Lindblom A - Search Results

1

A new polymorphism in the coding region of exon four in HSD17B2 in relation to risk of sporadic and hereditary breast cancer.

Jansson A, Carlsson J, Olsson A, Storm P, Margolin S, Gunnarsson C, Stenmark-Askmalm M, Lindblom A, Persson B, Stål O. Jansson A, et al. Among authors: lindblom a. Breast Cancer Res Treat. 2007 Nov;106(1):57-64. doi: 10.1007/s10549-006-9477-4. Epub 2007 Jan 27. Breast Cancer Res Treat. 2007. PMID: 17260097

2

Familial breast cancer and genes involved in breast carcinogenesis.

Lindblom A. Lindblom A. Breast Cancer Res Treat. 1995 May;34(2):171-83. doi: 10.1007/BF00665789. Breast Cancer Res Treat. 1995. PMID: 7647334 Review.

3

Hereditary breast cancer in Sweden: a predominance of maternally inherited cases.

Lindblom A, Rotstein S, Larsson C, Nordenskjöld M, Iselius L. Lindblom A, et al. Breast Cancer Res Treat. 1992;24(2):159-65. doi: 10.1007/BF01961248. Breast Cancer Res Treat. 1992. PMID: 8443403

4

ATM mutations in cancer families.

Vorechovský I, Luo L, Lindblom A, Negrini M, Webster AD, Croce CM, Hammarström L. Vorechovský I, et al. Among authors: lindblom a. Cancer Res. 1996 Sep 15;56(18):4130-3. Cancer Res. 1996. PMID: 8797579

5

A screening for BRCA1 mutations in breast and breast-ovarian cancer families from the Stockholm region.

Zelada-Hedman M, Wasteson Arver B, Claro A, Chen J, Werelius B, Kok H, Sandelin K, Håkansson S, Andersen TI, Borg A, Børresen Dale AL, Lindblom A. Zelada-Hedman M, et al. Among authors: lindblom a. Cancer Res. 1997 Jun 15;57(12):2474-7. Cancer Res. 1997. PMID: 9192828

6

The role of ataxia-telangiectasia heterozygotes in familial breast cancer.

Chen J, Birkholtz GG, Lindblom P, Rubio C, Lindblom A. Chen J, et al. Among authors: lindblom a, lindblom p. Cancer Res. 1998 Apr 1;58(7):1376-9. Cancer Res. 1998. PMID: 9537233

7

Hereditary cancer.

Lindblom A, Nordenskjöld M. Lindblom A, et al. Acta Oncol. 1999;38(4):439-47. doi: 10.1080/028418699431960. Acta Oncol. 1999. PMID: 10418710 Review.

8

Low frequency of E-cadherin alterations in familial breast cancer.

Salahshor S, Haixin L, Huo H, Kristensen VN, Loman N, Sjöberg-Margolin S, Borg A, Børresen-Dale AL, Vorechovsky I, Lindblom A. Salahshor S, et al. Among authors: lindblom a. Breast Cancer Res. 2001;3(3):199-207. doi: 10.1186/bcr295. Epub 2001 Mar 9. Breast Cancer Res. 2001. PMID: 11305955 Free PMC article.

9

BRCA1 mutations in a population-based study of breast cancer in Stockholm County.

Margolin S, Werelius B, Fornander T, Lindblom A. Margolin S, et al. Among authors: lindblom a. Genet Test. 2004 Summer;8(2):127-32. doi: 10.1089/gte.2004.8.127. Genet Test. 2004. PMID: 15345109

10

High incidence of skewed X chromosome inactivation in young patients with familial non-BRCA1/BRCA2 breast cancer.

Kristiansen M, Knudsen GP, Maguire P, Margolin S, Pedersen J, Lindblom A, Ørstavik KH. Kristiansen M, et al. Among authors: lindblom a. J Med Genet. 2005 Nov;42(11):877-80. doi: 10.1136/jmg.2005.032433. Epub 2005 May 6. J Med Genet. 2005. PMID: 15879497 Free PMC article.

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