Overview
Haiying Wu practices practicing medicine in Suzhou, China.
Wu is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Coffin-Siris Syndrome, Precocious Puberty, Cytochrome P450 Oxidoreductase Deficiency, and Graves Disease.
They are actively involved in clinical research, co-authoring 27 peer reviewed articles.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Haiying Wu
Is Haiying Wu a top-rated expert for Coffin-Siris Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Haiying Wu is classified as an Advanced expert for Coffin-Siris Syndrome, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Haiying Wu participate in research or clinical trials?
Yes. Haiying Wu has published 27 articles and abstracts on conditions like Coffin-Siris Syndrome. You can view a list of Haiying Wu's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Coffin-Siris Syndrome
- Precocious Puberty
- Experienced
- Acanthosis NigricansWu isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaWu isExperienced. Learn about Achondroplasia.
- Atelosteogenesis Type 1Wu isExperienced. Learn about Atelosteogenesis Type 1.
- BrachydactylyWu isExperienced. Learn about Brachydactyly.
- Cytochrome P450 Oxidoreductase Deficiency
- Diabetic KetoacidosisWu isExperienced. Learn about Diabetic Ketoacidosis.
- Familial Glucocorticoid Deficiency
- Familial Hyperthyroidism due to Mutations in TSH Receptor
- Generalized Resistance to Thyroid Hormone
- Graves DiseaseWu isExperienced. Learn about Graves Disease.
- Hirsutism in WomenWu isExperienced. Learn about Hirsutism in Women.
- HyperthyroidismWu isExperienced. Learn about Hyperthyroidism.
- Idiopathic Short Stature (ISS)
- Infant HyperglycemiaWu isExperienced. Learn about Infant Hyperglycemia.
- Neonatal HypothyroidismWu isExperienced. Learn about Neonatal Hypothyroidism.
- Nijmegen Breakage Syndrome
- Short Stature (Growth Disorders)