Overview
Jingbin Yan practices practicing medicine in Shanghai, China.
Their clinical expertise encompasses Ballinger-Wallace Syndrome, Down Syndrome, Infant Epilepsy with Migrant Focal Crisis, and Allan-Herndon-Dudley Syndrome.
They are actively involved in clinical research, co-authoring 19 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 Jingbin Yan
Is Jingbin Yan a top-rated expert for Ballinger-Wallace Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Jingbin Yan is classified as an Experienced expert for Ballinger-Wallace 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 Jingbin Yan participate in research or clinical trials?
Yes. Jingbin Yan has published 19 articles and abstracts on conditions like Ballinger-Wallace Syndrome. You can view a list of Jingbin Yan'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
- Experienced
- Allan-Herndon-Dudley Syndrome
- Ballinger-Wallace Syndrome
- Congenital Myasthenic Syndrome
- Down SyndromeYan isExperienced. Learn about Down Syndrome.
- HypotoniaYan isExperienced. Learn about Hypotonia.
- Infant Epilepsy with Migrant Focal Crisis
- RUNX1 Familial Platelet Disorder