| Two patients with Canavan disease and structural modeling of a novel mutation OK Zaki, N Krishnamoorthy, HS El Abd, SA Harche, RA Mattar, RS Al Disi, ... Metabolic brain disease 32, 171-177, 2017 | 37 | 2017 |
| Herpes simplex virus type 2 seroprevalence among different national populations of Middle East and North African men SR Dargham, GK Nasrallah, ES Al-Absi, LI Mohammed, RS Al-Disi, ... Sexually transmitted diseases 45 (7), 482-487, 2018 | 33 | 2018 |
| Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history E Hassanin, P May, R Aldisi, I Spier, AJ Forstner, MM Nöthen, S Aretz, ... Genetics in Medicine 24 (3), 576-585, 2022 | 32 | 2022 |
| Re-curation and rational enrichment of knowledge graphs in Biological Expression Language CT Hoyt, D Domingo-Fernández, R Aldisi, L Xu, K Kolpeja, S Spalek, ... Database 2019, baz068, 2019 | 30 | 2019 |
| Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence E Hassanin, I Spier, DR Bobbili, R Aldisi, H Klinkhammer, F David, ... BMC Medical Genomics 16 (1), 42, 2023 | 18 | 2023 |
| Performance evaluation of four type-specific commercial assays for detection of herpes simplex virus type 1 antibodies in a Middle East and North Africa population RS Aldisi, MS Elsidiq, SR Dargham, AS Sahara, ES Al-Absi, MY Nofal, ... Journal of Clinical Virology 103, 1-7, 2018 | 14 | 2018 |
| Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss SK Henne, R Aldisi, S Sivalingam, LM Hochfeld, O Borisov, PM Krawitz, ... Nature Communications 14 (1), 5492, 2023 | 8 | 2023 |
| GenRisk: a tool for comprehensive genetic risk modeling R Aldisi, E Hassanin, S Sivalingam, A Buness, H Klinkhammer, A Mayr, ... Bioinformatics 38 (9), 2651-2653, 2022 | 7 | 2022 |
| Assessing the role of polygenic background on the penetrance of monogenic forms in Parkinson’s disease E Hassanin, P May, R Aldisi, P Krawitz, C Maj, DR Bobbili Medrxiv, 2021.06. 06.21253270, 2021 | 5 | 2021 |
| Gene-based burden scores identify rare variant associations for 28 blood biomarkers R Aldisi, E Hassanin, S Sivalingam, A Buness, H Klinkhammer, A Mayr, ... BMC Genomic Data 24 (1), 50, 2023 | 2 | 2023 |
| Is happiness always a personal (ity) thing? A quasi-replication and extension of previous well-being studies M Deppe, CKL Pahnke, C Maj, R Aldisi, MM Nöthen, M Diewald, ... A Quasi-Replication and Extension of Previous Well-Being Studies, 2024 | | 2024 |
| Pathway-specific analysis of the burden of rare variants in complex phenotypes R Aldisi, H Froehlich, A Mayr, P Krawitz, C Maj EUROPEAN JOURNAL OF HUMAN GENETICS 32, 769-770, 2024 | | 2024 |
| Trans-ancestry polygenic models for the prediction of LDL blood levels: an analysis of the United Kingdom Biobank and Taiwan Biobank E Hassanin, KH Lee, TC Hsieh, R Aldisi, YL Lee, D Bobbili, P Krawitz, ... Frontiers in Genetics 14, 1286561, 2023 | | 2023 |
| Colorectal cancer risk: the interplay of polygenic background, high-impact monogenic variants, and family history C Maj, E Hassanin, H Klinkhammer, F David, D Bobbili, R Aldisi, ... EUROPEAN JOURNAL OF HUMAN GENETICS 31, 12-12, 2023 | | 2023 |
| Trans-ancestry polygenic models for the prediction of LDL blood levels: An analysis of the UK Biobank and Taiwan Biobank E Hassanin, KH Lee, TC Hsieh, R Aldisi, YL Lee, D Bobbili, P Krawitz, ... medRxiv, 2023.08. 03.23293320, 2023 | | 2023 |
| 303 The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank SK Henne, R Aldisi, S Sivalingam, LM Hochfeld, C Maj, O Borisov, ... Journal of Investigative Dermatology 142 (12), S232, 2022 | | 2022 |
| Colorectal cancer risk: the interplay of polygenic risk, high-impact monogenic variants, and family history E Hassanin, D Bobbili, R Aldisi, F David, H Klinkhammer, N Duenas, ... ONCOLOGY RESEARCH AND TREATMENT 45 (SUPPL 3), 66-67, 2022 | | 2022 |
| FAIR Genomes: a metadata model and guidelines for reuse of NGS data E Hassanin, R Aldisi, P May, P Krawitz, DR Bobbili, C Maj EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 83-84, 2022 | | 2022 |
| GenRisk: a tool to derive individual-level gene scores based on the load of rare damaging variants RS Aldisi, O Borisov, E Hassanin, A Mayr, P Krawitz, C Maj EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 488-489, 2022 | | 2022 |
| Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence 2022.01. 20.22269585 E Hassanin, I Spier, DR Bobbili, R Aldisi, H Klinkhammer, F David, ... Cold Spring Harbor Laboratory Press, 2022 | | 2022 |
