Author

Mohammed Uddin

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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Genetics· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Organism:mouse· 1 Assay:proteomics· 1

Frequent Co-Authors

Ahmed Khalifa· 1 shared Alawi A.A. Alsheikh-AliiD· 1 shared Alexandr MelnikoviD· 1 shared Alexandra Maria Chitroceanu· 1 shared Andreas KindiD· 1 shared Annika WinkleriD· 1 shared Bakhrom K. BerdieviD· 1 shared Bassam Adnan Jamalalail· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Ahmed Khalifa

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Author profile →

2 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

Lung microvascular rarefaction impairs pulmonary gas exchange and exacerbates heart failure with preserved ejection fraction

Ceren Koçana, Lara Jaeschke, Alexandra Maria Chitroceanu, Qi Zhang, Niklas Hegemann, Pengchao Sang, Q. Li, Mariya M. Kucherenko, Kristin Kräker, K. Franz, Alexandr Melnikov, David Faidel, Leonardo A. von der Ohe, Paul-Lennard Perret, Jonathan L. Gillan, , Wolfgang Michael Kuebler

This study identifies pulmonary microvascular rarefaction as a novel mechanism in heart failure, linking it to impaired gas exchange and worsened cardiac function.

bioRxiv · Mar 9, 2026 · PreprintPhysiology