Characterizing genetic variants for clinical action (Q28655937)

21 June 2017

Characterizing genetic variants for clinical action (English)

1 reference

21 June 2017

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8

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30

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18

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21 June 2017

9

Gail P Jarvik

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Corina Din-Lovinescu

2

Corina Din-Lovinescu

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Helen M. Colhoun

Helen M Colhoun

16

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Robert C. Green

21

Robert C Green

1 reference

21 June 2017

13

Leslie G Biesecker

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21 June 2017

20

Eric D Green

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21 June 2017

Teri A Manolio

33

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Stephen T Sherry

11

Stephen T Sherry

1 reference

21 June 2017

28

Donna Maglott

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21 June 2017

35

Marc S Williams

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21 June 2017

34

Rex L Chisholm

1 reference

21 June 2017

29

Howard L McLeod

1 reference

21 June 2017

1

Erin M Ramos

1 reference

21 June 2017

25

David H Ledbetter

1 reference

21 June 2017

2

Corina Din-Lovinescu

1 reference

21 June 2017

3

Jonathan S Berg

1 reference

21 June 2017

22

Matthew Hurles

1 reference

21 June 2017

Christopher J O'Donnell

10

Christopher O'Donnell

1 reference

21 June 2017

Lisa D Brooks

4

1 reference

21 June 2017

Michael Dunn

6

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21 June 2017

Peter Good

7

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21 June 2017

Naomi Aronson

12

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21 June 2017

Bruce Blumberg

14

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21 June 2017

Ned Calonge

15

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21 June 2017

Robert S Epstein

17

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21 June 2017

Erynn S Gordon

19

1 reference

21 June 2017

Kensaku Kawamoto

23

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21 June 2017

William Knaus

24

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21 June 2017

Howard P Levy

26

1 reference

21 June 2017

Elaine Lyon

27

1 reference

21 June 2017

Gurvaneet Randhawa

31

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21 June 2017

Catherine Wicklund

32

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21 June 2017

Audrey Duncanson

5

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21 June 2017

language of work or name

English

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publication date

13 March 2014

1 reference

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

21 June 2017

1 reference

21 June 2017

166C

1 reference

21 June 2017

93-104

1 reference

21 June 2017

1

1 reference

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

21 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Beyond base pairs to bedside: a population perspective on how genomics can improve health

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

A map of human genome variation from population-scale sequencing

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Finding the missing heritability of complex diseases

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

The A's, G's, C's, and T's of health disparities

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

A haplotype map of the human genome

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Integrating common and rare genetic variation in diverse human populations

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Cancer pharmacogenomics: early promise, but concerted effort needed

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Crossing the omic chasm: a time for omic ancillary systems

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Implementing genomic medicine in the clinic: the future is here

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Communicating new knowledge on previously reported genetic variants

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Exploring concordance and discordance for return of incidental findings from clinical sequencing

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Molecular genetic studies of complex phenotypes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Technical desiderata for the integration of genomic data into Electronic Health Records

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Motivations and perceptions of early adopters of personalized genomics: perspectives from research participants

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Charting a course for genomic medicine from base pairs to bedside

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Evaluation of the validity and utility of genetic testing for rare diseases

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Results of a survey of an online physician community regarding use of electronic medical records in office practices.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4158437

Warfarin genotyping reduces hospitalization rates results from the MM-WES (Medco-Mayo Warfarin Effectiveness study).

3 June 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31386

Evaluating the utility of personal genomic information.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31386

Deflating the Genomic Bubble

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31386

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.C.31386

Genetic risk estimation in the Coriell Personalized Medicine Collaborative

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24634402

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/AJMG.C.31386

1 reference

21 June 2017

0 references

1 reference