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

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Elisabeth Mangold 1.9k 1.4k 1.4k 1.2k 1.0k 117 4.0k
Ludwine Messiaen 661 0.4× 2.2k 1.5× 932 0.6× 491 0.4× 397 0.4× 145 5.0k
David Gisselsson 459 0.2× 2.7k 1.9× 966 0.7× 1.1k 0.9× 1.4k 1.4× 151 5.0k
Conxi Lázaro 838 0.4× 1.5k 1.0× 1.0k 0.7× 631 0.5× 673 0.7× 147 3.6k
Athena M. Cherry 399 0.2× 2.2k 1.5× 1.3k 0.9× 654 0.5× 322 0.3× 81 4.7k
Daniel L. Van Dyke 853 0.5× 1.8k 1.2× 1.9k 1.3× 586 0.5× 416 0.4× 183 4.7k
Masashi Sanada 441 0.2× 2.2k 1.5× 733 0.5× 633 0.5× 920 0.9× 118 4.1k
Daynna J. Wolff 392 0.2× 1.0k 0.7× 1.2k 0.8× 511 0.4× 822 0.8× 80 2.8k
Timothy T. Stenzel 379 0.2× 1.6k 1.1× 794 0.6× 551 0.5× 464 0.5× 45 3.8k
Eric Schoenmakers 443 0.2× 2.5k 1.7× 2.1k 1.5× 574 0.5× 705 0.7× 76 5.2k
Raymonda Varon 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.
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
6.
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
7.
Birtel, Johannes, Martin Gliem, Elisabeth Mangold, et al.. (2018). Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa. PLoS ONE. 13(12). e0207958–e0207958. 76 indexed citations
8.
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
9.
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
10.
Forstner, Andreas J., Kerstin U. Ludwig, Anne C. Böhmer, et al.. (2017). Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxiety. Psychiatric Genetics. 27(3). 96–102. 24 indexed citations
11.
Ludwig, Kerstin U., Anne C. Böhmer, Andrea Hofmann, et al.. (2016). Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene. PLoS Genetics. 12(3). e1005914–e1005914. 60 indexed citations
12.
Gliem, Martin, Philipp L. Müller, Elisabeth Mangold, et al.. (2015). Reticular Pseudodrusen in Sorsby Fundus Dystrophy. Ophthalmology. 122(8). 1555–1562. 57 indexed citations
13.
Assis, Nilma Almeida de, Stefanie Nowak, Kerstin U. Ludwig, et al.. (2010). SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients. International Journal of Pediatric Otorhinolaryngology. 75(1). 49–52. 9 indexed citations
14.
Rahner, Nils, Nicolaus Friedrichs, Verena Steinke, et al.. (2007). Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome. The Journal of Pathology. 214(1). 10–16. 54 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.
Lamberti, C., Elisabeth Mangold, Constanze Pagenstecher, et al.. (2006). Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany. Digestion. 74(1). 58–67. 23 indexed citations
17.
Mangold, Elisabeth, Nils Rahner, Nicolaus Friedrichs, et al.. (2006). MSH6 mutation in Muir?Torre syndrome: could this be a rare finding?. British Journal of Dermatology. 156(1). 158–162. 26 indexed citations
18.
Pistorius, Steffen, Heike Görgens, Stefan Krüger, et al.. (2005). N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC). Cancer Letters. 241(1). 150–157. 4 indexed citations
19.
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
20.
Kruse, Roland, Thomas Ruzicka, Arno Rütten, et al.. (2001). ‘‘Second Hit’’ in Sebaceous Tumors from Muir–Torre Patients with Germline Mutations in MSH2: Allele Loss is Not the Preferred Mode of Inactivation. Journal of Investigative Dermatology. 116(3). 463–465. 34 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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