(Q57577799)

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19 January 2020

title

Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing (English)

1 reference

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Erratum: Spectra of BRCA1 and BRCA2 mutations in Korean patients with breast cancer: the importance of whole-gene sequencing

19 January 2020

corrigendum / erratum

0 references

author

Jeong Eon Lee

2

1 reference

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19 January 2020

Chang-Seok Ki

4

1 reference

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19 January 2020

author name string

Ja-Hyun Jang

1

1 reference

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19 January 2020

Min-Jung Kwon

3

1 reference

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19 January 2020

Jong-Won Kim

5

1 reference

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19 January 2020

Seok Jin Nam

6

1 reference

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19 January 2020

Jung-Hyun Yang

7

1 reference

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19 January 2020

publication date

5 January 2012

1 reference

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Journal of Human Genetics

19 January 2020

published in

1 reference

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19 January 2020

volume

57

1 reference

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19 January 2020

issue

3

1 reference

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19 January 2020

page(s)

212-215

1 reference

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https://scigraph.springernature.com/pub.10.1038/jhg.2011.139

19 January 2020

exact match

0 references

cites work

Association between clinical characteristics and risk-reduction interventions in women who underwent BRCA1 and BRCA2 testing: a single-institution study

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Chronological changing patterns of clinical characteristics of Korean breast cancer patients during 10 years (1996-2006) using nationwide breast cancer registration on-line program: biannual update.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Prediction of deleterious human alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

PANTHER: a library of protein families and subfamilies indexed by function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Cataloging coding sequence variations in human genome databases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2 transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

inferred from DOI database lookup

7 January 2021

based on heuristic

Mutation analysis of BRCA1 and BRCA2 from 793 Korean patients with sporadic breast cancer

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

inferred from DOI database lookup

7 January 2021

based on heuristic

BRCA1 and BRCA2 genetic testing in Italian breast and/or ovarian cancer families: mutation spectrum and prevalence and analysis of mutation prediction models

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2011.139

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/JHG.2011.139

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22217648%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference