Mark Vermeulen

1.7k total citations
11 papers, 747 citations indexed

About

Mark Vermeulen is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Mark Vermeulen has authored 11 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Mark Vermeulen's work include Forensic and Genetic Research (6 papers), Genetic diversity and population structure (5 papers) and Molecular Biology Techniques and Applications (4 papers). Mark Vermeulen is often cited by papers focused on Forensic and Genetic Research (6 papers), Genetic diversity and population structure (5 papers) and Molecular Biology Techniques and Applications (4 papers). Mark Vermeulen collaborates with scholars based in Netherlands, Germany and United Kingdom. Mark Vermeulen's co-authors include Manfred Kayser, Peter de Knijff, Andreas Wollstein, Sofia B. Zuniga, Óscar Lao, Kaye N. Ballantyne, Arwin Ralf, Victoria Keerl, Lutz Roewer and Kristiaan J. van der Gaag and has published in prestigious journals such as Cell stem cell, Journal of General Virology and Human Gene Therapy.

In The Last Decade

Mark Vermeulen

11 papers receiving 730 citations

Peers

Mark Vermeulen

GENET

ARCHE

HEMAT

Lotte Henke Germany

H. Xiao United States

Toshimichi Yamamoto Japan

Alla G. Reddy India

Ali Hellani Saudi Arabia

Klaus Olek Germany

Mark Barash Australia

Abdelaziz Chafik Morocco

Alexandra Rosa Portugal

Mayra Eduardoff Austria

Lotte Henke Germany

Mark Vermeulen

757 ×1.5

GENET

571 ×1.5

79 ×1.0

95 ×1.4

ARCHE

52 ×0.8

HEMAT

Citations per year, relative to Mark Vermeulen Mark Vermeulen (= 1×) peers Lotte Henke

Countries citing papers authored by Mark Vermeulen

Since Specialization

Citations

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

Fields of papers citing papers by Mark Vermeulen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Vermeulen

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

All Works

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

11 of 11 papers shown

Vujadinovic, Marija, Kerstin Wunderlich, Benoît Callendret, et al.. (2017). Adenoviral Type 35 and 26 Vectors with a Bidirectional Expression Cassette in the E1 Region Show an Improved Genetic Stability Profile and Potent Transgene-Specific Immune Response. Human Gene Therapy. 29(3). 337–351. 1 indexed citations

Liu, Fan, Óscar Lao, Ariadne H.A.G. Ooms, et al.. (2014). PHOX2B polyalanine repeat length is associated with sudden infant death syndrome and unclassified sudden infant death in the Dutch population. International Journal of Legal Medicine. 128(4). 621–9. 26 indexed citations

Wunderlich, Kerstin, et al.. (2014). An alternative to the adenovirus inverted terminal repeat sequence increases the viral genome replication rate and provides a selective advantage in vitro. Journal of General Virology. 95(7). 1574–1584. 3 indexed citations

Oven, Mannis van, Mark Vermeulen, & Manfred Kayser. (2011). Multiplex genotyping system for efficient inference of matrilineal genetic ancestry with continental resolution. PubMed. 2(1). 6–6. 26 indexed citations

Gruijter, Johanna M. de, Óscar Lao, Mark Vermeulen, et al.. (2011). Contrasting signals of positive selection in genes involved in human skin-color variation from tests based on SNP scans and resequencing. PubMed. 2(1). 24–24. 13 indexed citations

Ballantyne, Kaye N., Victoria Keerl, Andreas Wollstein, et al.. (2011). A new future of forensic Y-chromosome analysis: Rapidly mutating Y-STRs for differentiating male relatives and paternal lineages. Forensic Science International Genetics. 6(2). 208–218. 179 indexed citations

Vermeulen, Mark, Andreas Wollstein, Kristiaan J. van der Gaag, et al.. (2009). Improving global and regional resolution of male lineage differentiation by simple single-copy Y-chromosomal short tandem repeat polymorphisms. Forensic Science International Genetics. 3(4). 205–213. 75 indexed citations

Robin, Catherine, Karine Bollérot, Sandra Mendes, et al.. (2009). Human Placenta Is a Potent Hematopoietic Niche Containing Hematopoietic Stem and Progenitor Cells throughout Development. Cell stem cell. 5(4). 385–395. 155 indexed citations

Goedbloed, Miriam, Mark Vermeulen, Rixun Fang, et al.. (2009). Comprehensive mutation analysis of 17 Y-chromosomal short tandem repeat polymorphisms included in the AmpFlSTR® Yfiler® PCR amplification kit. International Journal of Legal Medicine. 123(6). 471–482. 110 indexed citations

10.

Corach, Daniel, Óscar Lao, Cecilia Bobillo, et al.. (2009). Inferring Continental Ancestry of Argentineans from Autosomal, Y‐Chromosomal and Mitochondrial DNA. Annals of Human Genetics. 74(1). 65–76. 128 indexed citations

11.

Kayser, Manfred, Mark Vermeulen, Hans Knoblauch, et al.. (2007). Relating two deep-rooted pedigrees from Central Germany by high-resolution Y-STR haplotyping. Forensic Science International Genetics. 1(2). 125–128. 31 indexed citations

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