Overview
Hilary Vernon is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Vernon has been practicing medicine for over 21 years is highly rated in 9 conditions, according to our data. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Inborn Amino Acid Metabolism Disorder, and Progressive External Ophthalmoplegia.
Her clinical research consists of co-authoring 75 peer reviewed articles and participating in 3 clinical trials. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Locations
600 N Wolf St, Baltimore, MD 21287
601 N Caroline St, Baltimore, MD 21287
200 N Wolfe St, Baltimore, MD 21287
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.
3 Clinical Trials
Johns Hopkins University
Julie Hoover-Fong is a Medical Genetics specialist and a Geriatrics provider in Baltimore, Maryland. Dr. Hoover-Fong is highly rated in 39 conditions, according to our data. His top areas of expertise are Achondroplasia, Rhizomelic Syndrome, Spondyloepimetaphyseal Dysplasia Strudwick Type, Myringotomy, and Adenoidectomy. Dr. Hoover-Fong is currently accepting new patients.
Nancy Braverman is a Pediatrics specialist and a Medical Genetics provider in Baltimore, Maryland. Dr. Braverman is highly rated in 14 conditions, according to our data. Her top areas of expertise are Zellweger Syndrome, Chondrodysplasia Punctata Syndrome, X-Linked Chondrodysplasia Punctata 2, and Acromesomelic Dysplasia.
William Gahl is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Gahl is highly rated in 33 conditions, according to our data. His top areas of expertise are Oculocutaneous Albinism Type 2, Oculocutaneous Albinism, Oculocutaneous Albinism Type 1, and Hermansky-Pudlak Syndrome.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Distinguished
- Propionic Acidemia
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Beta-Ketothiolase Deficiency
- Inborn Amino Acid Metabolism Disorder
- Inborn Renal Aminoaciduria
- Infantile Neutropenia
- Ornithine Transcarbamylase Deficiency
- Experienced
- Achalasia Microcephaly Syndrome
- Albinism
- Alkaptonuria
- Autism Spectrum Disorder
- Brachydactyly Type B
- Carbamoyl Phosphate Synthetase 1 Deficiency