Dr. Caleb P. Bupp
Overview
Caleb Bupp is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Bupp has been practicing medicine for over 17 years and is rated as an Experienced provider by MediFind in the treatment of Cortical Dysplasia. His top areas of expertise are Marshall-Smith Syndrome, Hypotonia, Campomelia Cumming Type, and Campomelic Dysplasia.
His clinical research consists of co-authoring 72 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Cortical Dysplasia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
Locations
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
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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Linda Rossetti is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Rossetti has been practicing medicine for over 10 years and is rated as an Advanced provider by MediFind in the treatment of Cortical Dysplasia. Her top areas of expertise are Smith-Magenis Syndrome, Miller-Dieker Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion.
Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Advanced provider by MediFind in the treatment of Cortical Dysplasia. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.
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
- HypotoniaDr. Bupp isAdvanced. Learn about Hypotonia.
- Marshall-Smith SyndromeDr. Bupp isAdvanced. Learn about Marshall-Smith Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeDr. Bupp isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Bupp isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Albright's Hereditary Osteodystrophy
- Autism Spectrum DisorderDr. Bupp isExperienced. Learn about Autism Spectrum Disorder.
- Campomelia Cumming TypeDr. Bupp isExperienced. Learn about Campomelia Cumming Type.
- Campomelic DysplasiaDr. Bupp isExperienced. Learn about Campomelic Dysplasia.