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BMC Medical Genomics
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July 12, 2023
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history
Emadeldin Hassanin, Carlo Maj, Hannah Klinkhammer, et al.
NPJ Parkinson'S Disease
|
June 12, 2025
Penetrance of Parkinson's disease in GBA1 carriers depends on variant severity and polygenic background
Emadeldin Hassanin, Zied Landoulsi, Sinthuja Pachchek, et al.
BMC Genomic Data
|
September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkers
Rana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)
|
March 10, 2022
GenRisk: a tool for comprehensive genetic risk modeling
Rana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history
Emadeldin Hassanin, Patrick May, Rana Aldisi, et al.
Frontiers in Genetics
|
December 11, 2023
Trans-ancestry polygenic models for the prediction of LDL blood levels: an analysis of the United Kingdom Biobank and Taiwan Biobank
Emadeldin Hassanin, Ko-Han Lee, Tzung-Chien Hsieh, et al.
Journal of Medical Genetics
|
June 15, 2023
Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome
Nuria Dueñas, Hannah Klinkhammer, Nuria Bonifaci, et al.
Scientific Reports
|
December 7, 2025
Modifiable lifestyle factors and genetic risk of obesity in Indians
Emadeldin Hassanin, Rakesh Kalapala, Nitin Jagtap, et al.
BMC Medical Genomics
|
March 5, 2023
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
Emadeldin Hassanin, Isabel Spier, Dheeraj R Bobbili, et al.
American Journal of Human Genetics
|
October 2, 2024
Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS
Xiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
BMC Medical Genomics
|
July 12, 2023
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history
Emadeldin Hassanin, Carlo Maj, Hannah Klinkhammer, et al.
NPJ Parkinson'S Disease
|
June 12, 2025
Penetrance of Parkinson's disease in GBA1 carriers depends on variant severity and polygenic background
Emadeldin Hassanin, Zied Landoulsi, Sinthuja Pachchek, et al.
BMC Genomic Data
|
September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkers
Rana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)
|
March 10, 2022
GenRisk: a tool for comprehensive genetic risk modeling
Rana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history
Emadeldin Hassanin, Patrick May, Rana Aldisi, et al.
Frontiers in Genetics
|
December 11, 2023
Trans-ancestry polygenic models for the prediction of LDL blood levels: an analysis of the United Kingdom Biobank and Taiwan Biobank
Emadeldin Hassanin, Ko-Han Lee, Tzung-Chien Hsieh, et al.
Journal of Medical Genetics
|
June 15, 2023
Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome
Nuria Dueñas, Hannah Klinkhammer, Nuria Bonifaci, et al.
Scientific Reports
|
December 7, 2025
Modifiable lifestyle factors and genetic risk of obesity in Indians
Emadeldin Hassanin, Rakesh Kalapala, Nitin Jagtap, et al.
BMC Medical Genomics
|
March 5, 2023
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
Emadeldin Hassanin, Isabel Spier, Dheeraj R Bobbili, et al.
American Journal of Human Genetics
|
October 2, 2024
Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS
Xiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
Page
of 2