Overview
Molly Sheridan is a Medical Genetics provider in Baltimore, Maryland. Her top areas of expertise are Microcephaly Deafness Syndrome, Immune Defect due to Absence of Thymus, DiGeorge Syndrome, and Albright's Hereditary Osteodystrophy.
Her clinical research consists of co-authoring 14 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
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Locations
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.
Johns Hopkins University
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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
- Achalasia Microcephaly SyndromeDr. Sheridan isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Albright's Hereditary OsteodystrophyDr. Sheridan isExperienced. Learn about Albright's Hereditary Osteodystrophy.
- Cortical DysplasiaDr. Sheridan isExperienced. Learn about Cortical Dysplasia.
- DiGeorge SyndromeDr. Sheridan isExperienced. Learn about DiGeorge Syndrome.
- Immune Defect due to Absence of ThymusDr. Sheridan isExperienced. Learn about Immune Defect due to Absence of Thymus.
- MicrocephalyDr. Sheridan isExperienced. Learn about Microcephaly.