Whole-genome sequence-based analysis of thyroid function. - Wikidata - wikimedia - TriplyDB

Whole-genome sequence-based analysis of thyroid function.

Whole-genome sequence-based analysis of thyroid function.

http://www.wikidata.org/entity/Q30316724

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Subclinical Hypothyroidism and Type 2 Diabetes: A Systematic Review and Meta-Analysis Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers Progress in methods for rare variant association Data Resource Profile: Accessible Resource for Integrated Epigenomic Studies (ARIES).The impact of rare and low-frequency genetic variants in common disease Detecting association of rare and common variants based on cross-validation prediction error.The UK10K project identifies rare variants in health and disease Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer.A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.GSA: Genome Sequence Archive.Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Hypothyroid Patients Encoding Combined MCT10 and DIO2 Gene Polymorphisms May Prefer L-T3 + L-T4 Combination Treatment - Data Using a Blind, Randomized, Clinical Study.Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.Maturation in serum thyroid function parameters over childhood and puberty: results of a longitudinal study.Thyroxine replacement: a clinical endocrinologist's viewpoint.Association of STAT4 polymorphisms with hepatitis B virus infection and clearance in Chinese Han population.Thyroid function and ischemic heart disease: a Mendelian randomization study.Database Resources of the BIG Data Center in 2018.Association of increased eomesodermin, BCL6, and granzyme B expression with major clinical manifestations of Hashimoto's thyroiditis - an observational study.Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study.New insights into thyroid hormone action.Human genetics: Strength in numbers in the low-frequency spectrum.Genome-Wide Association Studies of Autoimmune Thyroid Diseases, Thyroid Function, and Thyroid Cancer.Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

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Erratum: Whole-genome sequence-based analysis of thyroid function

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Whole-genome sequence-based analysis of thyroid function.

http://www.wikidata.org/entity/Q30316724

description

2015 nî lūn-bûn

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2015 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի մարտին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

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2015年论文

@wuu

name

Whole-genome sequence-based analysis of thyroid function.

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Whole-genome sequence-based analysis of thyroid function.

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type

label

Whole-genome sequence-based analysis of thyroid function.

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Whole-genome sequence-based analysis of thyroid function.

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prefLabel

Whole-genome sequence-based analysis of thyroid function.

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Whole-genome sequence-based analysis of thyroid function.

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Nature Communications

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Whole-genome sequence-based analysis of thyroid function

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Andrew D Johnson

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Daniela Toniolo

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David Schlessinger

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Dawn Muddyman

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Ee M Lim

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Eleonora Porcu

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Elin Grundberg

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Frank Dudbridge

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Gabriela L Surdulescu

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Goncalo Abecasis

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Erratum: Whole-genome sequence-based analysis of thyroid function

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A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

An integrated encyclopedia of DNA elements in the human genome

A high-resolution map of human evolutionary constraint using 29 mammals

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

Transthyretin stability as a key factor in amyloidogenesis: X-ray analysis at atomic resolution

A method and server for predicting damaging missense mutations

The Genotype-Tissue Expression (GTEx) project

Discovery of common variants associated with low TSH levels and thyroid cancer risk

A new multipoint method for genome-wide association studies by imputation of genotypes

GCTA: a tool for genome-wide complex trait analysis

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5681

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scholarly article

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10.1038/NCOMMS6681

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6

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George Davey Smith

Eleftheria Zeggini

Nicholas J. Timpson

Francesco Cucca

Michael R. Barnes

Caroline L. Relton

Vincenzo Forgetta

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2015-03-06T00:00:00Z

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273139119

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1012196256

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25743335

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4366514

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