![]() | HASSANIN, E., Kalapala, R., Jagtap, N., Vishnubhotla, R., Andhi, N., Mamidi, S., Vyshnavi, S., Jilla, S., Samudrala, M., Shriya, P. S., Chawla, K., Maj, C., MAY, P., BOBBILI, D. R., & Reddy, D. N. (2025). Modifiable lifestyle factors and genetic risk of obesity in Indians. Scientific Reports. doi:10.1038/s41598-025-30530-3 Peer Reviewed verified by ORBi |
![]() | HASSANIN, E., LANDOULSI, Z., PACHCHEK, S., NCER-PD Consortium, Krawitz, P., Maj, C., KRÜGER, R., MAY, P., & BOBBILI, D. R. (12 June 2025). Penetrance of Parkinson's disease in GBA1 carriers depends on variant severity and polygenic background. NPJ Parkinson's Disease, 11 (1), 162. doi:10.1038/s41531-025-00997-y Peer Reviewed verified by ORBi |
![]() | HASSANIN, E., LANDOULSI, Z., PACHCHEK, S., Krawitz, P., Maj, C., KRÜGER, R., MAY, P., & BOBBILI, D. R. (2025). Penetrance of Parkinson's disease in GBA1 carriers is depending on the variant severity and polygenic background. (2025.01.23.25320896). ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/63892. doi:10.1101/2025.01.23.25320896 |
![]() | Leu, C., Avbersek, A., Stevelink, R., Martins Custodio, H., Chen, S., Speed, D., Bennett, C., Jonsson, L., Unnsteinsdóttir, U., Jorgensen, A., Cavalleri, G., Delanty, N., Craig, J., Depondt, C., Johnson, M., Koeleman, B., HASSANIN, E., Omidvar, M., KRAUSE, R., ... Sisodiya, S. (2025). Genome-wide association meta-analyses of drug-resistant epilepsy. EBioMedicine. doi:10.1016/j.ebiom.2025.105675 Peer Reviewed verified by ORBi |
![]() | LANDOULSI, Z., Ashok Kumar Sreelatha, A., Schulte, C., BOBBILI, D. R., Montanucci, L., Leu, C., Niestroj, L. M., HASSANIN, E., Domenighetti, C., Sugier, P. E., Radivojkov Blagojevic, M., Lichtner, P., Portugal, B., Edsall, C., Kruger, J., Hernandez, D. G., Blauwendraat, C., Mellick, G. D., Zimprich, A., ... MAY, P. (2024). Genome-wide association study of copy number variations in Parkinson's disease. ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/61869. doi:10.1101/2024.08.21.24311915 |
![]() | HASSANIN, E. S. F. E., Lee, K.-H., Hsieh, T.-C., Aldisi, R., Lee, Y.-L., BOBBILI, D. R., Krawitz, P., MAY, P., Chen, C.-Y., & Maj, C. (23 November 2023). Trans-ancestry polygenic models for the prediction of LDL blood levels: an analysis of the United Kingdom Biobank and Taiwan Biobank. Frontiers in Genetics, 14. doi:10.3389/fgene.2023.1286561 Peer Reviewed verified by ORBi Dataset: 10.17881/8wqn-x712 |
![]() | Dueñas, N., Klinkhammer, H., Bonifaci, N., Spier, I., Mayr, A., HASSANIN, E., Diez-Villanueva, A., Moreno, V., Pineda, M., Maj, C., Capellà, G., Aretz, S., & Brunet, J. (November 2023). Ability of a polygenic risk score to refine colorectal cancer risk in Lynch syndrome. Journal of Medical Genetics, 60 (11), 1044 - 1051. doi:10.1136/jmg-2023-109344 Peer Reviewed verified by ORBi |
![]() | Aldisi, R., HASSANIN, E., Sivalingam, S., Buness, A., Klinkhammer, H., Mayr, A., Fröhlich, H., Krawitz, P., & Maj, C. (04 September 2023). Gene-based burden scores identify rare variant associations for 28 blood biomarkers. BMC genomic data, 24 (1), 50. doi:10.1186/s12863-023-01155-0 Peer reviewed |
![]() | Stevelink, R., Campbell, C., Chen, S., Abou-Khalil, B., Adesoji, O. M., Afawi, Z., Amadori, E., Anderson, A., Anderson, J., Andrade, D. M., Annesi, G., Auce, P., Avbersek, A., Bahlo, M., Baker, M. D., Balagura, G., Balestrini, S., Barba, C., Barboza, K., ... Epilepsies, I. L. A. E. C. O. C. (2023). GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Nature Genetics. doi:10.1038/s41588-023-01485-w Peer Reviewed verified by ORBi |
![]() | HASSANIN, E. S. F. S., MAY, P., & BOBBILI, D. R. (2023). Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history. BMC Medical Genomics. doi:10.1186/s12920-023-01598-5 Peer Reviewed verified by ORBi |
![]() | HASSANIN, E. S. F. S., Spier, I., BOBBILI, D. R., Aldisi, R., Klinkhammer, H., David, F., Dueñas, N., Hüneburg, R., Perne, C., Brunet, J., Capella, G., Nöthen, M. M., Forstner, A. J., Mayr, A., Krawitz, P., MAY, P., Aretz, S., & Maj, C. (23 March 2023). Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence. BMC Medical Genomics, 16 (1), 42. doi:10.1186/s12920-023-01469-z Peer Reviewed verified by ORBi |
![]() | HASSANIN, E. S. F. S., Maj, C., Krawitz, P., MAY, P., & BOBBILI, D. R. (2023). Transferability of European-derived cardiometabolic polygenic risk scores in the South Asians and their interplay with family history 2023.03.20.23287470. ORBilu-University of Luxembourg. https://orbilu.uni.lu/handle/10993/55242. doi:10.1101/2023.03.20.23287470 |