(Q35052005)

6 August 2017

title

Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data (English)

1 reference

genome-wide association study

6 August 2017

main subject

0 references

1 reference

6 August 2017

Gail P Jarvik

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Jyotishman Pathak

series ordinal

object named as

Jyotishman Pathak

1 reference

6 August 2017

Jonathan D Mosley

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Sarah A Pendergrass

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Paul K Crane

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Catherine A McCarty

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Jennifer A Pacheco

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Marylyn D Ritchie

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6 August 2017

Dana C Crawford

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6 August 2017

Jonathan L Haines

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6 August 2017

Teri A Manolio

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Lisa Bastarache

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6 August 2017

Jill M Pulley

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6 August 2017

Lucia A Hindorff

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6 August 2017

Christopher G Chute

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6 August 2017

Joshua C Denny

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6 August 2017

Hua Xu

1 reference

6 August 2017

Dan M Roden

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6 August 2017

Robert J Carroll

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6 August 2017

Rex L Chisholm

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6 August 2017

Abel N Kho

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6 August 2017

David R Crosslin

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6 August 2017

Iftikhar J Kullo

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6 August 2017

Suzette J Bielinski

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6 August 2017

David S Carrell

1 reference

6 August 2017

Murray H Brilliant

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6 August 2017

Daniel R Masys

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6 August 2017

Melissa A Basford

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6 August 2017

Raquel Zink

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6 August 2017

Julie R Field

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6 August 2017

Erica Bowton

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6 August 2017

Peggy L Peissig

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6 August 2017

Andrea H Ramirez

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6 August 2017

Rongling Li

series ordinal

1 reference

6 August 2017

Eric B Larson

series ordinal

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6 August 2017

publication date

1 December 2013

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6 August 2017

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6 August 2017

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6 August 2017

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6 August 2017

page(s)

1102-1110

1 reference

describes a project that uses

6 August 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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A Germline Variant in the Interferon Regulatory Factor 4 Gene as a Novel Skin Cancer Risk Locus

8 July 2018

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8 July 2018

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8 July 2018

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Quality control procedures for genome-wide association studies

8 July 2018

1 reference

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The "meaningful use" regulation for electronic health records

8 July 2018

1 reference

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8 July 2018

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8 July 2018

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8 July 2018

1 reference

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

8 July 2018

1 reference

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Does MC1R genotype convey information about melanoma risk beyond risk phenotypes?

8 July 2018

1 reference

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A genome-wide association analysis of serum iron concentrations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

8 July 2018

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

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

1 reference

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Probing genetic overlap among complex human phenotypes.

8 July 2018

1 reference

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A common variant on chromosome 9p21 affects the risk of myocardial infarction

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Principal components analysis corrects for stratification in genome-wide association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Automated encoding of clinical documents based on natural language processing

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Inference of population structure using multilocus genotype data

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

Casemix adjustment of managed care claims data using the clinical classification for health policy research method

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3969265

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNBT.2749

21 January 2018

Dyskeratosis Congenita

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNBT.2749

Sample size requirements for association studies of gene-gene interaction

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNBT.2749

Marshfield Clinic Personalized Medicine Research Project (PMRP): design, methods and recruitment for a large population-based biobank

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24270849

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NBT.2749

1 reference

6 August 2017

1 reference

6 August 2017

1 reference