Author

Sumaya Almansoori

Mohammed Bin Rashid University of Medicine and Health SciencesORCID 0009-0000-4752-3616Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Assay:long-read sequencing· 2 Research Focus:variant calling· 2 Approach:Bayesian inference· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Ahmed Abou Tayoun· 1 shared Alexandra I. F. BlakemoreiD· 1 shared Andrianos M. Yiorkas· 1 shared Aswathy VijayakumariD· 1 shared Bakhrom K. BerdieviD· 1 shared Binte ZehraiD· 1 shared Carel Wynand le RouxiD· 1 shared Dale HandleyiD· 1 shared

Activity by Year

2023-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Ahmed Abou Tayoun

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 18, 2026

Structural variation landscape of Middle Eastern and North African individuals from long-read nanopore sequencing reveals medically relevant variants

Talal Al‐Yazeedi, Sophie Tandonnet, Sven Hauns…·Omer S. Alkhnbashi

The paper identifies structural variants in MENA individuals using long-read sequencing, revealing previously unreported variants and population-specific disease-related variants.

DOI 10.64898/2026.02.20.26346743

humanlong-read sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintApr 3, 2026

Isoform-Resolved Genetic Architecture of Epilepsy and SUDEP Reveals Divergent Brain and Heart Channelopathy Signatures

Binte Zehra, Shuhd Bineshaq, Muhammad Faizan…·Bakhrom K. Berdiev

The paper identifies tissue- and isoform-level genetic regulation differences between epilepsy and SUDEP, revealing distinct cardiac and neuronal gene expression patterns.

DOI 10.64898/2026.03.31.715736

humanscRNA-seq

𝕏 PostBluesky

Genetic & Genomic MedicinemedRxivPreprintAug 4, 2023

Severe obesity may be an oligogenic condition: evidence from 1,714 adults seeking treatment in the UK National Health Service

Sumaya Almansoori, Hasnat A Amin, Suzanne Alsters…·Alexandra I. F. Blakemore

This study identifies rare genetic variants in obesity-related genes in a UK cohort of severe obesity patients, suggesting an oligogenic inheritance pattern and demonstrating the utility of custom genotyping arrays.

DOI 10.1101/2023.08.04.23293229

humanwhole-exome sequencing

𝕏 PostBluesky