| The status of Her2 amplification and Kras mutations in mucinous ovarian carcinoma |
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| Head-and-neck squamous cell carcinoma risk in smokers: no association detected between phenotype and AHR, CYP1A1, CYP1A2, or CYP1B1 genotype |
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| Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients |
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| Transcriptome analysis reveals manifold mechanisms of cyst development in ADPKD |
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| A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive d |
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| Navigating the dynamic landscape of long noncoding RNA and protein-coding gene annotations in GENCODE |
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| Novel genetic risk variants for pediatric celiac disease |
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| An efficient method for protein function annotation based on multilayer protein networks |
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| A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies |
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| Variation of global DNA methylation levels with age and in autistic children |
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| Major influence of repetitive elements on disease-associated copy number variants (CNVs) |
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| MicroRNAs in acute kidney injury |
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| Transcriptome sequencing of gingival biopsies from chronic periodontitis patients reveals novel gene expression and splicing patterns |
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| Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta |
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| A comparative study of k-spectrum-based error correction methods for next-generation sequencing data analysis |
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| Identification of protein complexes from multi-relationship protein interaction networks |
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| The clinical significance of snail protein expression in gastric cancer: a meta-analysis |
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| The up-regulation of Myb may help mediate EGCG inhibition effect on mouse lung adenocarcinoma |
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| Association of six CpG-SNPs in the inflammation-related genes with coronary heart disease |
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| Hypomethylation coordinates antagonistically with hypermethylation in cancer development: a case study of leukemia |
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| Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree |
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| Letter to the editor for “Update of the human and mouse Fanconi anemia genes” |
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| Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders |
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| AMD and the alternative complement pathway: genetics and functional implications |
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| Proposed nomenclature for microhaplotypes |
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| Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population |
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| Systematic analysis of the molecular mechanism underlying atherosclerosis using a text mining approach |
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| Human genome meeting 2016 |
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| Exploring the interaction among EPHX1, GSTP1, SERPINE2, and TGFB1 contributing to the quantitative traits of chronic obstructive pulmonary disease in Chinese Han population |
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✓ |
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Chinese Han population |
| Multiplex SNaPshot—a new simple and efficient CYP2D6 and ADRB1 genotyping method |
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| Organization, evolution and functions of the human and mouse Ly6/uPAR family genes |
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| Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry |
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| The impact of common polymorphisms in CETP and ABCA1 genes with the risk of coronary artery disease in Saudi Arabians |
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| Reviewer acknowledgement 2015 |
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| A review of the new HGNC gene family resource |
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| The clinical trial landscape in oncology and connectivity of somatic mutational profiles to targeted therapies |
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| Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments |
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| Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes |
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| Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility |
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| Intragraft transcriptional profiling of renal transplant patients with tubular dysfunction reveals mechanisms underlying graft injury and recovery |
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