Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis (Q34531775)

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

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2 August 2017

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

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2 August 2017

language development

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Ingrid A Holm

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Leah C. Kottyan

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Leah C Kottyan

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Isaac S Kohane

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Marylyn D. Ritchie

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Marylyn D Ritchie

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John B Harley

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Joshua C. Denny

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Joshua C Denny

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Bahram Namjou

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Shefali Setia Verma

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Shefali S Verma

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Beth L Cobb

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Keith Marsolo

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Todd Lingren

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Susan D Thompson

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Susan D Thompson

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author name string

Robert J Caroll

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Aleksey Porollo

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Cassandra Perry

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Marc E Rothenberg

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publication date

18 November 2014

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2 August 2017

Frontiers in Genetics

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2 August 2017

5

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401

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2 August 2017

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

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7 July 2018

Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease

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7 July 2018

R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment

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7 July 2018

Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence

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Phenome-wide association studies on a quantitative trait: application to TPMT enzyme activity and thiopurine therapy in pharmacogenomics

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

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

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Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network

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Inhibition of interleukin-5 for the treatment of eosinophilic diseases.

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Genotype imputation with thousands of genomes

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Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13

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SLC22A4 and SLC22A5 gene polymorphisms and Crohn's disease in the Chinese Han population

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10.3389/FGENE.2014.00401

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Europe PubMed Central

PubMed publication ID

2 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 August 2017

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