(Q34158088)

31 July 2017

title

Fine mapping of 14q24.1 breast cancer susceptibility locus (English)

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31 July 2017

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26

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31 July 2017

Montserrat García-Closas

14

Montserrat Garcia-Closas

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Meredith Yeager

9

Meredith Yeager

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Charles Kooperberg

24

Charles Kooperberg

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31 July 2017

Ludmila Prokunina-Olsson

Ludmila Prokunina-Olsson

4

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Kevin B. Jacobs

Kevin B Jacobs

8

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Catherine A. McCarty

Catherine A McCarty

18

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Stephen Chanock

34

Stephen J Chanock

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31 July 2017

28

Louise A Brinton

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31 July 2017

3

Jonine D Figueroa

1 reference

Heather Spencer Feigelson

31 July 2017

19

Heather Spencer Feigelson

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31 July 2017

12

Amy Hutchinson

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31 July 2017

13

Nilanjan Chatterjee

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31 July 2017

21

Ryan Diver

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31 July 2017

33

David J Hunter

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31 July 2017

11

Susan E Hankinson

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31 July 2017

29

Margaret Tucker

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31 July 2017

7

Zhaoming Wang

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31 July 2017

27

Beata Peplonska

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31 July 2017

15

Regina G Ziegler

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31 July 2017

17

Saundra S Buys

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31 July 2017

16

Christine D Berg

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31 July 2017

25

Rowan Chlebowski

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31 July 2017

Joseph F. Fraumeni, Jr.

30

Joseph F Fraumeni

1 reference

31 July 2017

Jesús González Bosquet

5

Jesus Gonzalez-Bosquet

1 reference

31 July 2017

6

Peter Kraft

1 reference

31 July 2017

31

Robert N Hoover

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31 July 2017

20

Michael J Thun

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31 July 2017

Phoebe Lee

1

1 reference

31 July 2017

Yi-Ping Fu

2

1 reference

31 July 2017

Marie-Josèphe Horner

10

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31 July 2017

Ross Prentice

22

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31 July 2017

Rebecca Jackson

23

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31 July 2017

Gilles Thomas

32

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31 July 2017

publication date

30 September 2011

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31 July 2017

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31 July 2017

volume

131

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31 July 2017

issue

3

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31 July 2017

page(s)

479-490

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https://scigraph.springernature.com/pub.10.1007/s00439-011-1088-4

31 July 2017

exact match

0 references

cites work

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Identification and Management of Women With BRCA Mutations or Hereditary Predisposition for Breast and Ovarian Cancer

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

A map of human genome variation from population-scale sequencing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Integrating common and rare genetic variation in diverse human populations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

5 July 2018

Cancer statistics, 2010

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Genome-wide association studies in common cancers--what have we learnt?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Discovering moderate-risk breast cancer susceptibility genes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Rare variants create synthetic genome-wide associations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Polygenic susceptibility to breast cancer: current state-of-the-art

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Recombination activator function of the novel RAD51- and RAD51B-binding protein, human EVL.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

PLINK: a tool set for whole-genome association and population-based linkage analyses

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

The Polycomb group protein EZH2 impairs DNA repair in breast epithelial cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

The XRCC genes: expanding roles in DNA double-strand break repair

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Mediator function of the human Rad51B-Rad51C complex in Rad51/RPA-catalyzed DNA strand exchange

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

RAD51C interacts with RAD51B and is central to a larger protein complex in vivo exclusive of RAD51

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

A New Statistical Method for Haplotype Reconstruction from Population Data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

The Rad51 paralog Rad51B promotes homologous recombinational repair

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

The human REC2/RAD51B gene acts as a DNA damage sensor by inducing G1 delay and hypersensitivity to ultraviolet irradiation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

Linkage of early-onset familial breast cancer to chromosome 17q21

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4159746

SequenceLDhot: detecting recombination hotspots.

5 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1088-4

snp.plotter: an R-based SNP/haplotype association and linkage disequilibrium plotting package.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1088-4

Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1088-4

Disruption and aberrant expression of HMGA2 as a consequence of diverse chromosomal translocations in myeloid malignancies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1088-4

10.1007/S00439-011-1088-4

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

31 July 2017

0 references

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31 July 2017

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