Overview
Jingmin Yang practices practicing medicine in Shanghai, China.
Yang is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Pyruvate Carboxylase Deficiency, Snyder-Robinson Syndrome, Smith-Lemli-Opitz Syndrome, and Walker-Warburg Syndrome.
They are actively involved in clinical research, co-authoring 17 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 Jingmin Yang
Is Jingmin Yang a top-rated expert for Pyruvate Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Jingmin Yang is classified as an Advanced expert for Pyruvate Carboxylase Deficiency, 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 Jingmin Yang participate in research or clinical trials?
Yes. Jingmin Yang has published 17 articles and abstracts on conditions like Pyruvate Carboxylase Deficiency. You can view a list of Jingmin Yang'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
- Pyruvate Carboxylase Deficiency
- Experienced
- Alport SyndromeYang isExperienced. Learn about Alport Syndrome.
- Chronic Granulomatous Disease
- Familial Exudative Vitreoretinopathy
- Fukuyama Type Muscular Dystrophy
- Gitelman SyndromeYang isExperienced. Learn about Gitelman Syndrome.
- Hereditary SpherocytosisYang isExperienced. Learn about Hereditary Spherocytosis.
- Lactic AcidosisYang isExperienced. Learn about Lactic Acidosis.
- LissencephalyYang isExperienced. Learn about Lissencephaly.
- Low Potassium LevelYang isExperienced. Learn about Low Potassium Level.
- Smith-Lemli-Opitz SyndromeYang isExperienced. Learn about Smith-Lemli-Opitz Syndrome.
- Snyder-Robinson SyndromeYang isExperienced. Learn about Snyder-Robinson Syndrome.
- Walker-Warburg SyndromeYang isExperienced. Learn about Walker-Warburg Syndrome.