Monika Ziegler

756 total citations
36 papers, 345 citations indexed

About

Monika Ziegler is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Monika Ziegler has authored 36 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 21 papers in Plant Science and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Monika Ziegler's work include Genomic variations and chromosomal abnormalities (32 papers), Chromosomal and Genetic Variations (21 papers) and Prenatal Screening and Diagnostics (16 papers). Monika Ziegler is often cited by papers focused on Genomic variations and chromosomal abnormalities (32 papers), Chromosomal and Genetic Variations (21 papers) and Prenatal Screening and Diagnostics (16 papers). Monika Ziegler collaborates with scholars based in Germany, Greece and Italy. Monika Ziegler's co-authors include Thomas Liehr, Anja Weise, Emmanouil Manolakos, Nadezda Kosyakova, Heike Starke, Ioannis Papoulidis, Elisabeth Ewers, Uwe Claussen, Ahmed B. Hamid and Annalisa Vetro and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Journal of Histochemistry & Cytochemistry.

In The Last Decade

Monika Ziegler

35 papers receiving 305 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Monika Ziegler Germany 13 261 169 117 116 32 36 345
Sigrid Sahlén Sweden 11 327 1.3× 148 0.9× 115 1.0× 243 2.1× 26 0.8× 21 466
Jean‐Louis Taillemite France 12 247 0.9× 98 0.6× 80 0.7× 193 1.7× 19 0.6× 15 368
Sugandhi A. Tharapel United States 10 215 0.8× 94 0.6× 142 1.2× 83 0.7× 26 0.8× 19 337
Mauricette Jamar Belgium 10 160 0.6× 43 0.3× 72 0.6× 79 0.7× 53 1.7× 17 268
L. Wiśniewski Poland 11 305 1.2× 129 0.8× 115 1.0× 134 1.2× 42 1.3× 28 390
Jiansheng Xie China 8 190 0.7× 29 0.2× 142 1.2× 129 1.1× 59 1.8× 33 341
T. M. Schroeder-Kurth Germany 7 143 0.5× 135 0.8× 47 0.4× 227 2.0× 10 0.3× 10 330
Nadja Kokalj-Vokač Slovenia 11 176 0.7× 73 0.4× 51 0.4× 276 2.4× 17 0.5× 19 406
Jill K. Northup United States 8 155 0.6× 39 0.2× 26 0.2× 115 1.0× 27 0.8× 13 224
G. R. Stalder Switzerland 12 256 1.0× 87 0.5× 98 0.8× 146 1.3× 53 1.7× 21 387

Countries citing papers authored by Monika Ziegler

Since Specialization
Citations

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

Fields of papers citing papers by Monika Ziegler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monika Ziegler

This figure shows the co-authorship network connecting the top 25 collaborators of Monika Ziegler. A scholar is included among the top collaborators of Monika Ziegler 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 Monika Ziegler. Monika Ziegler 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.
Liehr, Thomas, Monika Ziegler, Anja Weise, et al.. (2023). Small supernumerary marker chromosomes derived from human chromosome 11. Frontiers in Genetics. 14. 1293652–1293652. 1 indexed citations
2.
Ziegler, Monika, et al.. (2021). About Cryptic Acrocentric Pericentromeric Abnormalities in Infertile. 5(3). 1–10. 2 indexed citations
3.
Liehr, Thomas, et al.. (2021). Small supernumerary marker chromosomes derived from chromosome 14 and/or 22. Molecular Cytogenetics. 14(1). 13–13. 3 indexed citations
4.
Sismani, Carolina, Athina Theodosiou, Maria Syrrou, et al.. (2020). Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population. Journal of Human Genetics. 65(9). 783–795. 9 indexed citations
5.
Liehr, Thomas, et al.. (2019). Recombinant Chromosomes Resulting From Parental Pericentric Inversions—Two New Cases and a Review of the Literature. Frontiers in Genetics. 10. 1165–1165. 8 indexed citations
6.
Liehr, Thomas, Isolde Schreyer, Alma Kuechler, et al.. (2018). Parental origin of deletions and duplications – about the necessity to check for cryptic inversions. Molecular Cytogenetics. 11(1). 20–20. 9 indexed citations
7.
Liehr, Thomas, et al.. (2018). Assessing Skewed X‐Chromosome Inactivation. Current Protocols in Human Genetics. 98(1). e66–e66. 2 indexed citations
8.
Galarza, Juan A., et al.. (2017). Unusual de novo Partial Trisomy 17p12p11.2 due to Unbalanced Insertion into 5p13.1 in a Severely Affected Boy. Journal of Pediatric Genetics. 6(3). 165–168. 4 indexed citations
9.
Manolakos, Emmanouil, Annalisa Vetro, Antonios Garas, et al.. (2014). Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature. Experimental and Therapeutic Medicine. 7(4). 953–957. 16 indexed citations
10.
Varvagiannis, Konstantinos, Ioannis Papoulidis, Theodora Koromila, et al.. (2014). De novo 393kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features. Meta Gene. 2. 274–282. 4 indexed citations
11.
Manolakos, Emmanouil, Γεώργιος Μαρκόπουλος, Thomas Liehr, et al.. (2014). An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review. Cytogenetic and Genome Research. 142(4). 227–238. 6 indexed citations
12.
Ziegler, Monika, Elisabeth Klein, Ahmed B. Hamid, et al.. (2014). Mitotic stability of small supernumerary marker chromosomes depends on their shape and telomeres — A long term in vitro study. Gene. 552(2). 246–248. 6 indexed citations
13.
Manolakos, Emmanouil, Annalisa Vetro, Eirini Papadopoulou, et al.. (2013). Partial Trisomy 2p and Partial Monosomy 2q Arising from a Paternal Intrachromosomal 2q-into-2p Between-Arm Insertion and Paracentric Inversion: Molecular Cytogenetic Characterization of a Four-Break Rearrangement. Cytogenetic and Genome Research. 140(1). 12–20. 12 indexed citations
14.
Klein, Elisabeth, Mariano Rocchi, Nadezda Kosyakova, et al.. (2012). Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin. Cytogenetic and Genome Research. 136(3). 163–166. 15 indexed citations
15.
Manvelyan, Marina, Friedrich W. Cremer, Christina Kelbova, et al.. (2011). New cytogenetically visible copy number variant in region 8q21.2. Molecular Cytogenetics. 4(1). 1–1. 15 indexed citations
16.
Liehr, Thomas, Jim Schröder, Monika Ziegler, et al.. (2011). Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements. SHILAP Revista de lepidopterología. 14(2). 13–6. 14 indexed citations
17.
Manolakos, Emmanouil, Panagiotis Peitsidis, Makarios Eleftheriades, et al.. (2010). Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: Molecular cytogenetic analysis and review of the literature. Journal of obstetrics and gynaecology research. 36(2). 435–440. 13 indexed citations
18.
Sheth, Frenny, Elisabeth Ewers, Nadezda Kosyakova, et al.. (2009). A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report. Molecular Cytogenetics. 2(1). 22–22. 13 indexed citations
19.
Lončarević, Ivan, Heike Starke, Anita Heller, et al.. (2002). Heterogenic molecular basis for loss of ABL1‐BCR transcription: Deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR‐ABL1‐positive chronic myeloid leukemia. Genes Chromosomes and Cancer. 34(2). 193–200. 28 indexed citations
20.
Liehr, Thomas, Matthias Schmidt, Heike Starke, et al.. (2002). First Case of Trisomy 13 plus Mosaic Trisomy 1q. Fetal Diagnosis and Therapy. 17(3). 133–136. 5 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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