Robert Nussbaum
Affiliations: | Genomic Medicine | University of California, San Francisco, San Francisco, CA |
Area:
Medical GeneticsWebsite:
http://profiles.ucsf.edu/robert.nussbaumGoogle:
"Robert Nussbaum"Bio:
http://cancer.ucsf.edu/people/profiles/nussbaum_robert.3571
http://www.ucsfhealth.org/robert.nussbaum
Mean distance: 11.41
Cross-listing: DevTree
Children
Sign in to add trainee| Jeannie T. Lee | grad student | 1993 | Penn |
| Jonathan F. Russell | grad student | 2013 | UCSF |
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Publications
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| Hammami Bomholtz S, Refaat M, Buur Steffensen A, et al. (2020) Functional phenotype variations of two novel K 7.1 mutations identified in patients with Long QT syndrome. Pacing and Clinical Electrophysiology : Pace |
| Callis TE, Truty R, Esplin ED, et al. (2020) Cardiologists Beware: Clinical Limitations Of Genotyping- Versus Sequencing-Based Strategies For Cardiomyopathy Evaluation Journal of the American College of Cardiology. 75: 6 |
| Parikh VN, Caleshu C, Reuter C, et al. (2019) Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy. Circulation. Heart Failure. 12: e005371 |
| Esplin E, Haverfield E, Yang S, et al. (2019) Abstract P4-03-06: Limitations of direct-to-consumer genetic screening for HBOC: False negatives, false positives and everything in between Cancer Research. 79 |
| Cline MS, Liao RG, Parsons MT, et al. (2018) BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2. Plos Genetics. 14: e1007752 |
| Kidambi TD, Goldberg D, Nussbaum R, et al. (2018) Novel variant of unknown significance in MUTYH in a patient with MUTYH-associated polyposis: a case to reclassify. Clinical Journal of Gastroenterology |
| Lincoln S, Truty R, Zook J, et al. (2018) Abstract PD1-03: Clinically actionable pathogenic mutations that may be missed by conventional NGS-based testing: An analysis of 80,000 patients Cancer Research. 78 |
| Lincoln S, Zook J, Truty R, et al. (2018) Abstract P4-06-08: An interlaboratory study of complex mutation detection in genes associated with hereditary breast and ovarian cancer highlights both successes and current challenges Cancer Research. 78 |
| Blanco A, Yang S, Michalski S, et al. (2018) Abstract P4-06-02: Germline analysis of breast cancer patients with abnormal somatic results: Ancillary assessment or critical co-diagnostic? Cancer Research. 78 |
| Esplin E, Michalski S, Yang S, et al. (2018) Abstract P3-03-01: Clinical utility of finding pathogenic mutations beyond BRCA1/2 in breast cancer patients Cancer Research. 78 |