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The 185delAG BRCA1 Mutation Originated before the Dispersion of Jews in the Diaspora and Is Not Limited to Ashkenazim

Human molecular genetics, 1998-05, Vol.7 (5), p.801-805

1998

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

British journal of cancer, 2000-07, Vol.83 (2), p.153-155

2000

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

European journal of cancer (1990), 2000-05, Vol.36 (8), p.983-986

2000

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Rates of Jewish ancestral mutations in BRCA1 and BRCA2 in borderline ovarian tumors

JNCI : Journal of the National Cancer Institute, 1998-07, Vol.90 (13), p.995-1000

1998

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Immunohistochemical analyses of sporadic and familial (185delAG carriers) ovarian cancer in Israel

European journal of cancer (1990), 2000-06, Vol.36 (9), p.1120-1124

2000

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The Tyr978X BRCA1 Mutation in Non-Ashkenazi Jews: Occurrence in High-Risk Families, General Population and Unselected Ovarian Cancer Patients

Community genetics, 2001, Vol.4 (1), p.50-55

2001

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Could the 185delAG BRCA1 Mutation Be an Ancient Jewish Mutation?

European journal of human genetics : EJHG, 1997-11, Vol.5 (6), p.413-416

1997

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

British journal of cancer, 1998-06, Vol.77 (11), p.1880-1883

1998

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Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

Human mutation, 2000-12, Vol.16 (6), p.491-501

2000

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Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast

Cancer genetics and cytogenetics, 2003-04, Vol.142 (2), p.145-148

2003

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Genetic analyses of male breast cancer in Israel

Genetic testing, 2000, Vol.4 (3), p.313-317

2000

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Hormone replacement therapy is more prevalent among Jewish BRCA1/2 mutation carriers

European journal of cancer (1990), 2006-03, Vol.42 (5), p.650-655

2006

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Lack of the predominant BRCA1 and BRCA2 mutations in Jewish ovarian carcinoma patients who previously underwent ovulation induction

European journal of gynaecological oncology, 1999, Vol.20 (5-6), p.371

1999

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Experience at Sheba Hospital in oncogenetic counseling and genetic testing of women with a high risk for breast and ovarian cancer

הרפואה, 1998-04, Vol.134 (8), p.593

1998

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Double Heterozygotes for the Ashkenazi Founder Mutations in BRCA1 and BRCA2 Genes

American journal of human genetics, 1998-10, Vol.63 (4), p.1224-1227

1998

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Rates of Jewish Ancestral Mutations in BRCAI and BRCA2 in Borderline Ovarian Tumors

JNCI : Journal of the National Cancer Institute, 1998-07, Vol.90 (13), p.995-1000

1998

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Insulin-like growth factor I polymorphism and breast cancer risk in Jewish women

The Israel Medical Association journal, 2002-10, Vol.4 (10), p.759-762

2002

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Adrenal tumors in BRCA1/BRCA2 mutation carriers

American journal of medical genetics, 2001-01, Vol.98 (3), p.277-279

2001

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Familial Aggregation of Glioma: A Pooled Analysis

American journal of epidemiology, 2010-11, Vol.172 (10), p.1099-1107

2010

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Genome-Wide High-Density SNP Linkage Search for Glioma Susceptibility Loci: Results from the Gliogene Consortium

Cancer research (Chicago, Ill.), 2011-12, Vol.71 (24), p.7568-7575

2011

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Description of selected characteristics of familial glioma patients – Results from the Gliogene Consortium

European journal of cancer (1990), 2013-04, Vol.49 (6), p.1335-1345

2013

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A Variable Age of Onset Segregation Model for Linkage Analysis, with Correction for Ascertainment, Applied to Glioma

Cancer epidemiology, biomarkers & prevention, 2012-12, Vol.21 (12), p.2242-2251

2012

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Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes

American journal of human genetics, 1998, Vol.63 (4), p.1224-1227

1998

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High Frequency of BRCA1 185delAG Mutation in Ovarian Cancer in Israel

JAMA : the journal of the American Medical Association, 1996-12, Vol.276 (22), p.1823

Modan, Baruch

1996

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The 185delAG BRCA1 Mutation Originated before the Dispersion of Jews in the Diaspora and Is Not Limited to Ashkenazim

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

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

Rates of Jewish ancestral mutations in BRCA1 and BRCA2 in borderline ovarian tumors

Immunohistochemical analyses of sporadic and familial (185delAG carriers) ovarian cancer in Israel

The Tyr978X BRCA1 Mutation in Non-Ashkenazi Jews: Occurrence in High-Risk Families, General Population and Unselected Ovarian Cancer Patients

Could the 185delAG BRCA1 Mutation Be an Ancient Jewish Mutation?

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

Mutational analyses of BRCA1 and BRCA2 in Ashkenazi and non-Ashkenazi Jewish women with familial breast and ovarian cancer

Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast

Genetic analyses of male breast cancer in Israel

Hormone replacement therapy is more prevalent among Jewish BRCA1/2 mutation carriers

Lack of the predominant BRCA1 and BRCA2 mutations in Jewish ovarian carcinoma patients who previously underwent ovulation induction

Experience at Sheba Hospital in oncogenetic counseling and genetic testing of women with a high risk for breast and ovarian cancer

Double Heterozygotes for the Ashkenazi Founder Mutations in BRCA1 and BRCA2 Genes

Rates of Jewish Ancestral Mutations in BRCAI and BRCA2 in Borderline Ovarian Tumors

Insulin-like growth factor I polymorphism and breast cancer risk in Jewish women

Adrenal tumors in BRCA1/BRCA2 mutation carriers

Familial Aggregation of Glioma: A Pooled Analysis

Genome-Wide High-Density SNP Linkage Search for Glioma Susceptibility Loci: Results from the Gliogene Consortium

Description of selected characteristics of familial glioma patients – Results from the Gliogene Consortium

A Variable Age of Onset Segregation Model for Linkage Analysis, with Correction for Ascertainment, Applied to Glioma

Double heterozygotes for the Ashkenazi founder mutations in BRCA1 and BRCA2 genes

High Frequency of BRCA1 185delAG Mutation in Ovarian Cancer in Israel

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