(Q34531775)

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

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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

14

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Leah C. Kottyan

object named as

Leah C Kottyan

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Isaac S Kohane

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2 August 2017

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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2 August 2017

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Bahram Namjou

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2 August 2017

Shefali Setia Verma

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Shefali S Verma

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Beth L Cobb

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2 August 2017

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Keith Marsolo

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Todd Lingren

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2 August 2017

Susan D Thompson

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object named as

Susan D Thompson

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2 August 2017

author name string

Robert J Caroll

3

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2 August 2017

Aleksey Porollo

8

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2 August 2017

Cassandra Perry

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Marc E Rothenberg

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2 August 2017

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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2 August 2017

401

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2 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4235428

7 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4235428

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

1 reference

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

1 reference

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1 reference

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

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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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The use of phenome-wide association studies (PheWAS) for exploration of novel genotype-phenotype relationships and pleiotropy discovery

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The rationale for lowering serum cholesterol levels in American children

1 reference

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12 December 2020

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

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.3389/FGENE.2014.00401

1 reference

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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