Brown K - Search Results

1

A family with three germline mutations in BRCA1 and BRCA2.

Liede A, Metcalfe K, Offit K, Brown K, Miller S, Narod SA, Moslehi R. Liede A, et al. Among authors: brown k. Clin Genet. 1998 Sep;54(3):215-8. doi: 10.1111/j.1399-0004.1998.tb04287.x. Clin Genet. 1998. PMID: 9788724

2

Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer.

Neuhausen S, Gilewski T, Norton L, Tran T, McGuire P, Swensen J, Hampel H, Borgen P, Brown K, Skolnick M, Shattuck-Eidens D, Jhanwar S, Goldgar D, Offit K. Neuhausen S, et al. Among authors: brown k. Nat Genet. 1996 May;13(1):126-8. doi: 10.1038/ng0596-126. Nat Genet. 1996. PMID: 8673092

3

Germline BRCA1 185delAG mutations in Jewish women with breast cancer.

Offit K, Gilewski T, McGuire P, Schluger A, Hampel H, Brown K, Swensen J, Neuhausen S, Skolnick M, Norton L, Goldgar D. Offit K, et al. Among authors: brown k. Lancet. 1996 Jun 15;347(9016):1643-5. doi: 10.1016/s0140-6736(96)91484-1. Lancet. 1996. PMID: 8642955

4

Quantitating familial cancer risk: a resource for clinical oncologists.

Offit K, Brown K. Offit K, et al. Among authors: brown k. J Clin Oncol. 1994 Aug;12(8):1724-36. doi: 10.1200/JCO.1994.12.8.1724. J Clin Oncol. 1994. PMID: 8040684 Review.

5

Decision-making about genetic testing among women at familial risk for breast cancer.

Jacobsen PB, Valdimarsdottier HB, Brown KL, Offit K. Jacobsen PB, et al. Among authors: brown kl. Psychosom Med. 1997 Sep-Oct;59(5):459-66. doi: 10.1097/00006842-199709000-00001. Psychosom Med. 1997. PMID: 9316177

6

Familial acute myeloid leukemia and DiGuglielmo syndrome.

Siebert R, Jhanwar S, Brown K, Berman E, Offit K. Siebert R, et al. Among authors: brown k. Leukemia. 1995 Jun;9(6):1091-4. Leukemia. 1995. PMID: 7596175

7

Psychosocial predictors of BRCA counseling and testing decisions among urban African-American women.

Thompson HS, Valdimarsdottir HB, Duteau-Buck C, Guevarra J, Bovbjerg DH, Richmond-Avellaneda C, Amarel D, Godfrey D, Brown K, Offit K. Thompson HS, et al. Among authors: brown k. Cancer Epidemiol Biomarkers Prev. 2002 Dec;11(12):1579-85. Cancer Epidemiol Biomarkers Prev. 2002. PMID: 12496047

8

Tolerance for uncertainty and perceived risk among women receiving uninformative BRCA1/2 test results.

O'Neill SC, DeMarco T, Peshkin BN, Rogers S, Rispoli J, Brown K, Valdimarsdottir H, Schwartz MD. O'Neill SC, et al. Among authors: brown k. Am J Med Genet C Semin Med Genet. 2006 Nov 15;142C(4):251-9. doi: 10.1002/ajmg.c.30104. Am J Med Genet C Semin Med Genet. 2006. PMID: 17024668

9

Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction.

Schwartz MD, Valdimarsdottir HB, DeMarco TA, Peshkin BN, Lawrence W, Rispoli J, Brown K, Isaacs C, O'Neill S, Shelby R, Grumet SC, McGovern MM, Garnett S, Bremer H, Leaman S, O'Mara K, Kelleher S, Komaridis K. Schwartz MD, et al. Among authors: brown k. Health Psychol. 2009 Jan;28(1):11-19. doi: 10.1037/a0013147. Health Psychol. 2009. PMID: 19210013 Free PMC article. Clinical Trial.

10

Telephone genetic counseling for high-risk women undergoing BRCA1 and BRCA2 testing: rationale and development of a randomized controlled trial.

Peshkin BN, Demarco TA, Graves KD, Brown K, Nusbaum RH, Moglia D, Forman A, Valdimarsdottir H, Schwartz MD. Peshkin BN, et al. Among authors: brown k. Genet Test. 2008 Mar;12(1):37-52. doi: 10.1089/gte.2006.0525. Genet Test. 2008. PMID: 18373403

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