Lev G. Goldfarb

Human spongiform encephalopathy: The national institutes of health series of 300 cases of experimentally transmitted disease

Paul S. Brown, Clarence J. Gibbs, Pamela Rodgers‐Johnson et al. · Annals of Neurology · 1994 · 816 citations

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton et al. · Science · 1992 · 716 citations

Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V

Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin et al. · The American Journal of Human Genetics · 2003 · 555 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +5

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Lev G. Goldfarb, Kyeyoon Park, Larisa Červen̆áková et al. · Nature Genetics · 1998 · 503 citations

Missense Mutations, Cardiomyopathy, Mendelian Disorder +7

Apolipoprotein E ∈4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases

Ann M. Saunders, Allen D. Roses, Jeffery M. Vance et al. · The Lancet · 1993 · 500 citations

Allele Distributions, Alzheimer's Disease, Apolipoprotein E +11