Overview
Laurie Seaver is a Medical Genetics provider practicing medicine in Grand Rapids, Michigan.
Dr. Seaver is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Hypotonia, 1p36 Deletion Syndrome, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome.
She is actively involved in clinical research, co-authoring 40 peer reviewed articles and participating in 1 clinical trial. Dr. Seaver 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
- HMO
- INDEMNITY
- 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.
1 Clinical Trials
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Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Priestley is highly rated in 21 conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics. Dr. Priestley is currently accepting new patients.
Corewell Health Grand Rapids Hospitals Cancer Genetics - Lemmen-Holton
Paul Mark is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Mark is highly rated in 4 conditions, according to our data. His clinical expertise encompasses VACTERL Association, Chromosome 21q Deletion, Peters Plus Syndrome, and Hypotonia. Dr. Mark is board certified in American Board Of Medical Genetics And Genomics. Dr. Mark is currently accepting new patients.
Frequently Asked Questions about Dr. Laurie H. Seaver
How do I make an appointment with Dr. Laurie H. Seaver?
You can book an appointment with Dr. Laurie H. Seaver by calling their office at 616-391-2700. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Laurie H. Seaver a top-rated expert for Hypotonia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Laurie H. Seaver is classified as an Advanced expert for Hypotonia, 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. Laurie H. Seaver specialize in?
While Dr. Laurie H. Seaver is a Medical Genetics, they have specific expertise in Hypotonia, 1p36 Deletion Syndrome, and Smith-Magenis Syndrome. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Laurie H. Seaver participate in research or clinical trials?
Yes. Dr. Laurie H. Seaver has published 40 articles and abstracts on conditions like Hypotonia. You can view a list of Dr. Laurie H. Seaver's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Laurie H. Seaver accept my insurance?
Dr. Laurie H. Seaver accepts most major insurance plans, including Blue Cross Blue Shield and Humana. We recommend calling the office directly at 616-391-2700 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
- 1p36 Deletion SyndromeDr. Seaver isAdvanced. Learn about 1p36 Deletion Syndrome.
- HypotoniaDr. Seaver isAdvanced. Learn about Hypotonia.
- Smith-Magenis SyndromeDr. Seaver isAdvanced. Learn about Smith-Magenis Syndrome.
- Experienced
- Aplasia Cutis CongenitaDr. Seaver isExperienced. Learn about Aplasia Cutis Congenita.
- Arthrogryposis Multiplex CongenitaDr. Seaver isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Cardiofaciocutaneous SyndromeDr. Seaver isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Clouston SyndromeDr. Seaver isExperienced. Learn about Clouston Syndrome.
- Congenital ContracturesDr. Seaver isExperienced. Learn about Congenital Contractures.
- Costello SyndromeDr. Seaver isExperienced. Learn about Costello Syndrome.
- Ectodermal DysplasiasDr. Seaver isExperienced. Learn about Ectodermal Dysplasias.
- Familial Short Stature (FSS)Dr. Seaver isExperienced. Learn about Familial Short Stature (FSS).
- Idiopathic Short Stature (ISS)Dr. Seaver isExperienced. Learn about Idiopathic Short Stature (ISS).
- MosaicismDr. Seaver isExperienced. Learn about Mosaicism.
- Potocki-Lupski SyndromeDr. Seaver isExperienced. Learn about Potocki-Lupski Syndrome.
- Pyruvate Carboxylase DeficiencyDr. Seaver isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- RASopathiesDr. Seaver isExperienced. Learn about RASopathies.
- Short Stature (Growth Disorders)Dr. Seaver isExperienced. Learn about Short Stature (Growth Disorders).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency