Overview
Bryce Mendelsohn is a Medical Genetics provider in Oakland, California. Dr. Mendelsohn is rated as an Experienced provider by MediFind in the treatment of Turner Syndrome. His top areas of expertise are Chromosome 10q Deletion, Chromosome 13q Duplication, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
His clinical research consists of co-authoring 43 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Turner Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- OTHER MEDICAID
- STATE MEDICAID
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.
1 Clinical Trials
Svetlana Yatsenko is a Medical Genetics provider in Stanford, California. Dr. Yatsenko is rated as a Distinguished provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Mosaicism, Turner Syndrome, 46XX Testicular Disorder of Sex Development, Intersex, and Hormone Replacement Therapy (HRT).
Ucsf Medical Group Business Services
Mary Norton is an Obstetrics and Gynecologist and a Medical Genetics provider in San Francisco, California. Dr. Norton is rated as an Elite provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are Fetal Edema, Hydrops Fetalis, Alpha Thalassemia, and Hemolytic Disease of the Newborn.
Lpch Medical Group Div Of Lucile
Suha Bachir is a Medical Genetics provider in Palo Alto, California. Dr. Bachir is rated as an Advanced provider by MediFind in the treatment of Turner Syndrome. Her top areas of expertise are 2q37 Deletion Syndrome, Costello Syndrome, Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects, and Currarino Triad.
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
- Biotinidase DeficiencyDr. Mendelsohn isAdvanced. Learn about Biotinidase Deficiency.
- Chromosome 10q DeletionDr. Mendelsohn isAdvanced. Learn about Chromosome 10q Deletion.
- Chromosome 13q DuplicationDr. Mendelsohn isAdvanced. Learn about Chromosome 13q Duplication.
- Classic GalactosemiaDr. Mendelsohn isAdvanced. Learn about Classic Galactosemia.
- Dihydropteridine Reductase DeficiencyDr. Mendelsohn isAdvanced. Learn about Dihydropteridine Reductase Deficiency.
- Fabry DiseaseDr. Mendelsohn isAdvanced. Learn about Fabry Disease.
- Experienced
- Activated PI3K Delta Syndrome (APDS)Dr. Mendelsohn isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adrenoleukodystrophy (ALD)Dr. Mendelsohn isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Arthrogryposis Multiplex CongenitaDr. Mendelsohn isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autism Spectrum DisorderDr. Mendelsohn isExperienced. Learn about Autism Spectrum Disorder.
- Autosomal Recessive Congenital Methemoglobinemia
- Branchio-Oculo-Facial Syndrome (BOFS)Dr. Mendelsohn isExperienced. Learn about Branchio-Oculo-Facial Syndrome (BOFS).