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Medrxiv - Genetic And Genomic Medicine Medrxiv-遗传与基因组医学

Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis

medRxiv - The Preprint Server for Health Sciences

Self-Directed Home-Based Dim-Light Melatonin Onset Collection: The Circadia Pilot Study

medRxiv - The Preprint Server for Health Sciences

Inflammatory breast cancer biomarker identification by simultaneous TGIRT-seq profiling of coding and non-coding RNAs in tumors and blood

medRxiv - The Preprint Server for Health Sciences

Multi-organ genetic causal connections inferred from imaging and clinical data through Mendelian randomization

medRxiv - The Preprint Server for Health Sciences

Relationship between branched chain amino acids and type 2 diabetes: a bidirectional Mendelian Randomization study

medRxiv - The Preprint Server for Health Sciences

PYCR1 Levels Track with Premature and Chronological Skin Aging

medRxiv - The Preprint Server for Health Sciences

FOG2 coding variant Ser657Gly is associated with Coronary Microvascular Disease through altered hypoxia-mediated gene transcription

medRxiv - The Preprint Server for Health Sciences

Association of neurotransmitter pathway polygenic risk with specific symptom profiles in psychosis

medRxiv - The Preprint Server for Health Sciences

Genetic architecture and shared mechanisms of common 'neglected' diseases

medRxiv - The Preprint Server for Health Sciences

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