Stephan Menzel

8.8k total citations · 1 hit paper
81 papers, 3.9k citations indexed

About

Stephan Menzel is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Stephan Menzel has authored 81 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 41 papers in Hematology and 26 papers in Molecular Biology. Recurrent topics in Stephan Menzel's work include Hemoglobinopathies and Related Disorders (51 papers), Iron Metabolism and Disorders (25 papers) and Blood groups and transfusion (24 papers). Stephan Menzel is often cited by papers focused on Hemoglobinopathies and Related Disorders (51 papers), Iron Metabolism and Disorders (25 papers) and Blood groups and transfusion (24 papers). Stephan Menzel collaborates with scholars based in United Kingdom, United States and France. Stephan Menzel's co-authors include Swee Lay Thein, Graeme I. Bell, Pamela J. Kaisaki, Kazuya Yamagata, Stefan S. Fajans, Naohisa Oda, Markus Stoffel, Steve Best, Nancy J. Cox and Tim D. Spector and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Stephan Menzel

77 papers receiving 3.9k 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.

Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1)

1996 764 citations Kazuya Yamagata, Hiroto Furuta et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephan Menzel United Kingdom	30	1.9k	1.6k	1.4k	1.2k	1.2k	81	3.9k
Melanie J. Percy United Kingdom	31	876 0.5×	1.1k 0.7×	787 0.5×	175 0.1×	677 0.6×	81	2.8k
Dieter Printz Austria	29	290 0.2×	911 0.6×	1.1k 0.8×	237 0.2×	185 0.2×	62	3.2k
G Stamatoyannopoulos United States	29	1.5k 0.8×	999 0.6×	1.1k 0.8×	66 0.1×	334 0.3×	104	2.6k
R. Galanello Italy	37	3.5k 1.9×	699 0.4×	3.0k 2.1×	81 0.1×	337 0.3×	128	4.3k
Lesley J. Bruce United Kingdom	29	415 0.2×	1.1k 0.7×	572 0.4×	212 0.2×	166 0.1×	80	2.7k
Michael J. Thirman United States	36	671 0.4×	2.3k 1.4×	2.4k 1.7×	87 0.1×	214 0.2×	90	4.0k
M Seip Norway	22	238 0.1×	702 0.4×	422 0.3×	141 0.1×	284 0.2×	81	1.9k
Joy D. Cogan United States	37	360 0.2×	1.4k 0.9×	58 0.0×	561 0.5×	962 0.8×	84	5.0k
Archana M. Agarwal United States	22	386 0.2×	647 0.4×	299 0.2×	108 0.1×	106 0.1×	104	1.6k
SJ Lauer United States	16	153 0.1×	586 0.4×	321 0.2×	292 0.2×	168 0.1×	19	1.6k

Countries citing papers authored by Stephan Menzel

Since Specialization

Citations

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

Fields of papers citing papers by Stephan Menzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Menzel

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

All Works

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20 of 20 papers shown

Stephanou, Coralea, Stephan Menzel, Sjaak Philipsen, & Petros Kountouris. (2024). Genetic Polymorphisms Associated with Fetal Hemoglobin (HbF) Levels and F-Cell Numbers: A Systematic Review of Genome-Wide Association Studies. International Journal of Molecular Sciences. 25(21). 11408–11408. 1 indexed citations

Adeyemo, Titilope A., et al.. (2021). Fetal‐haemoglobin enhancing genotype at BCL11A reduces HbA₂ levels in patients with sickle cell anaemia. SHILAP Revista de lepidopterología. 2(3). 459–461. 3 indexed citations

Brewin, John, Alexander Smith, Sanjay Tewari, et al.. (2020). Genetic Analysis of Patients With Sickle Cell Anemia and Stroke Before 4 Years of Age Suggest an Important Role for Apoliprotein E. Circulation Genomic and Precision Medicine. 13(5). 531–540. 8 indexed citations

Tewari, Sanjay, John Brewin, Kate Gardner, et al.. (2018). Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarction. Haematologica. 103(7). 1136–1142. 16 indexed citations

Menzel, Stephan, Tanja Holland, Alexander Boes, et al.. (2016). Optimized Blanching Reduces the Host Cell Protein Content and Substantially Enhances the Recovery and Stability of Two Plant-Derived Malaria Vaccine Candidates. Frontiers in Plant Science. 7. 159–159. 33 indexed citations

Stadhouders, Ralph, Süleyman Aktuna, Supat Thongjuea, et al.. (2014). HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers. Journal of Clinical Investigation. 124(4). 1699–1710. 142 indexed citations

Thein, Swee Lay, Stephan Menzel, Mark Lathrop, & C. Garner. (2009). Control of fetal hemoglobin: new insights emerging from genomics and clinical implications. Human Molecular Genetics. 18(R2). R216–R223. 183 indexed citations

Creary, Lisa E., Pinar Ulug, Stephan Menzel, et al.. (2009). Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients. PLoS ONE. 4(1). e4218–e4218. 68 indexed citations

Ulug, Pinar, Nisha Vasavda, Rohan Kumar, et al.. (2008). Hydroxyurea therapy lowers circulating DNA levels in sickle cell anemia. American Journal of Hematology. 83(9). 714–716. 7 indexed citations

10.

Creary, Lisa E., Stephan Menzel, Neil A. Hanchard, et al.. (2008). Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobin. British Journal of Haematology. 144(6). 954–960. 7 indexed citations

11.

Menzel, Stephan, et al.. (2007). Evaluation von Forschungsvorhaben nach einem positiven Votum einer Ethikkommission. DMW - Deutsche Medizinische Wochenschrift. 132(44). 2313–2317. 10 indexed citations

12.

Vasavda, Nisha, Stephan Menzel, Moji Awogbade, et al.. (2007). The linear effects of α‐thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease. British Journal of Haematology. 138(2). 263–270. 58 indexed citations

13.

Lai, Mei I, Jie Jiang, Nicholas Silver, et al.. (2006). α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia. British Journal of Haematology. 133(6). 675–682. 54 indexed citations

14.

Lai, Mei I, Stephan Menzel, Juan Jiang, Mitchell J. Weiss, & SL Thein. (2005). Alpha haemoglobin stabilizing protein expression in thalassaemia intermedia. Blood Cells Molecules and Diseases. 34(2). 1 indexed citations

15.

Garner, Chad, Steve Best, Stephan Menzel, et al.. (2005). Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin. European Journal of Human Genetics. 14(1). 101–108. 13 indexed citations

16.

Garner, C., Stephan Menzel, Charlotte Martin, et al.. (2005). Interaction Between Two Quantitative Trait Loci Affects Fetal Haemoglobin Expression. Annals of Human Genetics. 69(6). 707–714. 17 indexed citations

17.

Wiltshire, Steven, Timothy M. Frayling, Andrew T. Hattersley, et al.. (2002). Evidence for Linkage of Stature to Chromosome 3p26 in a Large U.K. Family Data Set Ascertained for Type 2 Diabetes. The American Journal of Human Genetics. 70(2). 543–546. 48 indexed citations

18.

Menzel, Stephan. (2002). Genetic and Molecular Analyses of Complex Metabolic Disorders: Genetic Linkage. Annals of the New York Academy of Sciences. 967(1). 249–257. 20 indexed citations

19.

McCarthy, Mark I. & Stephan Menzel. (2001). The genetics of type 2 diabetes. British Journal of Clinical Pharmacology. 51(3). 195–199. 29 indexed citations

20.

Yamagata, Kazuya, Hiroto Furuta, Naohisa Oda, et al.. (1996). Mutations in the hepatocyte nuclear factor-4α gene in maturity-onset diabetes of the young (MODY1). Nature. 384(6608). 458–460. 764 indexed citations breakdown →

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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