Assoc. Prof. Dr. Morteza Oladnabi | Genetic | Research Excellence Award

Golestan University of Medical Sciences | Iran

Assoc. Prof. Dr. Morteza Oladnabi is a medical genetics researcher with strong expertise in human genetics, molecular diagnostics, and translational genomics. His research focuses on identifying genetic variants underlying inherited disorders, including neurodevelopmental conditions, neuromuscular diseases, hereditary hearing loss, ectodermal dysplasia, and rare metabolic syndromes, using whole-exome sequencing, bioinformatics, and molecular modeling. He has contributed extensively to peer-reviewed journals, with a scholarly output of 74 documents, achieving an h-index of 19 and generating approximately 26,707 citations across 23,583 citing documents, reflecting strong academic influence. His professional experience includes academic research leadership, multidisciplinary collaboration, postgraduate supervision, and integration of computational genetics, artificial intelligence, and clinical genomics to improve diagnosis, counseling, and disease prevention strategies

Citation Metrics (Scopus)

30000

24000

18000

12000

6000

Citations
26,707

Documents
74

h-index
19

🟦 Citations 🟥 Documents 🟩 h-index

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Featured Publications

Molecular Dynamics Insights into De Novo Mutations in Ribosomal Proteins S19 and L26 Causing Diamond–Blackfan Anemia

– Journal of Biomolecular Structure and Dynamics

A Novel Bi-Allelic MCOLN1 Variant Underlying Mucolipidosis Type IV: Clinical, Genetic, and Structural Analysis

– BMC Medical Genomics

A Novel EDAR Splice-Site Variant in Hypohidrotic Ectodermal Dysplasia with Tooth Agenesis: Molecular Dynamics Insights

– BMC Medical Genomics

A Novel Biallelic IL10RB Deletion Causing Infant-Onset Inflammatory Bowel Disease: Molecular Docking Study

– Molecular Biology Reports

Identification of Genetic Variants Associated with Hereditary Hearing Loss Using Whole-Exome Sequencing

– Molecular Biology Reports

Prof. Dr. Seyed Mohammad Akrami | Genetics and Genomics | Best Researcher Award

Prof. Tehran University of Medical Sciences Iran

📚 Dr. Seyed Mohammad Akrami is a Professor of Medical Genetics at Tehran University of Medical Sciences (TUMS), Iran. With over two decades of experience, he has contributed significantly to genetic research, education, and clinical diagnostics. He specializes in molecular and cancer genetics, bioethics, and genetic counseling, actively advancing the field through innovative research and teaching.

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Education

🎓 Dr. Akrami earned his MD from Tehran University of Medical Sciences in 1995 and pursued a PhD in Genetics from Nottingham University, UK, in 2002. His PhD focused on “Diagnostic Application of Human DNA Copy Number Analysis,” using advanced techniques like MAPH, PCR, and Southern blotting.

Experience

🏥 Dr. Akrami has held various roles, including Assistant Professor at the Endocrine and Metabolism Research Center, Advisor at the Pasteur Institute of Iran, and Deputy for Strategic Planning at the Iran Red Crescent. He has been a full Professor at TUMS since 2023, teaching courses in molecular genetics, cancer genetics, and developmental genetics while supervising numerous research theses.

Research Interests

🔬 Dr. Akrami’s research revolves around molecular diagnostics, genetic counseling, and bioethics. He has contributed to understanding hereditary diseases like Holt-Oram syndrome, Charcot-Marie-Tooth disease, and cancer genetics, emphasizing innovative diagnostic methods.

Awards

🏆 Dr. Akrami has received numerous accolades, including the “Best Poster Prize” at Nottingham University, a full PhD scholarship from the Iranian Ministry of Health, and grants for international research collaborations. His work is recognized both nationally and internationally.