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Dr. Wu Bolin

吴柏林

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

基本信息At a glance

Where they practice, who they consult.

Hospital
Guangzhou Women and Children's Medical Center, Guangzhou
Experience
20+ years in pediatric genetics and genomic diagnostics
Languages
English, Mandarin
专长Specialties

What they personally lead.

Pediatric rare diseaseswhole exome sequencing for diagnostic odysseysmonogenic disease identificationpediatric genetic counselingneurodevelopmental genetic disorders
背景Background

Training and recognition

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

国际患者International patients

What to expect

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.

核实背景Verify credentials

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