Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies - Wikidata - awgldk - TriplyDB

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

http://www.wikidata.org/entity/Q35286565

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Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population Translational Bioinformatics: Past, Present, and Future Role of genomics in eliminating health disparities Biobanks and personalized medicine The challenges, advantages and future of phenome-wide association studies Mining electronic health records: towards better research applications and clinical care Integration of complex data sources to provide biologic insight into pulmonary vascular disease (2015 Grover Conference Series)Pleiotropy in complex traits: challenges and strategies Phenome-wide association studies on a quantitative trait: application to TPMT enzyme activity and thiopurine therapy in pharmacogenomics Surveying Recent Themes in Translational Bioinformatics: Big Data in EHRs, Omics for Drugs, and Personal Genomics Toward high-throughput phenotyping: unbiased automated feature extraction and selection from knowledge sources Extracting research-quality phenotypes from electronic health records to support precision medicine Size matters: how population size influences genotype-phenotype association studies in anonymized data SecureMA: protecting participant privacy in genetic association meta-analysis Secondary use of clinical data: the Vanderbilt approach Validation and enhancement of a computable medication indication resource (MEDI) using a large practice-based dataset The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future Development and evaluation of an ensemble resource linking medications to their indications Applying semantic web technologies for phenome-wide scan using an electronic health record linked Biobank Ethical issues in health research with novel online sources Novel associations for hypothyroidism include known autoimmune risk loci Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci.An evaluation of the NQF Quality Data Model for representing Electronic Health Record driven phenotyping algorithms Caveats for the use of operational electronic health record data in comparative effectiveness research.Applying active learning to high-throughput phenotyping algorithms for electronic health records data Extraction of echocardiographic data from the electronic medical record is a rapid and efficient method for study of cardiac structure and function.Phenome-Wide Association Studies: Leveraging Comprehensive Phenotypic and Genotypic Data for Discovery.FOXE1 association with differentiated thyroid cancer and its progression.Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank.eMERGEing progress in genomics-the first seven years.Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.Clinical phenotyping in selected national networks: demonstrating the need for high-throughput, portable, and computational methods.Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.R PheWAS: data analysis and plotting tools for phenome-wide association studies in the R environment Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.Improving the power of genetic association tests with imperfect phenotype derived from electronic medical records.Design patterns for the development of electronic health record-driven phenotype extraction algorithms.Disease risk factors identified through shared genetic architecture and electronic medical records

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P2860

Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies

http://www.wikidata.org/entity/Q35286565

description

2011 nî lūn-bûn

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2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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J.AJHG.2011.09.008

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American Journal of Human Genetics

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Abel N Kho

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Andrea H Ramirez

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Christopher G Chute

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Dan M Roden

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Daniel R Masys

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David Carrell

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Eric B Larson

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High Seng Chai

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Iftikhar J Kullo

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Jennifer A Pacheco

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P2860

Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae

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

Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

Inference of population structure using multilocus genotype data

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate

PLINK: a tool set for whole-genome association and population-based linkage analyses

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Marylyn D. Ritchie

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M Geoffrey Hayes

Lisa Bastarache

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2011-10-01T00:00:00Z

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21981779

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3188836

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