L. G. Goldfarb

1.6k total citations
19 papers, 715 citations indexed

About

L. G. Goldfarb is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, L. G. Goldfarb has authored 19 papers receiving a total of 715 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Neurology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in L. G. Goldfarb's work include Prion Diseases and Protein Misfolding (14 papers), Neurological diseases and metabolism (7 papers) and Mitochondrial Function and Pathology (3 papers). L. G. Goldfarb is often cited by papers focused on Prion Diseases and Protein Misfolding (14 papers), Neurological diseases and metabolism (7 papers) and Mitochondrial Function and Pathology (3 papers). L. G. Goldfarb collaborates with scholars based in United States, Israel and Russia. L. G. Goldfarb's co-authors include D. Carleton Gajdusek, Paul Brown, Joab Chapman, Amos D. Korczyn, Richard Rubenstein, Larisa Červen̆áková, Clarence J. Gibbs, D. C. Gajdusek, A Arlazoroff and Kimbra Kenney and has published in prestigious journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

L. G. Goldfarb

18 papers receiving 702 citations

Peers

Countries citing papers authored by L. G. Goldfarb

Since Specialization

Citations

This map shows the geographic impact of L. G. Goldfarb's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by L. G. Goldfarb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L. G. Goldfarb more than expected).

Fields of papers citing papers by L. G. Goldfarb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by L. G. Goldfarb. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by L. G. Goldfarb. The network helps show where L. G. Goldfarb may publish in the future.

Co-authorship network of co-authors of L. G. Goldfarb

This figure shows the co-authorship network connecting the top 25 collaborators of L. G. Goldfarb. A scholar is included among the top collaborators of L. G. Goldfarb based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with L. G. Goldfarb. L. G. Goldfarb is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Autosomal dominant spastic paraplegia in four generations of Yakut family linked to dynamin 2 mutation 2020 ·Yakut Medical Journal ·(unknown), L. G. Goldfarb, (unknown), (unknown), (unknown), Anna Sundborger, (unknown), Neil Renwick, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Jenny E. Hinshaw, (unknown)	0
2	[THE ANALYSIS OF LIFE SPAN AND MORTALITY OF PATIENTS WITH SPINOCEREBELLAR ATAXIA TYPE I]. 2016 ·PubMed ·(unknown), L. G. Goldfarb, (unknown), (unknown), (unknown), (unknown), Федор Алексеевич Платонов	1
3	Genetic Studies in Relation to Kuru: An Overview 2004 ·Current Molecular Medicine ·L. G. Goldfarb, Larisa Červen̆áková, D. C. Gajdusek	24
4	A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype 2000 ·Neurology ·(unknown), Paul Brown, (unknown), L. G. Goldfarb, Jun Tateishi	24
5	Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation 1996 ·Neurology ·Elizabeth J. Cochran, David A. Bennett, Larisa Červen̆áková, Kimbra Kenney, Bryan Bernard, Norman L. Foster, (unknown), L. G. Goldfarb, Patricia E. Brown	57
6	Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200 ^Lys mutation 1996 ·Neurology ·Joab Chapman, A Arlazoroff, L. G. Goldfarb, Larisa Červen̆áková, Miriam Y. Neufeld, (unknown), Mary Herbert, Paul Brown, D. C. Gajdusek, Amos D. Korczyn	53
7	Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy 1995 ·Annals of Neurology ·K Sivakumar, Larisa Červen̆áková, Marinos C. Dalakas, Marta Leon‐Monzon, Stuart Isaacson, James W. Nagle, Olavo M. Vasconcelos, L. G. Goldfarb	11
8	Clinical and genetic studies of fatal familial insomnia 1995 ·Neurology ·Anthony T. Reder, (unknown), Paul Brown, Jean‐Paul Spire, Eve Van Cauter, Robert L. Wollmann, (unknown), L. G. Goldfarb, (unknown), Fred Ovsiew, D. C. Gajdusek, Raymond P. Roos	47
9	Mutation analysis of spinocerebellar ataxia type 1 (SCA1) in a large Iakut kinship of Eastern Siberia 1994 ·The American Journal of Human Genetics ·L. G. Goldfarb, Astrid Lunkes, (unknown)	2
10	Autosomal Dominant Spinocerebellar Ataxia (SCA) in a Siberian Founder Population: Assignment to the SCA1 Locus 1994 ·Experimental Neurology ·Astrid Lunkes, L. G. Goldfarb, Федор Алексеевич Платонов, (unknown), (unknown), D. Carleton Gajdusek, (unknown)	12
11	Iatrogenic Creutzfeldt‐Jakob disease 1994 ·Neurology ·Paul A. Brown, (unknown), L. G. Goldfarb, W. Richard McCombie, Richard Rubenstein, Robert Will, Maurizio Pocchiari, Juan F. Martínez-Lage, C. Scalici, Carlo Masullo, (unknown), (unknown), D. Carleton Gajdusek	108
12	A new (two‐repeat) octapeptide coding insert mutation in Creutzfeldt‐Jakob disease 1993 ·Neurology ·L. G. Goldfarb, Paul Brown, (unknown), (unknown), Kimbra Kenney, C. J. Gibbs, D. Carleton Gajdusek	56
13	Effect of a Polymorphism on the Pathogenic 178Asn Mutation in the Prion Protein Gene 1993 ·Journal of Neuropathology & Experimental Neurology ·Robert B. Petersen, L. G. Goldfarb, Massimo Tabaton, Paul Brown, (unknown), P. Montagna, Pietro Cortelli, L. Monari, L. Autilio‐Gambetti, D. Carleton Gajdusek, E Lugaresi, Pierluigi Gambetti	1
14	Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation. 1993 ·Journal of Neurology Neurosurgery & Psychiatry ·Joab Chapman, Paul Brown, L. G. Goldfarb, A Arlazoroff, D. Carleton Gajdusek, Amos D. Korczyn	62
15	Transmission of spongiform encephalopathy from a familial Creutzfeldt‐Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation 1992 ·Neurology ·Joab Chapman, Paul Brown, J. M. Rabey, L. G. Goldfarb, Rivka Inzelberg, C. J. Gibbs, D. Carleton Gajdusek, Amos D. Korczyn	12
16	Atypical Creutzfeldt‐Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene 1992 ·Neurology ·P. Brown, L. G. Goldfarb, W. Richard McCombie, Ana Belén Nieto Librero, (unknown), William Sheremata, (unknown), M. S. Godec, Clarence J. Gibbs, D. Carleton Gajdusek	51
17	The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease 1991 ·European Journal of Epidemiology ·Paul Brown, L. G. Goldfarb, Clarence J. Gibbs, D. Carleton Gajdusek	46
18	Creutzfeldt-Jacob disease associated with the PRNP codon 200LYS mutation: An analysis of 45 families 1991 ·European Journal of Epidemiology ·L. G. Goldfarb, Paul Brown, (unknown), (unknown), Lynn R. Goldin, Amos D. Korczyn, Joab Chapman, Sergio Gálvez, L Cartier, Richard Rubenstein, D. Carleton Gajdusek	96
19	Clinical and molecular genetic study of a large German kindred with Gerstmann‐Straussler‐Scheinker syndrome 1991 ·Neurology ·Paul Brown, L. G. Goldfarb, W. Ted Brown, Dmitry Goldgaber, Richard Rubenstein, Regina Kascsak, Don C. Guiroy, Pedro Piccardo, (unknown), D. Carleton Gajdusek	52

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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