Overview
Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona.
Dr. Knoll is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Multiple Sulfatase Deficiency.
She is actively involved in clinical research, co-authoring 8 peer reviewed articles. Dr. Knoll is currently accepting new patients.
Specialties
Licenses
Languages Spoken
Gender
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.
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Kristin Lindstrom is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Phoenix, Arizona. Dr. Lindstrom is highly rated in 5 conditions, according to our data. Her clinical expertise encompasses 1p36 Deletion Syndrome, Phenylketonuria (PKU), Floating-Harbor Syndrome, and Kozlowski Warren Fisher Syndrome.
Frequently Asked Questions about Dr. Jasmine B. Knoll
How do I make an appointment with Dr. Jasmine B. Knoll?
You can book an appointment with Dr. Jasmine B. Knoll by calling their office at 602-933-0930. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Jasmine B. Knoll a top-rated expert for Fabry Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Jasmine B. Knoll is classified as an Advanced expert for Fabry Disease, 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. Jasmine B. Knoll specialize in?
While Dr. Jasmine B. Knoll is a Medical Genetics, they have specific expertise in Fabry Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), and Megalencephalic Leukoencephalopathy with Subcortical Cysts. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Jasmine B. Knoll participate in research or clinical trials?
Yes. Dr. Jasmine B. Knoll has published 8 articles and abstracts on conditions like Fabry Disease. You can view a list of Dr. Jasmine B. Knoll's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Jasmine B. Knoll accept my insurance?
Dr. Jasmine B. Knoll accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 602-933-0930 to verify that your specific plan is currently accepted before your visit.
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
- Beta-MannosidosisDr. Knoll isAdvanced. Learn about Beta-Mannosidosis.
- 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)
- Multiple Sulfatase DeficiencyDr. Knoll isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Phenylketonuria (PKU)Dr. Knoll isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- 15q11.2 MicrodeletionDr. Knoll isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Knoll isExperienced. Learn about 3p Deletion Syndrome.
- Alpha MannosidosisDr. Knoll isExperienced. Learn about Alpha Mannosidosis.
- 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.
- Chromosome 15q DeletionDr. Knoll isExperienced. Learn about Chromosome 15q Deletion.
- Chromosome 18p DeletionDr. Knoll isExperienced. Learn about Chromosome 18p Deletion.
- Chromosome 21q DeletionDr. Knoll isExperienced. Learn about Chromosome 21q Deletion.
- Chromosome 4q DeletionDr. Knoll isExperienced. Learn about Chromosome 4q Deletion.
- Chromosome 6q DeletionDr. Knoll isExperienced. Learn about Chromosome 6q Deletion.
- Chromosome 7p DeletionDr. Knoll isExperienced. Learn about Chromosome 7p Deletion.
- Chromosome 9p DeletionDr. Knoll isExperienced. Learn about Chromosome 9p Deletion.
- CitrullinemiaDr. Knoll isExperienced. Learn about Citrullinemia.
- Dihydropteridine Reductase DeficiencyDr. Knoll isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Distal 18q Deletion SyndromeDr. Knoll isExperienced. Learn about Distal 18q Deletion Syndrome.
- Gaucher DiseaseDr. Knoll isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Knoll isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Knoll isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Knoll isExperienced. Learn about Gaucher Disease Type 3.
- Glutaric Acidemia Type 1Dr. Knoll isExperienced. Learn about Glutaric Acidemia Type 1.
- Hemi 3 SyndromeDr. Knoll isExperienced. Learn about Hemi 3 Syndrome.
- HNRNPH2-Related DisorderDr. Knoll isExperienced. Learn about HNRNPH2-Related Disorder.
- HomocystinuriaDr. Knoll isExperienced. Learn about Homocystinuria.
- HyperlysinemiaDr. Knoll isExperienced. Learn about Hyperlysinemia.
- HypotoniaDr. Knoll isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Knoll isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Jacobsen SyndromeDr. Knoll isExperienced. Learn about Jacobsen Syndrome.
- Leigh SyndromeDr. Knoll isExperienced. Learn about Leigh Syndrome.
- MacroglossiaDr. Knoll isExperienced. Learn about Macroglossia.
- Marshall-Smith SyndromeDr. Knoll isExperienced. Learn about Marshall-Smith Syndrome.
- Maternal HyperphenylalaninemiaDr. Knoll isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Maternally Inherited Leigh SyndromeDr. Knoll isExperienced. Learn about Maternally Inherited Leigh Syndrome.
- Megalencephaly-Capillary Malformation Syndrome
- Methylmalonic AcidemiaDr. Knoll isExperienced. Learn about Methylmalonic Acidemia.
- MicrocephalyDr. Knoll isExperienced. Learn about Microcephaly.
- Miller-Dieker SyndromeDr. Knoll isExperienced. Learn about Miller-Dieker Syndrome.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A)
- Myhre SyndromeDr. Knoll isExperienced. Learn about Myhre Syndrome.
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- Niemann-Pick DiseaseDr. Knoll isExperienced. Learn about Niemann-Pick Disease.
- Ornithine Transcarbamylase DeficiencyDr. Knoll isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Ornithine Translocase DeficiencyDr. Knoll isExperienced. Learn about Ornithine Translocase Deficiency.
- Perlman SyndromeDr. Knoll isExperienced. Learn about Perlman Syndrome.
- Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy
- Propionic AcidemiaDr. Knoll isExperienced. Learn about Propionic Acidemia.
- Proteus SyndromeDr. Knoll isExperienced. Learn about Proteus Syndrome.
- Proteus-Like SyndromeDr. Knoll isExperienced. Learn about Proteus-Like Syndrome.
- Simpson-Golabi-Behmel SyndromeDr. Knoll isExperienced. Learn about Simpson-Golabi-Behmel Syndrome.
- Smith-Magenis SyndromeDr. Knoll isExperienced. Learn about Smith-Magenis Syndrome.
- Tyrosinemia Type 1Dr. Knoll isExperienced. Learn about Tyrosinemia Type 1.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- WAGR SyndromeDr. Knoll isExperienced. Learn about WAGR Syndrome.
- Weaver SyndromeDr. Knoll isExperienced. Learn about Weaver Syndrome.
- Y Chromosome InfertilityDr. Knoll isExperienced. Learn about Y Chromosome Infertility.