
Overview
Amna Othman is a Medical Genetics provider practicing medicine in Ann Arbor, Michigan.
Dr. Othman is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Rhizomelic Syndrome, Pfeiffer Syndrome, and Williams Syndrome.
She is actively involved in clinical research, co-authoring 6 peer reviewed articles.
Specialties
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Locations
1540 E Hospital Dr, Floor 6 Reception C, 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.
University Of Michigan Pediatric Genetics Clinic
Donna Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Martin is highly rated in 1 condition, according to our data. Her clinical expertise encompasses CHARGE Syndrome and Neurofibromatosis Type 1 (NF1). Dr. Martin is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2023. Dr. Martin is currently accepting new patients.
Taubman Center
Dr. Askari is interested in caring for patients with gastrointestinal problems with particular specialization in liver diseases. People interested in learning more about our Wilson Disease Clinic are encouraged to view the following web site: Wilson Disease Center of Excellence. Dr. Askari is highly rated in 37 conditions, according to our data. His clinical expertise encompasses Wilson Disease, Menkes Disease, Primary Biliary Cholangitis, Endoscopy, and Gastrectomy. Dr. Askari is board certified in Gastroenterology. Dr. Askari is currently accepting new patients.
Taubman Center
John K. Fink, MD, is a professor in the Department of Neurology and director of the Neurogenetic Disorders Program in the University of Michigan Medical School. He directs basic science laboratory research focused on identifying genes and mechanisms responsible for age-dependent neurologic degeneration; and on developing treatments for these conditions.Fink's laboratory investigates the molecular basis of inherited neurologic and psychiatric disorders. His clinical expertise focuses on inherited and degenerative disorders of the nervous system. Dr. Fink evaluates individuals of all ages, from infancy through senescence with these disorders, which include lysosomal storage disorders (such as Gaucher disease, Niemann-Pick disease and Fabry disease), ataxias (including Friedreich's ataxia), leukodystrophies (such as Krabbe, CADASIL and adrenoleukodystrophy), familial dystonia, primary lateral sclerosis, Wilson's disease, familial motor neuron disease (including familial amyotrophic lateral sclerosis), familial dementia, and a group of inherited spinal cord disorders known collectively as the Hereditary Spastic Paraplegias (HSPs).Dr. Fink came to the University of Michigan in 1990 as an assistant professor of neurology and director of the Neurogenetic Disorders Clinic. The program provides care and evaluation for individuals and families with inherited and degenerative neurologic disorders; and clinical and molecular laboratory training for physicians and scientists studying these disorders. He was promoted to associate professor in 1996 and professor in 2005.Board-certified in neurology and medical genetics, Dr. Fink received his medical degree in 1980 from the Medical College of Ohio in Toledo. Following internship at the Mayo Clinic in Rochester, Minnesota, he completed a neurology residency in 1984 at the University of Virginia in Charlottesville. Subsequently, he trained in developmental and metabolic neurology and medical genetics at the National Institutes of Health.Dr. Fink has served as the Medical Advisor to the Spastic Paraplegia Foundation since its establishment (2002), and serves as ad hoc reviewer for numerous journals and NIH study sections.A member of the American Society of Human Genetics, American Academy of Neurology, American Neurological Association and the American College of Genetics, Dr. Fink received the Derek Denny-Brown Neurological Scholar Award from the American Neurological Association in 2002. In addition, he has been elected by peers to Best Doctors in America annually since 2001. Dr. Fink is highly rated in 48 conditions, according to our data. His clinical expertise encompasses Spastic Paraplegia Type 7, Spastic Paraplegia Type 2, Primary Lateral Sclerosis, and CACH Syndrome. Dr. Fink is board certified in Neurology and Clinical Genetics. Dr. Fink is currently accepting new patients.
U Of M Pathology
Dr. Noah Brown received a B.S. in Biology from Stanford University in Stanford, California in 1999 and an M.D. from the University of Michigan in 2004. He also pursued both residency and fellowship training at the University of Michigan. His training included a residency in Anatomic and Clinical Pathology (2008-2013), and fellowships in Hematopathology (2011-2012) and Molecular and Genetic Pathology (2013-2014).Dr. Brown is board certified in Anatomic and Clinical Pathology, Hematopathology and Molecular and Genetic Pathology. He was recently awarded the Association for Molecular Pathology Young Investigator Award. He joined the faculty of the Department of Pathology at the University of Michigan in 2014 as an Assistant Professor. He is now the Medical Director of the Molecular Diagnostics Laboratory. Dr. Brown is highly rated in 15 conditions, according to our data. His clinical expertise encompasses Chronic Myelogenous Leukemia (CML), Philadelphia-Negative Chronic Myeloid Leukemia, Childhood Acute Myeloid Leukemia, and Acute Myeloid Leukemia (AML). Dr. Brown is board certified in Hematopathology, Pathology-Anatomic/Pathology-Clinical, and Pathology-Molecular Genetic.
University Of Michigan Pediatric Genetics Clinic
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Rachel Upjohn Building
Melvin Mcinnis is a Psychiatrist and a Medical Genetics provider practicing medicine in Ann Arbor, Michigan. Dr. Mcinnis is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Bipolar Disorder (BPD), Major Depression, Schizophrenia, and Post-Traumatic Stress Disorder (PTSD). Dr. Mcinnis is currently accepting new patients.
Frequently Asked Questions about Dr. Amna A. Othman
How do I make an appointment with Dr. Amna A. Othman?
You can book an appointment with Dr. Amna A. Othman by calling their office at 734-764-0579. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Amna A. Othman a top-rated expert for Rhizomelic Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Amna A. Othman is classified as an Advanced expert for Rhizomelic Syndrome, 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. Amna A. Othman specialize in?
While Dr. Amna A. Othman is a Medical Genetics, they have specific expertise in Rhizomelic Syndrome, Pfeiffer Syndrome, and Williams Syndrome. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Amna A. Othman participate in research or clinical trials?
Yes. Dr. Amna A. Othman has published 6 articles and abstracts on conditions like Rhizomelic Syndrome. You can view a list of Dr. Amna A. Othman's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Rhizomelic SyndromeDr. Othman isAdvanced. Learn about Rhizomelic Syndrome.
- Experienced
- Pfeiffer SyndromeDr. Othman isExperienced. Learn about Pfeiffer Syndrome.
- Williams SyndromeDr. Othman isExperienced. Learn about Williams Syndrome.





