Gilbert JR - Search Results

1

Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.

Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER. Ma DQ, et al. Among authors: gilbert jr. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):477-483. doi: 10.1002/ajmg.b.31003. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19588468 Free PMC article.

2

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium.

Sarfarazi M, Wijmenga C, Upadhyaya M, Weiffenbach B, Hyser C, Mathews K, Murray J, Gilbert J, Pericak-Vance M, Lunt P, et al. Sarfarazi M, et al. Am J Hum Genet. 1992 Aug;51(2):396-403. Am J Hum Genet. 1992. PMID: 1642237 Free PMC article.

3

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.

4

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.

5

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.

6

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

7

A novel splice site mutation (156 + 1G-->A) in the TSC2 gene.

Kumar A, Kandt RS, Wolpert C, Roses AD, Pericak-Vance MA, Gilbert JR. Kumar A, et al. Among authors: gilbert jr. Hum Mutat. 1997;9(1):64-5. doi: 10.1002/(SICI)1098-1004(1997)9:1<64::AID-HUMU12>3.0.CO;2-N. Hum Mutat. 1997. PMID: 8990012 No abstract available.

8

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.

9

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

10

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

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