Stefan Meyer

4.4k total citations · 1 hit paper
77 papers, 2.5k citations indexed

About

Stefan Meyer is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Stefan Meyer has authored 77 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 21 papers in Hematology and 16 papers in Genetics. Recurrent topics in Stefan Meyer's work include DNA Repair Mechanisms (22 papers), Blood groups and transfusion (11 papers) and Erythrocyte Function and Pathophysiology (9 papers). Stefan Meyer is often cited by papers focused on DNA Repair Mechanisms (22 papers), Blood groups and transfusion (11 papers) and Erythrocyte Function and Pathophysiology (9 papers). Stefan Meyer collaborates with scholars based in United Kingdom, Germany and Switzerland. Stefan Meyer's co-authors include Jan Clarkson, Tasneem Khalid, Martin G. McCabe, Helen V Worthington, Susan Furness, Paolo Dellabona, Giulia Casorati, Manfred Brockhaus, Antonio Lanzavecchia and Elisabetta Padovan and has published in prestigious journals such as Science, Blood and PLoS ONE.

In The Last Decade

Stefan Meyer

72 papers receiving 2.5k 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.

Interventions for treating oral mucositis for patients with cancer receiving treatment

2010 418 citations Stefan Meyer et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Stefan Meyer United Kingdom	22	863	548	526	525	428	77	2.5k
Juan Fang China	28	795 0.9×	257 0.5×	584 1.1×	439 0.8×	315 0.7×	87	2.4k
Phong T. Le United States	28	474 0.5×	99 0.2×	306 0.6×	926 1.8×	247 0.6×	61	2.1k
Atsushi Satō Japan	26	831 1.0×	429 0.8×	665 1.3×	299 0.6×	236 0.6×	190	2.6k
Anthony W.I. Lo Hong Kong	30	1.0k 1.2×	302 0.6×	514 1.0×	278 0.5×	55 0.1×	88	2.9k
Seunghee Kim‐Schulze United States	30	768 0.9×	188 0.3×	1.3k 2.5×	1.6k 3.0×	124 0.3×	113	3.4k
Deborah Phippard United States	26	773 0.9×	221 0.4×	410 0.8×	764 1.5×	104 0.2×	42	4.1k
Kunihiko Ito Japan	49	1.1k 1.3×	443 0.8×	834 1.6×	582 1.1×	78 0.2×	274	6.7k
Sung Ho Park South Korea	26	987 1.1×	146 0.3×	334 0.6×	1.2k 2.3×	129 0.3×	58	2.8k
Tsuyoshi Tanabe Japan	30	851 1.0×	624 1.1×	193 0.4×	697 1.3×	93 0.2×	85	2.7k
David P. Huston United States	33	484 0.6×	431 0.8×	263 0.5×	1.7k 3.3×	101 0.2×	102	3.6k

Countries citing papers authored by Stefan Meyer

Since Specialization

Citations

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

Fields of papers citing papers by Stefan Meyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Meyer

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan Meyer. A scholar is included among the top collaborators of Stefan Meyer 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 Stefan Meyer. Stefan Meyer 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:

20 of 20 papers shown

Whittle, Jessica S., et al.. (2025). Single-cell atlas of AML reveals age-related gene regulatory networks in t(8;21) AML. eLife. 14.

Thun, Gian Andri, Morgan Gueuning, Linda Schneider, et al.. (2024). Novel regulatory variant in ABO intronic RUNX1 binding site inducing A ₃ phenotype. Vox Sanguinis. 119(4). 377–382. 2 indexed citations

Gueuning, Morgan, Gian Andri Thun, Linda Schneider, et al.. (2024). Resolving Genotype–Phenotype Discrepancies of the Kidd Blood Group System Using Long-Read Nanopore Sequencing. Biomedicines. 12(1). 225–225. 3 indexed citations

Foster, Benjamin M., et al.. (2024). Small-Molecule Inhibition of CBX4/7 Hypersensitises Homologous Recombination-Impaired Cancer to Radiation by Compromising CtIP-Mediated DNA End Resection. Cancers. 16(11). 2155–2155. 1 indexed citations

Ma, Jie, Stefan Meyer, Johanna Olweus, Chuan Jin, & Di Yu. (2024). An adjusted droplet digital PCR assay for quantification of vector copy number in CAR-T cell and TCR-T cell products. Immuno-Oncology Technology. 25. 101031–101031.

Paredes, Roberto, et al.. (2021). EVI1 protein interaction dynamics: Targetable for therapeutic intervention?. Experimental Hematology. 107. 1–8. 4 indexed citations

Ellingford, Jamie M., Nick Telford, Jill Urquhart, et al.. (2021). High penetrance of myeloid neoplasia with diverse clinical and cytogenetic features in three siblings with a familial GATA2 deficiency. Cancer Genetics. 256-257. 77–80. 1 indexed citations

Gassner, Christoph, Gregory A. Denomme, Maja P. Mattle‐Greminger, et al.. (2020). Two Prevalent ∼100-kb <b><i>GYPB</i></b> Deletions Causative of the GPB-Deficient Blood Group MNS Phenotype S–s–U– in Black Africans. Transfusion Medicine and Hemotherapy. 47(4). 326–336. 7 indexed citations

Meyer, Stefan, et al.. (2017). A uniform method for the simultaneous blood group phenotyping of Fy^a, Fy^b, Jk^a, Jk^b, S, s, P1, k applying lateral‐flow technique. Vox Sanguinis. 113(2). 177–184. 10 indexed citations

10.

Stivaros, Stavros, Kate Chandler, Denise Bonney, et al.. (2015). Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imaging. British Journal of Radiology. 88(1056). 20150088–20150088. 19 indexed citations

11.

Meyer, Stefan, Marc Amoyel, Cora Bergantiños, et al.. (2014). An ancient defense system eliminates unfit cells from developing tissues during cell competition. Science. 346(6214). 1258236–1258236. 166 indexed citations

12.

Meyer, Stefan, Jochen Gottschalk, Behrouz Mansouri Taleghani, et al.. (2014). Implementation of a mandatory donor RHD screening in Switzerland. Transfusion and Apheresis Science. 50(2). 169–174. 31 indexed citations

13.

Gassner, Christoph, Stefan Meyer, Beat M. Frey, & Caren Vollmert. (2012). Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry–Based Blood Group Genotyping—The Alternative Approach. Transfusion Medicine Reviews. 27(1). 2–9. 53 indexed citations

14.

Strathdee, Gordon, Tessa L. Holyoake, Anton Parker, et al.. (2007). Inactivation of HOXA Genes by Hypermethylation in Myeloid and Lymphoid Malignancy is Frequent and Associated with Poor Prognosis. Clinical Cancer Research. 13(17). 5048–5055. 103 indexed citations

15.

Meyer, Stefan, William Fergusson, Anthony D. Whetton, et al.. (2007). Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes Chromosomes and Cancer. 46(4). 359–372. 24 indexed citations

16.

Meyer, Stefan, Wolfgang E. Kaminski, Péter Horn, et al.. (2005). Elastosis perforans serpiginosa-like pseudoxanthoma elasticum in a child with severe Moya Moya disease. British Journal of Dermatology. 153(2). 431–434. 11 indexed citations

17.

Meyer, Stefan, H. Tönnies, Quinten Waisfisz, et al.. (2005). Persistent chromosomal instability and cross-linker sensitivity in Fanconi anaemia derived leukaemia cell lines with bi-allelic FANCD1/BRCA2 mutations. British Journal of Haematology. 129. 81–81. 1 indexed citations

18.

Meyer, Stefan, Helen Kingston, A. Malcolm R. Taylor, et al.. (2004). Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site. Cancer Genetics and Cytogenetics. 154(2). 169–174. 29 indexed citations

19.

McGrath, Helen E., Stefan Meyer, Andrew Will, et al.. (2003). Constitutional sequence variation in the Fanconi anaemia group C (FANCC) gene in childhood acute myeloid leukaemia. British Journal of Haematology. 121(1). 57–62. 15 indexed citations

20.

Yarom, R., et al.. (1982). Metal Impregnation Abnormalities in Platelets of Patients with Idiopathic Scoliosis. Pathophysiology of Haemostasis and Thrombosis. 12(3). 282–288. 15 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.

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