Herdit M. Schüler

774 total citations
22 papers, 398 citations indexed

About

Herdit M. Schüler is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Herdit M. Schüler has authored 22 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Herdit M. Schüler's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Prenatal Screening and Diagnostics (3 papers). Herdit M. Schüler is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (5 papers) and Prenatal Screening and Diagnostics (3 papers). Herdit M. Schüler collaborates with scholars based in Germany, United States and Switzerland. Herdit M. Schüler's co-authors include Martin Zenke, Wolfgang Wagner, Bernd Denecke, Sylvia Joussen, Christoph V. Suschek, Anne Schellenberg, Norbert Pallua, Carmen Koch, Gudrun Walenda and Qiong Lin and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Frontiers in Immunology.

In The Last Decade

Herdit M. Schüler

21 papers receiving 373 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Herdit M. Schüler Germany 10 216 120 107 62 45 22 398
Stephanie M. Yan United States 6 122 0.6× 64 0.5× 98 0.9× 52 0.8× 18 0.4× 9 268
Yuri Uchiyama Japan 11 155 0.7× 84 0.7× 105 1.0× 43 0.7× 11 0.2× 52 400
Liat Samuelov Israel 15 202 0.9× 72 0.6× 41 0.4× 56 0.9× 15 0.3× 56 624
Jaclyn Schienda United States 10 538 2.5× 166 1.4× 157 1.5× 153 2.5× 41 0.9× 17 725
Ping Hong United States 6 250 1.2× 55 0.5× 89 0.8× 36 0.6× 9 0.2× 7 354
Elisabetta Lenzini Italy 11 212 1.0× 205 1.7× 105 1.0× 112 1.8× 71 1.6× 25 415
Rosita Bergström Sweden 8 647 3.0× 148 1.2× 34 0.3× 55 0.9× 28 0.6× 9 762
Élise Héon Canada 17 333 1.5× 146 1.2× 97 0.9× 65 1.0× 15 0.3× 33 807
M.J. Abeyta United States 5 530 2.5× 111 0.9× 22 0.2× 81 1.3× 74 1.6× 9 645
Anastasia Conti Italy 13 449 2.1× 140 1.2× 132 1.2× 21 0.3× 14 0.3× 17 653

Countries citing papers authored by Herdit M. Schüler

Since Specialization
Citations

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

Fields of papers citing papers by Herdit M. Schüler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Herdit M. Schüler. 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 Herdit M. Schüler. The network helps show where Herdit M. Schüler may publish in the future.

Co-authorship network of co-authors of Herdit M. Schüler

This figure shows the co-authorship network connecting the top 25 collaborators of Herdit M. Schüler. A scholar is included among the top collaborators of Herdit M. Schüler 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 Herdit M. Schüler. Herdit M. Schüler 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.
Helden, Josef van, et al.. (2025). Genetic Characterization of the Immortalized Human Nasopharyngeal Carcinoma Cell Line NPC/HK1. Cancer Medicine. 14(3). e70422–e70422.
2.
Sonntag, Roland, Herdit M. Schüler, Steffen K. Meurer, et al.. (2023). Transformation of primary murine peritoneal mast cells by constitutive KIT activation is accompanied by loss of Cdkn2a/Arf expression. Frontiers in Immunology. 14. 1154416–1154416. 3 indexed citations
3.
Toledo, Marcelo A. S., Paul Wanek, Herdit M. Schüler, et al.. (2022). CRISPR/Cas9-engineered human ES cells harboring heterozygous and homozygous c-KIT knockout. Stem Cell Research. 60. 102732–102732. 2 indexed citations
4.
Schröder, Sarah K., Herdit M. Schüler, Cinzia Tesauro, et al.. (2022). Genetic and Molecular Characterization of the Immortalized Murine Hepatic Stellate Cell Line GRX. Cells. 11(9). 1504–1504. 14 indexed citations
5.
Toledo, Marcelo A. S., Herdit M. Schüler, Stephanie Sontag, et al.. (2021). CRISPR/Cas9 mediated CXCL4 knockout in human iPS cells of polycythemia vera patient with JAK2 V617F mutation. Stem Cell Research. 55. 102490–102490. 1 indexed citations
6.
Han, Lijuan, Marcelo A. S. Toledo, Ivan G. Costa, et al.. (2021). CALR frameshift mutations in MPN patient-derived iPSCs accelerate maturation of megakaryocytes. Stem Cell Reports. 16(11). 2768–2783. 9 indexed citations
7.
Meyer, Robert, Matthias Begemann, Stephanie Demuth, et al.. (2020). Inherited cases of CNOT3‐associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies. Clinical Genetics. 98(4). 408–412. 11 indexed citations
8.
Kroh, Andreas, Herdit M. Schüler, Roman Eickhoff, et al.. (2019). A Newly Established Murine Cell Line as a Model for Hepatocellular Cancer in Non-Alcoholic Steatohepatitis. International Journal of Molecular Sciences. 20(22). 5658–5658. 6 indexed citations
9.
Sontag, Stephanie, Jie Qin, Paul Wanek, et al.. (2017). Modelling IRF8 Deficient Human Hematopoiesis and Dendritic Cell Development with Engineered iPS Cells. Stem Cells. 35(4). 898–908. 45 indexed citations
10.
Hemeda, Hatim, Michael Lenz, Jie Qin, et al.. (2013). To Clone or Not to Clone? Induced Pluripotent Stem Cells Can Be Generated in Bulk Culture. PLoS ONE. 8(5). e65324–e65324. 30 indexed citations
11.
Roos, Andreas, Constantin S. von Kaisenberg, Thomas Eggermann, et al.. (2013). Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies. Archives of Gynecology and Obstetrics. 288(5). 1153–1158. 5 indexed citations
12.
Schwanitz, Gesa, Isa Abdi Rad, Mir Davood Omrani, et al.. (2013). Patient with three euchromatic supernumerary marker chromosomes derived from chromosomes 1, 12, and 18: Characterization and evaluation of the aberrations. American Journal of Medical Genetics Part A. 164(3). 736–740. 3 indexed citations
13.
Engels, Hartmut, Herdit M. Schüler, Alexander M. Zink, et al.. (2012). A phenotype map for 14q32.3 terminal deletions. American Journal of Medical Genetics Part A. 158A(4). 695–706. 24 indexed citations
14.
Schellenberg, Anne, Qiong Lin, Herdit M. Schüler, et al.. (2011). Replicative senescence of mesenchymal stem cells causes DNA-methylation changes which correlate with repressive histone marks. Aging. 3(9). 873–888. 145 indexed citations
15.
Roos, Andreas, Miriam Elbracht, Michael Baudis, et al.. (2008). A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non‐pathogenic euchromatic variant. American Journal of Medical Genetics Part A. 146A(18). 2417–2420. 6 indexed citations
16.
Engels, Hartmut, Thomas Eggermann, Almuth Caliebe, et al.. (2008). Genetic counseling in Robertsonian translocations der(13;14): Frequencies of reproductive outcomes and infertility in 101 pedigrees. American Journal of Medical Genetics Part A. 146A(20). 2611–2616. 45 indexed citations
17.
Rudnik‐Schöneborn, Sabine, et al.. (2008). A new case of proximal monosomy 1p36, extending the phenotype. American Journal of Medical Genetics Part A. 146A(15). 2018–2022. 10 indexed citations
18.
Eggermann, Thomas, Ulrike Gamerdinger, Kristin Bosse, et al.. (2005). Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q. American Journal of Medical Genetics Part A. 134A(3). 305–308. 7 indexed citations
19.
Eggermann, Katja, et al.. (2005). Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22): New case and comparison with the literature. American Journal of Medical Genetics Part A. 134A(2). 226–228. 9 indexed citations
20.
Wuyts, Wim, Gérard Waeber, Peter Meinecke, et al.. (2004). Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects. European Journal of Human Genetics. 12(5). 400–406. 13 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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