Ikuti
Nour Albesher
Nour Albesher
Research Assistant Professor, King Abdulaziz City for Science and Technology
Email yang diverifikasi di kacst.gov.sa
Judul
Dikutip oleh
Dikutip oleh
Tahun
A nucleus-localized long non-coding RNA enhances drought and salt stress tolerance
T Qin, H Zhao, P Cui, N Albesher, L Xiong
Plant physiology 175 (3), 1321-1336, 2017
3282017
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
3052022
A first update on mapping the human genetic architecture of COVID-19
Writing group lead Andrews Shea J. 6 Kanai Masahiro 3 Cordioli Mattia 7, ...
Nature 608 (7921), E1-E10, 2022
1352022
Role of sphingolipid metabolism in neurodegeneration
M Alaamery, N Albesher, N Aljawini, M Alsuwailm, S Massadeh, ...
Journal of Neurochemistry 158 (1), 25-35, 2021
952021
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues
M D’Antonio, JP Nguyen, TD Arthur, H Matsui, BM Neale, M Daly, ...
Cell reports 37 (7), 2021
422021
Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart Disease
S Massadeh, M Albeladi, N Albesher, F Alhabshan, KD Kampe, ...
Genes 12 (5), 612, 2021
232021
Mapping the human genetic architecture of COVID-19: an update
COVID-19 Host Genetics Initiative, A Ganna
MedRxiv, 2021.11. 08.21265944, 2021
162021
Consanguinity and congenital heart disease susceptibility: insights into rare genetic variations in Saudi Arabia
N Albesher, S Massadeh, SM Hassan, M Alaamery
Genes 13 (2), 354, 2022
142022
The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank–Ter Haar Syndrome
S Massadeh, F Alhabshan, HN AlSudairi, S Alkwai, M Alsuwailm, ...
Genes 13 (2), 236, 2022
52022
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes
M Alaamery, J Alghamdi, S Massadeh, M Alsawaji, N Aljawini, N Albesher, ...
Frontiers in genetics 13, 886038, 2022
42022
Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia
M Alaamery, S Massadeh, M Aldarwish, N Albesher, N Aljawini, ...
Frontiers in Genetics 14, 1294214, 2024
22024
TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy
M Alaamery, N Albesher, F Alhabshan, P Barnett, M Salim Kabbani, ...
Journal of Cardiovascular Development and Disease 10 (11), 455, 2023
12023
Genomic Screening of Non-syndromic Congenital Heart Defects in the Saudi Population
N Albesher
KING ABDULAZIZ UNIVERSITY JEDDAH, 2023
2023
A Novel Non-coding RNA Regulates Drought Stress Tolerance in Arabidopsis thaliana
NH Albesher
2014
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