Mapping the human genetic architecture of COVID-19 Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ... Nature 600 (7889), 472-477, 2021 | 748 | 2021 |
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell Genomics 2 (10), 2022 | 210 | 2022 |
Improving bioinformatics prediction of microRNA targets by ranks aggregation A Quillet, C Saad, G Ferry, Y Anouar, N Vergne, T Lecroq, C Dubessy Frontiers in genetics 10, 1330, 2020 | 93 | 2020 |
One year of SARS-CoV-2: genomic characterization of COVID-19 outbreak in Qatar FM Benslimane, HA Al Khatib, O Al-Jamal, D Albatesh, S Boughattas, ... Frontiers in cellular and infection microbiology 11, 768883, 2021 | 69 | 2021 |
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 G Povysil, G Butler-Laporte, N Shang, C Wang, A Khan, M Alaamery, ... The Journal of clinical investigation 131 (14), 2021 | 68 | 2021 |
Meta-analysis fine-mapping is often miscalibrated at single-variant resolution M Kanai, R Elzur, W Zhou, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, ... Cell genomics 2 (12), 2022 | 53 | 2022 |
Qatar genome: Insights on genomics from the Middle East H Mbarek, G Devadoss Gandhi, S Selvaraj, W Al‐Muftah, R Badji, ... Human mutation 43 (4), 499-510, 2022 | 46 | 2022 |
Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits G Thareja, Y Al-Sarraj, A Belkadi, M Almotawa, ... Nature Communications 12 (1), 1250, 2021 | 41 | 2021 |
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ... PLoS genetics 18 (11), e1010367, 2022 | 36 | 2022 |
Thousands of Qatari genomes inform human migration history and improve imputation of Arab haplotypes RM Razali, J Rodriguez-Flores, M Ghorbani, H Naeem, W Aamer, ... Nature Communications 12 (1), 5929, 2021 | 29 | 2021 |
A second update on mapping the human genetic architecture of COVID-19 M Kanai, SJ Andrews, M Cordioli, C Stevens, BM Neale, M Daly, A Ganna, ... Nature 621 (7977), E7-E26, 2023 | 22 | 2023 |
Genetic predisposition to cancer across people of different ancestries in Qatar: a population-based, cohort study M Saad, Y Mokrab, N Halabi, J Shan, R Razali, K Kunji, N Syed, ... The Lancet Oncology 23 (3), 341-352, 2022 | 19 | 2022 |
Actionable genomic variants in 6045 participants from the Qatar Genome Program A Elfatih, B Mifsud, N Syed, R Badii, H Mbarek, F Abbaszadeh, ... Human Mutation 42 (12), 1584-1601, 2021 | 18 | 2021 |
Genetic predisposition to porto‐sinusoidal vascular disorder: A functional genomic‐based, multigenerational family study J Shan, A Megarbane, A Chouchane, D Karthik, R Temanni, AR Romero, ... Hepatology 77 (2), 501-511, 2023 | 11 | 2023 |
Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19 G Povysil, G Butler-Laporte, N Shang, C Weng, A Khan, M Alaamery, ... medRxiv, 2020 | 11 | 2020 |
DiNAMO: highly sensitive DNA motif discovery in high-throughput sequencing data C Saad, L Noé, H Richard, J Leclerc, MP Buisine, H Touzet, M Figeac BMC bioinformatics 19, 1-10, 2018 | 9 | 2018 |
Le séquençage de nouvelle génération (NGS) a-t-il déjà sa place dans nos laboratoires d’onco-hématologie A Marceau-Renaut, A Renneville, O Nibourel, O Jardin-Mathé, C Demay, ... Hématologie 19 (2), 112-122, 2013 | 5 | 2013 |
Analysis of incidental findings in Qatar genome participants reveals novel functional variants in LMNA and DSP A Elfatih, SI Da’as, D Abdelrahman, H Mbarek, I Mohammed, W Hasan, ... Human Molecular Genetics 31 (16), 2796-2809, 2022 | 2 | 2022 |
Poking COVID-19: insights on genomic constraints among immune-related genes between Qatari and Italian populations H Mbarek, M Cocca, Y Al-Sarraj, C Saad, M Mezzavilla, W AlMuftah, ... Genes 12 (11), 1842, 2021 | 2 | 2021 |
Caractérisation des erreurs de séquençage non aléatoires: application aux mosaïques et tumeurs hétérogènes C Saad Université de Lille, 2018 | 2 | 2018 |