基本信息
浏览量:48
职业迁徙
个人简介
Our team works on the molecular mechanism underlying human developmental disease. A special focus is on neurodevelopmental disorders and the genetic etiology of intellectual disability and autism, but also on the regulation of transcription factors in growth and development. Our work employs genome-editing, cell culture-based system as well as induced pluripotent stem cells and animal models. We aim at understanding how mutations correlate with disease, how genes are regulated and how they contribute to differentiation and development.
研究兴趣
论文共 327 篇作者统计合作学者相似作者
按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选
时间
引用量
主题
期刊级别
合作者
合作机构
Medizinische Genetik Mitteilungsblatt des Berufsverbandes Medizinische Genetik eVno. 3 (2024): 217-218
Medizinische Genetikno. 3 (2024): 217-218
Endocrine journalno. 9 (2024): 825-826
Birgit Weiss,Tim Ott,Philipp Vick,Julian C. Lui,Ralph Roeth, Sebastian Vogel, Stephan Waldmueller,Sandra Hoffmann,Jeffrey Baron,Jan M. Wit,Gudrun A. Rappold
Frontiers in endocrinology (2023)
Kristin Rädecke, Ambuj Gore, Karin Burau,Magdalena Laugsch,Katrin Köhler,Gudrun A Rappold,Sandra Hoffmann
Stem cell research (2023): 103089-103089
Nature Africa (2023)
DOAJ (DOAJ Directory of Open Access Journals) (2022)
Jing Wang,Henning Froehlich, Felipe Bodaleo Torres,Rangel Leal Silva,Gernot Poschet, Amit Agarwal,Gudrun A. Rappold
Proceedings of the National Academy of Sciencesno. 8 (2022)
加载更多
作者统计
#Papers: 331
#Citation: 16728
H-Index: 64
G-Index: 121
Sociability: 8
Diversity: 0
Activity: 1
合作学者
合作机构
D-Core
- 合作者
- 学生
- 导师
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn