(Q51701104)

English

Utility of clinical high-depth next generation sequencing for somatic variant detection in the PIK3CA-related overgrowth spectrum.

scientific article published on 16 June 2016

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

Utility of clinical high-depth next generation sequencing for somatic variant detection in the PIK3CA-related overgrowth spectrum. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

author name string

V Hucthagowder

1

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

A Shenoy

2

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

M Corliss

3

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

K A Vigh-Conrad

4

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

C Storer

5

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

D K Grange

6

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

C E Cottrell

7

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

publication date

16 June 2016

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

Clinical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

91

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

1

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

79-85

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

PIK3CA-related overgrowth spectrum (PROS): diagnostic and testing eligibility criteria, differential diagnosis, and evaluation

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Validation of a next-generation sequencing assay for clinical molecular oncology.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Design of targeted, capture-based, next generation sequencing tests for precision cancer therapy

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Assessing PIK3CA and PTEN in early-phase trials with PI3K/AKT/mTOR inhibitors

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Functional analysis of PIK3CA gene mutations in human colorectal cancer

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Expression of PIK3CA mutant E545K in the mammary gland induces heterogeneous tumors but is less potent than mutant H1047R.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Megalencephaly syndromes and activating mutations in the PI3K-AKT pathway: MPPH and MCAP.

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly

1 reference

https://api.crossref.org/works/10.1111%2FCGE.12819

21 January 2018

Identifiers

10.1111/CGE.12819

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 April 2018

http://europepmc.org/abstract/MED/27307077

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