Overview
Paul Mark is a Medical Genetics specialist and an Obstetrics and Gynecologist in Grand Rapids, Michigan. Dr. Mark is rated as a Distinguished provider by MediFind in the treatment of VACTERL Association. His top areas of expertise are VACTERL Association, Peters Plus Syndrome, Hypotonia, and Chromosome 21q Deletion. Dr. Mark is currently accepting new patients.
His clinical research consists of co-authoring 34 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 VACTERL Association.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- HMO
- POS
Locations
100 Michigan Ave Ne, Grand Rapids, MI 49503
25 Michigan St Ne, Corewell Health Grand Rapi, Grand Rapids, MI 49503
100 Michigan St Ne, 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.
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 VACTERL Association. 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 VACTERL Association. 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
- Distinguished
- VACTERL AssociationDr. Mark isDistinguished. Learn about VACTERL Association.
- Advanced
- HypotoniaDr. Mark isAdvanced. Learn about Hypotonia.
- Peters Plus SyndromeDr. Mark isAdvanced. Learn about Peters Plus Syndrome.
- Experienced
- Autism Spectrum DisorderDr. Mark isExperienced. Learn about Autism Spectrum Disorder.
- BlepharophimosisDr. Mark isExperienced. Learn about Blepharophimosis.
- Chromosome 21q DeletionDr. Mark isExperienced. Learn about Chromosome 21q Deletion.
- Imperforate AnusDr. Mark isExperienced. Learn about Imperforate Anus.
- Joubert SyndromeDr. Mark isExperienced. Learn about Joubert Syndrome.
- OmphaloceleDr. Mark isExperienced. Learn about Omphalocele.