Goldberg YP - Search Results

1

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.

Lafreniere RG, MacDonald ML, Dube MP, MacFarlane J, O'Driscoll M, Brais B, Meilleur S, Brinkman RR, Dadivas O, Pape T, Platon C, Radomski C, Risler J, Thompson J, Guerra-Escobio AM, Davar G, Breakefield XO, Pimstone SN, Green R, Pryse-Phillips W, Goldberg YP, Younghusband HB, Hayden MR, Sherrington R, Rouleau GA, Samuels ME. Lafreniere RG, et al. Among authors: goldberg yp. Am J Hum Genet. 2004 May;74(5):1064-73. doi: 10.1086/420795. Epub 2004 Apr 1. Am J Hum Genet. 2004. PMID: 15060842 Free PMC article.

2

Cloning and mapping of the alpha-adducin gene close to D4S95 and assessment of its relationship to Huntington disease.

Goldberg YP, Lin BY, Andrew SE, Nasir J, Graham R, Glaves ML, Hutchinson G, Theilmann J, Ginzinger DG, Schappert K, et al. Goldberg YP, et al. Hum Mol Genet. 1992 Dec;1(9):669-75. doi: 10.1093/hmg/1.9.669. Hum Mol Genet. 1992. PMID: 1284592

3

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.

Kremer B, Almqvist E, Theilmann J, Spence N, Telenius H, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: goldberg yp. Am J Hum Genet. 1995 Aug;57(2):343-50. Am J Hum Genet. 1995. PMID: 7668260 Free PMC article.

4

Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease.

Almqvist E, Spence N, Nichol K, Andrew SE, Vesa J, Peltonen L, Anvret M, Goto J, Kanazawa I, Goldberg YP, et al. Almqvist E, et al. Among authors: goldberg yp. Hum Mol Genet. 1995 Feb;4(2):207-14. doi: 10.1093/hmg/4.2.207. Hum Mol Genet. 1995. PMID: 7757069

5

Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms.

Lin B, Nasir J, Kalchman MA, McDonald H, Zeisler J, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Genomics. 1995 Feb 10;25(3):707-15. doi: 10.1016/0888-7543(95)80014-d. Genomics. 1995. PMID: 7759106

6

Genomic organization of the human alpha-adducin gene and its alternately spliced isoforms.

Lin B, Nasir J, McDonald H, Graham R, Rommens JM, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Genomics. 1995 Jan 1;25(1):93-9. doi: 10.1016/0888-7543(95)80113-z. Genomics. 1995. PMID: 7774961

7

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence.

Squitieri F, Andrew SE, Goldberg YP, Kremer B, Spence N, Zeisler J, Nichol K, Theilmann J, Greenberg J, Goto J, et al. Squitieri F, et al. Among authors: goldberg yp. Hum Mol Genet. 1994 Dec;3(12):2103-14. doi: 10.1093/hmg/3.12.2103. Hum Mol Genet. 1994. PMID: 7881406

8

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression.

Lin B, Rommens JM, Graham RK, Kalchman M, MacDonald H, Nasir J, Delaney A, Goldberg YP, Hayden MR. Lin B, et al. Among authors: goldberg yp. Hum Mol Genet. 1993 Oct;2(10):1541-5. doi: 10.1093/hmg/2.10.1541. Hum Mol Genet. 1993. PMID: 7903579

9

The molecular genetics of Huntington's disease.

Goldberg YP, Telenius H, Hayden MR. Goldberg YP, et al. Curr Opin Neurol. 1994 Aug;7(4):325-32. doi: 10.1097/00019052-199408000-00009. Curr Opin Neurol. 1994. PMID: 7952241 Review.

10

Familial predisposition to recurrent mutations causing Huntington's disease: genetic risk to sibs of sporadic cases.

Goldberg YP, Andrew SE, Theilmann J, Kremer B, Squitieri F, Telenius H, Brown JD, Hayden MR. Goldberg YP, et al. J Med Genet. 1993 Dec;30(12):987-90. doi: 10.1136/jmg.30.12.987. J Med Genet. 1993. PMID: 8133509 Free PMC article.

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