Eva Wohlleber

MicroRNA-mediated gene regulation and the resilience of multicellular animals

The Ensembl Variant Effect Predictor

Transcriptional Regulation and Its Misregulation in Disease

Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c

Reprogramming human fibroblasts to neurons by recapitulating an essential microRNA-chromatin switch

DECIPHER: database for the interpretation of phenotype-linked plausibly pathogenic sequence and copy-number variation

The Human Transcription Factors

Predicting the sequence specificities of DNA- and RNA-binding proteins by deep learning

Super-Enhancers in the Control of Cell Identity and Disease

Postnatal Loss of Mef2c Results in Dissociation of Effects on Synapse Number and Learning and Memory

Refining the phenotype associated with MEF2C haploinsufficiency

Haploinsufficiency of ARID1B, a Member of the SWI/SNF-A Chromatin-Remodeling Complex, Is a Frequent Cause of Intellectual Disability

A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients

Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression