Britta Baumann
University of Tübingen(DE)
Publications by Year
Research Areas
Retinal Development and Disorders, Retinal Diseases and Treatments, melanin and skin pigmentation, Connexins and lens biology, Glaucoma and retinal disorders
Most-Cited Works
- → Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia(2002)263 cited
- → CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia(2004)244 cited
- → Consequences of frameshift mutations at the immunoglobulin heavy chain locus of the mouse.(1985)193 cited
- → A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene(2009)184 cited
- → Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations inKCNV2(2008)84 cited
- → Spectral-Domain Optical Coherence Tomography Staging and Autofluorescence Imaging in Achromatopsia(2014)69 cited
- → Human Rod Monochromacy: Linkage Analysis and Mapping of a Cone Photoreceptor Expressed Candidate Gene on Chromosome 2q11(1998)68 cited
- → Mutations in CNGA3 impair trafficking or function of cone cyclic nucleotide-gated channels, resulting in achromatopsia(2008)63 cited
- → CNGB3 mutation spectrum including copy number variations in 552 achromatopsia patients(2017)63 cited
- → Mutation Analysis of the ND6 Gene in Patients with Lebers Hereditary Optic Neuropathy(1997)61 cited