(Q39991531)

16 September 2017

title

Mutational analysis of the breast cancer susceptibility gene BRIP1 /BACH1/FANCJ in high-risk non-BRCA1/BRCA2 breast cancer families (English)

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16 September 2017

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5

Jacques Simard

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16 September 2017

Frédéric Guénard

1

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16 September 2017

Yvan Labrie

2

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16 September 2017

Geneviève Ouellette

3

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16 September 2017

Charles Joly Beauparlant

4

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16 September 2017

Francine Durocher

6

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16 September 2017

INHERIT BRCAs

7

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16 September 2017

language of work or name

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15 April 2008

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Journal of Human Genetics

16 September 2017

published in

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16 September 2017

volume

53

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16 September 2017

issue

7

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16 September 2017

page(s)

579-591

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Dominant Negative ATM Mutations in Breast Cancer Families

16 September 2017

cites work

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Crossref

https://api.crossref.org/works/10.1007%2FS10038-008-0285-Z

Infrequent mutations in the PTEN/MMAC1 gene among primary breast cancers

21 January 2018

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Crossref

https://api.crossref.org/works/10.1007%2FS10038-008-0285-Z

The Bloom's syndrome gene product is homologous to RecQ helicases

21 January 2018

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12 December 2020

Automated detection of point mutations using fluorescent sequence trace subtraction

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12 December 2020

Are ATM mutations 7271T-->G and IVS10-6T-->G really high-risk breast cancer-susceptibility alleles?

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12 December 2020

BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function

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12 December 2020

Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families

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12 December 2020

BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families

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12 December 2020

Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer

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12 December 2020

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

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12 December 2020

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J

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12 December 2020

Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals

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12 December 2020

Antiestrogenic effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin are mediated by direct transcriptional interference with the liganded estrogen receptor. Cross-talk between aryl hydrocarbon- and estrogen-mediated signaling

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12 December 2020

No evidence of involvement of germline BACH1 mutations in Finnish breast and ovarian cancer families

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12 December 2020

LDA—a java-based linkage disequilibrium analyzer

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12 December 2020

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

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12 December 2020

The BRCT Domain Is a Phospho-Protein Binding Domain

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12 December 2020

Normal keratinization in a spontaneously immortalized aneuploid human keratinocyte cell line

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12 December 2020

BACH1 Ser919Pro variant and breast cancer risk

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12 December 2020

Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families

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12 December 2020

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

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12 December 2020

ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer

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12 December 2020

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

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12 December 2020

Germline mutations in the breast cancer susceptibility gene PTEN are rare in high-risk non-BRCA1/2 French Canadian breast cancer families

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12 December 2020

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

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12 December 2020

A novel functional polymorphism in the uridine diphosphate-glucuronosyltransferase 2B7 promoter with significant impact on promoter activity

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12 December 2020

Functional promoter SNPs in cell cycle checkpoint genes

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12 December 2020

Analysis of PALB2/FANCN-associated breast cancer families

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12 December 2020

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

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12 December 2020

A recurrent mutation in PALB2 in Finnish cancer families.

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12 December 2020

Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses

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12 December 2020

Association between common variation in 120 candidate genes and breast cancer risk

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12 December 2020

The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations

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12 December 2020

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12 December 2020

Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway

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12 December 2020

A New Statistical Method for Haplotype Reconstruction from Population Data

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12 December 2020

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

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12 December 2020

BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study

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12 December 2020

TP53 mutations in familial breast cancer: functional aspects

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12 December 2020

MatInspector and beyond: promoter analysis based on transcription factor binding sites

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12 December 2020

MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data

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12 December 2020

How many more breast cancer predisposition genes are there?

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12 December 2020

ESEfinder: A web resource to identify exonic splicing enhancers

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12 December 2020

Very high risk of cancer in familial Peutz-Jeghers syndrome

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12 December 2020

Prediction of pathogenic mutations in patients with early-onset breast cancer by family history

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12 December 2020

THE INTERACTION OF SELECTION AND LINKAGE. II. OPTIMUM MODELS

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12 December 2020

Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer

1 reference

12 December 2020

Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

1 reference

12 December 2020

A comparison of linkage disequilibrium measures for fine-scale mapping

1 reference

12 December 2020

Cancer in Fanconi anemia, 1927-2001

1 reference

12 December 2020

Polygenic inheritance of breast cancer: Implications for design of association studies

1 reference

12 December 2020

No mutations in the BACH1 gene in BRCA1 and BRCA2 negative breast-cancer families linked to 17q22

1 reference

12 December 2020

Kin-cohort estimates for familial breast cancer risk in relation to variants in DNA base excision repair, BRCA1 interacting and growth factor genes

1 reference

12 December 2020

Improved splice site detection in Genie

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12 December 2020

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

1 reference

12 December 2020

BACH1 517C-->T transition impairs protein translocation to nucleus: a role in breast cancer susceptibility?

1 reference

12 December 2020

Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer

1 reference

12 December 2020

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

1 reference

12 December 2020

Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease

1 reference

12 December 2020

Evaluation of genetic variation in the double-strand break repair pathway and bladder cancer risk.

1 reference

12 December 2020

c-Ha-ras oncogene expression in immortalized human keratinocytes (HaCaT) alters growth potential in vivo but lacks correlation with malignancy

1 reference

12 December 2020

Breast cancer, Cowden disease and PTEN-MATCHS syndrome

1 reference

12 December 2020

Positional cloning of the Werner's syndrome gene

1 reference

12 December 2020

Haplotype tagging for the identification of common disease genes

1 reference

12 December 2020

Genetic variants and haplotype analyses of the ZBRK1/ZNF350 gene in high-risk non BRCA1/2 French Canadian breast and ovarian cancer families.

1 reference

12 December 2020

The aryl hydrocarbon receptor displaces p300 from E2F-dependent promoters and represses S phase-specific gene expression

1 reference

12 December 2020

Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair

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12 December 2020

A comparison of bayesian methods for haplotype reconstruction from population genotype data

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12 December 2020

10.1007/S10038-008-0285-Z

Identifiers

DOI

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16 September 2017

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