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List of works by Naif A M Almontashiri

9p21.3 Coronary Artery Disease Risk Variants Disrupt TEAD Transcription Factor-Dependent Transforming Growth Factor β Regulation of p16 Expression in Human Aortic Smooth Muscle Cells

scientific article published on 20 October 2015

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

scientific article published on 01 October 2020

Clinical, molecular, and biochemical delineation of asparagine synthetase deficiency in Saudi cohort

scientific article published on 03 August 2020

Early Humoral Response Correlates with Disease Severity and Outcomes in COVID-19 Patients

scientific article published on 04 December 2020

Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion?

scientific article published on July 2014

IRF2BP2 Reduces Macrophage Inflammation and Susceptibility to Atherosclerosis

scientific article published on 20 July 2015

Interferon-γ activates expression of p15 and p16 regardless of 9p21.3 coronary artery disease risk genotype.

scientific article published on 28 November 2012

Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing: A Pilot Investigating Applications for Hypertrophic Cardiomyopathy.

scientific article

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

scientific article published on 15 September 2020

New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin

scientific article published on 06 August 2020

Plasma PCSK9 levels are elevated with acute myocardial infarction in two independent retrospective angiographic studies

scientific article

Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients

scientific article published on 19 October 2017

SPG7 variant escapes phosphorylation-regulated processing by AFG3L2, elevates mitochondrial ROS, and is associated with multiple clinical phenotypes

scientific article

The 9p21.3 risk locus for coronary artery disease: A 10-year search for its mechanism

scientific article published on 25 April 2017

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