Overview
Wenjuan Qiu practices practicing medicine in Shanghai, China.
Qiu is highly rated in 29 conditions, according to our data. Their clinical expertise encompasses Malonyl-CoA Decarboxylase Deficiency, Methylmalonic Acidemia, Multiple Carboxylase Deficiency, and Ornithine Transcarbamylase Deficiency.
They are actively involved in clinical research, co-authoring 147 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 Wenjuan J. Qiu
Is Wenjuan J. Qiu a top-rated expert for Malonyl-CoA Decarboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Wenjuan J. Qiu is classified as an Distinguished expert for Malonyl-CoA Decarboxylase Deficiency, 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 Wenjuan J. Qiu participate in research or clinical trials?
Yes. Wenjuan J. Qiu has published 147 articles and abstracts on conditions like Malonyl-CoA Decarboxylase Deficiency. You can view a list of Wenjuan J. Qiu'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
- Glycogen Storage Disease Type 6
- HomocystinuriaQiu isDistinguished. Learn about Homocystinuria.
- Malonyl-CoA Decarboxylase Deficiency
- Methylmalonic AcidemiaQiu isDistinguished. Learn about Methylmalonic Acidemia.
- Multiple Carboxylase Deficiency
- Ornithine Transcarbamylase Deficiency
- Advanced
- Acid Sphingomyelinase Deficiency (ASMD)
- AnorchiaQiu isAdvanced. Learn about Anorchia.
- Beta-Ketothiolase Deficiency
- Congenital Adrenal Hyperplasia (CAH)
- Congenital Lipoid Adrenal Hyperplasia
- Enlarged LiverQiu isAdvanced. Learn about Enlarged Liver.
- Gaucher Disease Type 2
- Glutaric Acidemia Type 1
- Glycogen Storage Disease Type 3
- Holocarboxylase Synthetase Deficiency
- HyperglycerolemiaQiu isAdvanced. Learn about Hyperglycerolemia.
- IntersexQiu isAdvanced. Learn about Intersex.
- Isovaleric AcidemiaQiu isAdvanced. Learn about Isovaleric Acidemia.
- Maple Syrup Urine Disease
- Metabolic AcidosisQiu isAdvanced. Learn about Metabolic Acidosis.
- Niemann-Pick Disease
- Phenylketonuria (PKU)
- Pompe DiseaseQiu isAdvanced. Learn about Pompe Disease.
- Pyruvate Carboxylase Deficiency
- Short Stature (Growth Disorders)
- SitosterolemiaQiu isAdvanced. Learn about Sitosterolemia.
- Urea Cycle Disorders (UCD)
- XanthomaQiu isAdvanced. Learn about Xanthoma.
- Experienced
- Achalasia Microcephaly Syndrome
- Acute PancreatitisQiu isExperienced. Learn about Acute Pancreatitis.
- Addison's DiseaseQiu isExperienced. Learn about Addison's Disease.
- Adrenal Insufficiency Pediatric
- Apolipoprotein C2 Deficiency
- Argininosuccinic AciduriaQiu isExperienced. Learn about Argininosuccinic Aciduria.
- Bile Duct ObstructionQiu isExperienced. Learn about Bile Duct Obstruction.
- Brachydactyly Mononen Type
- CardiomyopathyQiu isExperienced. Learn about Cardiomyopathy.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Childhood PancreatitisQiu isExperienced. Learn about Childhood Pancreatitis.
- CholestasisQiu isExperienced. Learn about Cholestasis.
- Chromosome 18p DeletionQiu isExperienced. Learn about Chromosome 18p Deletion.
- Common ColdQiu isExperienced. Learn about Common Cold.
- Common Variable Immune Deficiency
- Cortical DysplasiaQiu isExperienced. Learn about Cortical Dysplasia.
- DiarrheaQiu isExperienced. Learn about Diarrhea.
- Familial Glucocorticoid Deficiency
- Familial Hypertriglyceridemia
- Familial Lipoprotein Lipase Deficiency
- Fanconi Bickel SyndromeQiu isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeQiu isExperienced. Learn about Fanconi Syndrome.
- Farber LipogranulomatosisQiu isExperienced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseQiu isExperienced. Learn about Gaucher Disease.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Glutaric Acidemia Type 2Qiu isExperienced. Learn about Glutaric Acidemia Type 2.
- Glycogen Storage Disease Type 9
- Hashimoto ThyroiditisQiu isExperienced. Learn about Hashimoto Thyroiditis.
- High Blood Pressure in Infants
- High CholesterolQiu isExperienced. Learn about High Cholesterol.
- HistiocytosisQiu isExperienced. Learn about Histiocytosis.
- HypothyroidismQiu isExperienced. Learn about Hypothyroidism.
- Inborn Amino Acid Metabolism Disorder
- Increased Head Circumference
- Infantile Axonal Neuropathy
- Isolated ACTH DeficiencyQiu isExperienced. Learn about Isolated ACTH Deficiency.
- Krabbe DiseaseQiu isExperienced. Learn about Krabbe Disease.
- Leigh SyndromeQiu isExperienced. Learn about Leigh Syndrome.
- Low Blood SugarQiu isExperienced. Learn about Low Blood Sugar.
- Low Sodium LevelQiu isExperienced. Learn about Low Sodium Level.
- Lowe SyndromeQiu isExperienced. Learn about Lowe Syndrome.
- MalnutritionQiu isExperienced. Learn about Malnutrition.
- Maternal Hyperphenylalaninemia
- Methylmalonic Acidemia with Homocystinuria
- MicrocephalyQiu isExperienced. Learn about Microcephaly.
- Movement DisordersQiu isExperienced. Learn about Movement Disorders.
- Mucolipidosis 3Qiu isExperienced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Qiu isExperienced. Learn about Mucolipidosis Type 4.
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Newborn Low Blood SugarQiu isExperienced. Learn about Newborn Low Blood Sugar.
- Non-Langerhans-Cell Histiocytosis
- Osteochondritis DissecansQiu isExperienced. Learn about Osteochondritis Dissecans.
- OsteomalaciaQiu isExperienced. Learn about Osteomalacia.
- Pectus CarinatumQiu isExperienced. Learn about Pectus Carinatum.
- Pectus ExcavatumQiu isExperienced. Learn about Pectus Excavatum.
- Prader-Willi SyndromeQiu isExperienced. Learn about Prader-Willi Syndrome.
- Precocious PubertyQiu isExperienced. Learn about Precocious Puberty.
- Propionic AcidemiaQiu isExperienced. Learn about Propionic Acidemia.
- ReticulohistiocytomaQiu isExperienced. Learn about Reticulohistiocytoma.
- Rubinstein-Taybi SyndromeQiu isExperienced. Learn about Rubinstein-Taybi Syndrome.
- Small for Gestational AgeQiu isExperienced. Learn about Small for Gestational Age.
- SplenomegalyQiu isExperienced. Learn about Splenomegaly.
- Swyer SyndromeQiu isExperienced. Learn about Swyer Syndrome.
- Trisomy 12 MosaicismQiu isExperienced. Learn about Trisomy 12 Mosaicism.
- Turner SyndromeQiu isExperienced. Learn about Turner Syndrome.
- Ventricular Septal Defects
- Vitamin B12 Deficiency Anemia
- Von Gierke DiseaseQiu isExperienced. Learn about Von Gierke Disease.
- X-Linked HypophosphatemiaQiu isExperienced. Learn about X-Linked Hypophosphatemia.