Author

Shehzad Hanif

Mohammed Bin Rashid University of Medicine and Health Sciences

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· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:whole-genome sequencing· 3 Organism:human· 2 Approach:statistical model· 2 Organism:Arabidopsis· 1 Assay:bulk RNA-seq· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1

Frequent Co-Authors

Bassam Adnan Jamalalail· 3 shared Bipin BalaniD· 3 shared Hanan Abdelhalim ElSokary· 3 shared Nasna NassiriD· 3 shared Suhana Shiyas· 3 shared Alawi A.A. Alsheikh-AliiD· 2 shared Dasuki Kondaramage· 2 shared Dia AdvaniiD· 2 shared

Activity by Year

2025-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetics

Bassam Adnan Jamalalail

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3 papers

Recent·Most cited

Phenotype Dependent Segregation of a Novel EPS8 Variant for Hearing Loss and an HPDL Variant for Neurodevelopmental Disorders in a Complex Consanguineous Family

Bassam Adnan Jamalalail, Ahmed Khalifa, Bipin Balan, Shuhd Bineshaq, Dia Advani, Hanan Abdelhalim ElSokary, Dasuki Kondaramage, Suhana Shiyas, Nelson C. Soares, Shehzad Hanif, Samuel Tharakan, Zeinab Mohamdi, Mohammad Aburaidah, Sherin Kuttiankandy, Alawi A.A. Alsheikh-Ali, , Mohammed Uddin

The paper identifies two pathogenic variants in a consanguineous family, one causing hearing loss and the other neurodevelopmental disorder, through genomic and transcriptomic analysis.

bioRxiv · Jul 14, 2026 · PreprintGenetics

A draft Arab pangenome reference

Nasna Nassir, Mohamed A. Almarri, Muhammad Kumail, Nesrin Mohamed, Bipin Balan, Shehzad Hanif, Maryam AlObathani, Bassam Adnan Jamalalail, Hanan Abdelhalim ElSokary, Dasuki Kondaramage, Suhana Shiyas, Noor Kosaji, Dharana Satsangi, Madiha Hamdi Saif Abdelmotagali, Ahmad N. Abou Tayoun, , Mohammed J. Uddin

The paper presents the first Arab Pangenome Reference using long-read and Hi-C data, revealing novel sequences and variants specific to Arab populations.

Nature Communications · Jul 24, 2025Peer-reviewedGenomics

PanScan: A Tool for Tertiary Analysis of Human Pangenome Graphs

Bipin Balan, Shehzad Hanif, Mohammad Amiruddin Hashmi, Muhammad Kumail, Shuhd Bineshaq, Talal Al-Yazeedi, Richa Tambi, Munazza Murtaza, Bassam Adnan Jamalalail, Hanan Abdelhalim ElSokary, Maryam Al Obathani, Nesrin Mohamed, K Dasuki Hansana Perera, Dia Advani, Aysha Ibrahim Hamzah, , Mohammed J. Uddin

PanScan is a tool for tertiary analysis of human pangenome graphs, enabling detection of duplicated genes, novel variants, and complex genomic regions.

bioRxiv · May 1, 2025 · PreprintBioinformatics