Overview
Ting Chen practices practicing medicine in Shanghai, China.
Ms. Chen is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Multiple Carboxylase Deficiency, Hereditary Methemoglobinemia, Holocarboxylase Synthetase Deficiency, and Pyruvate Carboxylase Deficiency.
She is actively involved in clinical research, co-authoring 37 peer reviewed articles.
Gender
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 Ting S. Chen
Is Ting S. Chen a top-rated expert for Multiple Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Ting S. Chen is classified as an Advanced expert for Multiple 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 Ting S. Chen participate in research or clinical trials?
Yes. Ting S. Chen has published 37 articles and abstracts on conditions like Multiple Carboxylase Deficiency. You can view a list of Ting S. Chen'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
- Hereditary MethemoglobinemiaMs. Chen isAdvanced. Learn about Hereditary Methemoglobinemia.
- Holocarboxylase Synthetase Deficiency
- Multiple Carboxylase Deficiency
- Pyruvate Carboxylase Deficiency
- Experienced
- Diabetic NephropathyMs. Chen isExperienced. Learn about Diabetic Nephropathy.
- Glutaric Acidemia Type 2Ms. Chen isExperienced. Learn about Glutaric Acidemia Type 2.
- Inborn Amino Acid Metabolism Disorder
- Maple Syrup Urine DiseaseMs. Chen isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaMs. Chen isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Maturity Onset Diabetes of the Young
- MethemoglobinemiaMs. Chen isExperienced. Learn about Methemoglobinemia.
- Type 2 Diabetes (T2D)Ms. Chen isExperienced. Learn about Type 2 Diabetes (T2D).
- Wilson DiseaseMs. Chen isExperienced. Learn about Wilson Disease.