Overview
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ahmad is highly rated in 6 conditions, according to our data. Their top areas of expertise are Propionic Acidemia, Pompe Disease, Inborn Amino Acid Metabolism Disorder, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is currently accepting new patients.
Their clinical research consists of co-authoring 35 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance plans
- Priority Health
- Blue Cross Blue Shield
- McLaren Health
- Humana
Locations
1500 E Medical Ctr, Suite 0331, Ann Arbor, MI 48109
1500 E Medical Ctr Dr, Ann Arbor, MI 48109
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.
2 Clinical Trials
Donna Martin is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Martin is highly rated in 4 conditions, according to our data. Her top areas of expertise are CHARGE Syndrome, Chromosome 2p Duplication, Autism Spectrum Disorder, and Coloboma.
Kirit Pindolia is a Medical Genetics provider in Canton, Michigan. Dr. Pindolia is highly rated in 1 condition, according to our data. His top area of expertise is Biotinidase Deficiency.
Debbie Gipson is a Pediatrics specialist and a Nephrologist in Ann Arbor, Michigan. Dr. Gipson is highly rated in 10 conditions, according to our data. Her top areas of expertise are Minimal Change Disease, Focal Segmental Glomerulosclerosis, Nephrotic Syndrome, Glomerulonephritis, and Kidney Transplant. Dr. Gipson is currently accepting new patients.
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.
- Distinguished
- Pompe Disease
- Propionic Acidemia
- Advanced
- Homocystinuria
- Inborn Amino Acid Metabolism Disorder
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Phenylketonuria (PKU)
- Experienced
- Alpha Thalassemia
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly Taurinuria
- Carbamoyl Phosphate Synthetase 1 Deficiency