Michael Kwint

3.4k citations

19 papers · 813 · h-index 12

Impact in

Cancer Research top 10%
- Cancer Genomics and Diagnostics
Pathology and Forensic Medicine top 5%
- Genetic factors in colorectal cancer

Papers in

Molecular Biology 12
- Retinal Development and Disorders 5
- Genomics and Phylogenetic Studies 4
- CRISPR and Genetic Engineering 2
Genetics 7
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3

Co-authors: Joris A. Veltman (4 shared papers)Kornelia Neveling (6 shared papers)Huub J. M. Op den Camp (2 shared papers)Bas E. Dutilh (2 shared papers)Mike S. M. Jetten (2 shared papers)Lisenka E.L.M. Vissers (9 shared papers)Christian Gilissen (11 shared papers)Arjen R. Mensenkamp (2 shared papers)
Journals: European Journal of Human Genetics (4 papers)The American Journal of Human Genetics (2 papers)Human Genetics and Genomics Advances (1 paper)Environmental Microbiology Reports (1 paper)Archives of Medical Research (1 paper)
Partner nations: Netherlands United States Italy

In The Last Decade

Michael Kwint

17 papers receiving 809 citations

Peers

Countries citing papers authored by Michael Kwint

Since Specialization

Citations

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

Fields of papers citing papers by Michael Kwint

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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19 of 19 papers shown

#	Work
1	Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like Tumors Gastroenterology ·Arjen R. Mensenkamp, Ingrid P. Vogelaar, Wendy A.G. van Zelst–Stams, Monique Goossens, Hicham Ouchene, Sandra J. B. Hendriks-Cornelissen, Michael Kwint, Nicoline Hoogerbrugge, Irıs D. Nagtegaal, Marjolijn J. L. Ligtenberg	2013	230
2	Pyrosequencing of 16S rRNA gene amplicons to study the microbiota in the gastrointestinal tract of carp (Cyprinus carpio L.) AMB Express ·Maartje A. H. J. van Kessel, Bas E. Dutilh, Kornelia Neveling, Michael Kwint, Joris A. Veltman, Gert Flik, Mike S. M. Jetten, Peter H.M. Klaren, Huub J. M. Op den Camp	2011	204
3	Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation The American Journal of Human Genetics ·Rocío Acuña‐Hidalgo, Tan Bo, Michael Kwint, Maartje van de Vorst, Michele Pinelli, Joris A. Veltman, Alexander Hoischen, Lisenka E.L.M. Vissers, Christian Gilissen	2015	152
4	Ultra‐deep pyrosequencing of pmoA amplicons confirms the prevalence of Methylomonas and Methylocystis in Sphagnum mosses from a Dutch peat bog Environmental Microbiology Reports ·Nardy Kip, Bas E. Dutilh, Yao Pan, Levente Bodrossy, Kornelia Neveling, Michael Kwint, Mike S. M. Jetten, Huub J. M. Op den Camp	2011	52
5	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	28
6	Long-read trio sequencing of individuals with unsolved intellectual disability European Journal of Human Genetics ·Marc Pauper, Erdi Küçük, Aaron M. Wenger, Shreyasee Chakraborty, Primo Baybayan, Michael Kwint, Bart van der Sanden, Marcel Nelen, Ronny Derks, Han G. Brunner, Alexander Hoischen, Lisenka E.L.M. Vissers, Christian Gilissen	2020	24
7	Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis The American Journal of Human Genetics ·David Coman, Lisenka E.L.M. Vissers, Lisa G. Riley, Michael Kwint, Roxanna Hauck, Janet Koster, Sinje Geuer, Sarah Hopkins, Barbra Hallinan, Larry Sweetman, Udo F. H. Engelke, T. Burrow, John Cardinal, James McGill, Anita Inwood, Christine Gurnsey, Hans R. Waterham, John Christodoulou, Ron A. Wevers, James Pitt	2018	23
8	Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome European Journal of Human Genetics ·Michèl A.A.P. Willemsen, Lisenka E.L.M. Vissers, Marcel M. Verbeek, Bregje W.M. van Bon, Sinje Geuer, Christian Gilissen, Joerg Klepper, Michael Kwint, Wilhelmina G. Leen, Maartje Pennings, Ron A. Wevers, Joris A. Veltman, Erik‐Jan Kamsteeg	2017	19
9	Comprehensive de novo mutation discovery with HiFi long-read sequencing Genome Medicine ·Erdi Küçük, Bart van der Sanden, Luke O’Gorman, Michael Kwint, Ronny Derks, Aaron M. Wenger, Christine Lambert, Shreyasee Chakraborty, Primo Baybayan, William J. Rowell, Han G. Brunner, Lisenka E.L.M. Vissers, Alexander Hoischen, Christian Gilissen	2023	18
10	Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome Journal of the American Society of Nephrology ·Daan H.H.M. Viering, Marguerite Hureaux, Kornelia Neveling, Femke Latta, Michael Kwint, Anne Blanchard, Martin Konrad, René J.M. Bindels, Karl P. Schlingmann, Rosa Vargas‐Poussou, Jeroen H. F. de Baaij	2022	14
11	Long-read technologies identify a hidden inverted duplication in a family with choroideremia SHILAP Revista de lepidopterología ·Zeinab Fadaie, Kornelia Neveling, Tuomo Mantere, Ronny Derks, Lonneke Haer‐Wigman, Amber den Ouden, Michael Kwint, Luke O’Gorman, Dyon Valkenburg, Carel B. Hoyng, Christian Gilissen, Lisenka E.L.M. Vissers, Marcel Nelen, Frans P.M. Cremers, Alexander Hoischen, Susanne Roosing	2021	13
12	DeNovoCNN: a deep learning approach to de novo variant calling in next generation sequencing data Nucleic Acids Research ·Gelana Khazeeva, Karolis Šablauskas, Bart van der Sanden, Wouter Steyaert, Michael Kwint, Dmitrijs Rots, Max Hinne, Marcel van Gerven, Helger G. Yntema, Lisenka E.L.M. Vissers, Christian Gilissen	2022	11
13	Targeted Next Generation Sequencing Reveals a Novel Intragenic Deletion of the TPO Gene in a Family with Intellectual Disability Archives of Medical Research ·Zafar Iqbal, Kornelia Neveling, Attia Razzaq, Mohsin Shahzad, Muhammad Yasir Zahoor, Muhammad Qasim, Christian Gilissen, Nienke Wieskamp, Michael Kwint, Sabine Gijsen, Arjan P.M. de Brouwer, Joris A. Veltman, Sheikh Riazuddin, Hans van Bokhoven	2012	10
14	The Predicted Splicing Variant c.11+5G>A in RPE65 Leads to a Reduction in mRNA Expression in a Cell-Specific Manner Cells ·Irene Vázquez-Domínguez, Lonneke Duijkers, Zeinab Fadaie, Eef C. W. Alaerds, Merel A. Post, Edwin van Oosten, Luke O’Gorman, Michael Kwint, Louet Koolen, Anita D. M. Hoogendoorn, Hester Y. Kroes, Christian Gilissen, Frans P.M. Cremers, Rob W.J. Collin, Susanne Roosing, Alejandro Garanto	2022	8
15	Correction: Long-read trio sequencing of individuals with unsolved intellectual disability European Journal of Human Genetics ·Marc Pauper, Erdi Küçük, Aaron M. Wenger, Shreyasee Chakraborty, Primo Baybayan, Michael Kwint, Bart van der Sanden, Marcel Nelen, Ronny Derks, Han G. Brunner, Alexander Hoischen, Lisenka E.L.M. Vissers, Christian Gilissen	2021	5
16	Uncovering recessive alleles in rare Mendelian disorders by genome sequencing of 174 individuals with monoallelic pathogenic variants European Journal of Human Genetics ·Gaby Schobers, Maartje Pennings, Juliette de Vries, Michael Kwint, Jeroen van Reeuwijk, Jordi Corominas Galbany, Ronald van Beek, Eveline J. Kamping, Raoul Timmermans, Erik‐Jan Kamsteeg, Lonneke Haer‐Wigman, Frans P M Cremers, Susanne Roosing, Christian Gilissen, Hannie Kremer, Han G. Brunner, Helger G. Yntema, Lisenka E.L.M. Vissers	2024	1
17	Generation of a patient-derived induced pluripotent cell line (SCTCi016-A) carrying a homozygous variant in RPE65 Stem Cell Research ·Irene Vázquez-Domínguez, Michael Kwint, Hester Y. Kroes, Sílvia Albert, Luke O’Gorman, Christian Gilissen, Frans P.M. Cremers, Rob W.J. Collin, Susanne Roosing, Alejandro Garanto	2022	1
18	Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches Genome Research ·Merel Stemerdink, Tabea Riepe, Nick Zomer, Renee Salz, Michael Kwint, Jaap Oostrik, Raoul Timmermans, Barbara Ferrari, Stefano Ferrari, Alfredo Dueñas Rey, Emma Delanote, Suzanne E. de Bruijn, Hannie Kremer, Susanne Roosing, Frauke Coppieters, Alexander Hoischen, Frans P.M. Cremers, Peter A.C. ’t Hoen, Erwin van Wijk, Erik de Vrieze	2025	0
19	Targeted long-read cDNA sequencing reveals novel splice-altering pathogenic variants causing retinal dystrophies Human Genetics and Genomics Advances ·Dalila Capasso, Roberta Zeuli, Gavin Arno, Michael Kwint, Raoul Timmermans, Karla Alejandra Ruiz-Ceja, Marianthi Karali, Francesca Simonelli, Sabrina Signorini, Enza Maria Valente, Frans P.M. Cremers, Sandro Banfi, Susanne Roosing, Daan M. Panneman, Suzanne E. de Bruijn	2025	0

About Michael Kwint

Michael Kwint is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Immunology and Surgery, having authored 19 papers that have together received 813 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Retinal Development and Disorders (5 papers), Genomics and Phylogenetic Studies (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetic factors in colorectal cancer (2 papers), CRISPR and Genetic Engineering (2 papers), Microbial Community Ecology and Physiology (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Cancer Research (217 citations), Pathology and Forensic Medicine (235 citations), Aquatic Science (74 citations), Immunology (160 citations) and Genetics (208 citations). Michael Kwint has collaborated with scholars based in Netherlands, United States and Italy. Frequent co-authors include Joris A. Veltman, Kornelia Neveling, Huub J. M. Op den Camp, Bas E. Dutilh, Mike S. M. Jetten, Lisenka E.L.M. Vissers, Christian Gilissen, Arjen R. Mensenkamp, Hicham Ouchene and Alexander Hoischen. Their work appears in journals such as European Journal of Human Genetics, The American Journal of Human Genetics, Human Genetics and Genomics Advances, Environmental Microbiology Reports and Archives of Medical 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.

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Michael Kwint

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