(Q34339288)

1 August 2017

title

How genetic variant libraries effectively extend gene testing patents: implications for intellectual property and good clinical care (English)

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1 August 2017

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David A Asch

5

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Susan M Domchek

series ordinal

4

object named as

Susan M Domchek

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1 August 2017

Sean McElligott

1

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1 August 2017

Robert I Field

series ordinal

2

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1 August 2017

Mirar Bristol-Demeter

series ordinal

3

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1 August 2017

language of work or name

English

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publication date

16 July 2012

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Journal of Clinical Oncology

1 August 2017

published in

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1 August 2017

volume

30

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1 August 2017

issue

24

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1 August 2017

page(s)

2943-2945

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ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

Clinically applicable models to characterize BRCA1 and BRCA2 variants of uncertain significance

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

A full-likelihood method for the evaluation of causality of sequence variants from family data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

The breast cancer information core: database design, structure, and scope

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3417048

The case for locus-specific databases

6 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22802312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Realizing genomic medicine

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22802312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1200/JCO.2012.42.7757

1 reference

1 August 2017

1 reference

1 August 2017

1 reference