Author

Soada Ahmed Osman

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioinformatics· 4

Signature Assays, Organisms & Methods

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Assay:GWAS summary statistics· 4 Organism:human· 4 Approach:statistical model· 4 Research Focus:variant effect prediction· 3 Research Focus:differential expression· 1

Frequent Co-Authors

Tebyan A. AbdelhameediD· 4 shared Mohamed Ahmed Salih HassaniD· 3 shared Mujahed I. MustafaiD· 3 shared Fatima A. AbdelrhmaniD· 2 shared Mustafa ElhagiD· 2 shared Abdelrahman Hamza AbdelmoneimiD· 1 shared Adla M. Hassan· 1 shared Amal B. AhmediD· 1 shared

Activity by Year

2019-2019 · peak 4/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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4 shared papersBioinformatics

Tebyan A. AbdelhameedORCID

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Thirty two novel nsSNPs May effect on HEXA protein Leading to Tay-Sachs disease (TSD) Using a Computational Approach

Tebyan A. Abdelhameed, Mohamed Mustafa Osman Fadul, Dina Nasereldin Abdelrahman Mohamed, Amal Mohamed Mudawi, Sayaf Kamal Khalifa Fadul Allah, Ola Ahmed Elnour Ahmed, Sogoud Mohammednour Idrees Mohammeddeen, Aya Abdelwahab Taha khairi, Soada Ahmed Osman, Ebrahim Mohammed Al-Hajj, Mustafa Elhag, Mohamed Ahmed Hassan Salih

The paper predicts 32 novel non-synonymous SNPs in the HEXA gene that may contribute to Tay-Sachs disease using bioinformatics tools.

bioRxiv · Sep 9, 2019 · PreprintBioinformatics

Thirty five novel nsSNPs may affect ADAMTS13 protein leading to Thrombotic thrombocytopenic purpura (TTP) using bioinformatics approach

Tebyan A. Abdelhameed, Arwa I. Ahmed, Mujahed I. Mustafa, Amel N. Eltayeb, Fatima A. Abdelrhman, Amal B. Ahmed, Najla B. Ahmed, Hiba Y. Khadir, Adla M. Hassan, Huda K. Mohamed, Soada Ahmed Osman, Mustafa Elhag, Mohamed Ahmed Salih Hassan

The paper predicts 35 novel nsSNPs in ADAMTS13 that may cause TTP using bioinformatics tools.

bioRxiv · Sep 6, 2019 · PreprintBioinformatics

Novel deleterious nsSNPs within MEFV gene that could be used as Diagnostic Markers to Predict Hereditary Familial Mediterranean Fever: Using bioinformatics analysis

Mujahed I. Mustafa, Tebyan A. Abdelhameed, Fatima A. Abdelrhman, Soada Ahmed Osman, Mohamed Ahmed Salih Hassan

The paper identifies 23 novel deleterious nsSNPs in the MEFV gene using bioinformatics tools, which may serve as diagnostic markers for Familial Mediterranean Fever.

Advances in Bioinformatics · Jun 4, 2019Peer-reviewedBioinformatics

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

Mujahed I. Mustafa, Abdelrahman Hamza Abdelmoneim, Nafisa M. Elfadol, Soada Ahmed Osman, Tebyan A. Abdelhameed, Mohamed Ahmed Salih Hassan

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

bioRxiv · Jan 14, 2019 · PreprintBioinformatics