(Q38283284)

1 September 2017

title

Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice (English)

1 reference

1 September 2017

Jennifer Doherty

1

1 reference

1 September 2017

Danielle C Bonadies

series ordinal

2

1 reference

1 September 2017

Ellen T Matloff

series ordinal

3

1 reference

1 September 2017

language of work or name

1 reference

5 December 2014

1 reference

Journal of Genetic Counseling

1 September 2017

published in

1 reference

1 September 2017

volume

24

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1 September 2017

issue

4

1 reference

1 September 2017

page(s)

683-687

1 reference

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

1 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Infiltrating lobular carcinoma of the breast: tumor characteristics and clinical outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

F18-fluorodeoxyglucose-positron emission tomography/computed tomography screening in Li-Fraumeni syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

The integration of next-generation sequencing panels in the clinical cancer genetics practice: an institutional experience

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Rapid development of post-radiotherapy sarcoma and breast cancer in a patient with a novel germline 'de-novo' TP53 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Hereditary diffuse gastric cancer: association with lobular breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Lifetime cancer risks in individuals with germline PTEN mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10897-014-9796-2

Systematic review: comparative effectiveness of medications to reduce risk for primary breast cancer

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25475920

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic/familial high-risk assessment: breast and ovarian

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25475920

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10897-014-9796-2

1 reference

1 September 2017

1 reference