Dr. Nussbaum is on Doximity
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Office
513 Parnassus Ave
# HSE901E
San Francisco, CA 94143Phone+1 415-476-3200Fax+1 415-502-0720
Education & Training
- Baylor College of MedicineFellowship, 1978 - 1980
- Washington University/B-JH/SLCH ConsortiumResidency, Internal Medicine, 1975 - 1978
- Harvard Medical SchoolClass of 1975
Certifications & Licensure
- CA State Medical License 2006 - 2026
- NC State Medical License 2017 - 2024
- MD State Medical License 1995 - 2007
- PA State Medical License 1984 - 1994
- TX State Medical License 1981 - 1985
- American Board of Internal Medicine Internal Medicine
- American Board of Medical Genetics and Genomics Clinical Genetics
Awards, Honors, & Recognition
- CMS Meaningful Use Stage 1 Certification EpicCare Ambulatory EMR, Epic Systems Corporation, 2012-2013
- Elected Member Institute of Medicine, 2004
- Elected Member The American Society for Clinical Investigation, 1987
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Publications & Presentations
PubMed
- 4 citationsA Systematic Method for Detecting Abnormal mRNA Splicing and Assessing Its Clinical Impact in Individuals Undergoing Genetic Testing for Hereditary Cancer Syndromes.Nick Kamps-Hughes, Victoria E H Carlton, Laure Fresard, Steve Osazuwa, Elizabeth Starks
The Journal of Molecular Diagnostics. 2023-03-01 - 2 citationsGermline Cancer Testing in Unselected Patients with Gastric and Esophageal Cancers: A Multi-center Prospective Study.P L S Uson Jr, K L Kunze, M A Golafshar, G Botrus, D Riegert-Johnson
Digestive Diseases and Sciences. 2022-11-01 - 7 citationsComparison of Germline Genetic Testing Before and After a Medical Policy Covering Universal Testing Among Patients With Colorectal Cancer.Chad Moretz, Stacey DaCosta Byfield, Kathryn E Hatchell, Joline Dalton, Peter Nicholas Onglao
JAMA Network Open. 2022-10-03
Journal Articles
- Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients with Hereditary Cancer SyndromeScott Okuno, Luke Mountjoy, Cameron S Thorpe, Edward D Esplin, Robert L Nussbaum, Alan H Bryce, Tanios S Bekaii-Saab, Aleksandar Sekulic, JAMA Oncology
- Distinguishing Variant Pathogenicity from Genetic DiagnosisHeidi L Rehm, Robert L Nussbaum, JAMA
- Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization StudySusan M Domchek, Wendy K Chung, Patricia A Ganz, Robert L Nussbaum, Journal of the National Cancer Institute
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Press Mentions
- http://thesmarterbusiness.com/Thompson-Thompson-Genetics-in-Medicine-by-Nussbaum-Md-Robert-Mcinnes-Md-Phd-Frsc-Roderick-R-W-Saunders2007-Paperback-7th-Edition.pdfJune 27th, 2020
- Why Not All Genetic Testing Is Created Equal on Coast LiveJune 17th, 2019
- Invitae Study of 143,000 Patients Shows Importance of Routinely Including Deletion and Duplication Detection with Sequencing in Genetic TestingJune 13th, 2018
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Grant Support
- Combined BAC Transgenic And Knock-Out Mouse Model Of Lowe Syndrome NephropathyNational Institute Of Diabetes And Digestive And Kidney Diseases2012
- Glucocerebrosidase Mutations In A Mouse Synucleinopathy ModelNational Institute On Aging2011
- GI Endotoxin As An Environmental Trigger In An Alpha-Synuclein Transgenic MouseNational Institute Of Environmental Health Sciences2010–2011
- Combined BAC Transgenic And Knock-Out Mouse Model Of Lowe Syndrome NephropathyNational Institute Of Diabetes And Digestive And Kidney Diseases2010
- Glucocerebrosidase Mutations In A Mouse Synucleinopathy ModelNational Institute On Aging2009–2010
- Studies On Mouse VIT C TransporterNational Human Genome Research Institute2002–2005
- The Lowe Oculocerebrorenal SyndromeNational Human Genome Research Institute2000–2005
- Genetics Of Parkinson'S DiseaseNational Human Genome Research Institute1997–2005
- Outcomes Of Education And Counseling For HnpcctestingNational Human Genome Research Institute2004
- Lowe Oculocerebrorenal SyndromeNational Human Genome Research Institute1995–2004
- Positional Cloning Of Autosomal Dominant Fanconi SyndromNational Human Genome Research Institute2001
- Studies On Mouse Vitamin C TransporterNational Human Genome Research Institute2001
- Mouse Vitamin C TransporterNational Human Genome Research Institute2000
- Batten DiseaseNational Human Genome Research Institute2000
- Mouse Model For Batten'S DiseaseNational Human Genome Research Institute1999
- Genetics Of ParkinsonNational Human Genome Research Institute1998–1999
- Mice Defective In Phosphatidylinositol SignalingNational Human Genome Research Institute1995–1999
- Mutation Analysis In Patients With Lowe Oculocerebrorenal SyndromeNational Human Genome Research Institute1996–1998
- Triplet Repeat Amplification In The Fragile X SyndromeNational Human Genome Research Institute1995–1997
- Isolating The Gene For ChoroideremiaNational Eye Institute1987–1993
- Molecular Genetic Analysis Of Lowe'S SyndromeEunice Kennedy Shriver National Institute Of Child Health &Human Development1989–1992
- Postdoctoral Training In Molecular Genetic ResearchNational Institute Of General Medical Sciences1988–1992
- Genetic &Molecular Studies In Lowe'S SyndromeEunice Kennedy Shriver National Institute Of Child Health &Human Development1987–1988
- Molecular Analysis Of Fragile X In Somatic Cell HybridsEunice Kennedy Shriver National Institute Of Child Health &Human Development1985–1987
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