Isfahan University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the A Rare Combination of Compound Heterozygous Mutations in the Pah Gene in Three Unrelated Consanguineous Iranian Families With Classical Phenylketonuria
Majid Hosseinzadeh
Majid Hosseinzadeh

Assistant Professor of Genetics

Department of Genetics and Molecular Biology, School of Medicine

Isfahan University of Medical Sciences

All Documents
1. Bacterial Superinfection in Pregnant Women With Severe Covid-19: Prevalence, Resistance Patterns and Outcomes, Journal of Infection and Public Health (2026)
2. Association of Tlr9-Rs352140 Polymorphism and Serum Levels of Crp, Il-6, and Anti-Rbd Igg With the Chance of Developing Long Covid-19 Syndrome, Journal of Isfahan Medical School (2025)
3. Contribution of Bard1 Gene to Male Breast Cancer- Report of a Family With Different Types of Cancer, Current Problems in Cancer (2025)
4. Contribution of Bard1 Gene to Male Breast Cancer- Report of a Family With Different Types of Cancer, Current Problems in Cancer (2025)
5. Dync1h1 in Spinal Muscular Atrophy: Diagnostic Findings From Two Families and a Comprehensive Review of Its Role in Neuromuscular and Neurodevelopmental Disorders, Molecular Genetics and Genomic Medicine (2025)
6. Dync1h1 in Spinal Muscular Atrophy: Diagnostic Findings From Two Families and a Comprehensive Review of Its Role in Neuromuscular and Neurodevelopmental Disorders, Molecular Genetics and Genomic Medicine (2025)
7. Evaluation of Common Col2a1 Gene Variants in Iranian Patients Suspected With Stickler Syndrome Type I, Journal of Research in Medical Sciences (2025)
8. Mono-Allelic Mutyh Mutation As the Likely Inherited Etiology of Hereditary Breast Cancer in a Patient From a Multi-Cancer Family- Report of a Family and Literature Review, BMC Medical Genomics (2025)
9. Mono-Allelic Mutyh Mutation As the Likely Inherited Etiology of Hereditary Breast Cancer in a Patient From a Multi-Cancer Family- Report of a Family and Literature Review, BMC Medical Genomics (2025)
10. Prevalence of Novel and Recurrent Pathogenic Variants in Brca Genes in a Cohort of Iranian Hereditary Breast Cancer Patients, Advanced Biomedical Research (2025)
11. Prevalence of Novel and Recurrent Pathogenic Variants in Brca Genes in a Cohort of Iranian Hereditary Breast Cancer Patients, Advanced Biomedical Research (2025)
12. Bacterial Infections and Outcomes of Inpatients With Covid-19 in the Intensive Care Unit During the Delta-Dominant Phase: The Worst Wave of Pandemic in Iran, Frontiers in Public Health (2024)
13. Failure of Ceftazidime/Avibactam Experimental Therapy in the Treatment of Klebsiella Pneumoniae St11 Co-Producing Ndm-1 and Oxa-48 Carbapenemases Infection, European Journal of Clinical Microbiology and Infectious Diseases (2024)
14. First Case of New Delhi Metallo Β-Lactamase-1 (Ndm-1)-Producing Burkholderia Cepacia Complex in Iran, Heliyon (2024)
15. Outbreak of Colistin and Carbapenem-Resistant Klebsiella Pneumoniae St16 Co-Producing Ndm-1 and Oxa-48 Isolates in an Iranian Hospital, BMC Microbiology (2024)
16. Causative Variants Linked With Limb Girdle Muscular Dystrophy in an Iranian Population: 6 Novel Variants, Molecular Genetics and Genomic Medicine (2023)
17. Causative Variants Linked With Limb Girdle Muscular Dystrophy in an Iranian Population: 6 Novel Variants, Molecular Genetics and Genomic Medicine (2023)
18. Secondary Bacterial Infection Caused by St16 Ndm-1 and Oxa-48-Producing Colistin and Carbapenem-Resistant Klebsiella Pneumoniae Treated With Tigecycline in a Pregnant Woman With Covid-19, Journal of Pharmaceutical Policy and Practice (2023)
19. Association of Clinical Features With Spike Glycoprotein Mutations in Iranian Covid-19 Patients, Journal of Clinical Medicine (2022)
20. Dysregulation of Rna Interference Components in Covid-19 Patients, BMC Research Notes (2021)
21. Genetic Analysis of Mecp2 Gene in Iranian Patients With Rett Syndrome, Iranian Journal of Child Neurology (2019)
22. Genetic Analysis of Mecp2 Gene in Iranian Patients With Rett Syndrome, Iranian Journal of Child Neurology (2019)
23. Il-7Ra Association and Genotype-Dependent Severity and Response to Ifn-Β Therapy in Multiple Sclerosis, Acta Medica Iranica (2019)
24. A Novel Homozygous Dph1 Mutation Causes Intellectual Disability and Unique Craniofacial Features, Journal of Human Genetics (2018)
25. A Novel Homozygous Dph1 Mutation Causes Intellectual Disability and Unique Craniofacial Features, Journal of Human Genetics (2018)
26. Factors Influencing Sperm Retrieval Following Testicular Sperm Extraction in Nonobstructive Azoospermia Patients, Clinical and Experimental Reproductive Medicine (2017)
27. Factors Influencing Sperm Retrieval Following Testicular Sperm Extraction in Nonobstructive Azoospermia Patients, Clinical and Experimental Reproductive Medicine (2017)
28. Reciprocal 22Q11.2 Deletion and Duplication in Siblings With Karyotypically Normal Parents, Cytogenetic and Genome Research (2016)
29. Reciprocal 22Q11.2 Deletion and Duplication in Siblings With Karyotypically Normal Parents, Cytogenetic and Genome Research (2016)
30. A New Compound Heterozygous Mutation in Gjb2 Causes Nonsyndromic Hearing Loss in a Consanguineous Iranian Family, International Journal of Pediatric Otorhinolaryngology (2015)
31. Genotype and Phenotype Correlations in Iranian Patients With Hyperinsulinaemic Hypoglycaemia, BMC Research Notes (2015)
32. Mutation Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Central Iran, International Journal of Pediatric Otorhinolaryngology (2015)
33. Mutation Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Central Iran, International Journal of Pediatric Otorhinolaryngology (2015)
34. Significant Association Between Nonsyndromic Cleft Lip With or Without Cleft Palate and Irf6rs2235371 Polymorphism in Iranian Familiar Population, Molecular Biology (2015)
35. Significant Association Between Nonsyndromic Cleft Lip With or Without Cleft Palate and Irf6rs2235371 Polymorphism in Iranian Familiar Population, Molekuliarnaia biologiia (2015)