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Bassam Musa Sadik Al-Musawi

Department of Pathology & Forensic Medicine, College of Medicine · University of Baghdad

https://researchid.co/bassammusa
@uobaghdad.edu.iq
12Scopus Publications
151Google Scholar Citations
5Google Scholar h-index
4Google Scholar i10-index

Research Interests

Medical genetics Clinical genetics Molecular diagnosis Cancer genetics Rare diseases

Biography

A faculty member in the College of Medicine, University of Baghdad, Iraq since 1999. Teaches medical genetics and clinical genetics to undergraduate medical students and postgraduate medical students in different medical and surgical specialties (Diploma, MSc, Ph.D., Iraqi Board, and Arab Board for Medical Specializations). Supervised undergraduate and postgraduate students. Published many research works in the field of medical genetics, cytogenetics, molecular diagnosis, rare disorders, molecular hematology, birth defects, and cancer genetics. Serves as a reviewer for scientific journals and has reviewed more than 150 articles and case reports so far. The main goal of the project working on is ((to establish a molecular database for common and significant health problems in Iraq)).

Education

M.B.Ch.B. (1996) - College of Medicine, University of Baghdad, Iraq M.Sc. (2005) - College of Medicine, University of Baghdad, Iraq Ph.D. (2010) - College of Medicine, University of Baghdad, Iraq

Recent Scopus Publications

  1. Sequencing of Catalytic Serine Protease, Linker, and Activation Peptide Domains-Coding Regions of the F9 Gene in Iraqi Hemophilia B Patients
    Journal of the Faculty of Medicine Baghdad, 2026
  2. Assessment of Six Polymorphic Variants as Genetic Risks for Coronary Artery Disease: A Case–Control Study
    Medical Journal of Babylon, 2025
  3. Congenital Anomalies in Neonates: Findings from Six Baghdad Hospitals
    Journal of the Faculty of Medicine Baghdad, 2025
  4. Clinical and Molecular Analysis of ATP7B Variants Identified by Next-Generation Sequencing in Iraqi Adults With Wilson Disease
    Sultan Qaboos University Medical Journal, 2025
  5. Epigenomic and phenotypic characterization of DEGCAGS syndrome
    European Journal of Human Genetics, 2024

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