(Q48083405)

8 February 2018

title

Leading the way to genomic medicine (English)

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8 February 2018

2

Eric D Green

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8 February 2018

Teri A Manolio

1

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publication date

11 March 2014

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8 February 2018

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

published in

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8 February 2018

volume

166C

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8 February 2018

issue

1

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8 February 2018

page(s)

1-7

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8 February 2018

Whole-genome sequencing for optimized patient management

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Implementation Science six years on--our evolving scope and common reasons for rejection without review

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Genomics education for health care professionals in the 21st century.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

The National Institutes of Health Undiagnosed Diseases Program: insights into rare diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Charting a course for genomic medicine from base pairs to bedside

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

A mosaic activating mutation in AKT1 associated with the Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Implementing genomic medicine in the clinic: the future is here

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Characterizing genetic variants for clinical action

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

NT5E mutations and arterial calcifications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31384

21 January 2018

Identifiers

DOI

10.1002/AJMG.C.31384

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8 February 2018

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8 February 2018