Journal of Pediatrics Neonatal Biology

Dr. Sohier Yahia Abd ELrazek is a Professor of Pediatrics and Genetics and Head of the Genetics and Metabolic Unit at Mansoura University Children’s Hospital, Faculty of Medicine, Mansoura University, Egypt. She has extensive experience in pediatric care, with particular expertise in genetics, metabolic disorders, and neonatal diseases. She has actively contributed to education, research, and scientific leadership through supervision of numerous master’s and doctoral theses, participation in national research projects, and leadership in pediatric genetics programs.

• Pediatric Genetics and Metabolic Disorders
• Neonatology
• Endocrinology
• Neurodevelopmental Disorders
• Pediatric Hematology
• Immunogenetics
• Congenital Malformations

• Head of Genetics and Metabolic Unit, Mansoura University Children’s Hospital.

• Member of the National Scientific Committee for Promotion of Professors and Associate Professors in Pediatrics.

• Editorial board member and reviewer for numerous international journals including Scientific Reports, BMC Pediatrics, Pediatrics Research, and World Journal of Pediatrics.

• Organized and participated in over 180 national and international conferences as speaker, chairperson, and moderator.

• Editor of medical textbooks including Medical Genetics for Undergraduates and Special Feeding System in Metabolic Cases.

1. Segregation Analysis of p53, c-myc and DNA Ploidy in Childhood Leukemia. J. Med. Sci., 2006.
2. Neurophysiologic Evaluation of Peripheral Nerve Function in Uremic Egyptian Children. J. Pediatr. Neurol., 2006.
3. Increased DNA Damage in Children Caused by Passive Smoking. Mutation Research, 2007.
4. Markers of Apoptosis and Proliferation as Predictors in Childhood Leukemia. J. Hematology, 2007.
5. NPHS2 Mutations in Egyptian Children. Indian J. Pediatr., 2008.
6. Thyroid and Growth Hormones in Fanconi Anemia. Indian J. Pediatr., 2008.
7. Claudin16 Mutation in Familial Hypomagnesemia. Clin. Exp. Nephrol., 2009.
8. β-Thalassemia Mutations in Northeast Egypt. Hematology, 2010.
9. Expression of Lung Resistance Protein in Pediatric Leukemia. J. Oncol. Pharm. Pract., 2010.
10. Sirenomelia and Potter’s Syndrome Case Report. Afr. Health Sci., 2010.
11. MYH3 Mutation in Freeman–Sheldon Syndrome. Indian J. Pediatr., 2011.
12. Cytoprotective Effect of Honey in Fanconi Anemia. Indian J. Hum. Genet., 2011.
13. Cytogenetic and Comorbidity Profile of Down Syndrome. Indian J. Hum. Genet., 2011.
14. β-Glucosidase Acid Gene Mutations in Gaucher Disease. World J. Pediatr., 2011.
15. LMNA Mutation in Mandibuloacral Dysplasia. Eur. J. Hum. Genet., 2012.
16. HBV and HCV in Egyptian Thalassemic Patients. Hematol. Oncol. Stem Cell Ther., 2012.
17. hMPV in Acute Respiratory Infection. Indian J. Pediatr., 2012.
18. Leptin and Thyroid Hormones in Obese Down Syndrome Children. BMC Endocr. Disord., 2012.
19. Adhesion Molecules in Rheumatic Heart Disease. Pediatr. Cardiol., 2013.
20. Glucocorticoid Receptor Expression in Nephrotic Syndrome. Pediatr. Nephrol., 2013.
21. ACVR1 Mutation in Fibrodysplasia Ossificans Progressiva. Case Rep. Genet., 2013.
22. Predictors of Anxiety and Depression in Thalassemia. Int. J. Hematol., 2013.
23. Hidden Y Chromosome Mosaicism in Turner’s Syndrome. Genet. Res. Int., 2013.
24. Ewing’s Sarcoma after Retinoblastoma Case Report. J. Blood Lymph, 2013.
25. Community-Acquired Infections in Down Syndrome. Braz. J. Infect. Dis., 2013.
26. Familial Mediterranean Fever Database Update. Indian J. Hum. Genet., 2014.
27. Disruptive Behavior in Down Syndrome Children. Ann. Saudi Med., 2014.
28. Cognitive Function and QoL in Leukemia Children. J. Blood Disord. Transfus., 2015.
29. Sickle Cell Disease chapter in Inherited Hemoglobin Disorders, 2015.
30. Hyperbilirubinemia & Phototherapy on Genotoxicity. Eur. J. Pediatr., 2015.
31. Optimal Method for Cord Blood Collection. Transfusion, 2015.
32. IL-17A/F Polymorphisms in Juvenile Lupus. Autoimmunity, 2016.
33. Fibrillin-1 Mutation in Marfan Family. Saudi J. Kidney Dis. Transplant., 2017.
34. ACE Gene Polymorphism in Lupus Nephritis. Lupus, 2017.
35. Congenital Heart Disease in Down Syndrome. Ann. Saudi Med., 2017.
36. Rapunzel Syndrome Case Report. Paediatr. Int. Child Health., 2017.
37. Morbidity Profile of Genetic Unit Referrals. Am. J. Prev. Med. Public Health., 2017.
38. Morgagni Hernia Case Report. Pediatric Case Reports, 2018.
39. AT1R Gene Polymorphism in Lupus. Clin. Rheumatol., 2018.
40. Psychiatric Disorders in Chronic ITP. Indian J. Hematol. Blood Transfus., 2018.
41. Cytogenetic Profile of Genetic Disorders. Am. J. Prev. Med. Public Health., 2018.
42. AT2R Gene Polymorphism in Lupus. Lupus, 2019.
43. Mediators in Preterm Infants with Sepsis. J. Pediatr. Gastroenterol. Nutr., 2019.
44. Vitamin D Receptor Gene Polymorphism in Lupus. Lupus, 2019.
45. Neurocutaneous Melanosis Case. Indian J. Dermatol. Venereol. Leprol., 2020.
46. Serum Adiponectin and Obesity in Down Syndrome. J. Pediatr. Endocrinol. Metab., 2021.
47. Iron Deficiency and Thalassemia Carriers. J. Egypt. Public Health Assoc., 2021.
48. Cerebrolysin in High-Risk Preterm Infants. J. Neonatal-Perinatal Med., 2022.
49. EDN1 Gene Variant in Nephrotic Syndrome. J. Biochem. Mol. Toxicol., 2022.
50. Cerebrolysin in Down Syndrome Infants. J. Ment. Health Res. Intellect., 2022.
51. Chromosomal Abnormalities in Infertility. Middle East Fertil. Soc. J., 2022.
52. β-Thalassemia Carrier Rate in High School Children. Curr. Pediatr. Rev., 2023.
53. AZF & Inhibin B in Azoospermia. J. Med. Chem. Sci., 2023.
54. Death Markers in ITP. Indian J. Hematol. Blood Transfus., 2023.
55. Mothers’ Personality & Feeding Disorders. Middle East Curr. Psychiatry, 2023.
56. Serum Apelin-12 in Down Syndrome. Eur. J. Pediatr., 2024.
57. Wharton’s Jelly Stem Cells Yield Factors. Sci. Rep., 2024.
58. FTO Gene and Obesity in Down Syndrome. Eur. J. Pediatr., 2025.
59. Hearing in Mucopolysaccharidosis. Egypt. J. ENT Allied Sci., 2025.
60. Hearing Impairment in Down Syndrome. Sci. Rep., 2025.
61. Eating Disorders in Type 1 Diabetes. Eur. J. Pediatr., 2025.
62. Neonatal Sepsis Diagnosis Paradigm. Egypt. J. Med. Microbiol., 2025.
63. Knowledge on Cord Blood Banking. J. Health Popul. Nutr., 2025.
64. D-Bifunctional Protein Deficiency Case. Indian J. Pediatr., 2025.
65. Umbilical Cord Blood Unit Factors. Sci. Rep., 2025.
66. LPCAT1 rs9728 Variant & Neonatal RDS. Biomedicines, 2025.
67. Ambiguous Genitalia: Diagnostic Dilemmas. Benha Med. J., 2005.
68. Bone Mineral Density in Turner’s Syndrome. J. Pediatric Club, 2005.
69. Oxidative Stress and Antioxidants in Obese Children. J. Pediatric Club, 2006.
70. Lipid Metabolism and Atherogenic Index in Turner’s Syndrome. J. Egypt. Soc. Endocrinol. Metab. Diabetes, 2007.
71. MRSA Prevalence in Mansoura University Hospital. Egypt. Pediatr. Assoc. Gazette, 2008.
72. Pollution Effects on Chromosomes and Hormones. EJBMB, 2009.
73. Diagnosis of DiGeorge Syndrome. Egypt. Pediatr. Assoc. Gazette, 2011.
74. Sleep-Related Breathing Disorders in Obese Children. J. Pediatric Club, 2013.
75. Serum Amyloid A vs CRP in Sepsis. Res. Opin. Anesth. Intensive Care., 2019.