Claus‐Eric Ott

3.3k total citations
51 papers, 1.7k citations indexed

About

Claus‐Eric Ott is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Claus‐Eric Ott has authored 51 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 17 papers in Genetics and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Claus‐Eric Ott's work include Connective tissue disorders research (8 papers), Bone Metabolism and Diseases (8 papers) and RNA Research and Splicing (4 papers). Claus‐Eric Ott is often cited by papers focused on Connective tissue disorders research (8 papers), Bone Metabolism and Diseases (8 papers) and RNA Research and Splicing (4 papers). Claus‐Eric Ott collaborates with scholars based in Germany, United Kingdom and United States. Claus‐Eric Ott's co-authors include Stefan Mundlos, Peter N. Robinson, Johannes Grünhagen, Denise Horn, Sebastian Bauer, Eva Klopocki, Petra Knaus, Sebastian Köhler, Marcel H. Schulz and Peter Krawitz and has published in prestigious journals such as PLoS ONE, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Claus‐Eric Ott

47 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claus‐Eric Ott Germany 20 1.1k 698 319 123 118 51 1.7k
Jean McGowan‐Jordan Canada 15 690 0.7× 675 1.0× 208 0.7× 103 0.8× 146 1.2× 31 1.6k
Tristan Shaffer United States 4 748 0.7× 744 1.1× 271 0.8× 83 0.7× 76 0.6× 12 1.4k
San‐Pin Wu United States 23 1.1k 1.0× 418 0.6× 245 0.8× 175 1.4× 237 2.0× 64 2.3k
Shalini C. Reshmi United States 20 1.1k 1.0× 413 0.6× 312 1.0× 87 0.7× 45 0.4× 54 1.8k
Anas M. Alazami Saudi Arabia 22 857 0.8× 584 0.8× 95 0.3× 95 0.8× 52 0.4× 55 1.5k
Ramona Pop United States 22 1.4k 1.3× 288 0.4× 104 0.3× 214 1.7× 84 0.7× 31 1.9k
Tetsuya Ohbayashi Japan 21 882 0.8× 502 0.7× 175 0.5× 81 0.7× 114 1.0× 52 1.4k
Saurabh Baheti United States 21 701 0.7× 353 0.5× 267 0.8× 113 0.9× 130 1.1× 41 1.2k
Eul‐Ju Seo South Korea 24 796 0.8× 417 0.6× 106 0.3× 170 1.4× 157 1.3× 116 1.9k
Vaidehi Jobanputra United States 23 456 0.4× 521 0.7× 207 0.6× 159 1.3× 101 0.9× 79 1.3k

Countries citing papers authored by Claus‐Eric Ott

Since Specialization
Citations

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

Fields of papers citing papers by Claus‐Eric Ott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Claus‐Eric Ott. 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 Claus‐Eric Ott. The network helps show where Claus‐Eric Ott may publish in the future.

Co-authorship network of co-authors of Claus‐Eric Ott

This figure shows the co-authorship network connecting the top 25 collaborators of Claus‐Eric Ott. A scholar is included among the top collaborators of Claus‐Eric Ott 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 Claus‐Eric Ott. Claus‐Eric Ott 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.
Habringer, Stefan, Jana Ihlow, Max Schmidt, et al.. (2024). A diagnostic challenge of KIT p.V559D and BRAF p.G469A mutations in a paragastric mass. The Oncologist. 29(10). 908–912.
2.
Pantel, Jean Tori, et al.. (2024). Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study. Journal of Medical Internet Research. 26. e42904–e42904. 6 indexed citations
3.
Hülsemann, Wiebke, Johannes Grünhagen, Claus‐Eric Ott, et al.. (2023). HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families. Genetics in Medicine. 25(11). 100928–100928.
4.
Ott, Claus‐Eric, et al.. (2020). Prognostic significance of prenatal ultrasound in fetal arthrogryposis multiplex congenita. Archives of Gynecology and Obstetrics. 303(4). 943–953. 10 indexed citations
5.
Pantel, Jean Tori, Magdalena Danyel, Stefan Mundlos, et al.. (2020). Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study. Journal of Medical Internet Research. 22(10). e19263–e19263. 20 indexed citations
6.
Danyel, Magdalena, Claus‐Eric Ott, Bastian Salewsky, et al.. (2019). Evaluation of the role of STAP1 in Familial Hypercholesterolemia. Scientific Reports. 9(1). 11995–11995. 15 indexed citations
7.
Hartl, Daniela, Claus‐Eric Ott, Monika Osswald, et al.. (2015). Double NF1 Inactivation Affects Adrenocortical Function in NF1Prx1 Mice and a Human Patient. PLoS ONE. 10(3). e0119030–e0119030. 9 indexed citations
8.
Ott, Claus‐Eric, et al.. (2015). Brachydactyly Type C patient with compound heterozygosity for p.Gly319Val and p.Ile358Thr variants in the GDF5 proregion: benign variants or mutations?. Journal of Human Genetics. 60(8). 419–425. 3 indexed citations
9.
Fischer‐Zirnsak, Björn, Bert Callewaert, Paul Coucke, et al.. (2014). Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1. Molecular Genetics and Metabolism. 112(4). 310–316. 30 indexed citations
10.
Schwill, Simon, Philipp Seppelt, Johannes Grünhagen, et al.. (2013). The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta. Journal of Vascular Surgery. 57(6). 1628–1636.e3. 37 indexed citations
11.
Ott, Claus‐Eric, Silke B. Lohan, Jeannette Hoogeboom, et al.. (2012). Microduplications upstream ofMSX2are associated with a phenocopy of cleidocranial dysplasia. Journal of Medical Genetics. 49(7). 437–441. 12 indexed citations
12.
Ott, Claus‐Eric, Johannes Grünhagen, Marten Jäger, et al.. (2011). MicroRNAs Differentially Expressed in Postnatal Aortic Development Downregulate Elastin via 3′ UTR and Coding-Sequence Binding Sites. PLoS ONE. 6(1). e16250–e16250. 87 indexed citations
13.
Jäger, Marten, Claus‐Eric Ott, Johannes Grünhagen, et al.. (2011). Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing. BMC Genomics. 12(1). 158–158. 60 indexed citations
14.
Raff, Ulrike, Claus‐Eric Ott, Stefan John, et al.. (2010). Nitric Oxide and Reactive Hyperemia: Role of Location and Duration of Ischemia. American Journal of Hypertension. 23(8). 865–869. 18 indexed citations
15.
Thompson, Mark S., et al.. (2010). Quantification and significance of fluid shear stress field in biaxial cell stretching device. Biomechanics and Modeling in Mechanobiology. 10(4). 559–564. 11 indexed citations
16.
Köhler, Sebastian, Marcel H. Schulz, Peter Krawitz, et al.. (2009). Clinical Diagnostics in Human Genetics with Semantic Similarity Searches in Ontologies. The American Journal of Human Genetics. 85(4). 457–464. 349 indexed citations
17.
Dathe, Katarina, Klaus Kjaer, Anja Brehm, et al.. (2009). Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2. The American Journal of Human Genetics. 84(4). 483–492. 120 indexed citations
18.
Brunetti‐Pierri, Nicola, Daniela del Gaudio, Hartmut Peters, et al.. (2008). Robinow syndrome: Phenotypic variability in a family with a novel intragenic ROR2 mutation. American Journal of Medical Genetics Part A. 146A(21). 2804–2809. 16 indexed citations
19.
Klopocki, Eva, Harald Schulze, Gabriele Strauß, et al.. (2007). Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome. The American Journal of Human Genetics. 80(2). 232–240. 201 indexed citations
20.
Ott, Claus‐Eric & Stephen L. Huber. (2006). Die klinische Bedeutung von kosmischer Strahlenbelastung in der Luftfahrt. Praxis. 95(4). 99–106. 4 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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