Assist. Prof. Dr. Misbah Hanif | Human Genetics | Best Researcher Award
Dow University Of Health Sciences | Pakistan
Dr. Misbah Iqbal Hanif holds a Ph.D. in Human Genetics from the University of Karachi, with research focused on the genetic and cytogenetic causes of recurrent spontaneous miscarriages. Her doctoral work, “A comparative analysis of spontaneous miscarriage couples through QF-PCR with STR markers and conventional cytogenetic tools,” integrated molecular and cytogenetic methodologies to identify chromosomal abnormalities contributing to pregnancy loss. Her research interests encompass reproductive genetics, cytogenetic and molecular diagnostics, and the application of genetic counseling in clinical settings. Dr. Hanif has experience in genetic screening, QF-PCR assay development, and the interpretation of chromosomal aberrations associated with gynecological disorders. Her work also bridges clinical genetics and public health, emphasizing early detection and counseling for inherited and endocrine-related diseases. She has contributed to translational genetics through her involvement in clinical research projects, including those addressing pediatric endocrine disorders, congenital adrenal hyperplasia, and metabolic syndromes. With additional certification in genetic counseling, her research and clinical contributions aim to advance genetic diagnostics, improve patient outcomes, and strengthen genetic counseling services within healthcare and academic environments.
Profiles: Google Scholar | Scopus
Featured Publications:
Ali, A., Ali, N., Hanif, M. I., & Ali, S. R. (2024). Discovering Down’s syndrome: An account from a low middle income country. Pakistan Journal of Medical Sciences, 40(9).
Khan, H., Sher, S. A., Hanif, M. I., Zemawal, N. A., Ahmad, A., Khan, F., & Daftani, M. H. (2024). Prevalence, proportions, and identities of antibiotic-resistant bacteria in the oral microflora of healthy children. Cureus, 16(8), 1–9.
Hanif, M. I., Ahmed, H., Ibrahim, M. N., Raza, J., & Ahmed, S. A. (2024). A novel de novo likely pathogenic variant of WFS1 gene in a Pakistani child with non-classic WFS1 spectrum disorder. Journal of Ayub Medical College Abbottabad, 36(2), 433–435.
Hanif, M. I., Ahmed, F., Raza, J., & Ali, S. R. (2024). Clinical outcomes of neonatal admissions with respiratory distress at Sindh Institute of Child Health and Neonatology: An observational study. Pakistan Pediatric Journal, 48(1).
Hanif, M. I., Khan, S. W., Ali, S. R., & Raza, S. J. (2024). Neonatal disease presentations at a newly developed center in an LMIC: Insights from the spectrum of illness at SICHN. International Journal of Pediatrics and Neonatology, 6(1), 14–17.
Hanif, M. I., Mansoor, Q., Arif, A., Shoeb, E., Ismail, M., Khan, A., & Ahmed, S. A. (2024). Genetic evaluation of spontaneous miscarriages and couples through conventional and modern diagnostic tools. Liaquat National Journal of Primary Care.