Vasileiou, Georgia
Friedrich-Alexander-Universität Erlangen-Nürnberg · Universitätsklinikum Erlangen
4 papers on CoChatORCID 0000-0002-1993-1134
Most cited papers
- Verified
Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling
Vasileiou, G., Ekici, A. B., Uebe, S., Zweier, C., Hoyer, J., Engels, H., Behrens, J., Reis, A., & Hadjihannas, M. V. (2015) · The American Journal of Human Genetics
Chromatin Remodeling and CancerWnt/β-catenin signaling in development and cancer
Cited by 81
- Verified
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings
Hebebrand, M., Vasileiou, G., Krumbiegel, M., Kraus, C., Uebe, S., Ekici, A. B., Thiel, C. T., Reis, A., & Popp, B. (2019) · American Journal of Medical Genetics Part A
Connective tissue disorders researchGenomics and Rare Diseases
Cited by 18
- Verified
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Bosch, E., Güse, E., Kirchner, P., Winterpacht, A., Walther, M., Alders, M., Kerkhof, J., Ekici, A. B., Sticht, H., Sadikovic, B., et al. (2024) · Human Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 9
- Verified
The missing link: ARID1B non-truncating variants causing Coffin-Siris syndrome due to protein aggregation
Bosch, E., Güse, E., Kirchner, P., Winterpacht, A., Walther, M., Alders, M., Kerkhof, J., Ekici, A. B., Sticht, H., Sadikovic, B., et al. (2024) · Human Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 9
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