The 20 Best GABA-Transaminase Deficiency Doctors Near Me in Ann Arbor, MI
Find the Top GABA-Transaminase Deficiency Experts and Specialists
U Of M Radiology
Gary Luker is a Radiologist and a Pediatric Radiologist practicing medicine in Ann Arbor, Michigan. Dr. Luker is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Myeloproliferative Neoplasms (MPN), Tracheoesophageal Fistula, Posterior Urethral Valves, Chondrodystrophy, and Hepato-Pancreato-Biliary Surgery. Dr. Luker is board certified in Diagnostic Radiology and Pediatric Radiology.
C. S. Mott Children's Hospital
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of GABA-Transaminase Deficiency. He is also highly rated in 129 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Maple Syrup Urine Disease. Dr. Quinonez is board certified in Pediatrics, Clinical Biochemical Genetics, and Clinical Genetics & Genomics.
Domino's Farms
Dr. Lee earned her M.D. from Ross University School of Medicine in 2013, and completed Pediatric Residency at Ascension St. John Hospital in Grosse Point, MI, where she served as a Chief Pediatric Resident during her final year of residency. She completed Categorical Medical Genetics Residency at the University of Michigan in 2019. Following this she accepted a dual faculty position as a Clinical Lecturer in the Department of Pediatrics and Department of Internal Medicine for one year, before returning to Fellowship in 2020 to complete additional dedicated training in Medical Biochemical Genetics. After completion of Medical Biochemical Genetics Fellowship, she resumed her faculty position as a Clinical Assistant Professor in 2021. She is board certified in Pediatrics, and in Clinical and General Genetics.She has a dual faculty appointment in the Department of Pediatrics and the Department of Internal Medicine. As a faculty member in the Department of Pediatrics, she sees patients in the Pediatric Genetics and Biochemical Genetics Clinics, in addition to the newly created Multidisciplinary Genetics of Hearing Loss Clinic. As a faculty member in the Department of Internal Medicine, she sees patients in the Adult Medical Genetics and Cancer Genetics Clinics, in addition to patients with atypical diabetes and/or lipodystrophy in collaboration with MEND.In addition to her clinical responsibilities, Dr. Lee also enjoys spending time teaching and discussing various aspects of genetics with fellows, pediatric residents, medical students, and genetic counseling students. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 138 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome. Dr. Lee is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.
Domino's Farms
Cooking, spending time with my family. Dr. Ames is rated as an Advanced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Cardiomyopathic Lentiginosis, Cardiofaciocutaneous Syndrome, and Noonan Syndrome. Dr. Ames is board certified in Pediatrics, Clinical Genetics & Genomics, and Medical Biochemical Genetics.
C. S. Mott Children's Hospital
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 50 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome). Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics.
IM Hospital Medicine
Vijay Singh, M.D., M.P.H., M.S., F.A.A.F.P., Clinical Associate Professor in the Departments of Internal Medicine, Emergency Medicine, and Family Medicine, earned his medical degree from Northwestern University’s Feinberg School of Medicine, and master’s degree in public health and post-doctoral research fellowship from the Bloomberg School of Public Health at Johns Hopkins University. His family medicine residency training was at the University of California at Los Angeles, where he served as an academic chief resident. He additionally obtained a master's degree in health and health care research at the University of Michigan, where he completed the Robert Wood Johnson Foundation Clinical Scholars Program.Dr. Singh is a board-certified family medicine physician who works clinically in Medical Short Stay Unit, part of the Division of Hospital Medicine. His research interest is in health care identification of and response to intimate partner violence and adolescent dating violence. His research has been supported by grants from the World Health Organization, American Academy of Family Physicians Foundation, Society of Teachers of Family Medicine Foundation, and Michigan Institute for Clinical and Health Research. He is a fellow of the American Academy of Family Physicians, member of the University of Michigan Injury Prevention Center and Institute for Healthcare Policy and Innovation. Dr. Singh is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. His clinical expertise encompasses Malonyl-CoA Decarboxylase Deficiency, Succinic Semialdehyde Dehydrogenase Deficiency, GABA-Transaminase Deficiency, and X-Linked Creatine Deficiency.
IM Hospital Medicine
Jigisha Patel is an Internal Medicine provider practicing medicine in Ann Arbor, Michigan. Dr. Patel is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 1 other condition, according to our data. Her clinical expertise encompasses GABA-Transaminase Deficiency, Malonyl-CoA Decarboxylase Deficiency, Succinic Semialdehyde Dehydrogenase Deficiency, Colonoscopy, and Endoscopy. Dr. Patel is board certified in Internal Medicine.
C. S. Mott Children's Hospital
Dr. Thomas Michniacki was raised in Memphis, Michigan and attended the University of Michigan for his undergraduate studies. Following graduation from the University of Michigan Medical School, he completed his pediatric residency training at the University of Colorado/Children’s Hospital Colorado. Dr. Michniacki returned to his home state of Michigan for his fellowship training in pediatric hematology/oncology at the University of Michigan and is now a faculty member within the department. His clinical and research interests include immune-mediated hematologic disorders, bone marrow failure syndromes/aplastic anemia and primary immunodeficiencies. He enjoys attending University of Michigan sporting events and exploring the city of Ann Arbor with his wife. Dr. Michniacki is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. He is also highly rated in 22 other conditions, according to our data. His clinical expertise encompasses Aplastic Anemia, Febrile Neutropenia, Hereditary Spherocytosis, Hemophagocytic Lymphohistiocytosis, and Bone Marrow Transplant. Dr. Michniacki is board certified in Pediatric Hematology-Oncology and Pediatrics.
C. S. Mott Children's Hospital
Christina Sloan is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Sloan is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Duplication, Chromosome 8p Deletion, Delayed Growth, and Fragile XE Syndrome. Dr. Sloan is board certified in Medical Biochemical Genetics and Clinical Genetics & Genomics.
C. S. Mott Children's Hospital
Amy Filbrun is a Pediatrics specialist and a Pediatric Pulmonologist practicing medicine in Ann Arbor, Michigan. Dr. Filbrun is rated as an Experienced provider by MediFind in the treatment of GABA-Transaminase Deficiency. She is also highly rated in 18 other conditions, according to our data. Her clinical expertise encompasses Congenital Unilateral Pulmonary Hypoplasia, Cystic Fibrosis, Secondary Immunodeficiency (SID), and Newborn Jaundice.
Last Updated: 04/28/2026






