Overview
Francine Cormier is a Pediatrics provider practicing medicine in Poughkeepsie, New York.
Dr. Cormier is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses Hereditary Ataxia, Hereditary Spastic Paraparesis, Hypertension, and Obesity in Children.
Dr. Cormier 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
- OTHER COMMERCIAL
- OTHER MEDICARE
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- PPO
- 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
2507 South Rd, Poughkeepsie, NY 12601
Bradhurst Avenue Specialty Office
Mitchell Cairo is a Pediatrics provider practicing medicine in Hawthorne, New York. Dr. Cairo is highly rated in 7 conditions, according to our data. His clinical expertise encompasses Primary Mediastinal B-Cell Lymphoma (PMBCL), Anemia, Embryonal Tumor with Multilayered Rosettes, and Gliomatosis Cerebri.
Vassar Brothers Medical Center
Adam Czynski is a Pediatrics provider practicing medicine in Poughkeepsie, New York. Dr. Czynski is highly rated in 1 condition, according to our data. His clinical expertise encompasses Neonatal Abstinence Syndrome and Infant Respiratory Distress Syndrome.
CUIMC/NewYork-Presbyterian Morgan Stanley Children's Hospital
Joshua Milner is a leader in the field of discovery and immunopathogenesis of genetic diseases that lead to allergic symptoms. Among the disorders he has described and/or found major mechanistic insight are PLAID—an immune disorder that leads to lifelong cold urticaria, the glycosylation disorder PGM3 deficiency, ERBIN mutation, CARD11 dominant negative mutations, STAT3 gain-of-function, Hereditary Alpha Tryptasemia Syndrome, IL-6 receptor deficiency, and others. Dr. Milner graduated with an SB in biology from the Massachusetts Institute of Technology (MIT) in 1995 and an MD with distinction in immunology from the Albert Einstein College of Medicine. He completed his residency in pediatrics at the Children’s National Medical Center in Washington, DC, and, as the recipient of the Pediatric Scientist Development Program Fellowship, did his fellowship in allergy and immunology at NIAID. He completed a postdoctoral fellowship with Dr. William E. Paul, NIAID, examining issues of mouse T-cell receptor repertoires before beginning as an investigator in the Laboratory of Allergic Diseases in the NIAID, where he was eventually named chief.Dr. Milner's vision is to establish how genetic variation can help inform diagnosis and care of all patients with allergic disease—rare and common, severe and mild. This is achieved by performing genetic sequencing on samples from patients with allergic disease of all sorts, as well as performing functional studies on the same patient samples, which together help point to specific immune pathways that may be fundamentally causing disease. This comprehensive analysis, when performed in larger populations, will help personalize medicine so that patients can be better categorized for targeted care. Furthermore, this type of research and care requires a coordinated and comprehensive interdisciplinary approach, taking advantage of the expertise across the department of pediatrics and at multiple outpatient sites. Dr. Milner is highly rated in 11 conditions, according to our data. His clinical expertise encompasses Autosomal Dominant Hyper IgE Syndrome, Hyper IgE Syndrome, Multisystem Inflammatory Syndrome in Children (MIS-C), and Hereditary Alpha-Tryptasemia. Dr. Milner is board certified in Allergy And Immunology. Dr. Milner is currently accepting new patients.
Frequently Asked Questions about Dr. Francine L. Cormier
How do I make an appointment with Dr. Francine L. Cormier?
You can book an appointment with Dr. Francine L. Cormier by calling their office at 845-471-2287. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Francine L. Cormier a top-rated expert for Hereditary Ataxia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Francine L. Cormier is classified as an Advanced expert for Hereditary Ataxia, 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. Francine L. Cormier specialize in?
While Dr. Francine L. Cormier is a Pediatrics, they have specific expertise in Hereditary Ataxia, Hereditary Spastic Paraparesis, and Hypertension. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Francine L. Cormier accept my insurance?
Dr. Francine L. Cormier accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 845-471-2287 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
- Hereditary AtaxiaDr. Cormier isAdvanced. Learn about Hereditary Ataxia.
- Hereditary Spastic ParaparesisDr. Cormier isAdvanced. Learn about Hereditary Spastic Paraparesis.
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Cormier isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Asthma in ChildrenDr. Cormier isExperienced. Learn about Asthma in Children.
- Atrial TachycardiaDr. Cormier isExperienced. Learn about Atrial Tachycardia.
- Atrioventricular Nodal Reentrant Tachycardia (AVNRT)
- Gastroesophageal Reflux Disease (GERD)Dr. Cormier isExperienced. Learn about Gastroesophageal Reflux Disease (GERD).
- HypertensionDr. Cormier isExperienced. Learn about Hypertension.
- Lyme DiseaseDr. Cormier isExperienced. Learn about Lyme Disease.
- Multisystem Inflammatory Syndrome in Children (MIS-C)
- Obesity in ChildrenDr. Cormier isExperienced. Learn about Obesity in Children.
- OsteoporosisDr. Cormier isExperienced. Learn about Osteoporosis.
- Paroxysmal Supraventricular Tachycardia (PSVT)
- Vitamin D DeficiencyDr. Cormier isExperienced. Learn about Vitamin D Deficiency.

