Friederike Hennig
Max Planck Institute for Molecular Genetics(DE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, RNA Research and Splicing, Single-cell and spatial transcriptomics, RNA modifications and cancer, Genomics and Rare Diseases
Most-Cited Works
- → CDKL5 variants(2017)83 cited
- → EIF2S3Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO(2017)82 cited
- → De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females(2016)68 cited
- → De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction(2017)65 cited
- → Deleterious de novo variants of X‐linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita(2019)46 cited
- → Single-cell, whole-embryo phenotyping of mammalian developmental disorders(2023)32 cited
- → EIF2S3 Mutations Associated with Severe X-Linked Intellectual Disability Syndrome MEHMO(2018)10 cited
- → Single cell, whole embryo phenotyping of pleiotropic disorders of mammalian development(2022)5 cited
- Update on X-linked intellectual disability(2015)