iSCAN: An RT-LAMP-coupled CRISPR-Cas12 module for rapid, sensitive detection of SARS-CoV-2 Z Ali, R Aman, A Mahas, GS Rao, M Tehseen, T Marsic, R Salunke, ... Virus research 288, 198129, 2020 | 265 | 2020 |
Lessons learned from large-scale, first-tier clinical exome sequencing in a highly consanguineous population D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ... The American Journal of Human Genetics 104 (6), 1182-1201, 2019 | 240 | 2019 |
Plasma PCSK9 levels are elevated with acute myocardial infarction in two independent retrospective angiographic studies NAM Almontashiri, RO Vilmundarson, N Ghasemzadeh, S Dandona, ... PLoS One 9 (9), e106294, 2014 | 108 | 2014 |
SARS-CoV-2 S1 and N-based serological assays reveal rapid seroconversion and induction of specific antibody response in COVID-19 patients A Algaissi, MA Alfaleh, S Hala, TS Abujamel, SS Alamri, SA Almahboub, ... Scientific reports 10 (1), 16561, 2020 | 101 | 2020 |
IRF2BP2 reduces macrophage inflammation and susceptibility to atherosclerosis HH Chen, K Keyhanian, X Zhou, RO Vilmundarson, NAM Almontashiri, ... Circulation research 117 (8), 671-683, 2015 | 87 | 2015 |
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease PB Martin, Y Kigoshi-Tansho, RB Sher, G Ravenscroft, JE Stauffer, ... Nature communications 11 (1), 4625, 2020 | 62 | 2020 |
Early humoral response correlates with disease severity and outcomes in COVID-19 patients AM Hashem, A Algaissi, SA Almahboub, MA Alfaleh, TS Abujamel, ... Viruses 12 (12), 1390, 2020 | 54 | 2020 |
9p21. 3 Coronary Artery Disease Risk Variants Disrupt TEAD Transcription Factor–Dependent Transforming Growth Factor β Regulation of p16 Expression in Human Aortic Smooth … NAM Almontashiri, D Antoine, X Zhou, RO Vilmundarson, SX Zhang, ... Circulation 132 (21), 1969-1978, 2015 | 54 | 2015 |
Functional genomics of the 9p21. 3 locus for atherosclerosis: clarity or confusion? HH Chen, NAM Almontashiri, D Antoine, AFR Stewart Current cardiology reports 16, 1-8, 2014 | 54 | 2014 |
Interferon-γ activates expression of p15 and p16 regardless of 9p21. 3 coronary artery disease risk genotype NAM Almontashiri, M Fan, BLM Cheng, HH Chen, R Roberts, ... Journal of the American College of Cardiology 61 (2), 143-147, 2013 | 48 | 2013 |
SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypes NAM Almontashiri, HH Chen, RJ Mailloux, T Tatsuta, ACT Teng, ... Cell reports 7 (3), 834-847, 2014 | 47 | 2014 |
SARS-CoV-2 genomes from Saudi Arabia implicate nucleocapsid mutations in host response and increased viral load T Mourier, M Shuaib, S Hala, S Mfarrej, F Alofi, R Naeem, A Alsomali, ... Nature communications 13 (1), 601, 2022 | 45 | 2022 |
Clinical validation of targeted and untargeted metabolomics testing for genetic disorders: a 3 year comparative study NAM Almontashiri, L Zha, K Young, T Law, MD Kellogg, OA Bodamer, ... Scientific reports 10 (1), 9382, 2020 | 36 | 2020 |
Identification of a phosphorylation-dependent nuclear localization motif in interferon regulatory factor 2 binding protein 2 ACT Teng, NAM Al-Montashiri, BLM Cheng, P Lou, P Ozmizrak, HH Chen, ... PLoS One 6 (8), e24100, 2011 | 35 | 2011 |
New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin H Alhebbi, AA Peer-Zada, AA Al‐Hussaini, S Algubaisi, A Albassami, ... Journal of Human Genetics 66 (2), 151-159, 2021 | 30 | 2021 |
Saudi Arabian SARS-CoV-2 genomes implicate a mutant Nucleocapsid protein in modulating host interactions and increased viral load in COVID-19 patients T Mourier, M Shuaib, S Hala, S Mfarrej, F Alofi, R Naeem, A Alsomali, ... medRxiv, 2021.05. 06.21256706, 2021 | 24 | 2021 |
Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients NAM Almontashiri, A Alswaid, A Oza, KA Al-Mazrou, O Elrehim, ... Genetics in Medicine 20 (5), 536-544, 2018 | 21 | 2018 |
The 9p21. 3 risk locus for coronary artery disease: A 10-year search for its mechanism NAM Almontashiri Journal of Taibah University medical sciences 12 (3), 199-204, 2017 | 18 | 2017 |
A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families E Olinger, IA Alawi, MS Al Riyami, IA Salmi, E Molinari, EA Faqeih, ... Human mutation 42 (10), 1221-1228, 2021 | 17 | 2021 |
Simultaneous detection and mutation surveillance of SARS-CoV-2 and multiple respiratory viruses by rapid field-deployable sequencing C Bi, G Ramos-Mandujano, Y Tian, S Hala, J Xu, S Mfarrej, CR Esteban, ... Med 2 (6), 689-700. e4, 2021 | 17 | 2021 |