Anna Floriane Hennig

Author

Charité - Universitätsmedizin Berlin ORCID

Also Known As

ANNA HENNIG, Anna F. Hennig, Anna Floriane Hennig, Floriane Hennig, Hennig, Anna Floriane

Publications

288

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin Max Planck Institute for Molecular Genetics Universitätsmedizin Göttingen Berlin Institute of Health at Charité - Universitätsmedizin Berlin Freie Universität Berlin

About

Anna Floriane Hennig is an author at Charité - Universitätsmedizin Berlin specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	141
2	Molecular Genetics	2	2	81
3	Natural Sciences	1	1	50
4	Biology	1	1	50
5	Cell Biology	1	1	10

Anna Floriane Hennig

Publications

287

Citations

H-Index

Page 1

	Year	Citations
Identification of Novel Nuclear Factor of Activated T Cell (NFAT)-associated Proteins in T Cells Christian Gabriel, Martin Karl, Heike Stephanowitz, Journal of Biological Chemistry	2016	64
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction Nadja Ehmke, Luitgard Graul‐Neumann, Lukasz Smorag, The American Journal of Human Genetics Mendelian DisorderMitochondrial DysfunctionGenetic DisorderGeneticsInherited Metabolic Disease	2017	64
Mitochondrial DNA distributions indicate colony propagation by single matri-lineages in the social spider Stegodyphus dumicola (Eresidae) Jes Johannesen, Anna Floriane Hennig, BIANCA DOMMERMUTH, Biological Journal of the Linnean Society Molecular Evolutionary EcologyGeneticsColony PropagationBiological EvolutionGenetic Diversity	2002	50
Efficient generation of osteoclasts from human induced pluripotent stem cells and functional investigations of lethal CLCN7-related osteopetrosis Uta Rössler, Anna Floriane Hennig, Nina Stelzer, Journal of Bone and Mineral Research	2020	47
Adult Osteosclerotic Metaphyseal Dysplasia With Progressive Osteonecrosis of the Jaws and Abnormal Bone Resorption Pattern Due to a LRRK1 Splice Site Mutation Antonia Howaldt, Anna Floriane Hennig, Tim Rolvien, Journal of Bone and Mineral Research	2020	22
Compound Heterozygous Frameshift Mutations in <i>MESD</i> Cause a Lethal Syndrome Suggestive of Osteogenesis Imperfecta Type XX Julian Stürznickel, Katharina Jähn, Jozef Zustin, Journal of Bone and Mineral Research Bone DiseaseDevelopmental BiologyMendelian DisorderBone Morphogenic ProteinGenetic Disorder	2020	17
Generation of a human induced pluripotent stem cell line (BIHi002-A) from a patient with CLCN7-related infantile malignant autosomal recessive osteopetrosis Anna Floriane Hennig, Uta Rössler, Franziska Boiti, Stem Cell Research	2018	13
Recruitment of Histone Methyltransferase Ehmt1 to Foxp3 TSDR Counteracts Differentiation of Induced Regulatory T Cells Martin Karl, Christian Gabriel, Katharina Hecklau, Journal of Molecular Biology Histone ModificationsChromatinChromatin RemodelingEpigenetic ChangeGenetics	2019	10

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