Catherine B. Kunst

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Annemieke J.M.H. Verkerk, Maura Pieretti, James S. Sutcliffe et al. · Cell · 1991 · 3.5K citations

Breakpoint Cluster Region, Fragile X Syndrome, Mendelian Disorder +11

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles

Catherine B. Kunst · Cell · 1994 · 360 citations

Allelic Variant, Linkage Disequilibrium, Genetic Disorder +13

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeat

Claude T. Ashley, James S. Sutcliffe, Catherine B. Kunst et al. · Nature Genetics · 1993 · 262 citations

Transcriptional Regulation, Translational Biology, Genetics +9

Copper Activation of Superoxide Dismutase 1 (SOD1) in Vivo

Paul J. Schmidt, Catherine B. Kunst, Valeria Culotta · Journal of Biological Chemistry · 2000 · 132 citations · Full text

Mutations in SOD1 associated with amyotrophic lateral sclerosis cause novel protein interactions

Catherine B. Kunst, Éva Mezey, Michael Brownstein et al. · Nature Genetics · 1997 · 123 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +5