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Emadeldin Hassanin

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BMC Medical Genomics|July 12, 2023
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family historyEmadeldin 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 backgroundEmadeldin Hassanin, Zied Landoulsi, Sinthuja Pachchek, et al.
BMC Genomic Data|September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkersRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)|March 10, 2022
GenRisk: a tool for comprehensive genetic risk modelingRana 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 historyEmadeldin 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 BiobankEmadeldin 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 syndromeNuria Dueñas, Hannah Klinkhammer, Nuria Bonifaci, et al.
Scientific Reports|December 7, 2025
Modifiable lifestyle factors and genetic risk of obesity in IndiansEmadeldin 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 incidenceEmadeldin 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 VUSXiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 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 historyEmadeldin 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 backgroundEmadeldin Hassanin, Zied Landoulsi, Sinthuja Pachchek, et al.
BMC Genomic Data|September 4, 2023
Gene-based burden scores identify rare variant associations for 28 blood biomarkersRana Aldisi, Emadeldin Hassanin, Sugirthan Sivalingam, et al.
Bioinformatics (Oxford, England)|March 10, 2022
GenRisk: a tool for comprehensive genetic risk modelingRana 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 historyEmadeldin 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 BiobankEmadeldin 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 syndromeNuria Dueñas, Hannah Klinkhammer, Nuria Bonifaci, et al.
Scientific Reports|December 7, 2025
Modifiable lifestyle factors and genetic risk of obesity in IndiansEmadeldin 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 incidenceEmadeldin 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 VUSXiaoyu Yin, Marcy Richardson, Andreas Laner, et al.
Pageof 2