Stefan Meyer

4.4k citations

77 papers · 2.5k indexed · 1 hit paper · h-index 22

Impact in

Otorhinolaryngology top 1%
- Head and Neck Cancer Studies
Hematology top 2%
- Blood groups and transfusion
- Acute Myeloid Leukemia Research

Papers in ⓘ

Hematology 21
- Blood groups and transfusion 11
- Acute Myeloid Leukemia Research 7
Genetics 9
- BRCA gene mutations in cancer 7
- Hemoglobinopathies and Related Disorders 7

Co-authors: Helen V Worthington (3 shared papers)Martin G. McCabe (3 shared papers)Tasneem Khalid (3 shared papers)Jan Clarkson (3 shared papers)Susan Furness (2 shared papers)Elisabetta Padovan (1 shared paper)Manfred Brockhaus (1 shared paper)Giulia Casorati (1 shared paper)
Journals: British Journal of Haematology (7 papers)Transfusion (3 papers)Cochrane Database of Systematic Reviews (3 papers)Science (2 papers)Genes Chromosomes and Cancer (2 papers)
Partner nations: United Kingdom Germany Switzerland

In The Last Decade

Stefan Meyer

72 papers receiving 2.5k citations

Hit Papers

align trajectories log scale

Interventions for treating oral mucositis for patients with cancer receiving treatment 2010 · 418 citations

Peers

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-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 77 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Expression of Two T Cell Receptor α Chains: Dual Receptor T Cells Science ·Elisabetta Padovan, Giulia Casorati, Paolo Dellabona, Stefan Meyer, Manfred Brockhaus, Antonio Lanzavecchia	1993	440
2	Interventions for treating oral mucositis for patients with cancer receiving treatment Cochrane Database of Systematic Reviews ·Jan Clarkson, Helen V Worthington, Susan Furness, Martin G. McCabe, Tasneem Khalid, Stefan Meyer Hit paper breakdown →	2010	418
3	Interventions for preventing oral mucositis for patients with cancer receiving treatment Cochrane Database of Systematic Reviews ·Helen V Worthington, Jan Clarkson, Gemma Bryan, Susan Furness, Anne‐Marie Glenny, Anne Littlewood, Martin G. McCabe, Stefan Meyer, Tasneem Khalid, Philip Riley	2011	174
4	An ancient defense system eliminates unfit cells from developing tissues during cell competition Science ·Stefan Meyer, Marc Amoyel, Cora Bergantiños, Claire de la Cova, Claus Schertel, Konrad Basler, Laura A. Johnston	2014	166
5	Chromosome instability syndromes Nature Reviews Disease Primers ·A. Malcolm R. Taylor, Cynthia Rothblum‐Oviatt, Nathan A. Ellis, Ian D. Hickson, Stefan Meyer, Thomas O. Crawford, Agata Smogorzewska, Barbara Pietrucha, Corry M.R. Weemaes, Grant S. Stewart	2019	123
6	Inactivation of HOXA Genes by Hypermethylation in Myeloid and Lymphoid Malignancy is Frequent and Associated with Poor Prognosis Clinical Cancer Research ·Gordon Strathdee, Tessa L. Holyoake, Alyson Sim, Anton Parker, David Oscier, Junia V. Melo, Stefan Meyer, Tim Eden, Anne M. Dickinson, Joanne C. Mountford, Heather G. Jørgensen, Richard Soutar, Robert Brown	2007	103
7	Aberrant DNA hypermethylation signature in acute myeloid leukemia directed by EVI1 Blood ·Sanne Lugthart, María E. Figueroa, Eric M. Bindels, Lucy Skrabanek, Peter J.M. Valk, Yushan Li, Stefan Meyer, Claudia Erpelinck-Verschueren, John M. Greally, Bob Löwenberg, Ari Melnick, Ruud Delwel	2010	83
8	Acupuncture to Alleviate Chemotherapy-induced Nausea and Vomiting in Pediatric Oncology – A Randomized Multicenter Crossover Pilot Trial Klinische Pädiatrie ·Sven Gottschling, Tobias Reindl, Stefan Meyer, Jens Berrang, G. Henze, Simon Y. Graeber, Marcus Eng Hock Ong, Norbert Graf	2008	68
9	Fanconi anaemia: genetics, molecular biology, and cancer – implications for clinical management in children and adults Clinical Genetics ·Marion Schneider, Kate Chandler, Marc Tischkowitz, Stefan Meyer	2014	54
10	Matrix-Assisted Laser Desorption/Ionisation, Time-of-Flight Mass Spectrometry–Based Blood Group Genotyping—The Alternative Approach Transfusion Medicine Reviews ·Christoph Gassner, Stefan Meyer, Beat M. Frey, Caren Vollmert	2012	53
11	A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell–based assay Blood ·Kajal Biswas, Ranabir Das, Blanche P. Alter, Sergey G. Kuznetsov, Stacey Stauffer, Susan L. North, Sandra Burkett, Lawrence C. Brody, Stefan Meyer, R. Andrew Byrd, Shyam K. Sharan	2011	49
12	Intraoperative Impedance-Based Estimation of Cochlear Implant Electrode Array Insertion Depth IEEE Transactions on Biomedical Engineering ·Philipp Aebischer, Stefan Meyer, Marco Caversaccio, Wilhelm Wimmer	2020	44
13	Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling Journal of Medical Genetics ·Stefan Meyer, Marc Tischkowitz, Kate Chandler, Alan Gillespie, Jillian M. Birch, D. Gareth Evans	2013	41
14	High‐throughput Kell, Kidd, and Duffy matrix‐assisted laser desorption/ionization, time‐of‐flight mass spectrometry–based blood group genotyping of 4000 donors shows close to full concordance with serotyping and detects new alleles Transfusion ·Stefan Meyer, Caren Vollmert, Nadine Trost, Chantal Brönnimann, Jochen Gottschalk, Andreas Buser, Beat M. Frey, Christoph Gassner	2014	38
15	Phosphorylation of the Leukemic Oncoprotein EVI1 on Serine 196 Modulates DNA Binding, Transcriptional Repression and Transforming Ability PLoS ONE ·Daniel J. White, Richard D. Unwin, Eric M. Bindels, Andrew Pierce, Hsiang-Ying Teng, Joanne Muter, Brigit Greystoke, Tim D.D. Somerville, John R. Griffiths, Simon C. Lovell, Tim C. P. Somervaille, Ruud Delwel, Anthony D. Whetton, Stefan Meyer	2013	38
16	Epigenetic inactivation of TWIST2 in acute lymphoblastic leukemia modulates proliferation, cell survival and chemosensitivity Haematologica ·S. H. Thathia, Stuart J. Ferguson, Hannah E. Gautrey, Sanne D. van Otterdijk, M. Hili, Vikki Rand, Anthony V. Moorman, Stefan Meyer, Robert Brown, Gordon Strathdee	2011	35
17	Implementation of a mandatory donor RHD screening in Switzerland Transfusion and Apheresis Science ·Sofia Lejon Crottet, Christine Henny, Stefan Meyer, Franziska Still, Martin Stolz, Jochen Gottschalk, Kathrin Neuenschwander, Behrouz Mansouri Taleghani, Peter Gowland, Beat M. Frey, Stefano Fontana, Hein Hustinx, Christoph Niederhauser, Christoph Gassner	2014	31
18	Physical Exercise Induces Specific Adaptations Resulting in Reduced Organ Injury and Mortality During Severe Polymicrobial Sepsis Critical Care Medicine ·Maik Soßdorf, Jacqueline Fischer, Stefan Meyer, Katja Dahlke, Bianka Wissuwa, C. Seidel, Andrea Schrepper, Clemens L. Bockmeyer, Amelie Lupp, Sophie Neugebauer, Diana Schmerler, Jürgen Rödel, Ralf A. Claus, Gordon P Otto	2013	29
19	Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site Cancer Genetics and Cytogenetics ·Stefan Meyer, Helen Kingston, A. Malcolm R. Taylor, Phillip J. Byrd, James I. Last, Bernadette Brennan, Steve Trueman, Anna Kelsey, Geoffrey Taylor, Osborn B. Eden	2004	29
20	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 ·Stefan Meyer, William Fergusson, Anthony D. Whetton, Flávia Moreira-Leite, Stuart D Pepper, Crispin Miller, Emma Saunders, Daniel J. White, Andrew Will, Tim Eden, Hideyuki Ikeda, Reinhard Ullmann, Seval Tuerkmen, Antje Gerlach, Eva Klopocki, Holger Tönnies	2007	24

About Stefan Meyer

Stefan Meyer is a scholar working on Hematology, Genetics, Molecular Biology, Genetics and Aging, having authored 77 papers that have together received 2.5k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (22 papers), Blood groups and transfusion (11 papers), Erythrocyte Function and Pathophysiology (9 papers), Acute Myeloid Leukemia Research (7 papers), BRCA gene mutations in cancer (7 papers), Hemoglobinopathies and Related Disorders (7 papers), Acute Lymphoblastic Leukemia research (7 papers) and CRISPR and Genetic Engineering (5 papers). The work is most often cited by research in Otorhinolaryngology (307 citations), Hematology (428 citations), Immunology (525 citations), Oncology (526 citations) and Pulmonary and Respiratory Medicine (548 citations). Stefan Meyer has collaborated with scholars based in United Kingdom, Germany and Switzerland. Frequent co-authors include Helen V Worthington, Martin G. McCabe, Tasneem Khalid, Jan Clarkson, Susan Furness, Elisabetta Padovan, Manfred Brockhaus, Giulia Casorati, Paolo Dellabona and Antonio Lanzavecchia. Their work appears in journals such as British Journal of Haematology, Transfusion, Cochrane Database of Systematic Reviews, Science and Genes Chromosomes and Cancer.

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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