Dr. Wu Bolin

Chief Physician; Professor; Director of the Genetics and Endocrinology Department

Established one of China's most productive clinical programs for diagnosing pediatric rare diseases using whole exome sequencing (WES) and whole genome sequencing (WGS); his team has achieved diagnostic rates exceeding 40% for previously undiagnosed children with suspected genetic conditions, ending years-long diagnostic odysseys for hundreds of families; contributed to the discovery of novel disease-causing genes through international collaborative research; played a key role in building Guangzhou Women and Children's Medical Center into a national referral center for pediatric genetic diseases in southern China; published in American Journal of Human Genetics, Genetics in Medicine, and European Journal of Human Genetics

Dr. Wu is highly recommended for families with children who have unexplained developmental delay, intellectual disability, multiple congenital anomalies, or suspected genetic conditions that have not been diagnosed despite extensive prior testing. His team is experienced in coordinating comprehensive genomic diagnostic workups and providing clear, family-centered genetic counseling about results and management options.

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