Overview
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 highly rated in 138 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. She is actively involved in clinical research, co-authoring 9 peer reviewed articles.
Graduate Institution
Residency
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
24 Frank Lloyd Wright Dr Ste 1300, Lobby C, Ann Arbor, MI 48105
1540 E Hospital Dr, Floor 2 Reception A, Ann Arbor, MI 48109
Additional Areas of Focus
Dr. Lee 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 practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is highly rated in 50 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.
C. S. Mott Children's Hospital
Donna Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Martin is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses CHARGE Syndrome, Autism Spectrum Disorder, Coloboma, and Ulnar-Mammary Syndrome.
Kirit Pindolia is a Medical Genetics provider practicing medicine in Canton, Michigan. Dr. Pindolia is highly rated in 1 condition, according to our data. His clinical expertise encompasses Biotinidase Deficiency.
Frequently Asked Questions about Dr. Kristen N. Lee
How do I make an appointment with Dr. Kristen N. Lee?
You can book an appointment with Dr. Kristen N. Lee by calling their office at 734-647-8902. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Kristen N. Lee a top-rated expert for Biotinidase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Kristen N. Lee is classified as an Advanced expert for Biotinidase Deficiency, 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. Kristen N. Lee specialize in?
While Dr. Kristen N. Lee is a Medical Genetics, they have specific expertise in Biotinidase Deficiency, Delayed Growth, and Beta-Ketothiolase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Kristen N. Lee participate in research or clinical trials?
Yes. Dr. Kristen N. Lee has published 9 articles and abstracts on conditions like Biotinidase Deficiency. You can view a list of Dr. Kristen N. Lee's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Kristen N. Lee accept my insurance?
Dr. Kristen N. Lee accepts most major insurance plans, including Blue Cross Blue Shield and Health Alliance Plan. We recommend calling the office directly at 734-647-8902 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
- 15q11.2 MicrodeletionDr. Lee isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Lee isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Lee isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Lee isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Lee isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Lee isAdvanced. Learn about Aase Syndrome.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- AchondroplasiaDr. Lee isExperienced. Learn about Achondroplasia.
- Acro-Pectoro-Renal Field DefectDr. Lee isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- AcrocephalopolydactylyDr. Lee isExperienced. Learn about Acrocephalopolydactyly.
- Acromegaloid Facial Appearance Syndrome
- Acropectoral SyndromeDr. Lee isExperienced. Learn about Acropectoral Syndrome.