Overview
Timothy Moss is a Medical Genetics provider in Grand Rapids, Michigan. Dr. Moss is highly rated in 10 conditions, according to our data. His top areas of expertise are Proteus-Like Syndrome, Proteus Syndrome, Weaver Syndrome, and Simpson-Golabi-Behmel Syndrome.
His clinical research consists of co-authoring 33 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- HMO
- POS
Locations
Additional Areas of Focus
Dr. Moss has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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 highly rated in 3 conditions, according to our data. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Smith-Magenis Syndrome, and Potocki-Lupski Syndrome. Dr. Seaver is currently accepting new patients.
Robert Conway is a Medical Genetics specialist and a Pediatrics provider in Grand Rapids, Michigan. Dr. Conway is highly rated in 7 conditions, according to our data. 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.
Spectrum Health Hospitals
Paul Mark is a Medical Genetics specialist and an Obstetrics and Gynecologist in Grand Rapids, Michigan. Dr. Mark is highly rated in 3 conditions, according to our data. His top areas of expertise are VACTERL Association, Peters Plus Syndrome, Hypotonia, and Chromosome 21q Deletion. Dr. Mark 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
- Beckwith-Wiedemann SyndromeDr. Moss isAdvanced. Learn about Beckwith-Wiedemann Syndrome.
- Cantu SyndromeDr. Moss isAdvanced. Learn about Cantu Syndrome.
- Hemi 3 SyndromeDr. Moss isAdvanced. Learn about Hemi 3 Syndrome.
- Marshall-Smith SyndromeDr. Moss isAdvanced. Learn about Marshall-Smith Syndrome.
- Megalencephaly-Capillary Malformation Syndrome
- Perlman SyndromeDr. Moss isAdvanced. Learn about Perlman Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Moss isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Moss isExperienced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Moss isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Moss isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Moss isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Moss isExperienced. Learn about Aase Syndrome.