Overview
Jie-yuan Jin practices practicing medicine in Shaoxing, China.
Jin is highly rated in 16 conditions, according to our data. Their clinical expertise encompasses Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Taurinuria, Camptodactyly Syndrome Guadalajara Type 1, and Camptodactyly Syndrome Guadalajara Type 2.
They are actively involved in clinical research, co-authoring 61 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 Jie-yuan Y. Jin
Is Jie-yuan Y. Jin a top-rated expert for Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Jie-yuan Y. Jin is classified as an Distinguished expert for Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, 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 Jie-yuan Y. Jin participate in research or clinical trials?
Yes. Jie-yuan Y. Jin has published 61 articles and abstracts on conditions like Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia. You can view a list of Jie-yuan Y. Jin'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
- Arthrogryposis Multiplex Congenita
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaJin isDistinguished. Learn about Camptodactyly Taurinuria.
- Congenital Contractural Arachnodactyly
- Congenital ContracturesJin isDistinguished. Learn about Congenital Contractures.
- Distal ArthrogryposisJin isDistinguished. Learn about Distal Arthrogryposis.
- Distal Arthrogryposis Type 6Jin isDistinguished. Learn about Distal Arthrogryposis Type 6.
- Advanced
- Achard SyndromeJin isAdvanced. Learn about Achard Syndrome.
- AEC SyndromeJin isAdvanced. Learn about AEC Syndrome.
- ArachnodactylyJin isAdvanced. Learn about Arachnodactyly.
- Familial Ventricular Tachycardia
- Greig Cephalopolysyndactyly Syndrome
- PolydactylyJin isAdvanced. Learn about Polydactyly.
- Proximal Symphalangism
- Experienced
- Acanthosis NigricansJin isExperienced. Learn about Acanthosis Nigricans.
- AchondroplasiaJin isExperienced. Learn about Achondroplasia.
- Acromegaloid Facial Appearance Syndrome
- Acromicric DysplasiaJin isExperienced. Learn about Acromicric Dysplasia.
- ADULT SyndromeJin isExperienced. Learn about ADULT Syndrome.
- CardiomyopathyJin isExperienced. Learn about Cardiomyopathy.
- Chiari MalformationJin isExperienced. Learn about Chiari Malformation.
- Chiari Malformation Type 1
- Chiari Malformation Type 2
- ClubfootJin isExperienced. Learn about Clubfoot.
- Cockayne SyndromeJin isExperienced. Learn about Cockayne Syndrome.
- Cockayne Syndrome Type 1Jin isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Jin isExperienced. Learn about Cockayne Syndrome Type 2.
- Collins Pope SyndromeJin isExperienced. Learn about Collins Pope Syndrome.
- Cortical DysplasiaJin isExperienced. Learn about Cortical Dysplasia.
- Dent DiseaseJin isExperienced. Learn about Dent Disease.
- Diabetes Insipidus (DI)Jin isExperienced. Learn about Diabetes Insipidus (DI).
- Dilated Cardiomyopathy (DCM)
- Factor 11 DeficiencyJin isExperienced. Learn about Factor 11 Deficiency.
- FaintingJin isExperienced. Learn about Fainting.
- Familial Hypertriglyceridemia
- Familial Periodic Paralysis
- Hajdu-Cheney SyndromeJin isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hearing LossJin isExperienced. Learn about Hearing Loss.
- Hereditary Multiple Osteochondromas
- Hereditary Sensory and Autonomic Neuropathy Type 2
- High CholesterolJin isExperienced. Learn about High Cholesterol.
- High Molecular Weight Kininogen Deficiency
- Hirsutism in WomenJin isExperienced. Learn about Hirsutism in Women.
- Hypertrichosis-Acromegaloid Facial Appearance Syndrome
- HyperventilationJin isExperienced. Learn about Hyperventilation.
- Hypokalemic Periodic Paralysis
- HypophosphatemiaJin isExperienced. Learn about Hypophosphatemia.
- HypotoniaJin isExperienced. Learn about Hypotonia.
- Increased Head Circumference
- Low Blood PressureJin isExperienced. Learn about Low Blood Pressure.
- Low Potassium LevelJin isExperienced. Learn about Low Potassium Level.
- Marfan SyndromeJin isExperienced. Learn about Marfan Syndrome.
- MicrognathiaJin isExperienced. Learn about Micrognathia.
- Mucolipidosis 3Jin isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Jin isExperienced. Learn about Mucolipidosis Type 4.
- MyelomeningoceleJin isExperienced. Learn about Myelomeningocele.
- NephrocalcinosisJin isExperienced. Learn about Nephrocalcinosis.
- Nephrogenic Diabetes Insipidus
- OsteochondromaJin isExperienced. Learn about Osteochondroma.
- Paroxysmal Supraventricular Tachycardia (PSVT)
- Premature Ovarian FailureJin isExperienced. Learn about Premature Ovarian Failure.
- PseudoachondroplasiaJin isExperienced. Learn about Pseudoachondroplasia.
- Restrictive Cardiomyopathy (RCM)
- RicketsJin isExperienced. Learn about Rickets.
- ScoliosisJin isExperienced. Learn about Scoliosis.
- SialidosisJin isExperienced. Learn about Sialidosis.
- Waardenburg SyndromeJin isExperienced. Learn about Waardenburg Syndrome.
- Waardenburg Syndrome Type 1
- X-Linked HypophosphatemiaJin isExperienced. Learn about X-Linked Hypophosphatemia.