Dr. Hanaa Skhoun-Human genetics-Best Scholar Award
Mohammed V Military Instruction Hospital of Rabat-Morocco
Author profile
Early Academic Pursuits
Dr. Hanaa Skhoun began her academic journey with a strong foundation in genetics and biosecurity. Graduating with a Master of Research EuroAfrican in Biosecurity and Biosafety in 2016, she demonstrated early promise in the field of biological sciences.
Professional Endeavors
Dr. Skhoun's professional career reflects her commitment to cutting-edge research. Her doctoral thesis at the Mohammed V Military Training Hospital delved into the intricate genetic mechanisms underlying acute lymphoblastic leukemia in Moroccan children, showcasing her expertise in genetic analysis and molecular biology techniques.
Contributions and Research Focus
Her research contributions are significant, particularly in understanding the roles of tumor suppressor gene TP53 and oncogenes RAS in leukemia pathogenesis. Her work on the BCR/ABL fusion gene in chronic myeloid leukemia has also expanded diagnostic and therapeutic avenues for adult patients.
Accolades and Recognition
Dr. Skhoun's excellence has been recognized with prestigious awards such as the Excellence Prize from Mohammed V University in 2017 and a CNRST Excellence Scholarship from 2017 to 2020. These accolades underscore her dedication and impact in the scientific community.
Impact and Influence on Human genetics
Her publications in esteemed journals like Archives de Pédiatrie and Molecular Biology Reports highlight her impactful research on cytogenetic abnormalities and gene polymorphisms associated with leukemia risk. Her findings have implications for diagnosis, prognosis, and personalized treatment strategies.
One of the key goals of human genetics is to unravel the genetic basis of various traits and diseases, leading to advancements in personalized medicine and targeted therapies. By studying human DNA, genes, and chromosomes, researchers can identify genetic mutations associated with diseases, develop genetic tests for diagnosis and prognosis, and explore gene therapies for treating genetic disorders. Human genetics research has profound implications for healthcare, as it provides insights into the underlying mechanisms of diseases and facilitates the development of tailored interventions and preventive strategies based on an individual's genetic makeup.
Legacy and Future Contributions
Dr. Skhoun's legacy lies in advancing our understanding of genetic factors in leukemia and fostering a new generation of researchers. Her mastery of genetic techniques, bioinformatics tools, and pedagogical skills positions her as a leader in translational genomics, paving the way for future breakthroughs in cancer research.
In essence, Dr. Hanaa Skhoun's journey epitomizes dedication, excellence, and innovation in the realm of genetic research, leaving a lasting impact on scientific knowledge and patient care.
Human genetics is the branch of genetics that focuses on the study of inheritance in humans. It encompasses a wide range of topics, including the transmission of genetic traits from parents to offspring, the identification of genetic variations that contribute to human diversity, and the understanding of genetic disorders and diseases. Human genetics also explores the role of genetics in complex traits such as behavior, intelligence, and susceptibility to common diseases like diabetes and cancer.
Notable Publications
- Association of TP53 gene polymorphisms with the risk of acute lymphoblastic leukemia in Moroccan children
- B/T mixed phenotype acute leukemia with high hyperdiploidy and lineage switch to B-cell acute leukemia
- A prognostic approach on a case of pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia with monosomy-7
- Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature