Overview
Dr. Keegan is a physician-scientist boarded in Medical Genetics. She completed her Medical Genetics training at University of Michigan in 2001 and has been a faculty member in the Department of Pediatrics since 2002. She currently serves as Director of the Division of Genetics, Metabolism, and Genomic Medicine in the Department of Pediatrics. She has served as the Program Director for the Medical Genetics and Genomics Residency Program since 2017. She is Co-Director of the Michigan Medicine NORD Center of Excellence and Medical Director of the Michigan Medical Genetics Laboratory. As a practicing Pediatric Medical Geneticist, she cares for patients with a wide variety of known or suspected genetic disorders and has an interest in undiagnosed rare genetic diseases. She has significant clinical expertise in genetic evaluation of patients with Differences of Sex Development (DSDs). She also participates in a multidisciplinary clinic for patients with Turner syndrome.In her spare time, she likes to travel and spend time at her cottage in Northern Michigan.
Dr. Keegan is highly rated in 3 conditions, according to our data. Her top areas of expertise are Intersex, Aarskog Syndrome, Turner Syndrome, and Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius.
Her clinical research consists of co-authoring 47 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- HMO
- POS
Locations
1540 E Hospital Dr, Floor 6 Reception C, Ann Arbor, MI 48109
Ann Arbor, MI 48109
Additional Areas of Focus
Dr. Keegan 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.
C. S. Mott Children's Hospital
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Ahmad is highly rated in 50 conditions, according to our data. Her top areas of expertise are Pompe Disease, Propionic Acidemia, Von Gierke Disease, and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome).
C. S. Mott Children's Hospital
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, Autism Spectrum Disorder, Coloboma, and Ulnar-Mammary Syndrome.
C. S. Mott Children's Hospital
Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Hannibal is highly rated in 166 conditions, according to our data. His top areas of expertise are Aase Syndrome, CHARGE Syndrome, Cockayne Syndrome Type 2, and Hennekam Syndrome.
Frequently Asked Questions about Dr. Catherine E. Keegan
How do I make an appointment with Dr. Catherine E. Keegan?
You can book an appointment with Dr. Catherine E. Keegan 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. Catherine E. Keegan a top-rated expert for Intersex?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Catherine E. Keegan is classified as an Advanced expert for Intersex, 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. Catherine E. Keegan specialize in?
While Dr. Catherine E. Keegan is a Medical Genetics, they have specific expertise in Intersex, Aarskog Syndrome, and Turner Syndrome. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Catherine E. Keegan participate in research or clinical trials?
Yes. Dr. Catherine E. Keegan has published 47 articles and abstracts on conditions like Intersex. You can view a list of Dr. Catherine E. Keegan's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Catherine E. Keegan accept my insurance?
Dr. Catherine E. Keegan accepts most major insurance plans, including Blue Cross Blue Shield and Humana. We recommend calling the office directly at 734-764-0579 to verify that your specific plan is currently accepted before your visit.
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
- Aarskog SyndromeDr. Keegan isAdvanced. Learn about Aarskog Syndrome.
- IntersexDr. Keegan isAdvanced. Learn about Intersex.
- Turner SyndromeDr. Keegan isAdvanced. Learn about Turner Syndrome.
- Experienced
- 5-Alpha Reductase DeficiencyDr. Keegan isExperienced. Learn about 5-Alpha Reductase Deficiency.
- Brachydactyly Mononen TypeDr. Keegan isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Cortical DysplasiaDr. Keegan isExperienced. Learn about Cortical Dysplasia.
- Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius
- HypospadiasDr. Keegan isExperienced. Learn about Hypospadias.