Experienced in HNRNPH2-Related Disorder

Dr. Shagun Kaur

Pediatrics | Medical Genetics
1920 E Cambridge Ave Ste 201, 
Phoenix, AZ 
Accepting New Patients

Experienced in HNRNPH2-Related Disorder
1920 E Cambridge Ave Ste 201, 
Phoenix, AZ 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

Shagun Kaur is a Pediatrics specialist and a Medical Genetics provider in Phoenix, Arizona. Dr. Kaur is rated as an Experienced 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.

Her clinical research consists of co-authoring 11 peer reviewed articles. MediFind looks at clinical research from the past 15 years.

Specialties
Pediatrics
Medical Genetics
Licenses
Clinical Genetics in PA
Languages Spoken
English
Hindi
Punjabi
Gender
Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO
Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Health Net

Accepted plan types not found. Please verify directly with the provider.

Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Managed Medicaid
  • OTHER MANAGED MEDICAID
Medica
  • EPO
  • HMO
  • PPO
Medicaid
  • OTHER MEDICAID
  • STATE MEDICAID
MercyCare
  • EPO
  • HMO
UnitedHealthcare
  • EPO
  • HMO
  • POS
  • PPO
View 4 Less Insurance Carriers -

Locations

1920 E Cambridge Ave Ste 201, Phoenix, AZ 85006
Call: 602-933-0500

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.


11 Total Publications

Integration of Genome and Epigenetic Testing in the Diagnostic Evaluation of Developmental Delay: Differentiating Börjeson-Forssman-Lehmann (BFLS) and White-Kernohan (WHIKERS) Syndromes.
Integration of Genome and Epigenetic Testing in the Diagnostic Evaluation of Developmental Delay: Differentiating Börjeson-Forssman-Lehmann (BFLS) and White-Kernohan (WHIKERS) Syndromes.
Journal: Genes
Published: July 11, 2025
View All 11 Publications
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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 Congenital Bowing of Long Bones. Dr. Grebe is currently accepting new patients.

Experienced in HNRNPH2-Related Disorder
Dr. Jasmine B. Knoll
Medical Genetics | Pediatrics
Experienced in HNRNPH2-Related Disorder
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Medical Genetics | Pediatrics

Phoenix Children's Hospital

1919 E Thomas Rd, 
Phoenix, AZ 
 (1.1 miles away)
602-933-0930
Languages Spoken:
English
See accepted insurances
Accepting New Patients

Jasmine Knoll is a Medical Genetics specialist and a Pediatrics provider in Phoenix, Arizona. Dr. Knoll is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Fabry Disease, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Multiple Sulfatase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. Dr. Knoll is currently accepting new patients.

VIEW MORE HNRNPH2-RELATED DISORDER DOCTORS

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

Find Dr. Kaur's expertise for a condition
ConditionClose
      • Advanced
      • Classic Galactosemia
        Dr. Kaur is
        Advanced
        . Learn about Classic Galactosemia.
        See more Classic Galactosemia experts
      • Galactose Epimerase Deficiency
        Dr. Kaur is
        Advanced
        . Learn about Galactose Epimerase Deficiency.
        See more Galactose Epimerase Deficiency experts
      • Galactosemia
        Dr. Kaur is
        Advanced
        . Learn about Galactosemia.
        See more Galactosemia experts
      • Hydranencephaly
        Dr. Kaur is
        Advanced
        . Learn about Hydranencephaly.
        See more Hydranencephaly experts
      • Experienced
      • 2q37 Deletion Syndrome
        Dr. Kaur is
        Experienced
        . Learn about 2q37 Deletion Syndrome.
        See more 2q37 Deletion Syndrome experts
      • 47 XYY Syndrome
        Dr. Kaur is
        Experienced
        . Learn about 47 XYY Syndrome.
        See more 47 XYY Syndrome experts
      • Aase Syndrome
        Dr. Kaur is
        Experienced
        . Learn about Aase Syndrome.
        See more Aase Syndrome experts
      • Abruzzo-Erickson Syndrome
        Dr. Kaur is
        Experienced
        . Learn about Abruzzo-Erickson Syndrome.
        See more Abruzzo-Erickson Syndrome experts
      • Achalasia Microcephaly Syndrome
        Dr. Kaur is
        Experienced
        . Learn about Achalasia Microcephaly Syndrome.
        See more Achalasia Microcephaly Syndrome experts
      • Acrocephalopolydactyly
        Dr. Kaur is
        Experienced
        . Learn about Acrocephalopolydactyly.
        See more Acrocephalopolydactyly experts
      View All 144 Experienced Conditions
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