Gilbert JR - Search Results

1

Association analysis of genetic polymorphisms in the CDC2 gene with late-onset Alzheimer disease.

Liang X, Schnetz-Boutaud N, Bartlett J, Anderson BM, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: gilbert jr. Dement Geriatr Cogn Disord. 2007;23(2):126-32. doi: 10.1159/000097857. Epub 2006 Dec 8. Dement Geriatr Cogn Disord. 2007. PMID: 17159347

2

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Among authors: gilbert jr. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

3

Myotonic dystrophy: update on progress to define the gene.

Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH, et al. Roses AD, et al. Among authors: gilbert jr. Aust Paediatr J. 1988;24 Suppl 1:66-9. Aust Paediatr J. 1988. PMID: 3060077 Review.

4

Morphological, biochemical, and genetic support for an apolipoprotein E effect on microtubular metabolism.

Roses AD, Einstein G, Gilbert J, Goedert M, Han SH, Huang D, Hulette C, Masliah E, Pericak-Vance MA, Saunders AM, Schmechel DE, Strittmatter WJ, Weisgraber KH, Xi PT. Roses AD, et al. Ann N Y Acad Sci. 1996 Jan 17;777:146-57. doi: 10.1111/j.1749-6632.1996.tb34413.x. Ann N Y Acad Sci. 1996. PMID: 8624078 Review.

5

Mutation analysis of the TSC2 gene in an African-American family.

Kumar A, Kandt RS, Wolpert C, Roses AD, Pericak-Vance MA, Gilbert JR. Kumar A, et al. Among authors: gilbert jr. Hum Mol Genet. 1995 Dec;4(12):2295-8. doi: 10.1093/hmg/4.12.2295. Hum Mol Genet. 1995. PMID: 8634701

6

Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration.

De La Paz MA, Guy VK, Abou-Donia S, Heinis R, Bracken B, Vance JM, Gilbert JR, Gass JD, Haines JL, Pericak-Vance MA. De La Paz MA, et al. Among authors: gilbert jr. Ophthalmology. 1999 Aug;106(8):1531-6. doi: 10.1016/S0161-6420(99)90449-9. Ophthalmology. 1999. PMID: 10442900 Clinical Trial.

7

Genetic studies of autistic disorder and chromosome 7.

Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Ashley-Koch A, et al. Among authors: gilbert jr. Genomics. 1999 Nov 1;61(3):227-36. doi: 10.1006/geno.1999.5968. Genomics. 1999. PMID: 10552924

8

Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.

Maddox LO, Menold MM, Bass MP, Rogala AR, Pericak-Vance MA, Vance JM, Gilbert JR. Maddox LO, et al. Among authors: gilbert jr. Genomics. 1999 Dec 15;62(3):325-31. doi: 10.1006/geno.1999.6017. Genomics. 1999. PMID: 10644429

9

Analysis of association at single nucleotide polymorphisms in the APOE region.

Martin ER, Gilbert JR, Lai EH, Riley J, Rogala AR, Slotterbeck BD, Sipe CA, Grubber JM, Warren LL, Conneally PM, Saunders AM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, Vance JM. Martin ER, et al. Among authors: gilbert jr. Genomics. 2000 Jan 1;63(1):7-12. doi: 10.1006/geno.1999.6057. Genomics. 2000. PMID: 10662539

10

Physical and cDNA mapping in the DBH region of human chromosome 9q34.

Gilbert JR, Kumar A, Newey S, Rao N, Ioannou P, Qiu H, Lin D, Xu P, Pettenati MJ, Pericak-Vance MA. Gilbert JR, et al. Hum Hered. 2000 May-Jun;50(3):151-7. doi: 10.1159/000022905. Hum Hered. 2000. PMID: 10686491

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