Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants - Wikidata - awgldk - TriplyDB

Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants

Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants

http://www.wikidata.org/entity/Q33793911

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POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology.Mutations in LOXHD1 gene cause various types and severities of hearing loss.Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing loss.Expression quantitative trait locus analysis for translational medicine.Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels Clinical, Pathological, and Molecular Features of Lung Adenocarcinomas with AXL Expression.A Putative Association of a Single Nucleotide Polymorphism in GPR126 with Aggressive Periodontitis in a Japanese Population.The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population.Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients Targeted DNA and RNA sequencing of fine-needle biopsy FFPE specimens in patients with unresectable hepatocellular carcinoma treated with sorafenib.A novel MED12 mutation associated with non-specific X-linked intellectual disability.Attenuated familial adenomatous polyposis with desmoids caused by an APC mutation iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing.Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.Oncogene swap as a novel mechanism of acquired resistance to epidermal growth factor receptor-tyrosine kinase inhibitor in lung cancer Human genetic variation database, a reference database of genetic variations in the Japanese population.Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis.FGFR gene alterations in lung squamous cell carcinoma are potential targets for the multikinase inhibitor nintedanib.Tumor volume determines the feasibility of cell-free DNA sequencing for mutation detection in non-small cell lung cancer.Increased FGF19 copy number is frequently detected in hepatocellular carcinoma with a complete response after sorafenib treatment.Muscle RAS oncogene homolog (MRAS) recurrent mutation in Borrmann type IV gastric cancer.Population-specific genome-wide mapping of expression quantitative trait loci in the colon of Han Chinese.Sphingomyelin Phosphodiesterase 3 Enhances Cytodifferentiation of Periodontal Ligament Cells.Expression QTLs Mapping and Analysis: A Bayesian Perspective.Genotype-phenotype relationships in familial amyotrophic lateral sclerosis with FUS/TLS mutations in Japan.Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations.Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in Japan.Clinicopathological and genetic differences between low-grade and high-grade colorectal mucinous adenocarcinomas.Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patients.A novel heterozygous mutation in the ATP6V0A4 gene encoding the V-ATPase a4 subunit in an adult patient with incomplete distal renal tubular acidosis.CCDC88B is required for pathogenesis of inflammatory bowel disease Mutation status of RAD51C, PALB2 and BRIP1 in 100 Japanese familial breast cancer cases without BRCA1 and BRCA2 mutations.DBTSS/DBKERO for integrated analysis of transcriptional regulation.Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing.Association of autoimmune hepatitis with Src homology 2 adaptor protein 3 gene polymorphisms in Japanese patients.Effects of paraoxonase 1 on the cytodifferentiation and mineralization of periodontal ligament cells.Genome-wide association study of self-reported food reactions in Japanese identifies shrimp and peach specific loci in the HLA-DR/DQ gene region.A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN.

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Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variants

http://www.wikidata.org/entity/Q33793911

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2014 nî lūn-bûn

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2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2014 թվականի հունիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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Large-scale East-Asian eQTL ma ...... l effects of sequence variants

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Fumihiko Matsuda

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Kenichi Matsubara

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Koichiro Higasa

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Maiko Narahara

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Miho Ishii

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Yasuharu Tabara

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Genome-wide associations of gene expression variation in humans

Bioconductor: open software development for computational biology and bioinformatics

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Common genetic variants account for differences in gene expression among ethnic groups

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes

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

Genome regulation by long noncoding RNAs.

SHRiMP2: sensitive yet practical SHort Read Mapping

Capturing heterogeneity in gene expression studies by surrogate variable analysis

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