Overview
Caleb Bupp is a Medical Genetics provider in Grand Rapids, Michigan. Dr. Bupp is rated as an Experienced provider by MediFind in the treatment of Corpus Callosum Agenesis. 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 1 article in the study of Corpus Callosum Agenesis.
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.
Helga Toriello is a Medical Genetics provider in Grand Rapids, Michigan. Dr. Toriello is rated as an Advanced provider by MediFind in the treatment of Corpus Callosum Agenesis. Her top areas of expertise are Toriello-Carey Syndrome, Brachydactyly, Micrognathia, and Corpus Callosum Agenesis.
Spectrum Health Hospitals
Linda Rossetti is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Rossetti has been practicing medicine for over 9 years and is rated as an Advanced provider by MediFind in the treatment of Corpus Callosum Agenesis. Her top areas of expertise are Miller-Dieker Syndrome, Smith-Magenis Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion. Dr. Rossetti is currently accepting new patients.
Spectrum Health Primary Care Partners
Jessica Priestley is a Medical Genetics specialist and a Pediatrics provider in Kentwood, Michigan. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Corpus Callosum Agenesis. Her top areas of expertise are Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley 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.