Britta Baumann

Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

Susanne Kohl, Britta Baumann, Thomas Rosenberg et al. · The American Journal of Human Genetics · 2002 · 263 citations · Full text

Biology, Photoreceptor Cell, Genetic Disorder +6

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Susanne Kohl, Balázs Varsányi, Gesine Abadin Antunes et al. · European Journal of Human Genetics · 2004 · 244 citations · Full text

Autosomal Recessive Achromatopsia, Mendelian Disorder, Genetic Disorder +7

Consequences of frameshift mutations at the immunoglobulin heavy chain locus of the mouse.

Britta Baumann, Mary Jane Potash, Georges Köhler · The EMBO Journal · 1985 · 193 citations · Full text

Immunogenetics, Genetic Disorder, Genetics +6

A homologous genetic basis of the murine <i>cpfl1</i> mutant and human achromatopsia linked to mutations in the <i>PDE6C</i> gene

Bo Chang, Tanja Grau, Susann Dangel et al. · Proceedings of the National Academy of Sciences · 2009 · 184 citations · Full text

Retinal Cone Photoreceptors, Photoreceptor Cell, Signal Transduction +14

Cone Dystrophy with Supernormal Rod Response Is Strictly Associated with Mutations in<i>KCNV2</i>

Bernd Wissinger, Susann Dangel, Herbert Ja ̈gle et al. · Investigative Ophthalmology & Visual Science · 2008 · 83 citations · Full text