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PMC 3736582 An expansive human regulatory lexicon encoded in transcription factor footprints Abstract Regulatory factor binding to genomic DNA protects the underlying sequence from cleavage by DNaseI, leaving nu 35 KB 2025-10-02 5 0
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PMC 3090745 Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease Abstract The Alzheimer Disease Genetics Consortium (ADGC) performed a genome-wide associati 26 KB 2025-10-02 3 0
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PMC 10048713 Taste Preference-Related Genetic Polymorphisms Modify Alcohol Consumption Behavior of the Hungarian General and Roma Populations Abstract Harmful alcohol consumption has been considered a major publi 36.5 KB 2025-10-02 3 0
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PMC 3989221 Role of Genetic Variants of Autophagy Genes in Susceptibility for Non-Medullary Thyroid Cancer and Patients Outcome Autophagy Genetic Variants in Thyroid Carcinoma Abstract Autophagy is a central pro 21.3 KB 2025-10-02 5 0
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PMC 5444826 Lipidomic and metabolic changes in the P4-type ATPase ATP10D deficient C57BL/6J wild type mice upon rescue of ATP10D function Lipidomic and metabolic effects of ATP10D in mice Abstract Background Seq 34.9 KB 2025-10-02 5 0
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PMC 3492804 Progress in Multiple Sclerosis Genetics Abstract A genetic component in the susceptibility to multiple sclerosis (MS) has long been known, and the first and major genetic risk factor, the HLA region, 45.4 KB 2025-10-02 5 0
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PMC 6868576 High factor VIII levels and arterial thrombosis: illustrative case and literature review Abstract Thrombotic disorders are one of the most common causes of morbidity and mortality in developing and d 26.9 KB 2025-10-02 5 0
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PMC 7419288 Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses Abstract To investigate the diagnostic and clinical utility of 31.5 KB 2025-10-02 4 0
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PMC 8743587 Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study Abstract Background Epidemiological data have shown that vitamin D deficiency 38.3 KB 2025-10-02 3 0
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PMC 5844215 The SNPcurator: literature mining of enriched SNP-disease associations Abstract Abstract The uniqueness of each human genetic structure motivated the shift from the current practice of medicine to a 29.1 KB 2025-10-02 5 0
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