Analysis of BRCA1/BRCA2 genes' contribution to breast cancer susceptibility in high risk Jewish Ashkenazi women (Q81978444)

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14 January 2020

title

Analysis of BRCA1/BRCA2 genes' contribution to breast cancer susceptibility in high risk Jewish Ashkenazi women (English)

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14 January 2020

3

Yael Laitman

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14 January 2020

author name string

Tal Distelman-Menachem

1

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14 January 2020

Tal Shapira

2

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14 January 2020

Bella Kaufman

4

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14 January 2020

Frida Barak

5

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14 January 2020

Sean Tavtigian

6

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14 January 2020

Eitan Friedman

7

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14 January 2020

publication date

17 September 2008

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14 January 2020

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14 January 2020

volume

8

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14 January 2020

issue

2

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14 January 2020

page(s)

127-133

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BRCA1 and BRCA2 germline mutation analysis in the Indonesian population

14 January 2020

cites work

1 reference

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Large genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected families

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Color bar coding the BRCA1 gene on combed DNA: a useful strategy for detecting large gene rearrangements

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High occurrence of BRCA1 intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic

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Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions

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Detection of the CHEK2 1100delC mutation by MLPA BRCA1/2 analysis: a worthwhile strategy for its clinical applicability in 1100delC low-frequency populations?

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Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

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Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in western Denmark

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Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom-in array comparative genomic hybridization (aCGH).

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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Bar code screening on combed DNA for large rearrangements of the BRCA1 and BRCA2 genes in French breast cancer families

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Large BRCA1 gene deletions are found in 3% of German high-risk breast cancer families.

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The Cancer-predisposing Mutation C61G Disrupts Homodimer Formation in the NH2-terminal BRCA1 RING Finger Domain

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Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2

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Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families

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A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17

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Large genomic BRCA2 rearrangements and male breast cancer

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Hereditary cancer predisposition syndromes

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12 December 2020

Incidence of non-founder BRCA1 and BRCA2 mutations in high risk Ashkenazi breast and ovarian cancer families

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12 December 2020

Identification of novel BRCA large genomic rearrangements in Singapore Asian breast and ovarian patients with cancer

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12 December 2020

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

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12 December 2020

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion

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12 December 2020

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

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12 December 2020

BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland

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12 December 2020

Genomic rearrangements at the BRCA1 locus in Spanish families with breast/ovarian cancer.

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12 December 2020

Contribution ofBRCA1andBRCA2mutations to inherited ovarian cancer

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12 December 2020

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1

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12 December 2020

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

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12 December 2020

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families

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No Evidence of BRCA1/2 genomic rearrangements in high-risk French-Canadian breast/ovarian cancer families

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12 December 2020

DNA profiling of primary serous ovarian and fallopian tube carcinomas with array comparative genomic hybridization and multiplex ligation-dependent probe amplification

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12 December 2020

Large genomic deletions inactivate the BRCA2 gene in breast cancer families

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12 December 2020

Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations

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12 December 2020

Distinct BRCA1 rearrangements involving the BRCA1 pseudogene suggest the existence of a recombination hot spot

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12 December 2020

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

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