UOBScholar Hub
UOB Libraries created the UOBScholar Hub, an Institutional Repository (IR) for archiving and collecting all the research output of the UOB community. It aims to improve the visibility, usage and impact of research conducted at UOB. Materials included are: academic journal articles, conference papers and presentations, books and book chapters, ongoing research papers, reports and patents.
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Browsing by Author Zalloua, Pierre
Showing results 1 to 7 of 7
| Issue Date | Title | Author(s) |
|---|---|---|
| Mar-2023 | Ancient DNA investigation of the 17 Maronite patriarchs of Qanubin | Zalloua, Pierre; Elias, Nada; Senovska, Anna; Collins, Catherine; Gosling, Anna; Karam, Samar; Iskandar, Amine Jules; Matisoo-Smith, Elizabeth |
| 2021 | Autosomal genetics and Y-chromosome haplogroup L1b-M317 reveal Mount Lebanon Maronites as a persistently non-emigrating population | Platt, Daniel E; Artinian, Hovig; Mouzaya, Francis; Khalil, Wissam; Kamar, Francois G; Matisoo-Smith, Elizabeth; Calafell, Francesc; Taleb, Nassim Nicolas; Zalloua, Pierre |
| 22-Feb-2024 | HDL levels modulate the impact of type 2 diabetes susceptibility alleles in older adults | Sullivan, Siobhán O '; Al Hageh, Cynthia; Henschel, Andreas; Chacar, Stephanie; Abchee, Antoine; Zalloua, Pierre; Nader, Moni |
| 1-Jan-2021 | The impact of syrian refugees on patient demographics and type 2 diabetes across five public health centers in lebanon | Makhoul, Peter; Tcheroyan, Raya; Ammar, Walid; Hamadeh, Randa; Zalloua, Pierre; Nabbout, Ghassan |
| 2021 | Lies, Gosh Darn Lies, and not enough good statistics: why epidemic model parameter estimation fails | Platt, Daniel E; Parida, Laxmi; Zalloua, Pierre |
| 2021 | Mutations and variants of ONECUT1 in diabetes | Philippi, Anne; Heller, Sandra; Costa, Ivan G; Senée, Valérie; Breunig, Markus; Li, Zhijian; Kwon, Gino; Russell, Ronan; Illing, Anett; Lin, Qiong; Hohwieler, Meike; Degavre, Anne; Zalloua, Pierre; Liebau, Stefan; Schuster, Michael; Krumm, Johannes; Zhang, Xi; Geusz, Ryan; Benthuysen, Jacqueline R; Wang, Allen; Chiou, Joshua; Gaulton, Kyle; Neubauer, Heike; Simon, Eric; Klein, Thomas; Wagner, Martin; Nair, Gopika; Besse, Céline; Dandine-Roulland, Claire; Olaso, Robert; Deleuze, Jean-François; Kuster, Bernhard; Hebrok, Matthias; Seufferlein, Thomas; Sander, Maike; Boehm, Bernhard O; Oswald, Franz; Nicolino, Marc; Julier, Cécile; Kleger, Alexander |
| 12-Oct-2024 | PHACTR1 and APOC1 genetic variants are associated with multi-vessel coronary artery disease | Al Hageh, Cynthia; O'Sullivan, Siobhán; Henschel, Andreas; Abche, Antoine ; Hantouche, Mireille; Iakovidou, Nantia; Issa, Taly; Chacar, Stephanie; Nader, Moni; Zalloua, Pierre |