Eva Klopocki

8.5k total citations
103 papers, 3.7k citations indexed

About

Eva Klopocki is a scholar working on Molecular Biology, Genetics and Developmental Biology. According to data from OpenAlex, Eva Klopocki has authored 103 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Molecular Biology, 53 papers in Genetics and 13 papers in Developmental Biology. Recurrent topics in Eva Klopocki's work include Genomic variations and chromosomal abnormalities (32 papers), Congenital heart defects research (15 papers) and Congenital limb and hand anomalies (13 papers). Eva Klopocki is often cited by papers focused on Genomic variations and chromosomal abnormalities (32 papers), Congenital heart defects research (15 papers) and Congenital limb and hand anomalies (13 papers). Eva Klopocki collaborates with scholars based in Germany, United States and Netherlands. Eva Klopocki's co-authors include Stefan Mundlos, Denise Horn, Reinhard Ullmann, Edgar Dahl, Claus‐Eric Ott, Malte Spielmann, Glen Kristiansen, William B. Dobyns, Katarina Dathe and Jürgen Veeck and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Eva Klopocki

102 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Klopocki Germany 34 2.3k 1.5k 442 408 294 103 3.7k
Dagmar Wieczorek Germany 38 2.6k 1.2× 2.3k 1.5× 262 0.6× 518 1.3× 298 1.0× 137 4.9k
Hülya Kayserili Türkiye 35 2.8k 1.2× 1.7k 1.1× 197 0.4× 473 1.2× 229 0.8× 152 4.4k
Ruth Newbury‐Ecob United Kingdom 25 2.0k 0.9× 1.3k 0.8× 386 0.9× 238 0.6× 107 0.4× 64 3.2k
Hans G. Dauwerse Netherlands 25 2.1k 0.9× 1.2k 0.8× 277 0.6× 147 0.4× 142 0.5× 43 3.5k
Stefan J. White Netherlands 31 1.9k 0.8× 1.3k 0.9× 106 0.2× 301 0.7× 203 0.7× 76 3.3k
Gabriele Gillessen‐Kaesbach Germany 38 2.8k 1.3× 2.8k 1.9× 169 0.4× 949 2.3× 128 0.4× 133 4.7k
Tessa Homfray United Kingdom 25 3.3k 1.5× 1.1k 0.7× 651 1.5× 625 1.5× 236 0.8× 69 5.8k
Pao‐Tien Chuang United States 34 4.2k 1.9× 1.5k 1.0× 462 1.0× 100 0.2× 203 0.7× 52 5.1k
Cédric Le Caignec France 29 1.7k 0.8× 1.5k 1.0× 107 0.2× 770 1.9× 256 0.9× 76 3.1k
Weimin Bi United States 33 3.0k 1.3× 2.8k 1.9× 293 0.7× 719 1.8× 672 2.3× 92 5.5k

Countries citing papers authored by Eva Klopocki

Since Specialization
Citations

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

Fields of papers citing papers by Eva Klopocki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Klopocki

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Klopocki. A scholar is included among the top collaborators of Eva Klopocki 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 Eva Klopocki. Eva Klopocki 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.
2.
Strauß, Gabriele, et al.. (2023). Thrombocytopenia Absent Radius (TAR)-Syndrome: From Current Genetics to Patient Self-Empowerment. Hämostaseologie. 43(4). 252–260. 1 indexed citations
3.
Klopocki, Eva, et al.. (2020). Investigation of alpl expression and Tnap-activity in zebrafish implies conserved functions during skeletal and neuronal development. Scientific Reports. 10(1). 13321–13321. 8 indexed citations
4.
Schrama, David, Christian Adam, Cathrin Ritter, et al.. (2019). Characterization of six Merkel cell polyomavirus‐positive Merkel cell carcinoma cell lines: Integration pattern suggest that large T antigen truncating events occur before or during integration. International Journal of Cancer. 145(4). 1020–1032. 42 indexed citations
5.
Klein, Thomas, Chee Keong Kwok, Frank Edenhofer, et al.. (2019). Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy. Stem Cell Research. 35. 101396–101396. 4 indexed citations
6.
7.
Osterwalder, Marco, Wing-Lee Chan, Lars Wittler, et al.. (2017). Composition and dosage of a multipartite enhancer cluster control developmental expression of Ihh (Indian hedgehog). Nature Genetics. 49(10). 1539–1545. 85 indexed citations
8.
Spielmann, Malte & Eva Klopocki. (2013). CNVs of noncoding cis-regulatory elements in human disease. Current Opinion in Genetics & Development. 23(3). 249–256. 33 indexed citations
9.
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
10.
Rosenfeld, Jill A., Ryan N. Traylor, G. Bradley Schaefer, et al.. (2012). Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes. European Journal of Human Genetics. 20(7). 754–761. 82 indexed citations
11.
Klopocki, Eva, Christian M. Kähler, Nicola Foulds, et al.. (2012). Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly. European Journal of Human Genetics. 20(6). 705–708. 37 indexed citations
12.
Fiedler, Jenny L., Gabriele Strauß, Kerstin Seidel, et al.. (2011). Two patterns of thrombopoietin signaling suggest no coupling between platelet production and thrombopoietin reactivity in thrombocytopenia-absent radii syndrome. Haematologica. 97(1). 73–81. 20 indexed citations
13.
Klopocki, Eva, Bianca P. Hennig, Katarina Dathe, et al.. (2010). Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E. The American Journal of Human Genetics. 86(3). 434–439. 93 indexed citations
14.
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
15.
Najm, Juliane, Denise Horn, Isabella Wimplinger, et al.. (2008). Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nature Genetics. 40(9). 1065–1067. 202 indexed citations
16.
Schell-Apacik, Chayim, Birgit Ertl‐Wagner, Eva Klopocki, et al.. (2008). Expanding the phenotype of alopecia–contractures–dwarfism mental retardation syndrome (ACD syndrome): description of an additional case and review of the literature. European Journal of Pediatrics. 167(9). 1057–1062. 4 indexed citations
17.
Meyer, Stefan, William Fergusson, Anthony D. Whetton, et al.. (2007). Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes Chromosomes and Cancer. 46(4). 359–372. 24 indexed citations
18.
Yago, Tadayuki, Veronika I. Zarnitsyna, Eva Klopocki, Rodger P. McEver, & Cheng Zhu. (2006). Transport Governs Flow-Enhanced Cell Tethering through L-Selectin at Threshold Shear. Biophysical Journal. 92(1). 330–342. 68 indexed citations
19.
Weiß, Claudia, Sibylle Jakubiczka, Angela Huebner, et al.. (2006). Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalities. Muscle & Nerve. 35(3). 396–401. 5 indexed citations
20.
Dahl, Edgar, Jürgen Veeck, Hong‐Mei An, et al.. (2005). [Epigenetic inactivation of the WNT antagonist SFRP1 in breast cancer].. PubMed. 89. 169–77. 7 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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