Emadeldin Hassanin

This study conducts a genome-wide association study of copy number variations in Parkinson's disease, identifying a significant PRKN deletion but limited replication in an independent dataset.

This study shows that individuals of Indian ancestry with high genetic risk for obesity can reduce their risk through favorable lifestyle choices, as demonstrated in two cohorts.

The paper develops an improved polygenic score for idiopathic Parkinson's disease, showing higher discriminative performance and explaining variable penetrance in genetic forms of the disease.

This study shows that GBA1 variants increase Parkinson's disease risk, with severe variants having higher risk than risk variants, and polygenic scores further increase this risk.

This paper compares ancestry-specific and multi-ancestry polygenic risk scores for LDL prediction in East Asian populations using UK Biobank and Taiwan Biobank data, finding that multi-ancestry models are more generalizable.

This study evaluates the ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome individuals, finding weak associations in specific subgroups.

The paper assesses the transferability of European-derived polygenic risk scores for cardiometabolic diseases in South Asians and examines their interaction with family history.

This study assesses how polygenic risk scores, high-impact monogenic variants, and family history influence breast and prostate cancer risk using UK Biobank data.

This study examines how polygenic risk scores influence the penetrance of monogenic Parkinson's disease variants and family history in Parkinson's disease risk.