(Q28743906)

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

scientific article (publication date: 18 January 2011)

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scholarly article

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Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study (English)

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inferred from title

Geoffroy Durand

7

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Florence Le Calvez-Kelm

1

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object named as

Alun Thomas

12

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Fabienne Lesueur

object named as

Fabienne Lesueur

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Melissa C. Southey

object named as

Melissa C Southey

16

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Graham B Byrnes

13

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John L Hopper

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Irene L Andrulis

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object named as

Irene L Andrulis

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18

object named as

Esther M John

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author name string

Francesca Damiola

3

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Maxime Vallée

4

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Catherine Voegele

5

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Davit Babikyan

6

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Nathalie Forey

8

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Sandrine McKay-Chopin

9

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Nivonirina Robinot

10

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Tù Nguyen-Dumont

11

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Sean V Tavtigian

19

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publication date

18 January 2011

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Breast Cancer Research

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13

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1

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R6

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1 reference

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A method and server for predicting damaging missense mutations

1 reference

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Structure and activation mechanism of the CHK2 DNA damage checkpoint kinase

1 reference

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CHEK2 mutations affecting kinase activity together with mutations in TP53 indicate a functional pathway associated with resistance to epirubicin in primary breast cancer

1 reference

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Penetrance analysis of the PALB2 c.1592delT founder mutation

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Genome-wide association study identifies novel breast cancer susceptibility loci

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

1 reference

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16 March 2017

The CHEK2 gene and inherited breast cancer susceptibility

1 reference

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The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer

1 reference

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Structural and functional versatility of the FHA domain in DNA-damage signaling by the tumor suppressor kinase Chk2

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Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations

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Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome

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Amino acid difference formula to help explain protein evolution

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Testing for CHEK2 in the cancer genetics clinic: ready for prime time?

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Radiation exposure, the ATM Gene, and contralateral breast cancer in the women's environmental cancer and radiation epidemiology study

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Familial relative risks for breast cancer by pathological subtype: a population-based cohort study

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Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

1 reference

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Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis

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Classification of rare missense substitutions, using risk surfaces, with genetic- and molecular-epidemiology applications.

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Assessment of functional effects of unclassified genetic variants

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Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

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Genetic evidence and integration of various data sources for classifying uncertain variants into a single model

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Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories?

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Rapid detection of carriers with BRCA1 and BRCA2 mutations using high resolution melting analysis

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CHK2 kinase: cancer susceptibility and cancer therapy - two sides of the same coin?

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Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts

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Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

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Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?

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The genetic epidemiology of breast cancer genes

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CHEK2 is a multiorgan cancer susceptibility gene

1 reference

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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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American Society of Clinical Oncology Policy Statement Update: Genetic Testing for Cancer Susceptibility

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Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21244692

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based on heuristic

inferred from PubMed ID database lookup

Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/21244692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CHEK2-positive breast cancers in young Polish women

1 reference

https://pubmed.ncbi.nlm.nih.gov/21244692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline CHEK2 mutations in Jewish Ashkenazi women at high risk for breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/21244692

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/BCR2810

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Dimensions Publication ID

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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Springer Nature article ID

10.1186/bcr2810

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