Overview
Tizhen Yan practices practicing medicine in Dongguan, China.
Yan is highly rated in 7 conditions, according to our data. Their clinical expertise encompasses Thalassemia, Alpha Thalassemia, Beta Thalassemia, and Hemoglobinopathy.
They are actively involved in clinical research, co-authoring 60 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 Tizhen M. Yan
Is Tizhen M. Yan a top-rated expert for Thalassemia?
MediFind is an objective health platform that identifies experts based on real-world data. Tizhen M. Yan is classified as an Distinguished expert for Thalassemia, 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 Tizhen M. Yan participate in research or clinical trials?
Yes. Tizhen M. Yan has published 60 articles and abstracts on conditions like Thalassemia. You can view a list of Tizhen M. 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
- Distinguished
- Alpha ThalassemiaYan isDistinguished. Learn about Alpha Thalassemia.
- ThalassemiaYan isDistinguished. Learn about Thalassemia.
- Advanced
- AnemiaYan isAdvanced. Learn about Anemia.
- Beta ThalassemiaYan isAdvanced. Learn about Beta Thalassemia.
- Congenital Hemolytic Anemia
- HemoglobinopathyYan isAdvanced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaYan isAdvanced. Learn about Hemolytic Anemia.
- Experienced
- AlbinismYan isExperienced. Learn about Albinism.
- Allan-Herndon-Dudley Syndrome
- Atypical PneumoniaYan isExperienced. Learn about Atypical Pneumonia.
- Carnitine Palmitoyltransferase 1 Deficiency
- Chromosome 2 Uniparental Disomy
- CitrullinemiaYan isExperienced. Learn about Citrullinemia.
- ClubfootYan isExperienced. Learn about Clubfoot.
- Congenital Adrenal Hyperplasia (CAH)
- Congenital Heart Disease (CHD)
- DiGeorge SyndromeYan isExperienced. Learn about DiGeorge Syndrome.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Glutaric Acidemia Type 1Yan isExperienced. Learn about Glutaric Acidemia Type 1.
- Glutaric Acidemia Type 2Yan isExperienced. Learn about Glutaric Acidemia Type 2.
- Granuloma AnnulareYan isExperienced. Learn about Granuloma Annulare.
- Hallervorden-Spatz Disease
- Hearing LossYan isExperienced. Learn about Hearing Loss.
- Hemoglobin E DiseaseYan isExperienced. Learn about Hemoglobin E Disease.
- Hermansky-Pudlak SyndromeYan isExperienced. Learn about Hermansky-Pudlak Syndrome.
- HypoparathyroidismYan isExperienced. Learn about Hypoparathyroidism.
- Immune Defect due to Absence of Thymus
- Inborn Amino Acid Metabolism Disorder
- Infant Hearing LossYan isExperienced. Learn about Infant Hearing Loss.
- IntersexYan isExperienced. Learn about Intersex.
- Isovaleric AcidemiaYan isExperienced. Learn about Isovaleric Acidemia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Magnesium DeficiencyYan isExperienced. Learn about Magnesium Deficiency.
- MicrosporidiosisYan isExperienced. Learn about Microsporidiosis.
- Mitochondrial Trifunctional Protein Deficiency
- Mycoplasma PneumoniaYan isExperienced. Learn about Mycoplasma Pneumonia.
- Nonsyndromic Hearing LossYan isExperienced. Learn about Nonsyndromic Hearing Loss.
- Noonan SyndromeYan isExperienced. Learn about Noonan Syndrome.
- Oculocutaneous AlbinismYan isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- OmphaloceleYan isExperienced. Learn about Omphalocele.
- Primary Carnitine Deficiency
- Protein DeficiencyYan isExperienced. Learn about Protein Deficiency.
- RASopathiesYan isExperienced. Learn about RASopathies.
- RhabdomyolysisYan isExperienced. Learn about Rhabdomyolysis.
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Urea Cycle Disorders (UCD)
- Ventricular Septal Defects