Brody LC - Search Results

1

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.

Hacia JG, Fan JB, Ryder O, Jin L, Edgemon K, Ghandour G, Mayer RA, Sun B, Hsie L, Robbins CM, Brody LC, Wang D, Lander ES, Lipshutz R, Fodor SP, Collins FS. Hacia JG, et al. Among authors: brody lc. Nat Genet. 1999 Jun;22(2):164-7. doi: 10.1038/9674. Nat Genet. 1999. PMID: 10369258

2

The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals.

Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. Struewing JP, et al. Among authors: brody lc. Nat Genet. 1995 Oct;11(2):198-200. doi: 10.1038/ng1095-198. Nat Genet. 1995. PMID: 7550349

3

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.

Struewing JP, Brody LC, Erdos MR, Kase RG, Giambarresi TR, Smith SA, Collins FS, Tucker MA. Struewing JP, et al. Among authors: brody lc. Am J Hum Genet. 1995 Jul;57(1):1-7. Am J Hum Genet. 1995. PMID: 7611277 Free PMC article.

4

Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.

Russell MW, Dick M 2nd, Campbell RM, Hulse JE, Munroe DJ, Bric E, Housman DE, Collins FS, Brody LC. Russell MW, et al. Among authors: brody lc. Am J Hum Genet. 1995 Aug;57(2):503-7. Am J Hum Genet. 1995. PMID: 7668277 Free PMC article. No abstract available.

5

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer.

Castilla LH, Couch FJ, Erdos MR, Hoskins KF, Calzone K, Garber JE, Boyd J, Lubin MB, Deshano ML, Brody LC, et al. Castilla LH, et al. Among authors: brody lc. Nat Genet. 1994 Dec;8(4):387-91. doi: 10.1038/ng1294-387. Nat Genet. 1994. PMID: 7894491

6

KVLQT1 mutations in three families with familial or sporadic long QT syndrome.

Russell MW, Dick M 2nd, Collins FS, Brody LC. Russell MW, et al. Among authors: brody lc. Hum Mol Genet. 1996 Sep;5(9):1319-24. doi: 10.1093/hmg/5.9.1319. Hum Mol Genet. 1996. PMID: 8872472

7

Characterization of EZH1, a human homolog of Drosophila Enhancer of zeste near BRCA1.

Abel KJ, Brody LC, Valdes JM, Erdos MR, McKinley DR, Castilla LH, Merajver SD, Couch FJ, Friedman LS, Ostermeyer EA, Lynch ED, King MC, Welcsh PL, Osborne-Lawrence S, Spillman M, Bowcock AM, Collins FS, Weber BL. Abel KJ, et al. Among authors: brody lc. Genomics. 1996 Oct 15;37(2):161-71. doi: 10.1006/geno.1996.0537. Genomics. 1996. PMID: 8921387 Free article.

8

Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis.

Hacia JG, Brody LC, Chee MS, Fodor SP, Collins FS. Hacia JG, et al. Among authors: brody lc. Nat Genet. 1996 Dec;14(4):441-7. doi: 10.1038/ng1296-441. Nat Genet. 1996. PMID: 8944024

9

Cloning of the human NADH: ubiquinone oxidoreductase subunit B13: localization to chromosome 7q32 and identification of a pseudogene on 11p15.

Russell MW, du Manoir S, Collins FS, Brody LC. Russell MW, et al. Among authors: brody lc. Mamm Genome. 1997 Jan;8(1):60-1. doi: 10.1007/s003359900350. Mamm Genome. 1997. PMID: 9021153 Free article. No abstract available.

10

Chromosomal localization of 15 ion channel genes.

Russell MW, du Manoir S, Munroe DJ, Collins FS, Brody LC. Russell MW, et al. Among authors: brody lc. Somat Cell Mol Genet. 1996 Sep;22(5):425-31. doi: 10.1007/BF02369898. Somat Cell Mol Genet. 1996. PMID: 9039851 Free article.

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