Overview
Molly Crenshaw is a Medical Genetics provider in Charlotte, North Carolina. Her top areas of expertise are 15q11.2 Microdeletion, Molybdenum Cofactor Deficiency (MoCD), Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and X-Linked Spondyloepiphyseal Dysplasia Tarda.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- OTHER COMMERCIAL
- POS
- PPO
Locations
201 Queens Rd, Charlotte, NC 28204
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.
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Frequently Asked Questions about Dr. Molly Crenshaw
How do I make an appointment with Dr. Molly Crenshaw?
You can book an appointment with Dr. Molly Crenshaw by calling their office at 980-501-1676. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Molly Crenshaw a top-rated expert for 15q11.2 Microdeletion?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Molly Crenshaw is classified as an Experienced expert for 15q11.2 Microdeletion, 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. Molly Crenshaw specialize in?
While Dr. Molly Crenshaw is a Medical Genetics, they have specific expertise in 15q11.2 Microdeletion, Molybdenum Cofactor Deficiency (MoCD), and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Molly Crenshaw participate in research or clinical trials?
Yes. Dr. Molly Crenshaw has published 12 articles and abstracts on conditions like 15q11.2 Microdeletion. You can view a list of Dr. Molly Crenshaw's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Molly Crenshaw accept my insurance?
Dr. Molly Crenshaw accepts most major insurance plans, including Cigna and Medicaid. We recommend calling the office directly at 980-501-1676 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
- Experienced
- 15q11.2 MicrodeletionDr. Crenshaw isExperienced. Learn about 15q11.2 Microdeletion.
- Brachydactyly Mononen TypeDr. Crenshaw isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyDr. Crenshaw isExperienced. Learn about Chondrodystrophy.
- Molybdenum Cofactor Deficiency (MoCD)Dr. Crenshaw isExperienced. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- X-Linked Spondyloepiphyseal Dysplasia TardaDr. Crenshaw isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.
