The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk (Q33784408)

29 July 2017

The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk (English)

1 reference

Erratum: Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

29 July 2017

1 reference

corrigendum / erratum

1 reference

10.1038/S41523-017-0046-2

DOI

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/S41523-017-0046-2

18

Paolo Peterlongo

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Vignesh Ravichandran

Vignesh Ravichandran

7

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Kasmintan A Schrader

Kasmintan A Schrader

11

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Susan M Domchek

22

Susan M Domchek

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29 July 2017

5

Susan L Neuhausen

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29 July 2017

Katherine L Nathanson

25

Katherine L Nathanson

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29 July 2017

27

Fergus J Couch

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29 July 2017

4

Joseph Vijai

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29 July 2017

24

Kenneth Offit

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29 July 2017

26

Jeffrey N Weitzel

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29 July 2017

20

James M Ford

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29 July 2017

21

Judy E Garber

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29 July 2017

Thomas P Slavin

1

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29 July 2017

Kara N Maxwell

2

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29 July 2017

Jenna Lilyquist

3

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29 July 2017

Steven N Hart

6

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29 July 2017

Tinu Thomas

8

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29 July 2017

Ann Maria

9

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29 July 2017

Danylo Villano

10

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29 July 2017

Raymond Moore

12

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29 July 2017

Chunling Hu

13

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29 July 2017

Bradley Wubbenhorst

14

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29 July 2017

Brandon M Wenz

15

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29 July 2017

Kurt D'Andrea

16

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29 July 2017

Mark E Robson

17

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29 July 2017

Bernardo Bonanni

19

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29 July 2017

Csilla Szabo

23

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29 July 2017

9 June 2017

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29 July 2017

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3

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22

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Creative Commons Attribution 4.0 International

29 July 2017

start time

9 June 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/s41523-017-0024-8

0 references

cites work

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

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Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers

4 July 2018

1 reference

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Analysis of protein-coding genetic variation in 60,706 humans

4 July 2018

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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes

4 July 2018

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Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Counselling framework for moderate-penetrance cancer-susceptibility mutations

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.

4 July 2018

1 reference

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Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Gene-panel sequencing and the prediction of breast-cancer risk

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

4 July 2018

1 reference

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Second-generation PLINK: rising to the challenge of larger and richer datasets

4 July 2018

1 reference

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CODEX: a normalization and copy number variation detection method for whole exome sequencing

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

4 July 2018

1 reference

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Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

ClinVar: public archive of relationships among sequence variation and human phenotype

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Breast cancer phenotype in women with TP53 germline mutations: a Li-Fraumeni syndrome consortium effort

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

The variant call format and VCFtools

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Fast and accurate long-read alignment with Burrows-Wheeler transform

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

The Sequence Alignment/Map format and SAMtools

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Cancer susceptibility and the functions of BRCA1 and BRCA2

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Myelination and remyelination in the central nervous system by transplanted oligodendrocytes using the shiverer model. Discussion on the remyelinating cell population in adult mammals

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.

30 October 2018

1 reference

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Corrigendum: Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management

30 October 2018

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Detection of novel germline mutations for breast cancer in non-BRCA1/2 families.

30 October 2018

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Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5466608

BRCA1 and BRCA2: from molecular genetics to clinical medicine

30 October 2018

1 reference

https://api.crossref.org/works/10.1038%2FS41523-017-0024-8

7 January 2021

Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel

1 reference

https://api.crossref.org/works/10.1038%2FS41523-017-0024-8

7 January 2021

Frequency of triple-negative breast cancer in BRCA1 mutation carriers: comparison between common Ashkenazi Jewish and other mutations

1 reference

https://api.crossref.org/works/10.1038%2FS41523-017-0024-8

7 January 2021

Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology

1 reference

https://api.crossref.org/works/10.1038%2FS41523-017-0024-8

7 January 2021

Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France

1 reference

https://api.crossref.org/works/10.1038%2FS41523-017-0024-8

7 January 2021

10.1038/S41523-017-0024-8

Identifiers

DOI

1 reference

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

1 reference