A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing (Q50552807)

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scientific article published on 24 December 2010

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English	A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing	scientific article published on 24 December 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

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based on heuristic

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Uffe Birk Jensen

10

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

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Lone Sunde

8

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Anne-Marie Gerdes

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Anne-Marie Gerdes

13

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Ida Vogel

3

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Finn Cilius Nielsen

9

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Finn C Nielsen

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Thomas V O Hansen

4

object named as

Thomas V O Hansen

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

14

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Torben A Kruse

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

12

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Ake Borg

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

1

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Mads Thomassen

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Marie Luise Bisgaard

11

object named as

Marie Luise Bisgaard

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

author name string

Inge Søkilde Pedersen

2

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Charlotte Brasch-Andersen

5

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Claus L Brasen

6

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Dorthe Crüger

7

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

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publication date

24 December 2010

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Breast Cancer Research and Treatment

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

128

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

1

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

179-185

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

Breast cancer and breastfeeding: collaborative reanalysis of individual data from 47 epidemiological studies in 30 countries, including 50302 women with breast cancer and 96973 women without the disease

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Evaluation of two different models to predict BRCA1 and BRCA2 mutations in a cohort of Danish hereditary breast and/or ovarian cancer families.

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

A common Greenlandic Inuit BRCA1 RING domain founder mutation

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Integrated platform for detection of DNA sequence variants using capillary array electrophoresis

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age.

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

The variants BRCA1 IVS6-1G>A and BRCA2 IVS15+1G>A lead to aberrant splicing of the transcripts.

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Three per cent of Norwegian Ovarian Cancers are caused by BRCA1 1675delA or 1135insA

1 reference

https://api.crossref.org/works/10.1007%2FS10549-010-1272-6

21 January 2018

Identifiers

10.1007/S10549-010-1272-6

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/21184276

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