(Q42067358)

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The foundation of precision medicine: integration of electronic health records with genomics through basic, clinical, and translational research

scientific article published on 17 March 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

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The foundation of precision medicine: integration of electronic health records with genomics through basic, clinical, and translational research (English)

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

electronic health records

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Mariza de Andrade

2

0 references

Helena Kuivaniemi

3

0 references

Marylyn D. Ritchie

1

object named as

Marylyn D Ritchie

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Mariza de Andrade

2

object named as

Mariza de Andrade

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Helena Kuivaniemi

3

object named as

Helena Kuivaniemi

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

publication date

17 March 2015

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Frontiers in Genetics

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

6

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

104

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Imputation and quality control steps for combining multiple genome-wide datasets

1 reference

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5 June 2018

Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis

1 reference

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5 June 2018

Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records

1 reference

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5 June 2018

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

1 reference

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5 June 2018

Extension of GWAS results for lipid-related phenotypes to extreme obesity using electronic health record (EHR) data and the Metabochip

1 reference

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5 June 2018

Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example

1 reference

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5 June 2018

The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study

1 reference

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5 June 2018

eMERGEing progress in genomics-the first seven years

1 reference

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5 June 2018

Genetic-based prediction of disease traits: prediction is very difficult, especially about the future

1 reference

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5 June 2018

Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes

1 reference

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5 June 2018

Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.

1 reference

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Analysis pipeline for the epistasis search - statistical versus biological filtering

1 reference

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5 June 2018

Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts

1 reference

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5 June 2018

Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4362332

5 June 2018

Return of results in the genomic medicine projects of the eMERGE network

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4362332

5 June 2018

Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4362332

5 June 2018

The struggle to find reliable results in exome sequencing data: filtering out Mendelian errors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4362332

5 June 2018

EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children

1 reference

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5 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4362332

5 June 2018

Identifiers

10.3389/FGENE.2015.00104

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

ResearchGate publication ID

0 references

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