Amna I. Magrashi

Riyadh, Saudi Arabia

Last Updated: 09/26/2026

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Found 9 publications

Rare and novel genetic variants in sporadic and familial Alzheimer's disease: insights from the first Saudi cohort.

Rare and novel genetic variants in sporadic and familial Alzheimer's disease: insights from the first Saudi cohort.

Journal: Frontiers in aging
Published: December 11, 2025

Revealing co-infections in pneumonia: A case report on advancing diagnosis with metagenomic sequencing technologies.

Revealing co-infections in pneumonia: A case report on advancing diagnosis with metagenomic sequencing technologies.

Journal: Journal of infection and public health
Published: April 28, 2025

Diagnosis of donor-derived Malassezia restricta &Aspergillus species invasive fungal infection in renal transplant recipient using next generation sequencing - A report of 2 cases and literature review.

Diagnosis of donor-derived Malassezia restricta &Aspergillus species invasive fungal infection in renal transplant recipient using next generation sequencing - A report of 2 cases and literature review.

Journal: Journal of infection and public health
Published: December 14, 2024

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission.

Journal: European journal of human genetics : EJHG
Published: September 26, 2019

New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses.

New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses.

Journal: Oncotarget
Published: May 31, 2019

Estimating transfection efficiency in differentiated and undifferentiated neural cells.

Estimating transfection efficiency in differentiated and undifferentiated neural cells.

Journal: BMC research notes
Published: February 24, 2019

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.

Journal: Scientific reports
Published: August 10, 2018

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.

Journal: Scientific reports
Published: February 16, 2017

Parkinson's Disease in Saudi Patients: A Genetic Study.

Parkinson's Disease in Saudi Patients: A Genetic Study.

Journal: PloS one
Published: June 22, 2015
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Last Updated: 09/26/2026