(Q85247141)

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

scientific article published on 03 September 2014

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16 February 2020

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

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16 February 2020

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Judy E Garber

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16 February 2020

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Nadine Tung

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16 February 2020

Chiara Battelli

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16 February 2020

Brian Allen

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16 February 2020

Rajesh Kaldate

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16 February 2020

Satish Bhatnagar

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16 February 2020

Karla Bowles

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16 February 2020

Kirsten Timms

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16 February 2020

Christina Herold

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16 February 2020

Leif Ellisen

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16 February 2020

Jill Krejdovsky

11

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16 February 2020

Kim DeLeonardis

12

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16 February 2020

Kristin Sedgwick

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16 February 2020

Kathleen Soltis

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16 February 2020

Benjamin Roa

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16 February 2020

Richard J Wenstrup

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16 February 2020

Anne-Renee Hartman

17

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16 February 2020

publication date

3 September 2014

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16 February 2020

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16 February 2020

121

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16 February 2020

1

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16 February 2020

25-33

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16 February 2020

describes a project that uses

massive parallel sequencing

1 reference

based on heuristic

inferred from title

Comprehensive molecular portraits of human breast tumours

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer predisposing BARD1 mutations in breast-ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Variations in the NBN/NBS1 gene and the risk of breast cancer in non-BRCA1/2 French Canadian families with high risk of breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Nijmegen Breakage Syndrome mutations and risk of breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in BRIP1 confer high risk of ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline RAD51C mutations confer susceptibility to ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Lifetime cancer risks in individuals with germline PTEN mutations.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Relative frequency and morphology of cancers in STK11 mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer risk of heterozygotes with the NBN founder mutation.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutations in RAD51D confer susceptibility to ovarian cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

A PALB2 mutation associated with high risk of breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Rare germline mutations in PALB2 and breast cancer risk: a population-based study

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Multiple primary cancers in families with Li-Fraumeni syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

p53-deficient mice are extremely susceptible to radiation-induced tumorigenesis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer risks and mortality in heterozygous ATM mutation carriers

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

The PARP inhibitor olaparib induces significant killing of ATM-deficient lymphoid tumor cells in vitro and in vivo.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline PALB2 mutation analysis in breast-pancreas cancer families

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of colorectal cancer in monoallelic and biallelic carriers of MYH mutations: a population-based case-family study

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

International Cancer of the Pancreas Screening (CAPS) Consortium summit on the management of patients with increased risk for familial pancreatic cancer

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.29010

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/CNCR.29010

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25186627%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25186627%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

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