Overview
Tomoyasu Higashimoto is a Medical Genetics provider in Ann Arbor, Michigan. Dr. Higashimoto is highly rated in 13 conditions, according to our data. Their top areas of expertise are 3p Deletion Syndrome, Chromosome 9p Deletion, Chromosome 7p Deletion, and Jacobsen Syndrome.
Their clinical research consists of co-authoring 8 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance plans
- Priority Health
- Blue Cross Blue Shield
- McLaren Health
Locations
24 Frank Lloyd Wright Dr, Ann Arbor, MI 48105
1500 E Medical Ctr, Suite 0331, Ann Arbor, MI 48109
1500 E Medical Ctr Dr, Ann Arbor, MI 48109
Additional Areas of Focus
Dr. Higashimoto 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.
Donna Martin is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Martin is highly rated in 1 condition, according to our data. Her top areas of expertise are CHARGE Syndrome and Neurofibromatosis Type 1 (NF1).
Kirit Pindolia is a Medical Genetics provider in Canton, Michigan. Dr. Pindolia is highly rated in 1 condition, according to our data. Their top area of expertise is Biotinidase Deficiency.
Kristin Monaghan is a Medical Genetics provider in Detroit, Michigan. Dr. Monaghan is highly rated in 15 conditions, according to our data. Her top areas of expertise are Hypotonia, Microcephaly Deafness Syndrome, 1p36 Deletion Syndrome, and Early Infantile Epileptic Encephalopathy.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Advanced
- 15q11.2 Microdeletion
- 3p Deletion Syndrome
- Chromosome 12p Deletion
- Chromosome 15q Deletion
- Chromosome 18p Deletion
- Chromosome 21q Deletion
- Experienced
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Homocystinuria
- Maple Syrup Urine Disease
- Methylmalonic Acidemia
- Nevoid Basal Cell Carcinoma Syndrome