Elisabeth Mangold

10.5k total citations
117 papers, 4.0k citations indexed

About

Elisabeth Mangold is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Elisabeth Mangold has authored 117 papers receiving a total of 4.0k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Genetics, 42 papers in Molecular Biology and 40 papers in Pathology and Forensic Medicine. Recurrent topics in Elisabeth Mangold's work include Cleft Lip and Palate Research (48 papers), Genetic factors in colorectal cancer (39 papers) and Craniofacial Disorders and Treatments (36 papers). Elisabeth Mangold is often cited by papers focused on Cleft Lip and Palate Research (48 papers), Genetic factors in colorectal cancer (39 papers) and Craniofacial Disorders and Treatments (36 papers). Elisabeth Mangold collaborates with scholars based in Germany, United States and United Kingdom. Elisabeth Mangold's co-authors include Peter Propping, Waltraut Friedl, Constanze Pagenstecher, Kerstin U. Ludwig, Stefan Aretz, Siegfried Uhlhaas, Markus M. Nöthen, Gabriela Möslein, Micaela Mathiak and Karsten Schulmann and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Bioinformatics.

In The Last Decade

Elisabeth Mangold

113 papers receiving 3.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabeth Mangold Germany 36 1.9k 1.4k 1.4k 1.2k 1.0k 117 4.0k
Ludwine Messiaen United States 39 661 0.4× 2.2k 1.5× 932 0.6× 491 0.4× 397 0.4× 145 5.0k
David Gisselsson Sweden 40 459 0.2× 2.7k 1.9× 966 0.7× 1.1k 0.9× 1.4k 1.4× 151 5.0k
Conxi Lázaro Spain 35 838 0.4× 1.5k 1.0× 1.0k 0.7× 631 0.5× 673 0.7× 147 3.6k
Athena M. Cherry United States 29 399 0.2× 2.2k 1.5× 1.3k 0.9× 654 0.5× 322 0.3× 81 4.7k
Daniel L. Van Dyke United States 41 853 0.5× 1.8k 1.2× 1.9k 1.3× 586 0.5× 416 0.4× 183 4.7k
Masashi Sanada Japan 33 441 0.2× 2.2k 1.5× 733 0.5× 633 0.5× 920 0.9× 118 4.1k
Daynna J. Wolff United States 24 392 0.2× 1.0k 0.7× 1.2k 0.8× 511 0.4× 822 0.8× 80 2.8k
Timothy T. Stenzel United States 25 379 0.2× 1.6k 1.1× 794 0.6× 551 0.5× 464 0.5× 45 3.8k
Eric Schoenmakers Belgium 34 443 0.2× 2.5k 1.7× 2.1k 1.5× 574 0.5× 705 0.7× 76 5.2k
Raymonda Varon Germany 30 213 0.1× 2.9k 2.0× 813 0.6× 783 0.7× 1.0k 1.0× 62 3.5k

Countries citing papers authored by Elisabeth Mangold

Since Specialization
Citations

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

Fields of papers citing papers by Elisabeth Mangold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Mangold

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Mangold. A scholar is included among the top collaborators of Elisabeth Mangold 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 Elisabeth Mangold. Elisabeth Mangold 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.
Ludwig, Kerstin U., Evie Stergiakouli, Jonathan Sandy, et al.. (2025). Genetic heterogeneity and homogeneity among orofacial cleft subtypes: genome-wide association studies in the cleft collective. Human Molecular Genetics. 34(23). 1934–1950.
2.
Weinhold, Leonie, Axel Schmidt, Manuel Holtgrewe, et al.. (2022). Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations. Human Genetics and Genomics Advances. 4(1). 100166–100166. 2 indexed citations
3.
Dardani, Christina, Laurence J Howe, Nandita Mukhopadhyay, et al.. (2020). Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study. International Journal of Epidemiology. 49(4). 1282–1293. 23 indexed citations
4.
5.
Reutter, Heiko, Soyhan Bağcı, Florian Kipfmueller, et al.. (2018). Congenital diaphragmatic hernia in a case of Cat eye syndrome. Clinical Case Reports. 6(9). 1786–1790. 4 indexed citations
6.
Yusuf, Imran H., Martin Gliem, Johannes Birtel, et al.. (2018). The retinal phenotype associated with the frequent, synonymous c.783G > A mutation in CDHR1. Investigative Ophthalmology & Visual Science. 59(9). 3146–3146. 1 indexed citations
7.
Böhmer, Anne C., Lina Gölz, Thomas Kreusch, et al.. (2017). Investigation of dominant and recessive inheritance models in genome‐wide association studies data of nonsyndromic cleft lip with or without cleft palate. Birth Defects Research. 110(4). 336–341. 6 indexed citations
8.
Birtel, Johannes, Martin Gliem, Elisabeth Mangold, et al.. (2017). Novel Insights Into the Phenotypical Spectrum of KIF11 -Associated Retinopathy, Including a New Form of Retinal Ciliopathy. Investigative Ophthalmology & Visual Science. 58(10). 3950–3950. 47 indexed citations
9.
Gliem, Martin, Philipp L. Müller, Elisabeth Mangold, et al.. (2015). Reticular Pseudodrusen in Sorsby Fundus Dystrophy. Ophthalmology. 122(8). 1555–1562. 57 indexed citations
10.
Beaty, Terri H., Margaret A. Taub, Alan F. Scott, et al.. (2013). Confirming genes influencing risk to cleft lip with/without cleft palate in a case–parent trio study. Human Genetics. 132(7). 771–781. 112 indexed citations
11.
Pinheiro, Manuela, Carla Pinto, Ana Peixoto, et al.. (2012). The MSH2 c.388_389del mutation shows a founder effect in Portuguese Lynch syndrome families. Clinical Genetics. 84(3). 244–250. 11 indexed citations
12.
Mangold, Elisabeth, Kerstin U. Ludwig, & Markus M. Nöthen. (2011). Breakthroughs in the genetics of orofacial clefting. Trends in Molecular Medicine. 17(12). 725–733. 96 indexed citations
13.
Reutter, Heiko, Stefanie Birnbaum, Meinhard Mende, et al.. (2009). Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent. International Journal of Pediatric Otorhinolaryngology. 73(10). 1334–1338. 3 indexed citations
14.
Rahner, Nils, Gerald Höefler, Christoph Högenauer, et al.. (2008). Compound heterozygosity for two MSH6 mutations in a patient with early onset colorectal cancer, vitiligo and systemic lupus erythematosus. American Journal of Medical Genetics Part A. 146A(10). 1314–1319. 34 indexed citations
15.
Ollila, Saara, Laura Sarantaus, Reetta Kariola, et al.. (2006). Pathogenicity of MSH2 Missense Mutations Is Typically Associated With Impaired Repair Capability of the Mutated Protein. Gastroenterology. 131(5). 1408–1417. 54 indexed citations
16.
Engel, Christoph, Elke Holinski‐Feder, Constanze Pagenstecher, et al.. (2005). Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. International Journal of Cancer. 118(1). 115–122. 71 indexed citations
17.
Behrens, Peter, Micaela Mathiak, Elisabeth Mangold, et al.. (2003). Stromal expression of invasion‐promoting, matrix‐degrading proteases MMP‐1 and ‐9 and the Ets 1 transcription factor in HNPCC carcinomas and sporadic colorectal cancers. International Journal of Cancer. 107(2). 183–188. 48 indexed citations
18.
Wang, Yaping, Waltraut Friedl, Christof Lamberti, et al.. (2002). Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes. International Journal of Cancer. 103(5). 636–641. 87 indexed citations
19.
Wang, Yaping, Waltraut Friedl, Matthias Jungck, et al.. (2002). A modified multiplex PCR assay for detection of large deletions inMSH2 andMLH1. Human Mutation. 19(3). 279–286. 31 indexed citations
20.
Holinski‐Feder, Elke, Waltraut Friedl, Gabriela Möslein, et al.. (2001). DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2. Journal of Biochemical and Biophysical Methods. 47(1-2). 21–32. 82 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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