Andrew SE - Search Results

1

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: andrew se. Hum Mol Genet. 1994 Dec;3(12):2103-14. doi: 10.1093/hmg/3.12.2103. Hum Mol Genet. 1994. PMID: 7881406

2

Geographical distribution of haplotypes in Swedish families with Huntington's disease.

Almqvist E, Andrew S, Theilmann J, Goldberg P, Zeisler J, Drugge U, Grandell U, Tapper-Persson M, Winblad B, Hayden M, et al. Almqvist E, et al. Hum Genet. 1994 Aug;94(2):124-8. doi: 10.1007/BF00202856. Hum Genet. 1994. PMID: 8045558

3

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease.

Andrew S, Theilmann J, Almqvist E, Norremolle A, Lucotte G, Anvret M, Sorensen SA, Turpin JC, Hayden MR. Andrew S, et al. Clin Genet. 1993 Jun;43(6):286-94. doi: 10.1111/j.1399-0004.1993.tb03820.x. Clin Genet. 1993. PMID: 8370147

4

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. Among authors: andrew se. Hum Mol Genet. 1992 Dec;1(9):669-75. doi: 10.1093/hmg/1.9.669. Hum Mol Genet. 1992. PMID: 1284592

5

A transcription map of the region containing the Huntington disease gene.

Rommens JM, Lin B, Hutchinson GB, Andrew SE, Goldberg YP, Glaves ML, Graham R, Lai V, McArthur J, Nasir J, et al. Rommens JM, et al. Among authors: andrew se. Hum Mol Genet. 1993 Jul;2(7):901-7. doi: 10.1093/hmg/2.7.901. Hum Mol Genet. 1993. PMID: 7689900

6

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: andrew se. Hum Mol Genet. 1995 Feb;4(2):207-14. doi: 10.1093/hmg/4.2.207. Hum Mol Genet. 1995. PMID: 7757069

7

Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.

Telenius H, Kremer B, Goldberg YP, Theilmann J, Andrew SE, Zeisler J, Adam S, Greenberg C, Ives EJ, Clarke LA, et al. Telenius H, et al. Among authors: andrew se. Nat Genet. 1994 Apr;6(4):409-14. doi: 10.1038/ng0494-409. Nat Genet. 1994. PMID: 8054984

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. Among authors: andrew se. 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

Molecular analysis of late onset Huntington's disease.

Kremer B, Squitieri F, Telenius H, Andrew SE, Theilmann J, Spence N, Goldberg YP, Hayden MR. Kremer B, et al. Among authors: andrew se. J Med Genet. 1993 Dec;30(12):991-5. doi: 10.1136/jmg.30.12.991. J Med Genet. 1993. PMID: 8133510 Free PMC article.

10

A worldwide study of the Huntington's disease mutation. The sensitivity and specificity of measuring CAG repeats.

Kremer B, Goldberg P, Andrew SE, Theilmann J, Telenius H, Zeisler J, Squitieri F, Lin B, Bassett A, Almqvist E, et al. Kremer B, et al. Among authors: andrew se. N Engl J Med. 1994 May 19;330(20):1401-6. doi: 10.1056/NEJM199405193302001. N Engl J Med. 1994. PMID: 8159192 Free article.

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