Misbah Hanif | Human Genetics | Best Researcher Award

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.

Afolake Arowolo | Functional Genomics | Best Researcher Award

Assoc. Prof. Dr. Afolake Arowolo | Functional Genomics | Best Researcher Award

South African Medical Council and University of Cape Town | South Africa

Dr. Afolake Temitope Arowolo is a C2 NRF-rated Specialist Scientist at the South African Medical Research Council and Adjunct Professor at the University of Cape Town, with more than a decade of experience in biochemistry, molecular biology, and functional genomics. She earned her PhD in Biochemistry from Rhodes University, and earlier degrees from Obafemi Awolowo University. Her research has spanned teaching and supervising students at undergraduate, honours and postgraduate levels, delivering courses in molecular biology, structural biology, biochemistry, enzyme and protein characterisation, as well as quality control and molecular techniques such as CRISPR-Cas9 screening, PCR / qPCR, cloning, and electrophoresis. She has published over 20 peer-reviewed research articles, including a filed patent on novel inhibitors of human 5-alpha reductase for androgenetic alopecia, and has secured various international and local grants and fellowships. Her work has been cited in the scientific literature many times, reflecting a solid h-index (approximately mid- to high-teens) and citations in excess of one hundred. She is active in editorial and peer review duties, mentors, especially for scholars from under-represented backgrounds, and her current research interest is identifying novel therapeutic agents for diseases such as diabetes cardiomyopathy, cardiovascular disease, cancer, and fibrosing skin and hair disorders, applying functional genomics, nanobiotechnology, molecular biology and enzymology.

Profile: Google Scholar

Featured Publications:

Tambwe, N., Sinkala, M., Oluwole, O., Khumalo, N., & Arowolo, A. (2025). An integrative genotyping and gene expression profiling of the mutated human FAM111B gene and fibrosis-associated pathway in the POIKTMP syndrome. Journal of Cellular and Molecular Medicine. (Article in Press).

Oluwole, O. G., Arowolo, A., Musa, E., Levitt, N., & Matjila, M. (2025). The identification of a novel missense variant in the ChAT gene in a patient with gestational diabetes denotes a plausible genetic association. Open Medicine, 20(1), 1225.

Johnson, R., Shabalala, S., Mabasa, L., Kotzé-Hörstmann, L., Sangweni, N., Ramharack, P., Sharma, J., Pheiffer, C., Arowolo, A., & Sadie-Van Gijsen, H. (2025). Integrated profiling of adiponectin and cytokine signaling pathways in high-fat diet-induced MASLD reveals early markers of disease progression. Scientific Reports, 15(1), 1–5.

Naicker, D., Rhoda, C., Sunda, F., & Arowolo, A. (2024). Unravelling the intricate roles of FAM111A and FAM111B: From protease-mediated cellular processes to disease implications. International Journal of Molecular Sciences, 25(5), 2845.

Ntshingila, S., Oputu, O., Arowolo, A. T., & Khumalo, N. P. (2023). Androgenetic alopecia: An update. JAAD International, 13, 150–158.

Musa, E., Salazar-Petres, E., Arowolo, A., Levitt, N., Matjila, M., & Sferruzzi-Perri, A. N. (2023). Obesity and gestational diabetes independently and collectively induce specific effects on placental structure, inflammation and endocrine function in a cohort of South African women. The Journal of Physiology, 601(7), 1287–1306.