(Q35286565)

English

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

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scholarly article

1 reference

Europe PubMed Central

7 August 2017

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

1 reference

Europe PubMed Central

7 August 2017

Luke V. Rasmussen

15

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7 August 2017

24

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Gail P Jarvik

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Jyotishman Pathak

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Jyotishman Pathak

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7 August 2017

M. Geoffrey Hayes

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M Geoffrey Hayes

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Catherine A. McCarty

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Catherine A McCarty

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Marylyn D. Ritchie

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Marylyn D Ritchie

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2

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Dana C Crawford

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Teri A Manolio

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Lisa Bastarache

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Lisa Bastarache

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Christopher G. Chute

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Christopher G Chute

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Joshua C. Denny

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Joshua C Denny

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Mariza de Andrade

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Mariza de Andrade

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33

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Dan M Roden

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Jennifer A Pacheco

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Jennifer A Pacheco

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Rex L. Chisholm

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Rex L Chisholm

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Russell A Wilke

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Russell A Wilke

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Abel N Kho

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Rebecca L Zuvich

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Rebecca Zuvich

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Iftikhar J Kullo

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Iftikhar J Kullo

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Suzette J Bielinski

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Suzette J Bielinski

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David S Carrell

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David Carrell

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Daniel R. Masys

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Daniel R Masys

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Melissa A. Basford

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Melissa A Basford

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Peggy Peissig

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Yuki Bradford

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Martha E Matsumoto

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Martha Matsumoto

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Katherine M Newton

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Katherine M Newton

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7 August 2017

author name string

High Seng Chai

7

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Andrea H Ramirez

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7 August 2017

Xiaoming Wang

16

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Noah Weston

20

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Peter A Kopp

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7 August 2017

Rongling Li

25

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7 August 2017

Eric B Larson

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7 August 2017

language of work or name

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publication date

1 October 2011

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Europe PubMed Central

7 August 2017

number of pages

14

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American Journal of Human Genetics

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7 August 2017

89

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529-542

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7 August 2017

4

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7 August 2017

Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon alpha-modulated mechanism.

1 reference

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Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate

1 reference

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Using electronic health records to drive discovery in disease genomics

1 reference

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Iodine status of the U.S. population, National Health and Nutrition Examination Survey, 2005–2006 and 2007–2008.

1 reference

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Morphogenetics of early thyroid development

1 reference

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The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

1 reference

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The emerging role of electronic medical records in pharmacogenomics

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Genetic basis of autoantibody positive and negative rheumatoid arthritis risk in a multi-ethnic cohort derived from electronic health records

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

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A genome-wide association study of red blood cell traits using the electronic medical record.

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A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study

1 reference

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LocusZoom: regional visualization of genome-wide association scan results

1 reference

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METAL: fast and efficient meta-analysis of genomewide association scans

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Genetic susceptibility to autoimmune thyroid disease: past, present, and future

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12 July 2018

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record

1 reference

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A highly specific algorithm for identifying asthma cases and controls for genome-wide association studies

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

1 reference

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Electronic medical records for discovery research in rheumatoid arthritis

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12 July 2018

Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data

1 reference

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12 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3188836

12 July 2018

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

1 reference

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12 July 2018

Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association results

1 reference

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12 July 2018

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

1 reference

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12 July 2018

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

1 reference

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

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12 July 2018

Higher serum TSH in thyroid cancer patients occurs independent of age and correlates with extrathyroidal extension

1 reference

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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

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The effect of electronic prescribing on medication errors and adverse drug events: a systematic review

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Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

1 reference

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Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis

1 reference

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

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Genetics of congenital hypothyroidism

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1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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inferred from PubMed ID database lookup

Prospective study of the spontaneous course of subclinical hypothyroidism: prognostic value of thyrotropin, thyroid reserve, and thyroid antibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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inferred from PubMed ID database lookup

Reduce, recycle, reuse--iodotyrosine deiodinase in thyroid iodide metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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based on heuristic

inferred from PubMed ID database lookup

U.S. iodine nutrition: where do we stand?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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based on heuristic

inferred from PubMed ID database lookup

FOXE1 polyalanine tract length polymorphism in patients with thyroid hemiagenesis and subjects with normal thyroid

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association between thyroid malignancy and chronic lymphocytic thyroiditis: should it alter the surgical approach?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

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based on heuristic

inferred from PubMed ID database lookup

'Subclinical hypothyroidism'. Natural course of the syndrome during a prolonged follow-up study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21981779

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2011.09.008

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

1 reference

Europe PubMed Central

7 August 2017

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