Overview
Julia Geppert practices in Coventry, United Kingdom. Ms. Geppert is rated as an Advanced expert by MediFind in the treatment of Chromosome 13q Duplication. Her top areas of expertise are Tyrosinemia Type 1, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Trisomy 13, and Chromosome 13q Duplication.
Her clinical research consists of co-authoring 16 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Chromosome 13q Duplication.
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. Experts 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.
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
- Chromosome 13q DuplicationMs. Geppert isAdvanced. Learn about Chromosome 13q Duplication.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Trisomy 13Ms. Geppert isAdvanced. Learn about Trisomy 13.
- Trisomy 18Ms. Geppert isAdvanced. Learn about Trisomy 18.
- Tyrosinemia Type 1Ms. Geppert isAdvanced. Learn about Tyrosinemia Type 1.
- Experienced
- Down SyndromeMs. Geppert isExperienced. Learn about Down Syndrome.
- Lung CancerMs. Geppert isExperienced. Learn about Lung Cancer.
- Lung NodulesMs. Geppert isExperienced. Learn about Lung Nodules.
- Mitochondrial Trifunctional Protein Deficiency
- Protein DeficiencyMs. Geppert isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Geppert isExperienced. Learn about Rhabdomyolysis.