single-Cell Functional and Gene Expression Analysis Resolves Heterogeneity within Stem Cell Populations Cell stem cell ·Nicola K. Wilson, David G. Kent, Florian Buettner, Mona Shehata, Iain C. Macaulay, Fernando J. Calero‐Nieto, Manuel Sánchez Castillo, Caroline A. Oedekoven, Evangelia Diamanti, Reiner Schulte, Chris P. Ponting, Thierry Voet, Carlos Caldas, Julia Stingl, Anthony R. Green, Fabian J. Theis, Berthold Göttgens	2015	320
14	Single Cell Genomics: Advances and Future Perspectives PLoS Genetics ·Iain C. Macaulay, Thierry Voet	2014	261
15	Mosaic Copy Number Variation in Human Neurons Science ·Michael J. McConnell, Michael Lindberg, Kristen Brennand, Mintesnot Hawaze, Thierry Voet, Stephanie K. Demetriou, Jun-Long Cheng, Roger S. Lasken, Joris Vermeesch, Ira M. Hall, Fred H. Gage Hit paper breakdown →	2013	380
16	Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations Genome Research ·Caroline Robberecht, Thierry Voet, Masoud Zamani Esteki, Beata Nowakowska, Joris Vermeesch	2012	92
17	Single-cell copy number variation detection Genome biology ·Jie Cheng, Evelyne Vanneste, Peter Könings, Thierry Voet, Joris Vermeesch, Yves Moreau	2011	29
18	Genome-wide single cell array analysis for preimplantation genetic diagnosis of a complex chromosomal rearrangement carrier European Journal of Human Genetics ·Evelyne Vanneste, Cindy Melotte, Yana Kristin Siahaan, C. Staessen, I. Liebærs, Thierry Voet, Sophie Debrock, A. Pexsters, Carla Tomassetti, Jean‐Pierre Fryns, Thomas D’Hooghe, Joris Vermeesch	2010	2
19	Haplotyping of single human cells Chromosome Research ·Thierry Voet, Evelyne Vanneste, Hilde Peeters, Peter Könings, Jean‐Pierre Fryns, Thomas D’Hooghe, Yves Moreau, Joris Vermeesch	2009	1
20	Controlled transgene dosage and PAC-mediated transgenesis in mice using a chromosomal vector Genomics ·Thierry Voet, Erik Schoenmakers, Sébastien Carpentier, Peter Oluwatoyin Adewale, Peter Marynen	2003	20

About Thierry Voet

Thierry Voet is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Cancer Research, Molecular Biology and Biophysics, having authored 96 papers that have together received 8.6k indexed citations. Recurring topics across this work include Single-cell and spatial transcriptomics (26 papers), Prenatal Screening and Diagnostics (26 papers), Genomic variations and chromosomal abnormalities (22 papers), Cancer Genomics and Diagnostics (15 papers), Pluripotent Stem Cells Research (9 papers), Renal and related cancers (9 papers), Chromosomal and Genetic Variations (8 papers) and CRISPR and Genetic Engineering (7 papers). The work is most often cited by research in Cancer Research (1.5k citations), Biophysics (478 citations), Molecular Biology (5.5k citations), Pediatrics, Perinatology and Child Health (1.3k citations) and Genetics (1.5k citations). Thierry Voet has collaborated with scholars based in Belgium, United Kingdom and United States. Frequent co-authors include Iain C. Macaulay, Chris P. Ponting, Joris Vermeesch, Alejandro Sifrim, Katy Vandereyken, Bernard Thienpont, Magdalena Zernicka‐Goetz, Parveen Kumar, Niels van der Aa and Evelyne Vanneste. Their work appears in journals such as Nucleic Acids Research, Human Reproduction, Obstetrical & Gynecological Survey, Nature and Genome Research.

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.

Explore authors with similar magnitude of impact