| Overexpressed HSF1 cancer signature genes cluster in human chromosome 8q |
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| Early-life adversity and long-term neurobehavioral outcomes: epigenome as a bridge? |
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| Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients |
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Greek patients |
| Correction to: Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism |
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| Ethical frameworks for obtaining informed consent in tumour profiling: an evidence-based case for Singapore |
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| Yale school of public health symposium on lifetime exposures and human health: the exposome; summary and future reflections |
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| The peptidylglycine-α-amidating monooxygenase (PAM) gene rs13175330 A>G polymorphism is associated with hypertension in a Korean population |
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Korean population |
| Recessive VARS2 mutation underlies a novel syndrome with epilepsy, mental retardation, short stature, growth hormone deficiency, and hypogonadism |
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| Identification of functional single nucleotide polymorphisms in the branchpoint site |
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| Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti |
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| Identification of a novel genetic locus underlying tremor and dystonia |
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| Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydr |
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| Precision medicine at the crossroads |
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| Evaluating somatic tumor mutation detection without matched normal samples |
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| Distinct transcriptional and metabolic profiles associated with empathy in Buddhist priests: a pilot study |
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| Falling giants and the rise of gene editing: ethics, private interests and the public good |
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| Mutational analysis of COL1A1 and COL1A2 genes among Estonian osteogenesis imperfecta patients |
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| A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens |
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| Long non-coding RNAs as novel players in β cell function and type 1 diabetes |
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| Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome |
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| Inferring clonal structure in HTLV-1-infected individuals: towards bridging the gap between analysis and visualization |
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| Development and validation of a variant detection workflow for BRCA1 and BRCA2 genes and its clinical application based on the Ion Torrent technology |
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| The NF1 somatic mutational landscape in sporadic human cancers |
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| Genetic variation in neurodegenerative diseases and its accessibility in the model organism Caenorhabditis elegans |
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| A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasets |
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| Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics |
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| Identification of novel genes associated with HIV-1 latency by analysis of histone modifications |
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| Genome-wide DNA methylation analysis reveals hypomethylation in the low-CpG promoter regions in lymphoblastoid cell lines |
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| In silico prioritization and further functional characterization of SPINK1 intronic variants |
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| Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera |
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| Transcriptome analysis of bronchoalveolar lavage fluid from children with severe Mycoplasma pneumoniae pneumonia reveals novel gene expression and immunodeficiency |
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| The Israeli National Genetic database: a 10-year experience |
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| Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India |
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| Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity |
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| Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys |
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