Follow
Naif Almontashiri
Naif Almontashiri
Center for Genetics and Inherited Diseases, Taibah University
Verified email at taibahu.edu.sa
Title
Cited by
Cited by
Year
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
2572020
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
2322019
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
1072014
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
992020
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
872015
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
612020
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
542015
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
542014
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
512020
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
472014
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
472013
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
442022
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
352020
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
352011
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
302021
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
222021
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
212018
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
172021
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
162021
The leukodystrophy spectrum in Saudi Arabia: Epidemiological, clinical, radiological, and genetic data
M Alfadhel, M Almuqbil, F Al Mutairi, M Umair, M Almannai, M Alghamdi, ...
Frontiers in Pediatrics 9, 633385, 2021
162021
The system can't perform the operation now. Try again later.
Articles 1–20