Overview
Jinglan Liu is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania.
Dr. Liu is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Chromosome 22 Duplication, Chromosome 13q Deletion, Mosaic Trisomy 9, and Cornelia De Lange Syndrome.
She is actively involved in clinical research, co-authoring 15 peer reviewed articles.
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Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
Childrens Health Care Associates Inc
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Jennifer Kalish is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Kalish is highly rated in 19 conditions, according to our data. Her clinical expertise encompasses Beckwith-Wiedemann Syndrome, Macroglossia, Hemi 3 Syndrome, Glossectomy, and Pancreatectomy.
Nemours Children's Hospital, Delaware
Dr. Michael B. Bober is a pediatric geneticist and an authority on skeletal dysplasias, brittle bone disease, primordial dwarfism and other genetic disorders of the skeleton. He is a frequent guest lecturer, accomplished author and consultant for numerous television networks, here and abroad. Dr. Bober is highly rated in 69 conditions, according to our data. His clinical expertise encompasses Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2), Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1), Achondroplasia, Osteotomy, and Adenoidectomy. Dr. Bober is board certified in American Board Of Medical Genetics And Genomics.
Frequently Asked Questions about Dr. Jinglan W. Liu
How do I make an appointment with Dr. Jinglan W. Liu?
You can book an appointment with Dr. Jinglan W. Liu by calling their office at 215-955-6988. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Jinglan W. Liu a top-rated expert for Chromosome 22 Duplication?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Jinglan W. Liu is classified as an Distinguished expert for Chromosome 22 Duplication, 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.
What conditions does Dr. Jinglan W. Liu specialize in?
While Dr. Jinglan W. Liu is a Medical Genetics, they have specific expertise in Chromosome 22 Duplication, Chromosome 13q Deletion, and Mosaic Trisomy 9. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Jinglan W. Liu participate in research or clinical trials?
Yes. Dr. Jinglan W. Liu has published 15 articles and abstracts on conditions like Chromosome 22 Duplication. You can view a list of Dr. Jinglan W. Liu'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
- Chromosome 22 DuplicationDr. Liu isDistinguished. Learn about Chromosome 22 Duplication.
- Advanced
- Chromosome 13q DeletionDr. Liu isAdvanced. Learn about Chromosome 13q Deletion.
- Experienced
- Cornelia De Lange SyndromeDr. Liu isExperienced. Learn about Cornelia De Lange Syndrome.
- Mosaic Trisomy 9Dr. Liu isExperienced. Learn about Mosaic Trisomy 9.