Britt Johnson

Rates and Classification of Variants of Uncertain Significance in Hereditary Disease Genetic Testing

Elaine Chen, Flavia M. Facio, Kerry Aradhya et al. · JAMA Network Open · 2023 · 217 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The<i>nob2</i>mouse, a null mutation in<i>Cacna1f</i>: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses

Bo Chang, John R. Heckenlively, Philippa R. Bayley et al. · Visual Neuroscience · 2006 · 205 citations · Full text

Medicine, Neurobiology, Neuroscience +17

Multiple sclerosis susceptibility alleles in African Americans

Britt Johnson, Jane Wang, Elwood Taylor et al. · Genes and Immunity · 2009 · 126 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy

Rebecca Truty, Nila Patil, Raman Sankar et al. · Epilepsia Open · 2019 · 123 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Treatment with a Small Molecule Mutant IDH1 Inhibitor Suppresses Tumorigenic Activity and Decreases Production of the Oncometabolite 2-Hydroxyglutarate in Human Chondrosarcoma Cells

Luyuan Li, Ana C. Paz, Breelyn A. Wilky et al. · PLoS ONE · 2015 · 106 citations · Full text

Medicine, Cancer Biology, Oncology +12