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Robert Tjian grad student 1977-1982 UC Berkeley (Chemistry Tree)
 (T antigen : DNA interactions involved in SV40 DNA replication and regulation of viral gene expression.)
Tom Maniatis post-doc 1982-1985 Harvard


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Grant A Hartzog grad student 1992 UCSF (Chemistry Tree)
Holly K. Tabor grad student 2002 Stanford
James P. Noonan grad student 2004 Stanford
Nathan D. Trinklein grad student 2004 Stanford
Shelley J. Force Aldred grad student 2005 Stanford
Sara J. Cooper grad student 2006 Stanford
Anne N. Strehlow grad student 2006 Stanford
Diane I. Schroeder grad student 2008 Stanford
Alayne L. Brunner grad student 2010 Stanford
Ryne C. Ramaker grad student 2014-2017 HudsonAlpha Institute for Biotechnology (GenetiTree)
Nick Cochran post-doc 2015- HudsonAlpha Institute for Biotechnology
BETA: Related publications


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Gelfman S, Dugger SA, Araujo Martins Moreno C, et al. (2019) A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS. Genome Research
Patel N, Wang J, Shiozawa K, et al. (2019) HDAC2 Regulates Site-Specific Acetylation of MDM2 and Its Ubiquitination Signaling in Tumor Suppression. Iscience. 13: 43-54
Carvill GL, Engel KL, Ramamurthy A, et al. (2018) Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies. American Journal of Human Genetics. 103: 1022-1029
Hiatt SM, Neu MB, Ramaker RC, et al. (2018) De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay. Plos Genetics. 14: e1007671
Koch H, Starenki D, Cooper SJ, et al. (2018) powerTCR: A model-based approach to comparative analysis of the clone size distribution of the T cell receptor repertoire. Plos Computational Biology. 14: e1006571
Carlson J, Locke AE, Flickinger M, et al. (2018) Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans. Nature Communications. 9: 3753
Hagenauer MH, Schulmann A, Li JZ, et al. (2018) Inference of cell type content from human brain transcriptomic datasets illuminates the effects of age, manner of death, dissection, and psychiatric diagnosis. Plos One. 13: e0200003
Thompson ML, Finnila CR, Bowling KM, et al. (2018) Genomic sequencing identifies secondary findings in a cohort of parent study participants. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Myers RM, Kimberly RP, Roberts BS, et al. (2018) Discovery and validation of circulating biomarkers of colorectal adenoma by high-depth small RNA sequencing. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research
Ramaker RC, Savic D, Hardigan AA, et al. (2017) A genome-wide interactome of DNA-associated proteins in the human liver. Genome Research
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