Overview
Peih-shan Wu practices practicing medicine in Taiwan.
Wu is highly rated in 56 conditions, according to our data. Their clinical expertise encompasses Mosaicism, Chromosome 16 Trisomy, Trisomy 12 Mosaicism, and 15q11.2 Microdeletion.
They are actively involved in clinical research, co-authoring 216 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 Peih-shan W. Wu
Is Peih-shan W. Wu a top-rated expert for Mosaicism?
MediFind is an objective health platform that identifies experts based on real-world data. Peih-shan W. Wu 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 Peih-shan W. Wu participate in research or clinical trials?
Yes. Peih-shan W. Wu has published 216 articles and abstracts on conditions like Mosaicism. You can view a list of Peih-shan W. Wu'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
- 15q11.2 MicrodeletionWu isDistinguished. Learn about 15q11.2 Microdeletion.
- Cat Eye SyndromeWu isDistinguished. Learn about Cat Eye Syndrome.
- Chromosome 16 TrisomyWu isDistinguished. Learn about Chromosome 16 Trisomy.
- Chromosome 16q DuplicationWu isDistinguished. Learn about Chromosome 16q Duplication.
- Chromosome 20 TrisomyWu isDistinguished. Learn about Chromosome 20 Trisomy.
- Chromosome 21q DeletionWu isDistinguished. Learn about Chromosome 21q Deletion.
- Chromosome 22 DuplicationWu isDistinguished. Learn about Chromosome 22 Duplication.
- Chromosome 6q DuplicationWu isDistinguished. Learn about Chromosome 6q Duplication.
- Chromosome 9p DeletionWu isDistinguished. Learn about Chromosome 9p Deletion.
- Cri-Du-Chat SyndromeWu isDistinguished. Learn about Cri-Du-Chat Syndrome.
- Intrauterine Growth Restriction
- Jacobsen SyndromeWu isDistinguished. Learn about Jacobsen Syndrome.
- Mosaic Trisomy 7Wu isDistinguished. Learn about Mosaic Trisomy 7.
- Mosaic Trisomy 9Wu isDistinguished. Learn about Mosaic Trisomy 9.
- MosaicismWu isDistinguished. Learn about Mosaicism.
- Paris-Trousseau Thrombocytopenia
- Ring Chromosome 13Wu isDistinguished. Learn about Ring Chromosome 13.
- Tetrasomy 9pWu isDistinguished. Learn about Tetrasomy 9p.
- Trisomy 12 MosaicismWu isDistinguished. Learn about Trisomy 12 Mosaicism.
- Trisomy 17 MosaicismWu isDistinguished. Learn about Trisomy 17 Mosaicism.
- Trisomy 2 MosaicismWu isDistinguished. Learn about Trisomy 2 Mosaicism.
- Advanced
- Abdominal Cystic Lymphangioma
- Bilateral Hydronephrosis
- Cavernous Lymphangioma
- Chromosome 13q Duplication
- Chromosome 15q Duplication
- Chromosome 18p Deletion
- Chromosome 3q Duplication
- Chromosome 6 Uniparental Disomy
- Chromosome 7p Deletion
- Chromosome 8p Deletion
- Corpus Callosum Agenesis
- Cortical Dysplasia
- Cystic HygromaWu isAdvanced. Learn about Cystic Hygroma.
- Down SyndromeWu isAdvanced. Learn about Down Syndrome.
- Endocardial Cushion Defect
- Grix Blankenship Peterson Syndrome
- HydrocephalusWu isAdvanced. Learn about Hydrocephalus.
- Hygroma CervicalWu isAdvanced. Learn about Hygroma Cervical.
- Hypoparathyroidism
- LissencephalyWu isAdvanced. Learn about Lissencephaly.
- Lissencephaly 1Wu isAdvanced. Learn about Lissencephaly 1.
- MicrognathiaWu isAdvanced. Learn about Micrognathia.
- Miller-Dieker Syndrome
- Mosaic Trisomy 8Wu isAdvanced. Learn about Mosaic Trisomy 8.
- Pallister-Killian Mosaic Syndrome
- PolydactylyWu isAdvanced. Learn about Polydactyly.
- PolyhydramniosWu isAdvanced. Learn about Polyhydramnios.
- Rommen Mueller Sybert Syndrome
- Short Stature (Growth Disorders)
- Subcortical Band Heterotopia
- Triple X SyndromeWu isAdvanced. Learn about Triple X Syndrome.
- Trisomy 13Wu isAdvanced. Learn about Trisomy 13.
- Trisomy 14 Mosaicism
- Trisomy 18Wu isAdvanced. Learn about Trisomy 18.
- Wolf-Hirschhorn Syndrome
- Experienced
- 1p36 Deletion SyndromeWu isExperienced. Learn about 1p36 Deletion Syndrome.
- Absence SeizureWu isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly Syndrome
- AcrodysostosisWu isExperienced. Learn about Acrodysostosis.
- Acromicric DysplasiaWu isExperienced. Learn about Acromicric Dysplasia.
- Alagille SyndromeWu isExperienced. Learn about Alagille Syndrome.
- AnencephalyWu isExperienced. Learn about Anencephaly.
- Autism Spectrum Disorder
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly Taurinuria
- Chromosome 6p Duplication
- Chromosome 6q DeletionWu isExperienced. Learn about Chromosome 6q Deletion.
- Chromosome 7p Duplication
- ClubfootWu isExperienced. Learn about Clubfoot.
- Coarctation of the Aorta
- Congenital Diaphragmatic Hernia
- Cornelia De Lange Syndrome
- Crouzon SyndromeWu isExperienced. Learn about Crouzon Syndrome.
- Diaphragmatic HerniaWu isExperienced. Learn about Diaphragmatic Hernia.
- DiGeorge SyndromeWu isExperienced. Learn about DiGeorge Syndrome.
- Fetal Enterovirus Syndrome
- Generalized Tonic-Clonic Seizure
- GigantismWu isExperienced. Learn about Gigantism.
- HerniaWu isExperienced. Learn about Hernia.
- HoloprosencephalyWu isExperienced. Learn about Holoprosencephaly.
- HydronephrosisWu isExperienced. Learn about Hydronephrosis.
- Hypoplastic Left Heart Syndrome (HLHS)
- Immune Defect due to Absence of Thymus
- Increased Head Circumference
- IntersexWu isExperienced. Learn about Intersex.
- LymphangiomatosisWu isExperienced. Learn about Lymphangiomatosis.
- MicrocephalyWu isExperienced. Learn about Microcephaly.
- Muscle AtrophyWu isExperienced. Learn about Muscle Atrophy.
- OmphaloceleWu isExperienced. Learn about Omphalocele.
- Patent Ductus Arteriosus
- Patent Foramen OvaleWu isExperienced. Learn about Patent Foramen Ovale.
- PhocomeliaWu isExperienced. Learn about Phocomelia.
- Prader-Willi SyndromeWu isExperienced. Learn about Prader-Willi Syndrome.
- Roberts SyndromeWu isExperienced. Learn about Roberts Syndrome.
- SirenomeliaWu isExperienced. Learn about Sirenomelia.
- SyndactylyWu isExperienced. Learn about Syndactyly.
- Teratoma of the Mediastinum
- ThrombocytopeniaWu isExperienced. Learn about Thrombocytopenia.
- Total Anomalous Pulmonary Venous Return
- Transposition of the Great Arteries
- Trichorhinophalangeal Syndrome Type 2
- Tricuspid RegurgitationWu isExperienced. Learn about Tricuspid Regurgitation.
- Trophoblastic Tumor Placental Site
- Turner SyndromeWu isExperienced. Learn about Turner Syndrome.
- Umbilical HerniaWu isExperienced. Learn about Umbilical Hernia.
- UreteroceleWu isExperienced. Learn about Ureterocele.
- Ventricular Septal Defects