St George-Hyslop P - Search Results

1

Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's disease.

Lee JH, Barral S, Cheng R, Chacon I, Santana V, Williamson J, Lantigua R, Medrano M, Jimenez-Velazquez IZ, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R. Lee JH, et al. Neurogenetics. 2008 Feb;9(1):51-60. doi: 10.1007/s10048-007-0103-3. Epub 2007 Oct 17. Neurogenetics. 2008. PMID: 17940814 Free PMC article.

2

Homozygous inheritance of the Machado-Joseph disease gene.

Lang AE, Rogaeva EA, Tsuda T, Hutterer J, St George-Hyslop P. Lang AE, et al. Ann Neurol. 1994 Sep;36(3):443-7. doi: 10.1002/ana.410360318. Ann Neurol. 1994. PMID: 8080254

3

Linkage of polymorphic congenital cataract to the gamma-crystallin gene locus on human chromosome 2q33-35.

Rogaev EI, Rogaeva EA, Korovaitseva GI, Farrer LA, Petrin AN, Keryanov SA, Turaeva S, Chumakov I, St George-Hyslop P, Ginter EK. Rogaev EI, et al. Hum Mol Genet. 1996 May;5(5):699-703. doi: 10.1093/hmg/5.5.699. Hum Mol Genet. 1996. PMID: 8733140

4

Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease.

Rogaev EI, Sherrington R, Wu C, Levesque G, Liang Y, Rogaeva EA, Ikeda M, Holman K, Lin C, Lukiw WJ, de Jong PJ, Fraser PE, Rommens JM, St George-Hyslop P. Rogaev EI, et al. Genomics. 1997 Mar 15;40(3):415-24. doi: 10.1006/geno.1996.4523. Genomics. 1997. PMID: 9073509

5

Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease.

Brindle N, Song Y, Rogaeva E, Premkumar S, Levesque G, Yu G, Ikeda M, Nishimura M, Paterson A, Sorbi S, Duara R, Farrer L, St George-Hyslop P. Brindle N, et al. Hum Mol Genet. 1998 May;7(5):933-5. doi: 10.1093/hmg/7.5.933. Hum Mol Genet. 1998. PMID: 9536099

6

Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE.

Song YQ, Rogaeva E, Premkumar S, Brindle N, Kawarai T, Orlacchio A, Yu G, Levesque G, Nishimura M, Ikeda M, Pei Y, O'Toole C, Duara R, Barker W, Sorbi S, Freedman M, Farrer L, St George-Hyslop P. Song YQ, et al. Neurosci Lett. 1998 Jul 10;250(3):189-92. doi: 10.1016/s0304-3940(98)00470-4. Neurosci Lett. 1998. PMID: 9708864 Free article.

7

Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.

Rogaeva E, Premkumar S, Song Y, Sorbi S, Brindle N, Paterson A, Duara R, Levesque G, Yu G, Nishimura M, Ikeda M, O'Toole C, Kawarai T, Jorge R, Vilarino D, Bruni AC, Farrer LA, St George-Hyslop PH. Rogaeva E, et al. JAMA. 1998 Aug 19;280(7):614-8. doi: 10.1001/jama.280.7.614. JAMA. 1998. PMID: 9718052

8

A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease.

Ramirez-Dueñas MG, Rogaeva EA, Leal CA, Lin C, Ramirez-Casillas GA, Hernandez-Romo JA, St George-Hyslop PH, Cantu JM. Ramirez-Dueñas MG, et al. Ann Genet. 1998;41(3):149-53. Ann Genet. 1998. PMID: 9833068

9

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.

Kertesz A, Kawarai T, Rogaeva E, St George-Hyslop P, Poorkaj P, Bird TD, Munoz DG. Kertesz A, et al. Neurology. 2000 Feb 22;54(4):818-27. doi: 10.1212/wnl.54.4.818. Neurology. 2000. PMID: 10690970

10

Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees.

Orlacchio A, Kawarai T, Massaro AM, St George-Hyslop PH, Sorbi S. Orlacchio A, et al. Neurosci Lett. 2000 May 12;285(2):83-6. doi: 10.1016/s0304-3940(00)01032-6. Neurosci Lett. 2000. PMID: 10793232

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