Goldberg YP - Search Results

1

Papanikolaou G, Tzilianos M, Christakis JI, Bogdanos D, Tsimirika K, MacFarlane J, Goldberg YP, Sakellaropoulos N, Ganz T, Nemeth E. Papanikolaou G, et al. Among authors: goldberg yp. Blood. 2005 May 15;105(10):4103-5. doi: 10.1182/blood-2004-12-4844. Epub 2005 Jan 25. Blood. 2005. PMID: 15671438 Free PMC article.

2

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.

Papanikolaou G, Samuels ME, Ludwig EH, MacDonald ML, Franchini PL, Dubé MP, Andres L, MacFarlane J, Sakellaropoulos N, Politou M, Nemeth E, Thompson J, Risler JK, Zaborowska C, Babakaiff R, Radomski CC, Pape TD, Davidas O, Christakis J, Brissot P, Lockitch G, Ganz T, Hayden MR, Goldberg YP. Papanikolaou G, et al. Among authors: goldberg yp. Nat Genet. 2004 Jan;36(1):77-82. doi: 10.1038/ng1274. Epub 2003 Nov 30. Nat Genet. 2004. PMID: 14647275

3

A homozygous HAMP mutation in a multiply consanguineous family with pseudo-dominant juvenile hemochromatosis.

Delatycki MB, Allen KJ, Gow P, MacFarlane J, Radomski C, Thompson J, Hayden MR, Goldberg YP, Samuels ME. Delatycki MB, et al. Among authors: goldberg yp. Clin Genet. 2004 May;65(5):378-83. doi: 10.1111/j.0009-9163.2004.00254.x. Clin Genet. 2004. PMID: 15099344

4

Competitive regulation of hepcidin mRNA by soluble and cell-associated hemojuvelin.

Lin L, Goldberg YP, Ganz T. Lin L, et al. Among authors: goldberg yp. Blood. 2005 Oct 15;106(8):2884-9. doi: 10.1182/blood-2005-05-1845. Epub 2005 Jul 5. Blood. 2005. PMID: 15998830 Free article.

5

Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.

MacDonald ML, Goldberg YP, Macfarlane J, Samuels ME, Trese MT, Shastry BS. MacDonald ML, et al. Among authors: goldberg yp. Clin Genet. 2005 Apr;67(4):363-6. doi: 10.1111/j.1399-0004.2005.00408.x. Clin Genet. 2005. PMID: 15733276 No abstract available.

6

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

7

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.

8

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.

9

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing.

Andrew SE, Goldberg YP, Theilmann J, Zeisler J, Hayden MR. Andrew SE, et al. Among authors: goldberg yp. Hum Mol Genet. 1994 Jan;3(1):65-7. doi: 10.1093/hmg/3.1.65. Hum Mol Genet. 1994. PMID: 8162053

10

A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease.

Goldberg YP, Andrew SE, Clarke LA, Hayden MR. Goldberg YP, et al. Hum Mol Genet. 1993 Jun;2(6):635-6. doi: 10.1093/hmg/2.6.635. Hum Mol Genet. 1993. PMID: 8353482 No abstract available.

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