Overview
Jun-wei Su practices practicing medicine in Taitung, Taiwan.
Su is highly rated in 7 conditions, according to our data. Their clinical expertise encompasses Mosaicism, Trisomy 2 Mosaicism, Chromosome 3q Duplication, and 3p Deletion Syndrome.
They are actively involved in clinical research, co-authoring 77 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 Jun-wei W. Su
Is Jun-wei W. Su a top-rated expert for Mosaicism?
MediFind is an objective health platform that identifies experts based on real-world data. Jun-wei W. Su is classified as an Distinguished expert for Mosaicism, 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 Jun-wei W. Su participate in research or clinical trials?
Yes. Jun-wei W. Su has published 77 articles and abstracts on conditions like Mosaicism. You can view a list of Jun-wei W. Su'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
- MosaicismSu isDistinguished. Learn about Mosaicism.
- Trisomy 2 MosaicismSu isDistinguished. Learn about Trisomy 2 Mosaicism.
- Advanced
- 3p Deletion Syndrome
- Cat Eye SyndromeSu isAdvanced. Learn about Cat Eye Syndrome.
- Chromosome 3q Duplication
- Cri-Du-Chat Syndrome
- Mosaic Trisomy 7Su isAdvanced. Learn about Mosaic Trisomy 7.
- Experienced
- Achalasia Microcephaly Syndrome
- AchondroplasiaSu isExperienced. Learn about Achondroplasia.
- AcrocephalopolydactylySu isExperienced. Learn about Acrocephalopolydactyly.
- Acromicric DysplasiaSu isExperienced. Learn about Acromicric Dysplasia.
- Apert SyndromeSu isExperienced. Learn about Apert Syndrome.
- Chromosome 5q Duplication
- Chromosome 6q DeletionSu isExperienced. Learn about Chromosome 6q Deletion.
- Coarctation of the Aorta
- Cortical DysplasiaSu isExperienced. Learn about Cortical Dysplasia.
- Femur Fibula Ulna Syndrome
- HoloprosencephalySu isExperienced. Learn about Holoprosencephaly.
- HydrocephalusSu isExperienced. Learn about Hydrocephalus.
- HydronephrosisSu isExperienced. Learn about Hydronephrosis.
- Immune Defect due to Absence of Thymus
- Intrauterine Growth Restriction
- LissencephalySu isExperienced. Learn about Lissencephaly.
- MicrocephalySu isExperienced. Learn about Microcephaly.
- MicrognathiaSu isExperienced. Learn about Micrognathia.
- Osteogenesis ImperfectaSu isExperienced. Learn about Osteogenesis Imperfecta.
- Pfeiffer SyndromeSu isExperienced. Learn about Pfeiffer Syndrome.
- PolydactylySu isExperienced. Learn about Polydactyly.
- PolyhydramniosSu isExperienced. Learn about Polyhydramnios.
- Saethre-Chotzen Syndrome
- Short Rib-Polydactyly Syndrome Type 1
- SyndactylySu isExperienced. Learn about Syndactyly.
- Teratoma of the Mediastinum
- Trisomy 12 MosaicismSu isExperienced. Learn about Trisomy 12 Mosaicism.
- Trisomy 18Su isExperienced. Learn about Trisomy 18.
- VACTERL AssociationSu isExperienced. Learn about VACTERL Association.
- Ventricular Septal Defects