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Lev G. Goldfarb

Commissariat à l'Énergie Atomique et aux Énergies Alternatives FR

358
Publications
11,449
Citations
55
H-Index
124
i10-Index
0
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex . OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

358 total

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

Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin, Imke Puls, Annette Abel et al. - The American Journal of Human Genetics, 2003
Cited by 562 OpenAlex

Natural History of Fabry Renal Disease

Mary H. Branton, Raphael Schiffmann, Sharda G. Sabnis, Gary J. Murray, Jane M. Quirk et al. - Medicine, 2002
Cited by 459 OpenAlex

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene PDF

Marinos C. Dalakas, Kyeyoon Park, Cristina Semino‐Mora, Hee Suk Lee, Kumaraswamy Sivakumar et al. - New England Journal of Medicine, 2000
Cited by 452 OpenAlex

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

Lev G. Goldfarb, Kyeyoon Park, Larisa Červen̆áková, Svetlana Gorokhova, Hee-Suk Lee et al. - Nature Genetics, 1998
Cited by 504 OpenAlex

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, David M. Asher, Michael P. Sulima et al. - Annals of Neurology, 1994
Cited by 817 OpenAlex

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, Kenneth C. Dole, Warren J. Strittmatter et al. - The Lancet, 1993
Cited by 500 OpenAlex

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

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton, Paul Brown, Andréa C. LeBlanc et al. - Science, 1992
Cited by 718 OpenAlex

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. PDF

Lev G. Goldfarb, Paul Brown, W. Richard McCombie, Dmitry Goldgaber, Gary D. Swergold et al. - Proceedings of the National Academy of Sciences, 1991
Cited by 330 OpenAlex

Research Topics

Prion Diseases and Protein Misfolding (45) Genetic Neurodegenerative Diseases (44) Skin and Cellular Biology Research (42) Neurological diseases and metabolism (39) Cardiomyopathy and Myosin Studies (37)

Affiliations

Binghamton University
US 1998 - 1998
National Institutes of Health
US 2017 - 1988
American Red Cross
US 1998 - 1998
Howard Hughes Medical Institute
US 1988 - 1988
Tel Aviv University
IL 1996 - 1996

External Profiles

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