(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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1 reference

Tomas Kirchhoff

2

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Michael Dean

object named as

Michael Dean

18

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Larry Norton

object named as

Larry Norton

17

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Steven A. Narod

8

object named as

Steven Narod

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15 August 2017

20

Kenneth Offit

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15 August 2017

10

Peter Gregersen

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15 August 2017

7

Eitan Friedman

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15 August 2017

6

Judy Garber

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15 August 2017

16

Andrew G Clark

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1

Bert Gold

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14

Nathan A Ellis

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15 August 2017

Stefan Stefanov

3

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15 August 2017

James Lautenberger

4

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15 August 2017

Agnes Viale

5

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15 August 2017

Adam B Olshen

9

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15 August 2017

Kristi Kosarin

11

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15 August 2017

Adam Olsh

12

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15 August 2017

Julie Bergeron

13

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Robert J Klein

15

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15 August 2017

Jeff Boyd

19

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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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15 August 2017

4340-4345

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15 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

Genome-wide association study identifies novel breast cancer susceptibility loci

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

European population substructure: clustering of northern and southern populations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

The ubiquitin-proteasome pathway and its role in cancer

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

High-throughput SNP genotyping on universal bead arrays

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

MSH6 germline mutations are rare in colorectal cancer families.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

Polymorphisms in DNA repair genes and associations with cancer risk

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

A systematic review of genetic polymorphisms and breast cancer risk.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

The future of genetic studies of complex human diseases

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2393811

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

1 reference

12 December 2020

The genetic attributable risk of breast and ovarian cancer

1 reference

12 December 2020

A new inhibitor of mitochondrial fatty acid oxidation

1 reference

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

1 reference

15 August 2017

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1 reference

15 August 2017

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