Mark Drost

570 citations

16 papers · 302 · h-index 11

Impact in

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

Papers in

Pathology and Forensic Medicine 14
- Genetic factors in colorectal cancer 14
Cancer Research 13
- Cancer Genomics and Diagnostics 13

Co-authors: Niels de Wind (15 shared papers)Lene Juel Rasmussen (6 shared papers)Robert M.W. Hofstra (2 shared papers)Sean V. Tavtigian (3 shared papers)José B.M. Zonneveld (3 shared papers)Brigitte Royer‐Pokora (1 shared paper)Hans Morreau (2 shared papers)Hans F. A. Vasen (1 shared paper)
Journals: Human Mutation (6 papers)Clinical Cancer Research (1 paper)Molecular Carcinogenesis (1 paper)Familial Cancer (1 paper)Frontiers in Genetics (1 paper)
Partner nations: Netherlands Denmark Australia

In The Last Decade

Mark Drost

15 papers receiving 300 citations

Peers

Countries citing papers authored by Mark Drost

Since Specialization

Citations

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

Fields of papers citing papers by Mark Drost

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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16 of 16 papers shown

#	Work
1	Adjuvant Treatment for POLE Proofreading Domain–Mutant Cancers: Sensitivity to Radiotherapy, Chemotherapy, and Nucleoside Analogues Clinical Cancer Research ·Inge C. van Gool, Emily Rayner, Elisabeth M. Osse, Remi A. Nout, Carien L. Creutzberg, Ian Tomlinson, David N. Church, Vincent T.H.B.M. Smit, Niels de Wind, Tjalling Bosse, Mark Drost	2018	58
2	Pathological assessment of mismatch repair gene variants in Lynch syndrome: Past, present, and future Human Mutation ·Lene Juel Rasmussen, Christopher D. Heinen, Brigitte Royer‐Pokora, Mark Drost, Sean V. Tavtigian, Robert M.W. Hofstra, Niels de Wind	2012	48
3	A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1 Human Mutation ·Mark Drost, Jos é B.M. Zonneveld, Linda van Dijk, Hans Morreau, Carli M.J. Tops, Hans F. A. Vasen, Juul Wijnen, Niels de Wind	2009	48
4	A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants Human Mutation ·Mark Drost, José B.M. Zonneveld, Sandrine van Hees, Lene Juel Rasmussen, Robert M.W. Hofstra, Niels de Wind	2011	34
5	Inactivation of DNA Mismatch Repair by Variants of Uncertain Significance in the PMS2 Gene Human Mutation ·Mark Drost, Hester Koppejan, Niels de Wind	2013	22
6	Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome Genetics in Medicine ·Mark Drost, Yvonne Tiersma, Dylan M. Glubb, Scott D. Kathe, Sandrine van Hees, Fabienne M.G.R. Calléja, José B.M. Zonneveld, Kenneth M. Boucher, Renuka P.E. Ramlal, Bryony A. Thompson, Lene Juel Rasmussen, Marc S. Greenblatt, Andrea Lee, Amanda B. Spurdle, Sean V. Tavtigian, Niels de Wind	2020	16
7	Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome Proceedings of the National Academy of Sciences ·Mark Drost, Anne Lützen, Sandrine van Hees, Daniel Ferreira, Fabienne M.G.R. Calléja, José B.M. Zonneveld, Finn Cilius Nielsen, Lene Juel Rasmussen, Niels de Wind	2013	16
8	Functional characterization ofMLH1missense variants identified in lynch syndrome patients Human Mutation ·Sofie Dabros Andersen, Sascha Emilie Liberti, Anne Lützen, Mark Drost, Inge Bernstein, Mef Nilbert, Mev Dominguez–Valentin, Minna Nyström, Thomas van Overeem Hansen, Janus Wiese Christoffersen, Anne Charlotte Jäger, Niels de Wind, Finn Cilius Nielsen, Pernille Mathiesen Tørring, Lene Juel Rasmussen	2012	15
9	Consequences of germline variation disrupting the constitutional translational initiation codon start sites of MLH1 and BRCA2: Use of potential alternative start sites and implications for predicting variant pathogenicity Molecular Carcinogenesis ·Michael T. Parsons, Phillip J Whiley, Jonathan Beesley, Mark Drost, Niels de Wind, Bryony A. Thompson, Louise Marquart, John L. Hopper, Mark A. Jenkins, (unknown), Melissa A. Brown, Kathy Tucker, Linda Warwick, Daniel D. Buchanan, Amanda B. Spurdle	2013	12
10	Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation Frontiers in Genetics ·Bryony A. Thompson, Rhiannon Walters, Michael T. Parsons, Troy Dumenil, Mark Drost, Yvonne Tiersma, Noralane M. Lindor, Sean V. Tavtigian, Niels de Wind, Amanda B. Spurdle	2020	11
11	Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer Genes Chromosomes and Cancer ·Stephanie A Schubert, Dina Ruano, Yvonne Tiersma, Mark Drost, Niels de Wind, Maartje Nielsen, Liselotte P. van Hest, Hans Morreau, Noel F.C.C. de Miranda, Tom van Wezel	2020	10
12	Predictive functional assay‐based classification of PMS2 variants in Lynch syndrome Human Mutation ·Emily Rayner, Yvonne Tiersma, Cristina Fortuño, Sandrine van Hees‐Stuivenberg, Mark Drost, Bryony A. Thompson, Amanda B. Spurdle, Niels de Wind	2022	5
13	Induction of mismatch repair deficiency, compromised DNA damage signaling and compound hypermutagenesis by a dietary mutagen in a cell-based model for Lynch syndrome Carcinogenesis ·Robbert Ijsselsteijn, Sandrine van Hees, Mark Drost, Jacob G. Jansen, Niels de Wind	2021	4
14	Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity Familial Cancer ·Michael Farrell, David J. Hughes, Mark Drost, Andrew J. Wallace, Robert Cummins, Tracy Fletcher, Marie Meany, Elaine W. Kay, Niels de Wind, Derek G. Power, E. Andrews, Andrew Green, David Gallagher	2013	2
15	Functional implications of the p.Cys680Arg mutation in the MLH1 mismatch repair protein Molecular Genetics & Genomic Medicine ·Mev Dominguez–Valentin, Mark Drost, Christina Therkildsen, Eva Rambech, Hans Ehrencrona, Maria Angleys, Thomas Lau Hansen, Niels de Wind, Mef Nilbert, Lene Juel Rasmussen	2014	1
16	Chorionic Villus Sampling for Rapid Confirmation of High‐Risk NIPT Results for Trisomy 21, 18, and 13 Prenatal Diagnosis ·Malgorzata I. Srebniak, Marjolein J.A. Weerts, Marieke Joosten, Mark Drost, Robert‐Jan H. Galjaard, Vyne van der Schoot, Myrthe van den Born, Maarten F. C. M. Knapen, Krista Prinsen, Jérôme Cornette, Philip DeKoninck, Dimitri Papatsonis, Julia J. Spaan, Anneke Dijkman, Sabina de Weerd, Attie T. J. I. Go, Karin E. M. Diderich, Diane Van Opstal	2025	0

About Mark Drost

Mark Drost is a scholar working on Pathology and Forensic Medicine, Cancer Research, Genetics, Molecular Biology and Oncology, having authored 16 papers that have together received 302 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (14 papers), Cancer Genomics and Diagnostics (13 papers), RNA Research and Splicing (4 papers), Genomics and Rare Diseases (4 papers), DNA Repair Mechanisms (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Colorectal Cancer Treatments and Studies (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (214 citations), Cancer Research (165 citations), Obstetrics and Gynecology (48 citations), Reproductive Medicine (33 citations) and Genetics (76 citations). Mark Drost has collaborated with scholars based in Netherlands, Denmark and Australia. Frequent co-authors include Niels de Wind, Lene Juel Rasmussen, Robert M.W. Hofstra, Sean V. Tavtigian, José B.M. Zonneveld, Brigitte Royer‐Pokora, Hans Morreau, Hans F. A. Vasen, Carli M.J. Tops and Juul Wijnen. Their work appears in journals such as Human Mutation, Clinical Cancer Research, Molecular Carcinogenesis, Familial Cancer and Frontiers in Genetics.

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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