Osama M. Mustafa

Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways.

Olfat Al-Harazi, N. Kaya, D. Çolak, 2020, Omics : a journal of integrative biology.

Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking

J. Rosenfeld, D. Trabzuni, S. Arold, 2021, Brain : a journal of neurology.

RNA-Seq transcriptome profiling in three liver regeneration models in rats: comparative analysis of partial hepatectomy, ALLPS, and PVL

Olfat Al-Harazi, D. Çolak, D. Dhar, 2020, Scientific Reports.

Identification of novel genomic imbalances in Saudi patients with congenital heart disease

N. Kaya, D. Çolak, B. Levy, 2018, Molecular Cytogenetics.

The Role of CK20, p53 and p63 in Differentiation of Some Urothelial Lesions of Urinary Bladder, Immunohistochemical Study

Osama M. Mustafa, A. H. Ali, S. Raheem, 2014 .

KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability

N. Kaya, D. Çolak, M. D’Adamo, 2016, Journal of Medical Genetics.

Identification of novel genomic imbalances in Saudi patients with congenital heart disease

N. Kaya, D. Çolak, B. Levy, 2018, Molecular Cytogenetics.

RNA-Seq transcriptome profiling in three liver regeneration models in rats: comparative analysis of partial hepatectomy, ALLPS, and PVL

Olfat Al-Harazi, D. Çolak, D. Dhar, 2020, Scientific Reports.