Amna Magrashi
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View article: 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 Open
Pneumonia, a frequent and serious complication in kidney transplant recipients, is significantly increased by long-term immunosuppressive medication. This case report details a patient with lung cavitation, in which conventional microbiolo…
View article: 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 Open
Diagnosing donor-derived fungal infection in solid organ transplant recipients can be particularly challenging and is associated with high mortality. Here, we report two cases of Malassezia restricta and Aspergillus spp donor-derived funga…
View article: 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 Open
View article: Implementation of Next Generation Sequencing (Ngs) as a Diagnostic Tool in Infectious Diseases
Implementation of Next Generation Sequencing (Ngs) as a Diagnostic Tool in Infectious Diseases Open
View article: Revealing Co-Infections in Pneumonia: A Case Report on Advancing Diagnosis with Metagenomic Sequencing Technologiesrevealing 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 Technologiesrevealing Co-Infections in Pneumonia: A Case Report on Advancing Diagnosis with Metagenomic Sequencing Technologies Open
View article: 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 Open
Several types of genetic alterations occurring at numerous loci have been described in attention deficit hyperactivity disorder (ADHD). However, the role of rare single nucleotide variants (SNVs) remains under investigated. Here, we sought…
View article: 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 Open
Background: With a prevalence of 170 000 adults in the US alone, meningiomas are the most common primary intracranial tumors. The management of skull base meningiomas is challenging due to their complexity and proximity to crucial n…
View article: Estimating transfection efficiency in differentiated and undifferentiated neural cells
Estimating transfection efficiency in differentiated and undifferentiated neural cells Open
View article: 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 Open
Genetic studies of the familial forms of Parkinson’s disease (PD) have identified a number of causative genes with an established role in its pathogenesis. These genes only explain a fraction of the diagnosed cases. The emergence of Next G…
View article: 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 Open
View article: Parkinson’s Disease in Saudi Patients: A Genetic Study
Parkinson’s Disease in Saudi Patients: A Genetic Study Open
Parkinson's disease (PD) is one of the major causes of parkinsonism syndrome. Its characteristic motor symptoms are attributable to dopaminergic neurons loss in the midbrain. Genetic advances have highlighted underlying molecular mechanism…