Uwe Menzel

3.7k total citations
30 papers, 884 citations indexed

About

Uwe Menzel is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Uwe Menzel has authored 30 papers receiving a total of 884 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Uwe Menzel's work include Genomic variations and chromosomal abnormalities (4 papers), Neurofibromatosis and Schwannoma Cases (4 papers) and Genetics, Aging, and Longevity in Model Organisms (3 papers). Uwe Menzel is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Neurofibromatosis and Schwannoma Cases (4 papers) and Genetics, Aging, and Longevity in Model Organisms (3 papers). Uwe Menzel collaborates with scholars based in Sweden, Germany and United States. Uwe Menzel's co-authors include Jan P. Dumanski, Teresita Díaz de Ståhl, Matthias Platzer, Johanna Sandgren, Jan Komorowski, Arkadiusz Piotrowski, Robin Andersson, Carl E.G. Bruder, Marco Groth and Patrick G. Buckley and has published in prestigious journals such as Bioinformatics, PLoS ONE and Cancer Research.

In The Last Decade

Uwe Menzel

29 papers receiving 868 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Uwe Menzel Sweden 20 488 275 141 111 91 30 884
Johanna Sandgren Sweden 12 425 0.9× 335 1.2× 241 1.7× 71 0.6× 145 1.6× 21 818
Jean‐Pierre Desvignes France 17 603 1.2× 324 1.2× 72 0.5× 72 0.6× 37 0.4× 31 1.0k
Bérengère de Martinville United States 17 616 1.3× 389 1.4× 69 0.5× 94 0.8× 72 0.8× 27 980
Barbara K. Goodman United States 25 811 1.7× 360 1.3× 146 1.0× 109 1.0× 79 0.9× 48 1.5k
Ngan Ching Cheng Australia 13 681 1.4× 186 0.7× 236 1.7× 77 0.7× 31 0.3× 20 899
Sung Chun United States 11 771 1.6× 813 3.0× 206 1.5× 73 0.7× 53 0.6× 15 1.4k
Avni Santani United States 16 405 0.8× 439 1.6× 110 0.8× 48 0.4× 24 0.3× 39 781
Marie‐Laure Sobrier France 24 960 2.0× 834 3.0× 213 1.5× 67 0.6× 213 2.3× 50 2.0k
Jason A. Watts United States 12 862 1.8× 144 0.5× 87 0.6× 75 0.7× 74 0.8× 21 1.0k
Daniel A. Peiffer United States 14 554 1.1× 466 1.7× 135 1.0× 107 1.0× 110 1.2× 19 926

Countries citing papers authored by Uwe Menzel

Since Specialization
Citations

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

Fields of papers citing papers by Uwe Menzel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Uwe Menzel

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

All Works

20 of 20 papers shown
1.
Varotsis, Georgios, Uwe Menzel, Anders Wigren, et al.. (2022). Spatio-temporal predictions of COVID-19 test positivity in Uppsala County, Sweden: a comparative approach. Scientific Reports. 12(1). 15176–15176. 2 indexed citations
2.
Mattsson, Johanna Sofia Margareta, et al.. (2019). Programmed Cell Death Ligand 1 Immunohistochemistry: A Concordance Study Between Surgical Specimen, Biopsy, and Tissue Microarray. Clinical Lung Cancer. 20(4). 258–262.e1. 21 indexed citations
3.
Fischer, Klaus, et al.. (2016). EXPERIÊNCIA ALEMÃ COM TRATAMENTO MECÂNICO BIOLÓGICO DE RESÍDUOS SÓLIDOS URBANOS. 7(7).
4.
Marthandan, Shiva, Uwe Menzel, Stefan Priebe, et al.. (2016). Conserved genes and pathways in primary human fibroblast strains undergoing replicative and radiation induced senescence. Biological Research. 49(1). 34–34. 32 indexed citations
5.
Baumgart, Mario, Stefan Priebe, Marco Groth, et al.. (2016). Longitudinal RNA-Seq Analysis of Vertebrate Aging Identifies Mitochondrial Complex I as a Small-Molecule-Sensitive Modifier of Lifespan. Cell Systems. 2(2). 122–132. 98 indexed citations
6.
Holtze, Susanne, Ulrich Wachter, Uwe Menzel, et al.. (2016). Low sulfide levels and a high degree of cystathionine β-synthase (CBS) activation by S-adenosylmethionine (SAM) in the long-lived naked mole-rat. Redox Biology. 8. 192–198. 23 indexed citations
7.
Sponholz, Christoph, Uwe Menzel, Evangelos J. Giamarellos‐Bourboulis, et al.. (2015). Polymorphisms of cystathionine beta-synthase gene are associated with susceptibility to sepsis. European Journal of Human Genetics. 24(7). 1041–1048. 8 indexed citations
8.
Quickert, Stefanie, Christoph Sponholz, Uwe Menzel, et al.. (2015). Alternative Splicing of SMPD1 in Human Sepsis. PLoS ONE. 10(4). e0124503–e0124503. 12 indexed citations
9.
Sponholz, Christoph, Bianka Wissuwa, Ralf A. Claus, et al.. (2013). Alternative 5’ Untranslated Regions Are Involved in Expression Regulation of Human Heme Oxygenase-1. PLoS ONE. 8(10). e77224–e77224. 37 indexed citations
10.
Priebe, Stefan, Uwe Menzel, Kim Zarse, et al.. (2013). Extension of Life Span by Impaired Glucose Metabolism in Caenorhabditis elegans Is Accompanied by Structural Rearrangements of the Transcriptomic Network. PLoS ONE. 8(10). e77776–e77776. 19 indexed citations
11.
Nord, Helena, Ulrika Segersten, Johanna Sandgren, et al.. (2009). Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma. International Journal of Cancer. 126(6). 1390–1402. 55 indexed citations
12.
Ramos, Edward, Janet M. Young, Robert K. Tran, et al.. (2009). Tissue-specific variation in DNA methylation levels along human chromosome 1. Epigenetics & Chromatin. 2(1). 7–7. 45 indexed citations
13.
Mantripragada, Kiran K., Teresita Díaz de Ståhl, Uwe Menzel, et al.. (2009). Genome‐wide high‐resolution analysis of DNA copy number alterations in NF1‐associated malignant peripheral nerve sheath tumors using 32K BAC array. Genes Chromosomes and Cancer. 48(10). 897–907. 37 indexed citations
14.
Piotrowski, Arkadiusz, Carl E.G. Bruder, Robin Andersson, et al.. (2008). Somatic mosaicism for copy number variation in differentiated human tissues. Human Mutation. 29(9). 1118–1124. 150 indexed citations
15.
Piotrowski, Arkadiusz, Magdalena Benetkiewicz, Uwe Menzel, et al.. (2006). Microarray‐based survey of CpG islands identifies concurrent hyper‐ and hypomethylation patterns in tissues derived from patients with breast cancer. Genes Chromosomes and Cancer. 45(7). 656–667. 36 indexed citations
16.
Ståhl, Teresita Díaz de, Arkadiusz Piotrowski, Kiran K. Mantripragada, et al.. (2006). Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH. Genomics. 88(2). 152–162. 12 indexed citations
17.
Buckley, Patrick G., Uwe Menzel, Tiit Mathiesen, et al.. (2005). Comprehensive DNA Copy Number Profiling of Meningioma Using a Chromosome 1 Tiling Path Microarray Identifies Novel Candidate Tumor Suppressor Loci. Cancer Research. 65(7). 2653–2661. 38 indexed citations
18.
Buckley, Patrick G., Kiran K. Mantripragada, Teresita Díaz de Ståhl, et al.. (2005). Identification of genetic aberrations on chromosome 22 outside theNF2locus in schwannomatosis and neurofibromatosis type 2. Human Mutation. 26(6). 540–549. 21 indexed citations
19.
Ali, Haider, Carl E.G. Bruder, Ingegerd Fransson, et al.. (2003). Strong conservation of the human NF2 locus based on sequence comparison in five species. Mammalian Genome. 14(8). 526–536. 5 indexed citations
20.
Mantripragada, Kiran K., et al.. (2003). Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection. Journal of Molecular Medicine. 81(7). 443–451. 29 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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