Mona M. Almramhi

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Corrigendum to "Integrative in silico analysis identifies functionally and regulatively relevant nsSNPs in the TRIB3 gene" [Comput. Biol. Chem. 124 (2026) 109227].

Corrigendum to "Integrative in silico analysis identifies functionally and regulatively relevant nsSNPs in the TRIB3 gene" [Comput. Biol. Chem. 124 (2026) 109227].

Journal: Computational biology and chemistry
Published: August 12, 2026

Integrative in silico analysis identifies functionally and regulatively relevant nsSNPs in the TRIB3 gene.

Integrative in silico analysis identifies functionally and regulatively relevant nsSNPs in the TRIB3 gene.

Journal: Computational biology and chemistry
Published: April 21, 2026

Implications of occult hepatitis B infection for blood donor management: a five-year evaluation from Western Saudi Arabia.

Implications of occult hepatitis B infection for blood donor management: a five-year evaluation from Western Saudi Arabia.

Journal: BMC infectious diseases
Published: December 03, 2025

Immune Evasion Mechanisms of Neurotropic Dengue Virus.

Immune Evasion Mechanisms of Neurotropic Dengue Virus.

Journal: Reviews in medical virology
Published: October 16, 2025

Exploring the Role of Plasma Lipids and Statin Interventions on Multiple Sclerosis Risk and Severity: A Mendelian Randomization Study.

Exploring the Role of Plasma Lipids and Statin Interventions on Multiple Sclerosis Risk and Severity: A Mendelian Randomization Study.

Journal: Neurology
Published: October 12, 2022

The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study.

The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study.

Journal: Multiple sclerosis (Houndmills, Basingstoke, England)
Published: May 16, 2022

Mendelian Randomisation Finds No Causal Association between Urate and Parkinson's Disease Progression.

Mendelian Randomisation Finds No Causal Association between Urate and Parkinson's Disease Progression.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: November 27, 2020

Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome.

Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome.

Journal: Nature communications
Published: October 21, 2020

Using Mendelian randomization to understand and develop treatments for neurodegenerative disease.

Using Mendelian randomization to understand and develop treatments for neurodegenerative disease.

Journal: Brain communications
Published: January 16, 2020

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features.

A missense mutation in TRAPPC6A leads to build-up of the protein, in patients with a neurodevelopmental syndrome and dysmorphic features.

Journal: Scientific reports
Published: August 14, 2017

The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family.

The alkylglycerol monooxygenase (AGMO) gene previously involved in autism also causes a novel syndromic form of primary microcephaly in a consanguineous Saudi family.

Journal: Journal of the neurological sciences
Published: November 30, 2015

A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.

A novel homozygous PTH1R variant identified through whole-exome sequencing further expands the clinical spectrum of primary failure of tooth eruption in a consanguineous Saudi family.

Journal: Archives of oral biology
Published: October 04, 2015
Showing 1-12 of 17

Last Updated: 09/26/2026