Guozhuang Li
Genetics Clinic of Skeletal Deformity,
Peking Union Medical College Hospital, PUMC & CAMS
I'm Guozhuang Li from Peking Union Medical College Hospital in Beijing, China.
From January to June 2025, I will be a visiting fellow at Zou Lab, Johns Hopkins University School of Medicine.
My medical journey began in 2016 at Tongji Medical College, Huazhong University of Science and Technology, where I built a strong foundation in clinical medicine and excelled academically, marking the start of my aspirations in the medical field. Currently, I am pursuing a doctorate at Peking Union Medical College Hospital (PUMCH) under the mentorship of Professor Nan Wu, with a research focus on the medical genetics of skeletal deformities and rare disorders. As the core member of the Genetics Clinic of Skeletal Deformity at PUMCH, I have led collaborative efforts to develop integrated workflows and guidelines that combine deep phenotyping with genetic analysis. These innovations aim to advance diagnostic strategies and precision medicine for rare diseases.
Beyond my research, I contribute to patient care by providing genetic counseling as part of a multidisciplinary team, striving to improve outcomes for individuals with complex rare diseases. My work reflects a deep commitment to advancing precision medicine and enhancing clinical care for rare disorders.
From January to June 2025, I will be a visiting fellow at Zou Lab, Johns Hopkins University School of Medicine.
My medical journey began in 2016 at Tongji Medical College, Huazhong University of Science and Technology, where I built a strong foundation in clinical medicine and excelled academically, marking the start of my aspirations in the medical field. Currently, I am pursuing a doctorate at Peking Union Medical College Hospital (PUMCH) under the mentorship of Professor Nan Wu, with a research focus on the medical genetics of skeletal deformities and rare disorders. As the core member of the Genetics Clinic of Skeletal Deformity at PUMCH, I have led collaborative efforts to develop integrated workflows and guidelines that combine deep phenotyping with genetic analysis. These innovations aim to advance diagnostic strategies and precision medicine for rare diseases.
Beyond my research, I contribute to patient care by providing genetic counseling as part of a multidisciplinary team, striving to improve outcomes for individuals with complex rare diseases. My work reflects a deep commitment to advancing precision medicine and enhancing clinical care for rare disorders.
Sessions
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20-Mar-2025Featured Platform Presentations
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21-Mar-2025Medical Diagnostic Challenges (Adult and Cancer)
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