受强制性开放获取政策约束的文章 - Said Ismail了解详情
可在其他位置公开访问的文章：11 篇
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
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, UK …
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
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
N Shrine, AG Izquierdo, J Chen, R Packer, RJ Hall, AL Guyatt, C Batini, ...
Nature genetics 55 (3), 410-422, 2023
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
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
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, Wellcome …
Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women
M Monticelli, B Hay Mele, E Benetti, C Fallerini, M Baldassarri, S Furini, ...
Genes 12 (4), 596, 2021
强制性开放获取政策： Government of Italy
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
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council
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
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health, US …
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
C Fallerini, N Picchiotti, M Baldassarri, K Zguro, S Daga, F Fava, E Benetti, ...
Human genetics 141 (1), 147-173, 2022
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
A population study of clinically actionable genetic variation affecting drug response from the Middle East
PV Jithesh, M Abuhaliqa, N Syed, I Ahmed, M El Anbari, K Bastaki, ...
NPJ genomic medicine 7 (1), 10, 2022
强制性开放获取政策： UK Engineering and Physical Sciences Research Council, UK Medical Research …
Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations
G Thareja, A Belkadi, M Arnold, OME Albagha, J Graumann, F Schmidt, ...
Human molecular genetics 32 (6), 907-916, 2023
强制性开放获取政策： US National Institutes of Health, Helmholtz Association, Federal Ministry of …
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
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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