Corinna Menzel

2.8k total citations
28 papers, 2.1k citations indexed

About

Corinna Menzel is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Corinna Menzel has authored 28 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Genetics and 7 papers in Plant Science. Recurrent topics in Corinna Menzel's work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Chromosomal and Genetic Variations (7 papers). Corinna Menzel is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Chromosomal and Genetic Variations (7 papers). Corinna Menzel collaborates with scholars based in Germany, Netherlands and China. Corinna Menzel's co-authors include Wei Chen, Vera M. Kalscheuer, Philipp Khaitovich, Hans‐Hilger Ropers, Ying Xu, Hai Hu, Niels Tommerup, Reinhard Ullmann, Song Guo and Ning Fu and has published in prestigious journals such as Genome Research, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Corinna Menzel

28 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Corinna Menzel Germany 20 1.3k 942 456 233 168 28 2.1k
Kathleen A. Worringer United States 11 2.0k 1.5× 685 0.7× 302 0.7× 133 0.6× 221 1.3× 14 2.8k
Peter J. Skene United States 14 2.7k 2.0× 757 0.8× 224 0.5× 284 1.2× 91 0.5× 22 3.1k
Jennifer A. Erwin United States 16 2.5k 1.9× 609 0.6× 977 2.1× 337 1.4× 178 1.1× 25 3.0k
Mareike Albert Germany 18 1.5k 1.1× 338 0.4× 192 0.4× 98 0.4× 191 1.1× 24 2.1k
Yuping Luo China 18 1.3k 1.0× 538 0.6× 639 1.4× 124 0.5× 150 0.9× 47 1.7k
Anna Szekely United States 14 1.8k 1.3× 470 0.5× 258 0.6× 86 0.4× 326 1.9× 22 2.3k
Marjolein H. Willemsen Netherlands 20 1.3k 1.0× 1.5k 1.6× 244 0.5× 74 0.3× 238 1.4× 43 2.4k
Stephan P. Persengiev United States 22 1.6k 1.2× 395 0.4× 472 1.0× 123 0.5× 132 0.8× 39 2.2k
Robert S. Illingworth United Kingdom 22 3.8k 2.8× 1.2k 1.3× 251 0.6× 380 1.6× 65 0.4× 29 4.2k
Ronald G. Lafrenière Canada 22 2.9k 2.2× 2.0k 2.2× 948 2.1× 367 1.6× 351 2.1× 40 4.1k

Countries citing papers authored by Corinna Menzel

Since Specialization
Citations

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

Fields of papers citing papers by Corinna Menzel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Corinna Menzel

This figure shows the co-authorship network connecting the top 25 collaborators of Corinna Menzel. A scholar is included among the top collaborators of Corinna 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 Corinna Menzel. Corinna 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.
Shao, Ning‐Yi, Hai Hu, Yan Zheng, et al.. (2010). Comprehensive survey of human brain microRNA by deep sequencing. BMC Genomics. 11(1). 409–409. 127 indexed citations
2.
Tzschach, Andreas, Corinna Menzel, Fikret Erdogan, et al.. (2010). Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement. American Journal of Medical Genetics Part A. 152A(4). 1008–1012. 16 indexed citations
3.
Somel, Mehmet, Song Guo, Ning Fu, et al.. (2010). MicroRNA, mRNA, and protein expression link development and aging in human and macaque brain. Genome Research. 20(9). 1207–1218. 239 indexed citations
4.
Xu, Augix Guohua, Liu He, Zhongshan Li, et al.. (2010). Intergenic and Repeat Transcription in Human, Chimpanzee and Macaque Brains Measured by RNA-Seq. PLoS Computational Biology. 6(7). e1000843–e1000843. 45 indexed citations
5.
Hu, Hai, Yan Zheng, Ying Xu, et al.. (2009). Sequence features associated with microRNA strand selection in humans and flies. BMC Genomics. 10(1). 413–413. 127 indexed citations
6.
Hu, Hao, Klaus Wrogemann, Vera M. Kalscheuer, et al.. (2009). Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. HAL (Le Centre pour la Communication Scientifique Directe). 3(1-4). 41–49. 35 indexed citations
7.
Chen, Wei, Reinhard Ullmann, Corinna Menzel, et al.. (2009). Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing. European Journal of Human Genetics. 18(5). 539–543. 50 indexed citations
8.
Fu, Xing, Ning Fu, Song Guo, et al.. (2009). Estimating accuracy of RNA-Seq and microarrays with proteomics. BMC Genomics. 10(1). 161–161. 216 indexed citations
9.
Chen, Wei, Vera M. Kalscheuer, Andreas Tzschach, et al.. (2008). Mapping translocation breakpoints by next-generation sequencing. Genome Research. 18(7). 1143–1149. 102 indexed citations
10.
Møller, Rikke S., Maria Hoeltzenbein, Babett Heye, et al.. (2008). Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly. The American Journal of Human Genetics. 82(5). 1165–1170. 116 indexed citations
11.
Tzschach, Andreas, Christina Kelbova, Hartmut Peters, et al.. (2008). Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome in a Girl with Chromosome Translocation t(2;3)(q33;q23). Ophthalmic Genetics. 29(1). 37–40. 6 indexed citations
12.
Tzschach, Andreas, Christian Ramel, Christian Wüster, et al.. (2007). Hypergonadotropic hypogonadism in a patient with inv ins (2;4). International Journal of Andrology. 32(3). 226–230. 2 indexed citations
13.
Tzschach, Andreas, Corinna Menzel, Fikret Erdogan, et al.. (2007). Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH. American Journal of Medical Genetics Part A. 143A(4). 333–337. 14 indexed citations
14.
Erdogan, Fikret, Wei Chen, Maria Kirchhoff, et al.. (2006). Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation. Cytogenetic and Genome Research. 115(3-4). 247–253. 58 indexed citations
15.
Tzschach, Andreas, Maria Hoeltzenbein, Kirsten Hoffmann, et al.. (2006). Heterotaxy and cardiac defect in a girl with chromosome translocation t(X;1)(q26;p13.1) and involvement of ZIC3. European Journal of Human Genetics. 14(12). 1317–1320. 14 indexed citations
16.
Tzschach, Andreas, Corinna Menzel, Maria Hoeltzenbein, et al.. (2006). Molecular cytogenetic analysis of a de novo interstitial chromosome 10q22 deletion. American Journal of Medical Genetics Part A. 140A(10). 1108–1110. 8 indexed citations
17.
Tzschach, Andreas, Corinna Menzel, Vera M. Kalscheuer, et al.. (2006). Molecular cytogenetic analysis of a de novo interstitial deletion of 5q23.3q31.2 and its phenotypic consequences. American Journal of Medical Genetics Part A. 140A(5). 496–502. 10 indexed citations
18.
Borg, Isabella, Kristine Freude, Kirsten Hoffmann, et al.. (2005). Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome. European Journal of Human Genetics. 13(8). 921–927. 67 indexed citations
19.
Shoichet, Sarah A., Laurence Duprez, Vicki Waetzig, et al.. (2005). Truncation of the CNS-expressed JNK3 in a patient with a severe developmental epileptic encephalopathy. Human Genetics. 118(5). 559–567. 31 indexed citations
20.
Shoichet, Sarah A., Kirsten Hoffmann, Corinna Menzel, et al.. (2003). Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation. The American Journal of Human Genetics. 73(6). 1341–1354. 65 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

Breakdown of academic impact, for papers by Kathleen A. Worringer Breakdown of academic impact, for papers by Peter J. Skene Breakdown of academic impact, for papers by Jennifer A. Erwin Breakdown of academic impact, for papers by Mareike Albert Breakdown of academic impact, for papers by Yuping Luo Breakdown of academic impact, for papers by Anna Szekely Breakdown of academic impact, for papers by Marjolein H. Willemsen Breakdown of academic impact, for papers by Stephan P. Persengiev Breakdown of academic impact, for papers by Robert S. Illingworth Breakdown of academic impact, for papers by Ronald G. Lafrenière
Rankless by CCL
2026