Cannon-Albright LA - Search Results

1

Characterization of linkage disequilibrium structure, mutation history, and tagging SNPs, and their use in association analyses: ELAC2 and familial early-onset prostate cancer.

Camp NJ, Swensen J, Horne BD, Farnham JM, Thomas A, Cannon-Albright LA, Tavtigian SV. Camp NJ, et al. Genet Epidemiol. 2005 Apr;28(3):232-43. doi: 10.1002/gepi.20054. Genet Epidemiol. 2005. PMID: 15593091

2

Segregation and linkage analysis of nine Utah breast cancer pedigrees.

Bishop DT, Cannon-Albright L, McLellan T, Gardner EJ, Skolnick MH. Bishop DT, et al. Genet Epidemiol. 1988;5(3):151-69. doi: 10.1002/gepi.1370050303. Genet Epidemiol. 1988. PMID: 3169523

3

Genomic structure, expression and mutational analysis of the P15 (MTS2) gene.

Stone S, Dayananth P, Jiang P, Weaver-Feldhaus JM, Tavtigian SV, Cannon-Albright L, Kamb A. Stone S, et al. Oncogene. 1995 Sep 7;11(5):987-91. Oncogene. 1995. PMID: 7675459

4

Familiality of cancer in Utah.

Cannon-Albright LA, Thomas A, Goldgar DE, Gholami K, Rowe K, Jacobsen M, McWhorter WP, Skolnick MH. Cannon-Albright LA, et al. Cancer Res. 1994 May 1;54(9):2378-85. Cancer Res. 1994. PMID: 8162584

5

A large kindred with 17q-linked breast and ovarian cancer: genetic, phenotypic, and genealogical analysis.

Goldgar DE, Fields P, Lewis CM, Tran TD, Cannon-Albright LA, Ward JH, Swensen J, Skolnick MH. Goldgar DE, et al. J Natl Cancer Inst. 1994 Feb 2;86(3):200-9. doi: 10.1093/jnci/86.3.200. J Natl Cancer Inst. 1994. PMID: 8283492

6

Chromosome 17q linkage studies of 18 Utah breast cancer kindreds.

Goldgar DE, Cannon-Albright LA, Oliphant A, Ward JH, Linker G, Swensen J, Tran TD, Fields P, Uharriet P, Skolnick MH. Goldgar DE, et al. Am J Hum Genet. 1993 Apr;52(4):743-8. Am J Hum Genet. 1993. PMID: 8460640 Free PMC article.

7

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds.

Tavtigian SV, Simard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S, Thorlacius S, Offit K, Stoppa-Lyonnet D, Belanger C, Bell R, Berry S, Bogden R, Chen Q, Davis T, Dumont M, Frye C, Hattier T, Jammulapati S, Janecki T, Jiang P, Kehrer R, Leblanc JF, Mitchell JT, McArthur-Morrison J, Nguyen K, Peng Y, Samson C, Schroeder M, Snyder SC, Steele L, Stringfellow M, Stroup C, Swedlund B, Swense J, Teng D, Thomas A, Tran T, Tranchant M, Weaver-Feldhaus J, Wong AK, Shizuya H, Eyfjord JE, Cannon-Albright L, Tranchant M, Labrie F, Skolnick MH, Weber B, Kamb A, Goldgar DE. Tavtigian SV, et al. Nat Genet. 1996 Mar;12(3):333-7. doi: 10.1038/ng0396-333. Nat Genet. 1996. PMID: 8589730

8

Genetic heterogeneity and unmapped genes for colorectal cancer.

Lewis CM, Neuhausen SL, Daley D, Black FJ, Swensen J, Burt RW, Cannon-Albright LA, Skolnick MH. Lewis CM, et al. Cancer Res. 1996 Mar 15;56(6):1382-8. Cancer Res. 1996. PMID: 8640829

9

Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.

Swensen J, Lewis CM, Cannon-Albright LA. Swensen J, et al. Hum Mutat. 1997;10(1):80-1. doi: 10.1002/(SICI)1098-1004(1997)10:1<80::AID-HUMU12>3.0.CO;2-W. Hum Mutat. 1997. PMID: 9222765 No abstract available.

10

BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing.

Shattuck-Eidens D, Oliphant A, McClure M, McBride C, Gupte J, Rubano T, Pruss D, Tavtigian SV, Teng DH, Adey N, Staebell M, Gumpper K, Lundstrom R, Hulick M, Kelly M, Holmen J, Lingenfelter B, Manley S, Fujimura F, Luce M, Ward B, Cannon-Albright L, Steele L, Offit K, Thomas A, et al. Shattuck-Eidens D, et al. JAMA. 1997 Oct 15;278(15):1242-50. JAMA. 1997. PMID: 9333265

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