Eva Klopocki

8.5k citations

103 papers · 3.7k · h-index 33

Impact in

Developmental Biology top 1%
Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases

Papers in

Molecular Biology 58
- Congenital heart defects research 14
Genetics 47
- Genomic variations and chromosomal abnormalities 27
- Genetics and Neurodevelopmental Disorders 7
- Connective tissue disorders research 7

Co-authors: Stefan Mundlos (29 shared papers)Denise Horn (16 shared papers)Reinhard Ullmann (12 shared papers)Edgar Dahl (7 shared papers)Malte Spielmann (7 shared papers)Glen Kristiansen (3 shared papers)William B. Dobyns (3 shared papers)Claus‐Eric Ott (4 shared papers)
Journals: Stem Cell Research (10 papers)European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (6 papers)Journal of Medical Genetics (5 papers)The American Journal of Human Genetics (5 papers)
Partner nations: Germany United States Netherlands

In The Last Decade

Eva Klopocki

102 papers receiving 3.6k citations

Peers

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-authors

The 25 scholars most cited alongside Eva Klopocki, 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 Eva Klopocki Line = papers co-authored together Eva Klopocki links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 103 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Aberrant methylation of the Wnt antagonist SFRP1 in breast cancer is associated with unfavourable prognosis Oncogene ·Jürgen Veeck, Dieter Niederacher, Han‐Xiang An, Eva Klopocki, Frank Wiesmann, Beate Betz, Oliver Galm, Oumar Camara, Matthias Dürst, Glen Kristiansen, C Huszka, Ruth Knüchel, Edgar Dahl	2006	215
2	Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum Nature Genetics ·Juliane Najm, Denise Horn, Isabella Wimplinger, Jeffrey A. Golden, Victor V. Chizhikov, Jyotsna Sudi, Susan L. Christian, Reinhard Ullmann, Alma Kuechler, Carola A. Haas, Armin Flubacher, Lawrence Charnas, Gökhan Uyanık, Ulrich Frank, Eva Klopocki, William B. Dobyns, Kerstin Kutsche	2008	205
3	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	202
4	The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis Journal of Medical Genetics ·Fanny Kortüm, Soma Das, M. Flindt, Déborah Morris-Rosendahl, (unknown), Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, A. Roumer, Sulagna C. Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanık, Kerstin Kutsche, William B. Dobyns	2011	181
5	Negative enrichment by immunomagnetic nanobeads for unbiased characterization of circulating tumor cells from peripheral blood of cancer patients Journal of Translational Medicine ·Zhian Liu, Alberto Fusi, Eva Klopocki, Alexander Schmittel, Ingeborg Tinhofer, Anika Nonnenmacher, Ulrich Keilholz	2011	152
6	Loss of SFRP1 is associated with breast cancer progression and poor prognosis in early stage tumors International Journal of Oncology ·Eva Klopocki, Glen Kristiansen, Peter J. Wild, Irina Klaman, Esmeralda Castaños‐Vélez, Gad Singer, Robert Stöhr, Ronald Simon, Guido Sauter, H. Leibiger, Lutz Essers, Birgit Weber, K. Hermann, André Rosenthal, Arndt Hartmann, Edgar Dahl	2004	138
7	Deletions of chromosome 8p and loss of sFRP1 expression are progression markers of papillary bladder cancer Laboratory Investigation ·Robert Stoehr, Christoph Wissmann, Hiromu Suzuki, Ruth Knuechel, René C. Krieg, Eva Klopocki, Edgar Dahl, Peter J. Wild, Hagen Blaszyk, Guido Sauter, Ronald Simon, Ruediger Schmitt, Dirk Zaak, Ferdinand Hofstaedter, André Rosenthal, Stephen B. Baylin, Christian Pilarsky, Arndt Hartmann	2004	123
8	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	121
9	Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients American Journal of Medical Genetics Part A ·Chayim Schell-Apacik, Kristina Wagner, Moritz Bihler, Birgit Ertl‐Wagner, Uwe Heinrich, Eva Klopocki, Vera M. Kalscheuer, Maximilian Muenke, Hubertus von Voß	2008	120
10	Frequent loss of SFRP1 expression in multiple human solid tumours: association with aberrant promoter methylation in renal cell carcinoma Oncogene ·Edgar Dahl, Frank Wiesmann, Matthias Woenckhaus, Robert Stoehr, Peter J. Wild, Jürgen Veeck, Ruth Knüchel, Eva Klopocki, Guido Sauter, Ronald Simon, Wolf F. Wieland, Bernadette Walter, Stefan Denzinger, Arndt Hartmann, Christine G. Hammerschmied	2007	115
11	A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome Journal of Medical Genetics ·Eva Klopocki, (unknown), N Benatar, Reinhard Ullmann, Stefan Mundlos, Katarina Lehmann	2008	99
12	Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E The American Journal of Human Genetics ·Eva Klopocki, Bianca P. Hennig, Katarina Dathe, Randi Koll, Thomy de Ravel, Emiel Baten, Eveline W Blom, Y. Gillerot, Johannes Weigel, Gabriele Krüger, Olaf Hiort, Petra Seemann, Stefan Mundlos	2010	96
13	Composition and dosage of a multipartite enhancer cluster control developmental expression of Ihh (Indian hedgehog) Nature Genetics ·Anja J. Will, Giulia Cova, Marco Osterwalder, Wing-Lee Chan, Lars Wittler, Norbert Brieske, Verena Heinrich, Jean‐Pierre de Villartay, Martin Vingron, Eva Klopocki, Axel Visel, Darío G. Lupiáñez, Stefan Mundlos	2017	86
14	Homeotic Arm-to-Leg Transformation Associated with Genomic Rearrangements at the PITX1 Locus The American Journal of Human Genetics ·Malte Spielmann, Francesco Brancati, Peter Krawitz, Peter N. Robinson, Daniel M. Ibrahim, Martin Franke, Jochen Hecht, Silke B. Lohan, Katarina Dathe, Anna Maria Nardone, Paola Ferrari, Antonio Landi, Lars Wittler, Bernd Timmermann, Danny Chan, U Mennen, Eva Klopocki, Stefan Mundlos	2012	84
15	Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes European Journal of Human Genetics ·(unknown), Jill A. Rosenfeld, Ryan N. Traylor, G. Bradley Schaefer, Elizabeth McPherson, Blake C. Ballif, Eva Klopocki, Stefan Mundlos, Lisa G. Shaffer, Arthur S. Aylsworth	2012	83
16	DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics Clinical Genetics ·Barbara Vona, Michaela A. H. Hofrichter, Cordula Neuner, Jörg Schröder, Andrea Gehrig, Julia B. Hennermann, Fabian Kraus, Wafaa Shehata-Dieler, Eva Klopocki, I. Nanda, Thomas Haaf	2013	74
17	Expanded Clinical Spectrum in Hepatocyte Nuclear Factor 1B-Maturity-Onset Diabetes of the Young The Journal of Clinical Endocrinology & Metabolism ·Klemens Raile, Eva Klopocki, Martin Holder, Theda Wessel, Angela Galler, Dorothee Deiss, Dominik Müller, T Riebel, Denise Horn, Monika Maringa, Jürgen Weber, Reinhard Ullmann, Annette Grüters	2009	74
18	ITIH5, a novel member of the inter-α-trypsin inhibitor heavy chain family is downregulated in breast cancer Cancer Letters ·Marina Himmelfarb, Eva Klopocki, Susanne Grube, Eike Staub, Irina Klaman, Bernd Hinzmann, Glen Kristiansen, André Rosenthal, Matthias Dürst, Edgar Dahl	2003	69
19	Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis The American Journal of Human Genetics ·Eva Klopocki, Silke B. Lohan, Francesco Brancati, Randi Koll, Anja Brehm, Petra Seemann, Katarina Dathe, Sigmar Stricker, Jochen Hecht, Kristin Bosse, Regina C. Betz, Francesco Garaci, Bruno Dallapiccola, Mahim Jain, Maximilian Muenke, Vivian Ng, Wilson Chan, Danny Chan, Stefan Mundlos	2010	68
20	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

About Eva Klopocki

Eva Klopocki is a scholar working on Molecular Biology, Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health and Immunology, having authored 103 papers that have together received 3.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (27 papers), Congenital heart defects research (14 papers), Congenital limb and hand anomalies (13 papers), Prenatal Screening and Diagnostics (9 papers), Chromosomal and Genetic Variations (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Connective tissue disorders research (7 papers) and Platelet Disorders and Treatments (6 papers). The work is most often cited by research in Developmental Biology (210 citations), Genetics (1.3k citations), Molecular Biology (2.0k citations), Pediatrics, Perinatology and Child Health (351 citations) and Cancer Research (253 citations). Eva Klopocki has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Stefan Mundlos, Denise Horn, Reinhard Ullmann, Edgar Dahl, Malte Spielmann, Glen Kristiansen, William B. Dobyns, Claus‐Eric Ott, Katarina Dathe and Ruth Knüchel. Their work appears in journals such as Stem Cell Research, European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Medical Genetics and The American Journal of Human Genetics.

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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Eva Klopocki

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