Overview
Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider in Phoenix, Arizona. Dr. Knoll is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Fabry Disease, Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Knoll is currently accepting new patients.
Her clinical research consists of co-authoring 4 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- EPO
- HMO
- PPO
Accepted plan types not found. Please verify directly with the provider.
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1919 E Thomas Rd, Phoenix, AZ 85016
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.
Theresa Grebe is a Medical Genetics specialist and a Pediatrics provider in Phoenix, Arizona. Dr. Grebe is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Chromosome 6 Uniparental Disomy, Temple Syndrome, Hypotonia, and Chromosome 13q Duplication. Dr. Grebe is currently accepting new patients.
Phoenix Children's Hospital
Shagun Kaur is a Pediatrics specialist and a Medical Genetics provider in Phoenix, Arizona. Dr. Kaur has been practicing medicine for over 9 years and is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Classic Galactosemia, Galactose Epimerase Deficiency, Galactosemia, and Hydranencephaly. Dr. Kaur is currently accepting new patients.
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
- Advanced
- Fabry DiseaseDr. Knoll isAdvanced. Learn about Fabry Disease.
- Glycogen Storage Disease Type 3Dr. Knoll isAdvanced. Learn about Glycogen Storage Disease Type 3.
- Joubert SyndromeDr. Knoll isAdvanced. Learn about Joubert Syndrome.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Mucopolysaccharidoses (MPS)Dr. Knoll isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Experienced
- 15q11.2 MicrodeletionDr. Knoll isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Knoll isExperienced. Learn about 3p Deletion Syndrome.
- Beckwith-Wiedemann SyndromeDr. Knoll isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Cantu SyndromeDr. Knoll isExperienced. Learn about Cantu Syndrome.
- Chromosome 12p DeletionDr. Knoll isExperienced. Learn about Chromosome 12p Deletion.
- Chromosome 13q DuplicationDr. Knoll isExperienced. Learn about Chromosome 13q Duplication.