Author

Saqib Mahmood

Nur International UniversityORCID 0000-0003-2326-3025Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Abolfazl Heidari· 1 shared Abu BakariD· 1 shared Aisha Nasir HashmiiD· 1 shared Ali Amar· 1 shared Anna MikhailoviD· 1 shared Ansa RabiaiD· 1 shared Ashlyn Rodrigues· 1 shared Ayman Ali Mohammed AlameeniD· 1 shared

Activity by Year

2021-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abolfazl Heidari

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintSep 23, 2025

Identification of Novel Fusion Genes in Pediatric B-ALL patients Using Whole Transcriptome Sequencing

Osheen Sajjad, Ali Amar, Abu Bakar…·Saqib Mahmood

This study identifies 19 high-confidence fusion genes in 12 pediatric B-ALL patients using whole transcriptome sequencing, revealing novel and unreported fusion events.

DOI 10.1101/2025.09.23.677992

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintDec 24, 2021

Autism spectrum disorder trios from consanguineous populations are enriched for rare biallelic variants, identifying 32 new candidate genes

Ricardo Harripaul, Ansa Rabia, Nasim Vasli…·John B. Vincent

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky