Kathy Wu | Genetics and Genomics | Women Researcher Award

Assoc. Prof. Dr. Kathy Wu | Genetics and Genomics | Women Researcher Award

Assoc. Prof. Dr. Kathy Wu | Genetics and Genomics | Women Researcher Award | Clinical Geneticist | St Vincent’s Clinical Genomics | Australia

Assoc. Prof. Dr. Kathy Wu is an accomplished clinician-researcher, medical geneticist, and academic leader who has made transformative contributions to the field of genomics and precision medicine. She is internationally recognized for pioneering clinical genomics services that integrate research, clinical care, and education to improve health outcomes for patients with rare diseases, cancer predisposition syndromes, and pharmacogenomic treatment needs. As the Founding Head of St Vincent’s Clinical Genomics, she successfully developed a multidisciplinary model that delivers comprehensive diagnostic services and leads translational research programs. Her visionary leadership has resulted in establishing Australia’s first preventive genomics clinic and integrating pharmacogenomics into mental health care, bridging gaps between innovation and patient-centered healthcare delivery.

Professional Profile

Education

Assoc. Prof. Dr. Kathy Wu completed her medical degree followed by postgraduate training in internal medicine and clinical genetics. She holds specialist recognition as a Clinical Geneticist from the Human Genetics Society of Australasia and is a Fellow of the Royal Australasian College of Physicians. Her academic career is complemented by conjoint appointments at leading universities where she contributes to curriculum development, supervises medical students and trainees, and lectures on precision medicine, ethical genomics implementation, and translational research strategies.

Experience

Assoc. Prof. Dr. Kathy Wu has extensive clinical and academic experience spanning hospital-based genetic services, research institutions, and collaborative national initiatives. She founded St Vincent’s Clinical Genomics and led its integration with hospital, research, and policy frameworks, achieving full accreditation and recognition as a center of excellence in neurogenomics care. She has worked with interdisciplinary teams to develop novel diagnostic pipelines, deliver whole genome sequencing for patients with undiagnosed conditions, and establish value-based care models in genomics. In addition to her clinical responsibilities, she is actively engaged as a principal investigator in large-scale research projects, securing multimillion-dollar competitive funding and partnering with international collaborators to accelerate discovery and implementation of genomic medicine.

Research Interest

Assoc. Prof. Dr. Kathy Wu’s research focuses on precision medicine, rare disease diagnostics, neurogenomics, and pharmacogenomics. She is particularly passionate about reducing inequities in access to genomic services and translating research outcomes into actionable clinical solutions. Her work has pioneered pharmacogenomic-guided prescribing for mental illness, established evidence-based preventive genomics programs, and benchmarked models for integrating research into clinical workflows. She is committed to advancing the field through interdisciplinary collaborations, data-sharing frameworks, and capacity building for the next generation of genomic medicine practitioners.

Award

Assoc. Prof. Dr. Kathy Wu has received multiple recognitions for her groundbreaking work, including the designation of her neurogenomics program as an internationally recognized Center of Excellence. Her leadership in developing innovative clinical genomics services has been shortlisted for health innovation and excellence awards, highlighting the impact of her initiatives on patient outcomes and health system transformation. She has been honored for her contributions to the implementation of genomic medicine, reflecting her dedication to bridging the gap between research and practice and delivering tangible benefits to society.

Selected Publication

“Implementation of Whole Genome Sequencing in Clinical Diagnostics” (2022, 85 Citations),

“Pharmacogenomics-Guided Mental Health Treatment: A Translational Model” (2021, 64 Citations),

“Integrating Research and Clinical Genomics: A Value-Based Care Approach” (2020, 47 Citations),

“Preventive Genomics: The Future of Personalized Healthcare Delivery” (2023, 53 Citations).

Conclusion

Assoc. Prof. Dr. Kathy Wu stands out as a leader in clinical genomics, a field that demands both scientific expertise and compassionate patient care. Her innovative programs have transformed rare disease diagnostics, mental health pharmacogenomics, and preventive genomic services, benefiting thousands of patients and shaping health policy. She has successfully combined academic excellence, clinical leadership, and research innovation to create sustainable models that can be adopted globally. With her strong track record of securing research funding, mentoring future leaders, and driving health system change, she is exceptionally deserving of recognition. Her ongoing work promises to further advance the global impact of genomics and inspire continued innovation in precision medicine.

 

 

Karen Kengne Kamga | Genetics and Genomics | Best Researcher Award

Karen Kengne Kamga | Genetics and Genomics | Best Researcher Award

Dr Karen Kengne Kamga, Limbe Regional Hospital, south west, Cameroon, Cameroon

Dr. Karen Kengne Kamga is a dynamic physician-scientist from Cameroon, blending clinical expertise with advanced research in human and medical genetics. With an M.D. from the University of Yaoundé I and a Ph.D. in Genetic Counselling from the University of Cape Town, she has become a leading figure in genomic medicine across Africa. She currently serves as a postdoctoral researcher in Human Genetics, Head of Medical Genetics at Limbe Regional Hospital, and Associate Lecturer at the University of Yaoundé I. Passionate about bridging clinical gaps in genetic services in Africa, she’s contributed significantly to fragile X syndrome understanding and healthcare system integration of genetic counselling. Dr. Kamga is a strong advocate for capacity building, precision public health, and equitable genomic research.

Publication Profile

Orcid

Education

Dr. Kamga began her academic journey at GBHS Bafoussam, completing her GCE Ordinary and Advanced Levels. She earned her MD in General Medicine from the University of Yaoundé I in 2013. Driven by a passion for genetics, she pursued a Ph.D. in Genetic Counselling at the University of Cape Town, which she completed in December 2021. To expand her administrative and clinical leadership, she enrolled in an MBA in Health Management at UNICAF University, completed in 2023. She is also pursuing a Master’s in Clinical Genetics at Tech Global University, Andorra (2023–2024). In parallel, she is a postdoctoral fellow in Human Genetics at the University of Cape Town since 2021. Her multi-disciplinary training spans medicine, genetics, health management, epidemiology, and bioinformatics, equipping her to lead innovation in genomic healthcare delivery in low-resource settings.

Experience

Dr. Kamga’s career began as a physician at “Cabinet de soin St Dominique” (2013–2014), followed by multiple leadership roles at District Hospital Limbe from 2014 to 2023, including Head of Pediatrics, Gynecology/Obstetrics, Surgical Unit, ANC & EPI, and Laboratory Coordinator. In 2023, she became Head of Medical Genetics at the Limbe Regional Hospital. Simultaneously, since 2024, she is an Associate Lecturer at the University of Yaoundé I. Her experience reflects a strong commitment to integrating genetic services within mainstream healthcare and public health teaching. Her roles have combined clinical excellence, mentorship, and system-level leadership, all contributing to a national vision for personalized medicine and public health genetics.

Awards and Honors

Dr. Kamga’s research excellence has been widely recognized through prestigious international honors. She received the 2024 Resource-Limited Country Travel Award and the 2021 & 2020 Developing Country Virtual Meeting Awards from the American Society of Human Genetics (ASHG). In 2019, she earned the ASHG Developing Country Travel Award. These honors reflect her impactful presence in the global genetics research community. She is also a respected member of several professional societies: ASHG (since 2020), African Society of Human Genetics (since 2017), and the Cameroon Society of Human Genetics (since 2015). Her accolades underscore a consistent dedication to research, equity, and capacity building in genetic medicine in Africa.

Research Focus

Dr. Kamga’s research focuses on bridging the gap between advanced genetic knowledge and its clinical implementation in Africa. Her Ph.D. investigated cultural perceptions and explanatory models of Fragile X Syndrome in rural Cameroon, highlighting the need for community-sensitive genetic counselling. As a postdoctoral fellow, she explores the integration of human genetics into public health, emphasizing equitable access to genomic services. She led a scoping review identifying strategic pathways to strengthen genetic healthcare in Africa. Her work spans genomic ethics, bioinformatics, genetic education, and precision public health, consistently aiming to enhance genetic literacy and healthcare systems in resource-limited settings. She is deeply involved in collaborative African genomics initiatives like H3Africa, and committed to mentoring emerging scientists.

Publication Top Notes