ZFIN Person: Klopocki, Eva

ZFIN ID: ZDB-PERS-161220-5

Klopocki, Eva

Email:	eva.klopocki@uni-wuerzburg.de
URL:
Affiliation:	Klopocki Lab
Address:	Institute for Human Genetics University of Würzburg Biozentrum, Am Hubland 97074 Würzburg Germany
Country:	Germany
Phone:
Fax:
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Liedtke, D., Klopocki, E. (2022) Microarray expression profiling of fndc3a zebrafish mutants. microPublication. Biology. 2022:

Bauer, B., Liedtke, D., Jarzina, S., Stammler, E., Kreisel, K., Lalomia, V., Diefenbacher, M., Klopocki, E., Mally, A. (2021) Exploration of zebrafish larvae as an alternative whole-animal model for nephrotoxicity testing. Toxicology letters. 344:69-81

Liedtke, D., Hofmann, C., Jakob, F., Klopocki, E., Graser, S. (2020) Tissue-Nonspecific Alkaline Phosphatase-A Gatekeeper of Physiological Conditions in Health and a Modulator of Biological Environments in Disease. Biomolecules. 10(12):

Ohlebusch, B., Borst, A., Frankenbach, T., Klopocki, E., Jakob, F., Liedtke, D., Graser, S. (2020) Investigation of alpl expression and Tnap-activity in zebrafish implies conserved functions during skeletal and neuronal development. Scientific Reports. 10:13321

Liedtke, D., Orth, M., Meissler, M., Geuer, S., Knaup, S., Köblitz, I., Klopocki, E. (2019) ECM alterations in Fndc3a (Fibronectin Domain Containing Protein 3A) deficient zebrafish cause temporal fin development and regeneration defects. Scientific Reports. 9:13383

Blümel, R., Zink, M., Klopocki, E., Liedtke, D. (2019) On the traces of tcf12: Investigation of the gene expression pattern during development and cranial suture patterning in zebrafish (Danio rerio). PLoS One. 14:e0218286

Arndt, A.K., Schafer, S., Drenckhahn, J.D., Sabeh, M.K., Plovie, E.R., Caliebe, A., Klopocki, E., Musso, G., Werdich, A.A., Kalwa, H., Heinig, M., Padera, R.F., Wassilew, K., Bluhm, J., Harnack, C., Martitz, J., Barton, P.J., Greutmann, M., Berger, F., Hubner, N., Siebert, R., Kramer, H.H., Cook, S.A., MacRae, C.A., and Klaassen, S. (2013) Fine Mapping of the 1p36 Deletion Syndrome Identifies Mutation of PRDM16 as a Cause of Cardiomyopathy. American journal of human genetics. 93(1):67-77

Doelken, S.C., Köhler, S., Mungall, C.J., Gkoutos, G.V., Ruef, B.J., Smith, C., Smedley, D., Bauer, S., Klopocki, E., Schofield, P.N., Westerfield, M., Robinson, P.N., and Lewis, S.E. (2013) Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish. Disease models & mechanisms. 6(2):358-372

Klopocki, E., Lohan, S., Doelken, S.C., Stricker, S., Ockeloen, C.W., Thiele de Aguiar R.S., Lezirovitz, K., Netto, R.C.M., Jamsheer, A., Shah, H., Kurth, I., Habenicht, R., Warman, M., Devriendt, K., Kordass, U., Hempel, M., Rajabm, A., Mäkitie, O., Naveed, M., Radhakrishna, U., Antonarakis, S.E., Horn, D., and Mundlos, S. (2012) Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion. Journal of Medical Genetics. 49(2):119-125

NON-ZEBRAFISH PUBLICATIONS