Stefanie Weinert
Forschungsinstitut Havelhöhe(DE)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Ion Transport and Channel Regulation, Genomics and Rare Diseases, Ion channel regulation and function, COVID-19 and Mental Health
Most-Cited Works
- → X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes(2015)302 cited
- → Exome sequencing reveals new causal mutations in children with epileptic encephalopathies(2013)291 cited
- → Insect‐Derived Proline‐Rich Antimicrobial Peptides Kill Bacteria by Inhibiting Bacterial Protein Translation at the 70 S Ribosome(2014)242 cited
- → Lysosomal Pathology and Osteopetrosis upon Loss of H + -Driven Lysosomal Cl – Accumulation(2010)234 cited
- → Endosomal Chloride-Proton Exchange Rather Than Chloride Conductance Is Crucial for Renal Endocytosis(2010)177 cited
- → Cell Biology and Physiology of CLC Chloride Channels and Transporters(2012)148 cited
- → Stretch–Activation of Angiotensin II Type 1aReceptors Contributes to the Myogenic Response of Mouse Mesenteric and Renal Arteries(2014)130 cited
- → M line–deficient titin causes cardiac lethality through impaired maturation of the sarcomere(2006)105 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
- → Genetic analysis of adiponectin and obesity in Hispanic families: the IRAS Family Study(2005)68 cited