Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. (Q36670312)

15 August 2017

Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. (English)

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genome-wide association study

15 August 2017

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Tomas Kirchhoff

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Michael Dean

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Michael Dean

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Larry Norton

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Larry Norton

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Steven A. Narod

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object named as

Steven Narod

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Kenneth Offit

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Peter Gregersen

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Eitan Friedman

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Judy Garber

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Andrew G Clark

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Bert Gold

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Nathan A Ellis

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Stefan Stefanov

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James Lautenberger

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Agnes Viale

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Adam B Olshen

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Kristi Kosarin

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Adam Olsh

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Julie Bergeron

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Robert J Klein

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Jeff Boyd

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15 August 2017

language of work or name

English

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publication date

7 March 2008

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Proceedings of the National Academy of Sciences of the United States of America

15 August 2017

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15 August 2017

105

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4340-4345

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11

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describes a project that uses

15 August 2017

genome-wide association study

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Analysis of genetic variation in Ashkenazi Jews by high density SNP genotyping

inferred from title

cites work

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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

30 September 2017

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Genome-wide association study identifies novel breast cancer susceptibility loci

30 September 2017

1 reference

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

30 September 2017

1 reference

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Genetic and expression aberrations of E3 ubiquitin ligases in human breast cancer

30 September 2017

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European population substructure: clustering of northern and southern populations

30 September 2017

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Principal components analysis corrects for stratification in genome-wide association studies

30 September 2017

1 reference

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The ubiquitin-proteasome pathway and its role in cancer

30 September 2017

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High-throughput SNP genotyping on universal bead arrays

30 September 2017

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RNA interference-mediated silencing of the p53 tumor-suppressor protein drastically increases apoptosis after inhibition of endogenous fatty acid metabolism in breast cancer cells

30 September 2017

1 reference

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The New York Cancer Project: rationale, organization, design, and baseline characteristics

30 September 2017

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Fatty acid synthase inhibition triggers apoptosis during S phase in human cancer cells

30 September 2017

1 reference

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MSH6 germline mutations are rare in colorectal cancer families.

30 September 2017

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Polymorphisms in DNA repair genes and associations with cancer risk

30 September 2017

1 reference

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Cytochrome P450 polymorphisms as risk factors for steroid hormone-related cancers

30 September 2017

1 reference

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Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium

30 September 2017

1 reference

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Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

30 September 2017

1 reference

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Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland

30 September 2017

1 reference

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A systematic review of genetic polymorphisms and breast cancer risk.

30 September 2017

1 reference

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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

30 September 2017

1 reference

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The future of genetic studies of complex human diseases

30 September 2017

1 reference

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Family history, age, and risk of breast cancer. Prospective data from the Nurses' Health Study

30 September 2017

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30 September 2017

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800441105

Time to check CHEK2 in families with breast cancer?

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800441105

Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800441105

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0800441105

A comprehensive evaluation of family history and breast cancer risk. The Utah Population Database

21 January 2018

1 reference

12 December 2020

Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8

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12 December 2020

The genetic attributable risk of breast and ovarian cancer

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12 December 2020

A new inhibitor of mitochondrial fatty acid oxidation

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12 December 2020

Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0800441105

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15 August 2017

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15 August 2017

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