PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations (Q33808357)

29 July 2017

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

1 reference

29 July 2017

2

Marylyn D Ritchie

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29 July 2017

10

Dana C Crawford

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29 July 2017

5

Lisa Bastarache

1 reference

29 July 2017

4

Jill M Pulley

1 reference

29 July 2017

6

Kristin Brown-Gentry

1 reference

29 July 2017

1

Joshua C Denny

1 reference

29 July 2017

9

Dan M Roden

1 reference

29 July 2017

3

Melissa A Basford

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29 July 2017

7

Deede Wang

1 reference

29 July 2017

8

Dan R Masys

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PubMed ID

20335276

29 July 2017

language of work or name

English

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publication date

24 March 2010

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29 July 2017

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29 July 2017

26

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29 July 2017

9

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29 July 2017

1205-1210

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

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Acid-suppressive medication use and the risk for hospital-acquired pneumonia

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Phenomics: the systematic study of phenotypes on a genome-wide scale

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Active computerized pharmacovigilance using natural language processing, statistics, and electronic health records: a feasibility study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Collaborative genome-wide association studies of diverse diseases: programs of the NHGRI's office of population genomics

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Large scale association analysis of novel genetic loci for coronary artery disease

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Trends in the diagnosis of overweight and obesity in children and adolescents: 1999-2007.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Automated identification of acute hepatitis B using electronic medical record data to facilitate public health surveillance

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Development of a large-scale de-identified DNA biobank to enable personalized medicine.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Increased hospital mortality in patients with bedside hippus

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Genome-wide association with select biomarker traits in the Framingham Heart Study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Underdiagnosis of hypertension in children and adolescents

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Risk alleles for multiple sclerosis identified by a genomewide study

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Probing genetic overlap among complex human phenotypes.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Variants conferring risk of atrial fibrillation on chromosome 4q25.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Identifying UMLS concepts from ECG Impressions using KnowledgeMap.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

The search for genenotype/phenotype associations and the phenome scan

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Accuracy of Medicare claims-based diagnosis of acute myocardial infarction: estimating positive predictive value on the basis of review of hospital records

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2859132

Clinical phenome scanning

4 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTQ126

Molecular analysis of HLA-DRB1 allelic associations with systemic lupus erythematous and lupus nephritis in Taiwan

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20335276

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTQ126

1 reference

journals/bioinformatics/DennyRBPBBWMRC10

29 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

29 July 2017

1 reference

PubMed ID

20335276