Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes (Q36096070)

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English	Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes	scientific article

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scholarly article

1 reference

Europe PubMed Central

12 August 2017

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes (English)

1 reference

Europe PubMed Central

12 August 2017

Leslie G Biesecker

8

object named as

Leslie G Biesecker

1 reference

Europe PubMed Central

12 August 2017

James C Mullikin

7

object named as

James C Mullikin

1 reference

Europe PubMed Central

12 August 2017

author name string

Jennifer J Johnston

1

1 reference

Europe PubMed Central

12 August 2017

Wendy S Rubinstein

2

1 reference

Europe PubMed Central

12 August 2017

Flavia M Facio

3

1 reference

Europe PubMed Central

12 August 2017

David Ng

4

1 reference

Europe PubMed Central

12 August 2017

Larry N Singh

5

1 reference

Europe PubMed Central

12 August 2017

Jamie K Teer

6

1 reference

Europe PubMed Central

12 August 2017

language of work or name

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publication date

14 June 2012

1 reference

Europe PubMed Central

12 August 2017

American Journal of Human Genetics

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Europe PubMed Central

12 August 2017

91

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Europe PubMed Central

12 August 2017

1

1 reference

Europe PubMed Central

12 August 2017

97-108

1 reference

Europe PubMed Central

12 August 2017

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

1 reference

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Taxonomizing, sizing, and overcoming the incidentalome

1 reference

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VarSifter: visualizing and analyzing exome-scale sequence variation data on a desktop computer

1 reference

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SDH mutations in cancer

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Motivators for participation in a whole-genome sequencing study: implications for translational genomics research

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Carrier testing for severe childhood recessive diseases by next-generation sequencing

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Disclosure of individual genetic data to research participants: the debate reconsidered

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A map of human genome variation from population-scale sequencing

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Exome sequencing identifies the cause of a mendelian disorder

1 reference

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1 reference

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Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

1 reference

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1 reference

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Research ethics recommendations for whole-genome research: consensus statement

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Recommendations for locus-specific databases and their curation

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dbSNP: the NCBI database of genetic variation

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based on heuristic

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Identifiers

10.1016/J.AJHG.2012.05.021

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

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