Overview
Bryce Mendelsohn is a Medical Genetics provider practicing medicine in Oakland, California.
Dr. Mendelsohn is highly rated in 16 conditions, according to our data. His clinical expertise encompasses Chromosome 10q Deletion, Chromosome 13q Duplication, Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia.
He is actively involved in clinical research, co-authoring 48 peer reviewed articles and participating in 1 clinical trial.
Specialties
Licenses
Languages Spoken
Gender
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
Lpch Medical Group Div Of Lucile
David Stevenson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Stevenson is highly rated in 100 conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, RASopathies, Costello Syndrome, and Deep Brain Stimulation.
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Enns is highly rated in 54 conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.
Center For Complex Obstetric Medicine
Dr. Mary E. Norton is a perinatologist and clinical geneticist who cares for pregnant patients who have a fetus with a birth defect or genetic disorder or are at risk for such a condition. She performs obstetric ultrasounds, counsels patients with abnormal ultrasounds and performs prenatal tests like amniocentesis and chorionic villus sampling. She also interprets complex genetic tests, especially when abnormalities are found. Norton's areas of interest in research include applying new genetic tests to prenatal diagnosis and fetal disease, as well as patient decision-making around genetic testing and obstetrical ultrasound. She is co-director of the Center for Maternal-Fetal Precision Medicine at UCSF, as well as the David E. Thorburn, M.D. and Kate McKee Thorburn Endowed Chair in Perinatal Medicine and Genetics at UCSF. Norton earned her medical degree at the University of Washington. She completed a residency in obstetrics and gynecology at Tufts University followed by a fellowship in maternal-fetal medicine and clinical genetics at UCSF. After several years at Brigham and Women's Hospital and Harvard Medical School, she returned to San Francisco and joined UCSF Medical Center in 1998. Dr. Norton is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Fetal Edema, Hydrops Fetalis, Alpha Thalassemia, and Hemolytic Disease of the Newborn. Dr. Norton is board certified in American Board Of Obstetrics And Gynecology, Obstetrics & Gynecology, American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics, and American Board Of Obstetrics And Gynecology, Maternal-Fetal Medicine. Dr. Norton is currently accepting new patients.
Frequently Asked Questions about Dr. Bryce A. Mendelsohn
How do I make an appointment with Dr. Bryce A. Mendelsohn?
You can book an appointment with Dr. Bryce A. Mendelsohn by calling their office at 510-752-7691. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Bryce A. Mendelsohn a top-rated expert for Chromosome 10q Deletion?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Bryce A. Mendelsohn is classified as an Advanced expert for Chromosome 10q Deletion, 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. Bryce A. Mendelsohn specialize in?
While Dr. Bryce A. Mendelsohn is a Medical Genetics, they have specific expertise in Chromosome 10q Deletion, Chromosome 13q Duplication, and Dihydropteridine Reductase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Bryce A. Mendelsohn participate in research or clinical trials?
Yes. Dr. Bryce A. Mendelsohn has published 48 articles and abstracts on conditions like Chromosome 10q Deletion. You can view a list of Dr. Bryce A. Mendelsohn's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Bryce A. Mendelsohn accept my insurance?
Dr. Bryce A. Mendelsohn accepts most major insurance plans, including Medicaid. We recommend calling the office directly at 510-752-7691 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
- 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.
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Mendelsohn isAdvanced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Dihydropteridine Reductase DeficiencyDr. Mendelsohn isAdvanced. Learn about Dihydropteridine Reductase Deficiency.
- Fabry DiseaseDr. Mendelsohn isAdvanced. Learn about Fabry Disease.
- Glycogen Storage Disease Type 3Dr. Mendelsohn isAdvanced. Learn about Glycogen Storage Disease Type 3.
- Maternal HyperphenylalaninemiaDr. Mendelsohn isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Sulfatase DeficiencyDr. Mendelsohn isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Phenylketonuria (PKU)Dr. Mendelsohn isAdvanced. Learn about Phenylketonuria (PKU).
- Pyruvate Decarboxylase DeficiencyDr. Mendelsohn isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Mendelsohn isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Mendelsohn isAdvanced. Learn about Thymidine Kinase 2 Deficiency (TK2d).
- 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).
- Branchiootorenal SyndromeDr. Mendelsohn isExperienced. Learn about Branchiootorenal Syndrome.
- CitrullinemiaDr. Mendelsohn isExperienced. Learn about Citrullinemia.
- ColobomaDr. Mendelsohn isExperienced. Learn about Coloboma.
- Congenital Aplastic AnemiaDr. Mendelsohn isExperienced. Learn about Congenital Aplastic Anemia.
- Congenital ContracturesDr. Mendelsohn isExperienced. Learn about Congenital Contractures.
- Cortical DysplasiaDr. Mendelsohn isExperienced. Learn about Cortical Dysplasia.
- Danon DiseaseDr. Mendelsohn isExperienced. Learn about Danon Disease.
- Early Infantile Epileptic EncephalopathyDr. Mendelsohn isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Galactokinase DeficiencyDr. Mendelsohn isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDr. Mendelsohn isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Mendelsohn isExperienced. Learn about Galactosemia.
- Gaucher DiseaseDr. Mendelsohn isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Mendelsohn isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Mendelsohn isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Mendelsohn isExperienced. Learn about Gaucher Disease Type 3.
- HomocystinuriaDr. Mendelsohn isExperienced. Learn about Homocystinuria.
- HypotoniaDr. Mendelsohn isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Mendelsohn isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Increased Head CircumferenceDr. Mendelsohn isExperienced. Learn about Increased Head Circumference.
- Leber Hereditary Optic Neuropathy (LHON)Dr. Mendelsohn isExperienced. Learn about Leber Hereditary Optic Neuropathy (LHON).
- LeukodystrophyDr. Mendelsohn isExperienced. Learn about Leukodystrophy.
- Maple Syrup Urine DiseaseDr. Mendelsohn isExperienced. Learn about Maple Syrup Urine Disease.
- MELAS SyndromeDr. Mendelsohn isExperienced. Learn about MELAS Syndrome.
- Methylmalonic AcidemiaDr. Mendelsohn isExperienced. Learn about Methylmalonic Acidemia.
- MicrocephalyDr. Mendelsohn isExperienced. Learn about Microcephaly.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- NeurofibromatosisDr. Mendelsohn isExperienced. Learn about Neurofibromatosis.
- Neurofibromatosis Type 1 (NF1)Dr. Mendelsohn isExperienced. Learn about Neurofibromatosis Type 1 (NF1).
- Niemann-Pick DiseaseDr. Mendelsohn isExperienced. Learn about Niemann-Pick Disease.
- Ornithine Transcarbamylase DeficiencyDr. Mendelsohn isExperienced. Learn about Ornithine Transcarbamylase Deficiency.
- Ornithine Translocase DeficiencyDr. Mendelsohn isExperienced. Learn about Ornithine Translocase Deficiency.
- PEPCK 1 DeficiencyDr. Mendelsohn isExperienced. Learn about PEPCK 1 Deficiency.
- Pompe DiseaseDr. Mendelsohn isExperienced. Learn about Pompe Disease.
- Pyruvate Carboxylase DeficiencyDr. Mendelsohn isExperienced. Learn about Pyruvate Carboxylase Deficiency.
- Roberts SyndromeDr. Mendelsohn isExperienced. Learn about Roberts Syndrome.
- Turner SyndromeDr. Mendelsohn isExperienced. Learn about Turner Syndrome.
- Urea Cycle Disorders (UCD)Dr. Mendelsohn isExperienced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
