Lev Goldfarb - Publications

University of New Brunswick (Canada) 
Computer Science

65 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Tasca G, Odgerel Z, Monforte M, Aurino S, Clarke NF, Waddell LB, Udd B, Ricci E, Goldfarb LG. Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia. Muscle & Nerve. 46: 275-82. PMID 22806379 DOI: 10.1002/mus.23349  0.92
2012 Sambuughin N, Swietnicki W, Techtmann S, Matrosova V, Wallace T, Goldfarb L, Maynard E. KBTBD13 interacts with Cullin 3 to form a functional ubiquitin ligase. Biochemical and Biophysical Research Communications. 421: 743-9. PMID 22542517 DOI: 10.1016/j.bbrc.2012.04.074  0.92
2012 Liberski PP, Sikorska B, Lindenbaum S, Goldfarb LG, McLean C, Hainfellner JA, Brown P. Kuru: genes, cannibals and neuropathology. Journal of Neuropathology and Experimental Neurology. 71: 92-103. PMID 22249461 DOI: 10.1097/Nen.0B013E3182444Efd  0.92
2011 Goldfarb LG, Dalakas MC. Tragedy in a heartbeat: Malfunctioning desmin causes skeletal and cardiac muscle disease Journal of Clinical Investigation. 121: 455. DOI: 10.1172/JCI45852  0.92
2010 Odgerel Z, Sarkozy A, Lee HS, McKenna C, Rankin J, Straub V, Lochmüller H, Paola F, D'Amico A, Bertini E, Bushby K, Goldfarb LG. Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation. Neuromuscular Disorders : Nmd. 20: 438-42. PMID 20605452 DOI: 10.1016/j.nmd.2010.05.004  0.92
2010 Lee HS, Zhdanova SN, Vladimirtsev VA, Platonov FA, Osakovskiy VL, Subbotina EL, Broytman O, Danilova AP, Nikitina RS, Chepurnov AA, Krivoshapkin VG, Gajdusek DC, Savilov YD, Garruto RM, Goldfarb LG. Epidemiology of Viliuisk encephalomyelitis in Eastern Siberia. Epidemiology (Cambridge, Mass.). 21: 24-30. PMID 20010208 DOI: 10.1097/EDE.0b013e3181c30fd2  0.92
2010 Blumen SC, Drory VE, Sadeh M, El-Ad B, Soimu U, Groozman GB, Bouchard JP, Goldfarb LG. Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 11: 237-9. PMID 19412816 DOI: 10.3109/17482960902849823  0.92
2010 Goldfarb L. Representation before computation Natural Computing. 9: 365-379. DOI: 10.1007/s11047-009-9135-y  0.92
2009 Goldfarb LG, Vladimirtsev VA, Platanov FA, Lee HS, McLean CA, Masters CL. Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 cases. Folia Neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences. 47: 171-81. PMID 19618339  0.92
2009 McNeill A, Birchall D, Straub V, Goldfarb L, Reilich P, Walter MC, Schramm N, Lochmüller H, Chinnery PF. Lower limb radiology of distal myopathy due to the S60F myotilin mutation. European Neurology. 62: 161-6. PMID 19590214 DOI: 10.1159/000227266  0.92
2009 Shatunov A, Olivé M, Odgerel Z, Stadelmann-Nessler C, Irlbacher K, van Landeghem F, Bayarsaikhan M, Lee HS, Goudeau B, Chinnery PF, Straub V, Hilton-Jones D, Damian MS, Kaminska A, Vicart P, ... ... Goldfarb LG, et al. In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy. European Journal of Human Genetics : Ejhg. 17: 656-63. PMID 19050726 DOI: 10.1038/Ejhg.2008.226  0.92
2009 Goldfarb L, Scrimger I, Peter-Paul BR. ETS as a structural language for decision modeling and analysis: Planning, anticipation and monitoring Risk and Decision Analysis. 1: 85-101. DOI: 10.3233/RDA-2009-0008  0.92
2008 Fischer D, Kley RA, Strach K, Meyer C, Sommer T, Eger K, Rolfs A, Meyer W, Pou A, Pradas J, Heyer CM, Grossmann A, Huebner A, Kress W, Reimann J, ... ... Goldfarb L, et al. Distinct muscle imaging patterns in myofibrillar myopathies. Neurology. 71: 758-65. PMID 18765652 DOI: 10.1212/01.wnl.0000324927.28817.9b  0.92
2008 Lee HS, Goldfarb LG. Global distribution of Fatal familial insomnia: Founder or recurrent mutations Neurogenetics. 9: 301-302. PMID 18568368 DOI: 10.1007/s10048-008-0135-3  0.92
2007 Vladimirtsev VA, Nikitina RS, Renwick N, Ivanova AA, Danilova AP, Platonov FA, Krivoshapkin VG, McLean CA, Masters CL, Gajdusek DC, Goldfarb LG. Family clustering of Viliuisk encephalomyelitis in traditional and new geographic regions. Emerging Infectious Diseases. 13: 1321-6. PMID 18252102 DOI: 10.3201/Eid1309.061585  0.92
2007 Goldfarb L. On one unconventional framework for computation Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 4618: 77-90.  0.92
2006 Antonellis A, Lee-Lin SQ, Wasterlain A, Leo P, Quezado M, Goldfarb LG, Myung K, Burgess S, Fischbeck KH, Green ED. Functional analyses of glycyl-tRNA synthetase mutations suggest a key role for tRNA-charging enzymes in peripheral axons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10397-406. PMID 17035524 DOI: 10.1523/Jneurosci.1671-06.2006  0.92
2006 Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. Journal of Neuropathology and Experimental Neurology. 65: 642-51. PMID 16825951 DOI: 10.1097/01.Jnen.0000228198.81797.4D  0.92
2006 Shatunov A, Sambuughin N, Jankovic J, Elble R, Lee HS, Singleton AB, Dagvadorj A, Ji J, Zhang Y, Kimonis VE, Hardy J, Hallett M, Goldfarb LG. Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23. Brain : a Journal of Neurology. 129: 2318-31. PMID 16702189 DOI: 10.1093/Brain/Awl120  0.92
2006 Fischer D, Clemen CS, Olivé M, Ferrer I, Goudeau B, Roth U, Badorf P, Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Fürst DO, Vicart P, Goldfarb LG, Moza M, et al. Different early pathogenesis in myotilinopathy compared to primary desminopathy. Neuromuscular Disorders : Nmd. 16: 361-7. PMID 16684602 DOI: 10.1016/j.nmd.2006.03.007  0.92
2005 Sivakumar K, Kyriakides T, Puls I, Nicholson GA, Funalot B, Antonellis A, Sambuughin N, Christodoulou K, Beggs JL, Zamba-Papanicolaou E, Ionasescu V, Dalakas MC, Green ED, Fischbeck KH, Goldfarb LG. Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations. Brain : a Journal of Neurology. 128: 2304-14. PMID 16014653 DOI: 10.1093/Brain/Awh590  0.92
2003 Mulligan CJ, Robin RW, Osier MV, Sambuughin N, Goldfarb LG, Kittles RA, Hesselbrock D, Goldman D, Long JC. Allelic variation at alcohol metabolism genes ( ADH1B, ADH1C, ALDH2) and alcohol dependence in an American Indian population. Human Genetics. 113: 325-36. PMID 12884000 DOI: 10.1007/S00439-003-0971-Z  0.92
2003 Green AJ, Sivtseva TM, Danilova AP, Osakovsky VL, Vladimirtsev VA, Zeidler M, Knight RS, Platonov FA, Shatunov A, Alekseev VP, Krivoshapkin VG, Masters CL, Gajdusek DC, Goldfarb LG. Viliuisk encephalomyelitis: intrathecal synthesis of oligoclonal IgG. Journal of the Neurological Sciences. 212: 69-73. PMID 12810001 DOI: 10.1016/S0022-510X(03)00107-2  0.92
2003 Antonellis A, Ellsworth RE, Sambuughin N, Puls I, Abel A, Lee-Lin SQ, Jordanova A, Kremensky I, Christodoulou K, Middleton LT, Sivakumar K, Ionasescu V, Funalot B, Vance JM, Goldfarb LG, et al. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. American Journal of Human Genetics. 72: 1293-9. PMID 12690580 DOI: 10.1086/375039  0.92
2003 Uspensky I, Garruto RM, Goldfarb L. The taiga tick Ixodes persulcatus (Acari: Ixodidae) in the Sakha Republic (Yakutia) of Russia: distributional and reproductive ranges. Journal of Medical Entomology. 40: 119-22. PMID 12597666  0.92
2003 Goldfarb LG. Ataxia in Prion Diseases Genetics of Movement Disorders. 151-163. DOI: 10.1016/B978-012566652-7/50019-8  0.92
2002 Goldfarb LG. Kuru: the old epidemic in a new mirror. Microbes and Infection / Institut Pasteur. 4: 875-82. PMID 12270735 DOI: 10.1016/S1286-4579(02)01608-8  0.92
2002 Dagvadorj A, Petersen RB, Lee HS, Cervenakova L, Shatunov A, Budka H, Brown P, Gambetti P, Goldfarb LG. Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy. Annals of Neurology. 52: 355-9. PMID 12205650 DOI: 10.1002/Ana.10267  0.92
2002 Korkin D, Goldfarb L. Multiple genome rearrangement: a general approach via the evolutionary genome graph. Bioinformatics (Oxford, England). 18: S303-11. PMID 12169560  0.92
2002 Goldfarb LG. Genetics and infectious disease: convergence at the prion. Epidemiology (Cambridge, Mass.). 13: 379-81. PMID 12094090 DOI: 10.1097/00001648-200207000-00003  0.92
2002 Branton MH, Schiffmann R, Sabnis SG, Murray GJ, Quirk JM, Altarescu G, Goldfarb L, Brady RO, Balow JE, Austin Iii HA, Kopp JB. Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course. Medicine. 81: 122-38. PMID 11889412 DOI: 10.1097/00005792-200203000-00003  0.92
2001 Bushara KO, Goebel SU, Shill H, Goldfarb LG, Hallett M. Gluten sensitivity in sporadic and hereditary cerebellar ataxia. Annals of Neurology. 49: 540-3. PMID 11310636 DOI: 10.1002/ana.108  0.92
2001 Lee HS, Brown P, Cervenáková L, Garruto RM, Alpers MP, Gajdusek DC, Goldfarb LG. Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype. The Journal of Infectious Diseases. 183: 192-196. PMID 11120925 DOI: 10.1086/317935  0.92
2000 Bhavsar VC, Ghorbani AA, Goldfarb L. Inductive learning inability of artificial neural networks Canadian Conference On Electrical and Computer Engineering. 2: 712-716.  0.92
1998 Chapman J, Cervenáková L, Petersen RB, Lee HS, Estupinan J, Richardson S, Vnencak-Jones CL, Gajdusek DC, Korczyn AD, Brown P, Goldfarb LG. APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies. Neurology. 51: 548-53. PMID 9710033 DOI: 10.1212/Wnl.51.2.548  0.92
1998 Goldfarb LG, Park KY, Cervenáková L, Gorokhova S, Lee HS, Vasconcelos O, Nagle JW, Semino-Mora C, Sivakumar K, Dalakas MC. Missense mutations in desmin associated with familial cardiac and skeletal myopathy. Nature Genetics. 19: 402-3. PMID 9697706 DOI: 10.1038/1300  0.92
1996 Cochran EJ, Bennett DA, Cervenáková L, Kenney K, Bernard B, Foster NL, Benson DF, Goldfarb LG, Brown P. Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation. Neurology. 47: 727-33. PMID 8797471 DOI: 10.1212/Wnl.47.3.727  0.92
1996 Sivakumar K, Vasconcelos O, Goldfarb L, Dalakas MC. Late-onset muscle weakness in partial phosphofructokinase deficiency: A unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation Neurology. 46: 1337-1342. PMID 8628478 DOI: 10.1212/WNL.46.5.1337  0.92
1995 Reder AT, Mednick AS, Brown P, Spire JP, Van Cauter E, Wollmann RL, Cervenàkovà L, Goldfarb LG, Garay A, Ovsiew F. Clinical and genetic studies of fatal familial insomnia. Neurology. 45: 1068-75. PMID 7783865 DOI: 10.1212/Wnl.45.6.1068  0.92
1995 Goldfarb LG, Brown P. The transmissible spongiform encephalopathies Annual Review of Medicine. 46: 57-65. PMID 7598484 DOI: 10.1146/annurev.med.46.1.57  0.92
1995 Dranovsky A, Goldfarb L, Gajdusek DC, Goldgaber D. Brief report: Apolipoprotein e ε4 allele does not correlate with amyloid plaques in transmissible spongiform encephalopathies Amyloid. 2: 36-38. DOI: 10.3109/13506129509031886  0.92
1994 Haltia M, Viitanen M, Sulkava R, Ala-Hurula V, Poyhonen M, Goldfarb L, Brown P, Levy E, Houlden H, Crook R, Goate A, Clark R, Korenblat K, Pandit S, Keller HD, et al. Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description Annals of Neurology. 36: 362-367. PMID 8080244 DOI: 10.1002/Ana.410360307  0.92
1994 Camenga DL, Goldfarb LG, Bierke-Nelson D, Neff K. Familial Creutzfeldt-Jakob disease Annals of the New York Academy of Sciences. 724: 361-362. PMID 8030961 DOI: 10.1111/j.1749-6632.1994.tb38932.x  0.92
1994 Petersen RB, Goldfarb LG, Tabaton M, Brown P, Monari L, Cortelli P, Montagna P, Autilio-Gambetti L, Gajdusek DC, Lugaresi E. A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene). Molecular Neurobiology. 8: 99-103. PMID 7999319 DOI: 10.1007/Bf02780659  0.92
1994 Lunkes A, Goldfarb LG, Platonov FA, Alexeev VP, Duenas-Barajas E, Gajdusek DC, Auburger G. Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locus. Experimental Neurology. 126: 310-2. PMID 7925830 DOI: 10.1006/exnr.1994.1070  0.92
1993 Goldfarb LG, Brown P, Little BW, Cervenáková L, Kenney K, Gibbs CJ, Gajdusek DC. A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob disease. Neurology. 43: 2392-4. PMID 8232966 DOI: 10.1212/WNL.43.11.2392  0.92
1992 Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science (New York, N.Y.). 258: 806-8. PMID 1439789 DOI: 10.1126/Science.1439789  0.92
1992 Goldfarb LG, Gajdusek DC. Viliuisk encephalomyelitis in the Iakut people of Siberia. Brain : a Journal of Neurology. 115: 961-78. PMID 1393513 DOI: 10.1093/brain/115.4.961  0.92
1992 Chapman J, Brown P, Rabey JM, Goldfarb LG, Inzelberg R, Gibbs CJ, Gajdusek DC, Korczyn AD. Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutation. Neurology. 42: 1249-50. PMID 1351274 DOI: 10.1212/WNL.42.6.1249-a  0.92
1992 Goldfarb L. A cognitive theory without inductive learning Behavioral and Brain Sciences. 15: 446-447. DOI: 10.1017/S0140525X00069569  0.92
1992 Goldfarb L. What is distance and why do we need the metric model for pattern learning? Pattern Recognition. 25: 431-438. DOI: 10.1016/0031-3203(92)90091-V  0.92
1992 Chan TYT, Goldfarb L. Primitive pattern learning Pattern Recognition. 25: 883-889. DOI: 10.1016/0031-3203(92)90041-G  0.92
1991 Eldadah ZA, Asher DM, Godec MS, Pomeroy KL, Goldfarb LG, Feinstone SM, Levitan H, Gibbs CJ, Gajdusek DC. Detection of flaviviruses by reverse-transcriptase polymerase chain reaction. Journal of Medical Virology. 33: 260-7. PMID 1713265 DOI: 10.1002/jmv.1890330410  0.92
1991 Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, Cervenakova L, Baron H, Gibbs CJ, Gajdusek DC. Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. Proceedings of the National Academy of Sciences of the United States of America. 88: 10926-30. PMID 1683708 DOI: 10.1073/Pnas.88.23.10926  0.92
1991 Brown P, Goldfarb LG, Brown WT, Goldgaber D, Rubenstein R, Kascsak RJ, Guiroy DC, Piccardo P, Boellaard JW, Gajdusek DC. Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome. Neurology. 41: 375-9. PMID 1672447 DOI: 10.1212/Wnl.41.3.375  0.92
1991 Speer MC, Goldgaber D, Goldfarb LG, Roses AD, Pericak-Vance MA. Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter Genomics. 9: 366-368. PMID 1672296 DOI: 10.1016/0888-7543(91)90266-H  0.92
1990 Goldfarb LG, Brown P, Goldgaber D, Asher DM, Rubenstein R, Brown WT, Piccardo P, Kascsak RJ, Boellaard JW, Gajdusek DC. Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome. Experimental Neurology. 108: 247-50. PMID 2190844 DOI: 10.1016/0014-4886(90)90130-K  0.92
1990 Goldfarb L. On the foundations of intelligent processes-I. An evolving model for pattern learning Pattern Recognition. 23: 595-616. DOI: 10.1016/0031-3203(90)90037-L  0.92
1989 Goldgaber D, Goldfarb LG, Brown P, Asher DM, Brown WT, Lin S, Teener JW, Feinstone SM, Rubenstein R, Kascsak RJ, Boellaard JW, Gajdusek DC. Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome Experimental Neurology. 106: 204-206. PMID 2572450 DOI: 10.1016/0014-4886(89)90095-2  0.92
1988 Mora CA, Garruto RM, Brown P, Guiroy D, Morgan OSC, Rodgers-Johnson P, Ceroni M, Yanagihara R, Goldfarb LG, Gibbs CJ, Gajdusek DC. Seroprevalence of antibodies to HTLV-I in patients with chronic neurological disorders other than tropical spastic paraparesis Annals of Neurology. 23: S192-S195. PMID 2894813 DOI: 10.1002/ana.410230743  0.92
1986 Goldfarb LG. Epidemiological models of tick-borne infections (Acari: Ixodidae and Argasidae) Journal of Medical Entomology. 23: 125-131. PMID 3701796  0.92
1984 Goldfarb L. A unified approach to pattern recognition Pattern Recognition. 17: 575-582. DOI: 10.1016/0031-3203(84)90056-6  0.92
1982 Wong AKC, Goldfarb L. Pattern recognition of relational structures Pattern Recognition Theory and Applications. Proc. Nato Asi, Oxford, 1981. 157-175.  0.92
1981 Goldfarb LG, Gurevich GS. A simplified model for description of epidemic process in low intensity foci of tick-borne encephalitis Meditsinskaya Parazitologiya I Parazitarnye Bolezni. 50: 30-34. PMID 7254135  0.92
1978 Goldfarb L, Wong AKC. TOWARDS ANALYSIS OF STRUCTURAL AND MEASURABLE PATTERNS OF SYSTEMS STATES Proceedings of the Ieee Conference On Decision and Control. 1086-1093.  0.92
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