CNRGH
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Novel CAPN3 variant associated with an autosomal dominant calpainopathy
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Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus and intellectual disability
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PLCG2 protective variant p.P522R modulates tau pathology and disease progression in patients with mild cognitive impairment
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Routine CYP2C19 Genotyping to Adjust Thienopyridine Treatment After Primary PCI for STEMI
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Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use
Translational Psychiatry 2020, vol. 10, issue 1
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Genome sequencing in cytogenetics: Comparison of short‐read and linked‐read approaches for germline structural variant detection and characterization
Molecular Genetics & Genomic Medicine 2020, vol. 8, issue 3
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High degree of polyclonality hinders somatic mutation calling in lung brush samples of COPD cases and controls
Scientific Reports 2019, vol. 9, issue 1
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The Impact of Genetic Variations in ADORA2A in the Association between Caffeine Consumption and Sleep
Genes 2019, vol. 10, issue 12
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Heritability of a resting heart rate in a 20-year follow-up family cohort with GWAS data: Insights from the STANISLAS cohort
European Journal of Preventive Cardiology 2019
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Expression of miRNAs from the Imprinted DLK1/DIO3 Locus Signals the Osteogenic Potential of Human Pluripotent Stem Cells
Cells 2019, vol. 8, issue 12
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