Overview
Caleb Bupp is a Medical Genetics provider in Grand Rapids, Michigan. Dr. Bupp is rated as an Advanced provider by MediFind in the treatment of Hypotonia. His top areas of expertise are Marshall-Smith Syndrome, Hypotonia, Campomelia Cumming Type, and Campomelic Dysplasia. Dr. Bupp is currently accepting new patients.
His clinical research consists of co-authoring 70 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 3 articles in the study of Hypotonia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- HMO
- POS
Locations
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.
Spectrum Health Hospitals
Laurie Seaver is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Seaver is rated as an Advanced provider by MediFind in the treatment of Hypotonia. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.
Spectrum Health Hospitals
Paul Mark is a Medical Genetics specialist and an Obstetrics and Gynecologist in Grand Rapids, Michigan. Dr. Mark is rated as an Advanced provider by MediFind in the treatment of Hypotonia. His top areas of expertise are VACTERL Association, Peters Plus Syndrome, Hypotonia, and Chromosome 21q Deletion. Dr. Mark is currently accepting new patients.
Robert Conway is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Conway is rated as an Advanced provider by MediFind in the treatment of Hypotonia. His top areas of expertise are Hypermethioninemia, Biotinidase Deficiency, Phenylketonuria (PKU), and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Conway 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
- 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.