Overview
James Goldberg is a Medical Genetics specialist and a Neonatologist in San Francisco, California. Dr. Goldberg is rated as an Experienced provider by MediFind in the treatment of Fragile X Syndrome. His top areas of expertise are Smith-Lemli-Opitz Syndrome, Fragile X Syndrome, Trisomy 13, and Chromosome 13q Duplication.
His clinical research consists of co-authoring 34 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
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Accepted insurance plans:
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
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.
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 Fragile X Syndrome. Her top areas of expertise are 2q37 Deletion Syndrome, Costello Syndrome, Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects, and Currarino Triad.
Lpch Medical Group Div Of Lucile
Christina Tise is a Medical Genetics provider in Palo Alto, California. Dr. Tise is rated as an Advanced provider by MediFind in the treatment of Fragile X Syndrome. Her top areas of expertise are Zellweger Syndrome, 2q37 Deletion Syndrome, Adrenoleukodystrophy (ALD), and Urea Cycle Disorders (UCD).
Yael Wilnai-Ziskind is a Medical Genetics specialist and a Pediatrics provider in Palo Alto, California. Dr. Wilnai-Ziskind is rated as an Advanced provider by MediFind in the treatment of Fragile X Syndrome. Her top areas of expertise are Carnitine Palmitoyltransferase 2 Deficiency, Carnitine Palmitoyltransferase 1 Deficiency, Beta-Ketothiolase Deficiency, and Citrullinemia.
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
- Angelman SyndromeDr. Goldberg isExperienced. Learn about Angelman Syndrome.
- Chromosome 13q DuplicationDr. Goldberg isExperienced. Learn about Chromosome 13q Duplication.
- Fragile X SyndromeDr. Goldberg isExperienced. Learn about Fragile X Syndrome.
- Immune Defect due to Absence of ThymusDr. Goldberg isExperienced. Learn about Immune Defect due to Absence of Thymus.
- Prader-Willi SyndromeDr. Goldberg isExperienced. Learn about Prader-Willi Syndrome.
- Smith-Lemli-Opitz SyndromeDr. Goldberg isExperienced. Learn about Smith-Lemli-Opitz Syndrome.