Abdelrahman Hamza Abdelmoneim

Design of Epitope Based Peptide Vaccine against Brucella Abortus OmpW Family Protein using Immunoinformatics

This study identifies potential epitopes for a peptide vaccine against Brucella abortus OmpW protein using immunoinformatics tools.

Bio-informatic Analysis of Missense Single Nucleotide Polymorphisms (SNPs) in Human CD38 Gene Associated with B-Chronic Lymphocytic Leukemia

The paper analyzes CD38 gene SNPs in CLL patients to predict their impact on protein structure and function, identifying 12 deleterious SNPs associated with altered stability and potential functional changes.

In silico multi-epitope vaccine against covid19 showing effective interaction with HLA-B*15:03

This paper designs an in silico multi-epitope vaccine against SARS-CoV-2 that interacts with HLA-B*15:03, showing potential for cross-protection against SARS and MERS.

Extensive In Silico Analysis of ATL1 Gene: Discovered Five Mutations that may Cause Hereditary Spastic Paraplegia Type 3A

The paper analyzes nsSNPs in the ATL1 gene using bioinformatics tools to identify five deleterious mutations potentially linked to SPG3A and their implications for pharmacogenomics.

In Silico Analysis of B3GALTL Gene Reveling 13 Novel Mutations Associated with Peters'-plus syndrome

The paper identifies 13 novel deleterious mutations in the B3GALTL gene associated with Peters-plus syndrome using in silico analysis.

Extensive In Silico Analysis of the Functional and Structural Consequences of SNPs in Human ARX Gene

The paper identifies 11 nsSNPs in the ARX gene that may cause EIEE1 by analyzing their functional and structural impacts using in silico tools.

Design of multi epitope-based peptide vaccine against E protein of human COVID-19: An immunoinformatics approach

This study designs a multi-epitope peptide vaccine against the E protein of SARS-CoV-2 using immunoinformatics, identifying ten peptides with high population coverage for potential vaccine development.

Identification of Six novel missense single nucleotide polymorphisms in MAOA gene predisposing to aggressive behavior. Bioinformatics study.

This study identifies six novel missense SNPs in the MAOA gene associated with aggressive behavior using bioinformatics analysis.

Multi-epitope Peptide Vaccine Prediction for Candida albicans targeting Pyruvate Kinase Protein; an Immunoinformatics Approach

This paper predicts multi-epitope peptides for a Candida albicans vaccine targeting pyruvate kinase using immunoinformatics tools.

In silico analysis of CDC73 gene revealing 11 novel SNPs associated with Jaw Tumor Syndrome

The paper uses in-silico tools to analyze CDC73 SNPs and identifies 11 novel variants associated with Jaw Tumor Syndrome.

Identification of novel key biomarkers in Simpson-Golabi-Behmel Syndrome: Evidence from bioinformatics analysis

The paper identifies three novel missense mutations in the GPC3 gene associated with Simpson-Golabi-Behmel Syndrome using bioinformatics tools.

In silico analysis of coding SNPs and 3-UTR associated miRNAs in DCAF17 gene that may affect the regulation and pathogenesis of Woodhouse-Sakati Syndrome

The paper identifies 10 deleterious SNPs and one microRNA in the DCAF17 gene that may affect protein structure and function in Woodhouse-Sakati Syndrome through in silico analysis.

Comprehensive bioinformatics analysis of L1CAM gene revealed Novel Pathological mutations associated with L1 syndrome

The paper performs a bioinformatics analysis of L1CAM gene mutations to identify novel pathological variants associated with L1 syndrome and their potential diagnostic applications.

In silico analysis of IDH3A gene revealed Novel mutations associated with Retinitis Pigmentosa

The paper identifies 20 novel deleterious SNPs in the IDH3A gene associated with Retinitis Pigmentosa using bioinformatics tools.

In Silico Analysis and Modeling of Novel Pathogenic Single Nucleotide Polymorphisms (SNPs) in Human CD40LG Gene

The paper identifies 8 novel SNPs in the CD40LG gene using bioinformatics tools and suggests they may be diagnostic markers for hyper-IgM syndrome.

In Silico Genetics: Identification of pathogenic nsSNPs in human STAT3 gene associated with Job's syndrome

This study identifies eleven novel pathogenic nsSNPs in the STAT3 gene associated with Job's syndrome using in silico analysis of SNPs from dbSNP/NCBI.

Novel mutations within PRSS1 Gene that could potentially cause hereditary pancreatitis: Using Comprehensive in silico Approach

The paper identifies two novel deleterious mutations in the PRSS1 gene using in silico analysis of SNPs.

In Silico Genetics Revealing Novel Mutations in CEBPA Gene Associated with Acute Myeloid Leukemia

The paper identifies five novel nsSNPs in the CEBPA gene associated with AML using computational methods and suggests their potential as diagnostic markers.