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

Association Between Psychiatric Polygenic Scores, Healthcare Utilization and Comorbidity Burden

medRxiv - The Preprint Server for Health Sciences

Genome sequencing as a generic diagnostic strategy for rare disease

medRxiv - The Preprint Server for Health Sciences

Heterozygous loss-of-function SMC3 variants are associated with variable and incompletely penetrant growth and developmental features

medRxiv - The Preprint Server for Health Sciences

Blood-based multivariate methylation risk score for cognitive impairment and dementia

medRxiv - The Preprint Server for Health Sciences

Multimodal cell-free DNA whole-genome analysis combined with TET-Assisted Pyridine Borane Sequencing is sensitive and reveals specific cancer signals

medRxiv - The Preprint Server for Health Sciences

Genome-wide association analysis reveals insights into the molecular aetiology underlying dilated cardiomyopathy

medRxiv - The Preprint Server for Health Sciences

Multi-ancestry Polygenic Mechanisms of Type 2 Diabetes Elucidate Disease Processes and Clinical Heterogeneity

medRxiv - The Preprint Server for Health Sciences

Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes

medRxiv - The Preprint Server for Health Sciences

Clinically actionable pharmacogenomic landscape of antidepressants and antipsychotics in Qatar: A population-based cohort study

medRxiv - The Preprint Server for Health Sciences

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