Overview
Yongjia Yang practices practicing medicine in Changsha, China.
Yang is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Congenital Radioulnar Synostosis, Mosaic Variegated Aneuploidy Syndrome, 47 XYY Syndrome, and Micrognathia.
They are actively involved in clinical research, co-authoring 33 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 Yongjia Yang
Is Yongjia Yang a top-rated expert for Congenital Radioulnar Synostosis?
MediFind is an objective health platform that identifies experts based on real-world data. Yongjia Yang is classified as an Elite expert for Congenital Radioulnar Synostosis, 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 Yongjia Yang participate in research or clinical trials?
Yes. Yongjia Yang has published 33 articles and abstracts on conditions like Congenital Radioulnar Synostosis. You can view a list of Yongjia 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
- Elite
- Congenital Radioulnar Synostosis
- Advanced
- Mosaic Variegated Aneuploidy Syndrome
- Experienced
- 47 XYY SyndromeYang isExperienced. Learn about 47 XYY Syndrome.
- Brachydactyly Mononen TypeYang isExperienced. Learn about Brachydactyly Mononen Type.
- Childhood PancreatitisYang isExperienced. Learn about Childhood Pancreatitis.
- ChondrodystrophyYang isExperienced. Learn about Chondrodystrophy.
- Cohen SyndromeYang isExperienced. Learn about Cohen Syndrome.
- Cortical DysplasiaYang isExperienced. Learn about Cortical Dysplasia.
- CystinuriaYang isExperienced. Learn about Cystinuria.
- Ehlers-Danlos Syndrome (EDS)
- HypotoniaYang isExperienced. Learn about Hypotonia.
- Increased Head Circumference
- IntersexYang isExperienced. Learn about Intersex.
- MicrognathiaYang isExperienced. Learn about Micrognathia.
- Microvillus Inclusion Disease
- MosaicismYang isExperienced. Learn about Mosaicism.
- NephrocalcinosisYang isExperienced. Learn about Nephrocalcinosis.
- NeurofibromatosisYang isExperienced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)
- OsteopetrosisYang isExperienced. Learn about Osteopetrosis.
- Osteosclerosis Autosomal Dominant
- Pectus ExcavatumYang isExperienced. Learn about Pectus Excavatum.
- Pierre Robin SequenceYang isExperienced. Learn about Pierre Robin Sequence.
- Premature Ovarian FailureYang isExperienced. Learn about Premature Ovarian Failure.
- Primary HyperoxaluriaYang isExperienced. Learn about Primary Hyperoxaluria.
- Primary Hyperoxaluria Type 1
- Pyle DiseaseYang isExperienced. Learn about Pyle Disease.
- Schwartz-Jampel SyndromeYang isExperienced. Learn about Schwartz-Jampel Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda
- Xeroderma PigmentosumYang isExperienced. Learn about Xeroderma Pigmentosum.