Claus‐Eric Ott

3.3k citations

51 papers · 1.7k indexed · h-index 20

Impact in

Developmental Biology top 5%
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Connective tissue disorders research

Papers in ⓘ

Developmental Biology 3
- Congenital limb and hand anomalies 3
Anatomy 1

Co-authors: Stefan Mundlos (26 shared papers)Peter N. Robinson (15 shared papers)Johannes Grünhagen (13 shared papers)Denise Horn (6 shared papers)Sebastian Bauer (5 shared papers)Eva Klopocki (5 shared papers)Petra Knaus (5 shared papers)Sebastian Köhler (3 shared papers)
Journals: Journal of Hypertension (6 papers)Bone (5 papers)The American Journal of Human Genetics (3 papers)Scientific Reports (2 papers)Journal of Biomechanics (2 papers)
Partner nations: Germany United Kingdom United States

In The Last Decade

Claus‐Eric Ott

47 papers receiving 1.7k citations

Peers

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-authors

The 25 scholars most cited alongside Claus‐Eric Ott, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Claus‐Eric Ott Line = papers co-authored together Claus‐Eric Ott links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Clinical Diagnostics in Human Genetics with Semantic Similarity Searches in Ontologies The American Journal of Human Genetics ·Sebastian Köhler, Marcel H. Schulz, Peter Krawitz, Sebastian Bauer, Sandra Dölken, Claus‐Eric Ott, Christine Mundlos, Denise Horn, Stefan Mundlos, Peter N. Robinson	2009	349
2	Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome The American Journal of Human Genetics ·Eva Klopocki, Harald Schulze, Gabriele Strauß, Claus‐Eric Ott, Judith G. Hall, Fabienne Trotier, Silke Fleischhauer, Lynn Greenhalgh, Ruth Newbury‐Ecob, Luitgard M. Neumann, R. Habenicht, Rainer König, E Seemanová, André Mégarbané, Hans‐Hilger Ropers, Reinhard Ullmann, Denise Horn, Stefan Mundlos	2007	201
3	Duplications Involving a Conserved Regulatory Element Downstream of BMP2 Are Associated with Brachydactyly Type A2 The American Journal of Human Genetics ·Katarina Dathe, Klaus Kjaer, Anja Brehm, Peter Meinecke, Peter Nürnberg, Jordao C. Neto, Décio Brunoni, Niels Tommerup, Claus‐Eric Ott, Eva Klopocki, Petra Seemann, Stefan Mundlos	2009	120
4	miR-181a promotes osteoblastic differentiation through repression of TGF-β signaling molecules The International Journal of Biochemistry & Cell Biology ·Raghu Bhushan, Johannes Grünhagen, Jessica Becker, Peter N. Robinson, Claus‐Eric Ott, Petra Knaus	2012	118
5	A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome Journal of Medical Genetics ·Eva Klopocki, Claus‐Eric Ott, N Benatar, Reinhard Ullmann, Stefan Mundlos, Katarina Lehmann	2008	98
6	Deletions of chromosomal regulatory boundaries are associated with congenital disease Genome biology ·Jonas Ibn-Salem, Sebastian Köhler, Michael I. Love, Ho‐Ryun Chung, Ni Huang, Matthew E. Hurles, Melissa Haendel, Nicole Washington, Damian Smedley, Chris Mungall, Suzanna Lewis, Claus‐Eric Ott, Sebastian Bauer, Paul N. Schofield, Stefan Mundlos, Malte Spielmann, Peter N. Robinson	2014	90
7	MicroRNAs Differentially Expressed in Postnatal Aortic Development Downregulate Elastin via 3′ UTR and Coding-Sequence Binding Sites PLoS ONE ·Claus‐Eric Ott, Johannes Grünhagen, Marten Jäger, Daniel Horbelt, Simon Schwill, Klaus Kallenbach, Gao Guo, Thomas Manke, Petra Knaus, Stefan Mundlos, Peter N. Robinson	2011	87
8	Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing BMC Genomics ·Marten Jäger, Claus‐Eric Ott, Johannes Grünhagen, Jochen Hecht, Hanna Schell, Stefan Mundlos, Georg N. Duda, Peter N. Robinson, Jasmin Lienau	2011	60
9	MiR-497∼195 Cluster MicroRNAs Regulate Osteoblast Differentiation by Targeting BMP Signaling Journal of Bone and Mineral Research ·Johannes Grünhagen, Raghu Bhushan, Elisa Degenkolbe, Marten Jäger, Petra Knaus, Stefan Mundlos, Peter N. Robinson, Claus‐Eric Ott	2014	58
10	Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia Human Mutation ·Claus‐Eric Ott, Gundula Leschik, Fabienne Trotier, Louise Brueton, Han G. Brunner, Wim Brussel, Encarna Guillén‐Navarro, Claudia M. Haase, Juergen Kohlhase, Dieter Kotzot, Andrew Lane, Min Ae Lee‐Kirsch, Susanne Morlot, Marleen Simon, Elisabeth Steichen‐Gersdorf, David Tegay, Hartmut Peters, Stefan Mundlos, Eva Klopocki	2010	58
11	BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation Scientific Reports ·Isabelle Schreiber, Gina Dörpholz, Claus‐Eric Ott, Bjørt K. Kragesteen, Nancy Schanze, Cory Thomas Lee, Josef Köhrle, Stefan Mundlos, Karen Ruschke, Petra Knaus	2017	44
12	Effect of empagliflozin on ketone bodies in patients with stable chronic heart failure Cardiovascular Diabetology ·Robert Pietschner, Julie Kolwelter, Agnes Bosch, Kristina Striepe, Susanne Jung, Dennis Kannenkeril, Claus‐Eric Ott, Mario Schiffer, Stephan Achenbach, Roland E. Schmieder	2021	40
13	Biaxial cell stimulation: A mechanical validation Journal of Biomechanics ·Frederike Bieler, Claus‐Eric Ott, Mark S. Thompson, Robin Seidel, S Ahrens, Devakara R. Epari, Ulrich Wilkening, Klaus‐Dieter Schaser, Stefan Mundlos, Georg N. Duda	2009	37
14	The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta Journal of Vascular Surgery ·Simon Schwill, Philipp Seppelt, Johannes Grünhagen, Claus‐Eric Ott, Manfred Jugold, Arjang Ruhparwar, Peter N. Robinson, Matthias Karck, Klaus Kallenbach	2013	37
15	Severe congenital cutis laxa with cardiovascular manifestations due to homozygous deletions in ALDH18A1 Molecular Genetics and Metabolism ·Björn Fischer‐Zirnsak, Bert Callewaert, Phillipe Schröter, Paul Coucke, Claire Schlack, Claus‐Eric Ott, Manrico Morroni, Wolfgang Homann, Stefan Mundlos, Éva Morava, Anna Ficcadenti, Uwe Kornak	2014	30
16	Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice Human Molecular Genetics ·Gao Guo, (unknown), Claus‐Eric Ott, Johannes Grünhagen, Shaker A. Mousa, Angelika Pletschacher, Y. von Kodolitsch, Petra Knaus, Peter N. Robinson	2012	29
17	Promiscuous and Depolarization-Induced Immediate-Early Response Genes Are Induced by Mechanical Strain of Osteoblasts Journal of Bone and Mineral Research ·Claus‐Eric Ott, Sebastian Bauer, Thomas Manke, Susan Ahrens, Christian Rödelsperger, Johannes Grünhagen, Uwe Kornak, Georg N. Duda, Stefan Mundlos, Peter N. Robinson	2009	23
18	Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1 Bone ·Claus‐Eric Ott, Björn Fischer‐Zirnsak, Phillipe Schröter, Reyk Richter, Neerja Gupta, Nishant Verma, Madhulika Kabra, Stefan Mundlos, Anna Rajab, Heidemarie Neitzel, Uwe Kornak	2013	21
19	Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms Journal of Cardiovascular Electrophysiology ·Alexander Moscu‐Gregor, Christoph Marschall, Carsten Müntjes, Anne Schönecker, Franziska Schuessler‐Hahn, Felix Hohendanner, Abdul Shokor Parwani, Leif‐Hendrik Boldt, Claus‐Eric Ott, Anja Bennewiz, Thomas Paul, Ulrich Krause, Imma Rost	2020	21
20	Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study Journal of Medical Internet Research ·Jean Tori Pantel, Nurulhuda Hajjir, Magdalena Danyel, Jonas Elsner, Angela Teresa Abad‐Perez, Peter Hansen, Stefan Mundlos, Malte Spielmann, Denise Horn, Claus‐Eric Ott, Martin A. Mensah	2020	20

About Claus‐Eric Ott

Claus‐Eric Ott is a scholar working on Developmental Biology, Anatomy, Genetics, Molecular Biology and Orthopedics and Sports Medicine, having authored 51 papers that have together received 1.7k indexed citations. Recurring topics across this work include Connective tissue disorders research (8 papers), Bone Metabolism and Diseases (8 papers), RNA Research and Splicing (4 papers), MicroRNA in disease regulation (3 papers), Kruppel-like factors research (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital limb and hand anomalies (3 papers) and Aortic Disease and Treatment Approaches (3 papers). The work is most often cited by research in Developmental Biology (79 citations), Genetics (698 citations), Cancer Research (319 citations), Molecular Biology (1.1k citations) and Genetics (71 citations). Claus‐Eric Ott has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Stefan Mundlos, Peter N. Robinson, Johannes Grünhagen, Denise Horn, Sebastian Bauer, Eva Klopocki, Petra Knaus, Sebastian Köhler, Peter Krawitz and Marcel H. Schulz. Their work appears in journals such as Journal of Hypertension, Bone, The American Journal of Human Genetics, Scientific Reports and Journal of Biomechanics.

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.

Explore authors with similar magnitude of impact