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Katy Barwick
Research Associate at UCL, Great Ormond Street Institute of Child Health
Professional Background
Katy Barwick is an accomplished biomedical scientist with a rich background in the genetic and molecular basis of hereditary motor neuropathies. Her extensive research experience encompasses a variety of roles, contributing significantly to the field of medical genetics. Katy started her career as a research intern at the prestigious Vanderbilt University Medical Center, where she honed her skills in genetics and molecular biology. Following this foundational experience, she progressed to serve as a research assistant at University College London (UCL), further deepening her understanding of genetic conditions, especially hereditary motor neuropathies.
Throughout her career, Katy has offered her insights and findings at numerous prestigious conferences, including the European Society of Human Genetics and the Society for Neuroscience. These presentations not only showcased her research but also reflected her commitment to collaboration and sharing knowledge within the scientific community.
Education and Achievements
Katy's strong educational background laid the groundwork for her successful career in biomedical science. She began her academic journey at St. Edwards Oxford, where she completed her A-levels in Biology, Chemistry, Spanish, and Physics. This diverse educational foundation prepared her for the rigorous studies that lay ahead.
She then pursued her Bachelor of Science (BSc) in Biomedical Science at St. George's, University of London, obtaining a 2:1 degree, which carved a path for her further academic achievements. Katy continued her studies at the same institution, where she completed her Master of Research (MRes) in Biomedical Science specializing in Human/Medical Genetics, earning a distinction for her excellent work.
Katy's passion for genetics achieved its zenith when she completed not one, but two Doctor of Philosophy (PhD) programs. Her first PhD was completed at the University of Exeter, where she focused on investigating the genetic and molecular basis of hereditary motor neuropathies. Following that, she pursued another PhD on the same topic at St. George's, University of London, establishing herself as a leading expert in her field.
Notable Contributions
Katy has contributed significantly to the scientific community through her presentations at various conferences, which are vital for knowledge exchange in the field. Not only did she present at the AGTC-INDIA conference in 2014, but she also showcased her research at the European Society of Human Genetics conferences in both 2012 and 2015, indicating her ongoing commitment to staying at the forefront of her discipline.
Additionally, Katy participated in the Society for Neuroscience (SFN) Conference in 2012, where she effectively communicated her findings to an audience of her peers in neuroscience, highlighting her versatility across interdisciplinary platforms. Her role as a platform presenter at the GW4 Universities Early Career Neuroscientist Day (ECND) in 2015 further underscores her standing in the academic and scientific community.
Skills and Expertise
Katy's broad skill set is characterized by her expertise in genetic research, molecular biology, and biomedical applications. Her ability to convey complex scientific concepts to a diverse audience showcases her communication skills, essential for successful collaboration in research and academia. Furthermore, Katy's experience varies from account management at Weber Shandwick to office management at Grey Matter Recruitment, demonstrating her versatility and adaptability across different sectors.
As a dedicated scientist, Katy Barwick embodies the spirit of inquiry and excellence within biomedical research. Her dual PhD qualifications and her commitment to addressing genetic conditions affirm her as a leading figure in her area of expertise. Katy's work not only contributes to scientific knowledge but also holds significant promise for future advancements in the treatment and understanding of hereditary motor neuropathies.
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