Eitan Friedman

发表

Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

W. Chung, P. Hall, V. Pankratz, 2013, PLoS genetics.

Functional variant of KLOTHO: a breast cancer risk modifier among BRCA1 mutation carriers of Ashkenazi origin

B. Karlan, E. Friedman, M. Kuro-o, 2010, Oncogene.

Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas.

Z. Rappaport, Z. Ram, E. Friedman, 2001, Cancer genetics and cytogenetics.

A familial syndromic association between cutaneous malignant melanoma and neural system tumours

A. Scope, E. Friedman, E. Azizi, 2004, The British journal of dermatology.

ATM haplotypes and breast cancer risk in Jewish high-risk women

M Z Papa, R. Shamir, D. Lancet, 2006, British Journal of Cancer.

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.

Dieter Niederacher, Ute Hamann, Alfons Meindl, 2008, American journal of human genetics.

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Olufunmilayo I. Olopade, Mads Thomassen, Dieter Niederacher, 2016, Breast Cancer Research.

An identical novel mutation in BRCA1 and a common haplotype in familial ovarian cancer in non-Ashkenazi Jews.

B. Modan, M. Papa, E. Friedman, 1998, British Journal of Cancer.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

A. Whittemore, F. Couch, B. Bonanni, 2015 .

Significantly lower rates of BRCA1/BRCA2 founder mutations in Ashkenazi women with sporadic compared with familial early onset breast cancer.

R. Gershoni-baruch, E. Dagan, E. Friedman, 2000, European journal of cancer.

Rates of risk‐reducing surgery in Israeli BRCA1 and BRCA2 mutation carriers

R. Berger, E. Friedman, S. Narod, 2014, Clinical genetics.

Oncotype-DX recurrence score distribution in breast cancer patients with BRCA1/2 mutations

E. Friedman, D. Tsoref, I. Ben-Aharon, 2016, Breast Cancer Research and Treatment.

Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers

R. Gershoni-baruch, E. Friedman, A. Figer, 2000, British Journal of Cancer.

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Jane E. Carpenter, Jaana M. Hartikainen, A. Whittemore, 2016, Breast Cancer Research.