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Russ Altman, M.D./Ph.D.

Affiliations: 
Stanford University, Palo Alto, CA 
Google:
"Russ Altman"
Bio:

https://books.google.com/books?id=tpQvAQAAIAAJ

Parents

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Bruce Gardner Buchanan grad student 1989 Stanford (Computer Science Tree)
 (Exclusion methods for the determination of protein structure from experimental data.)
Oleg Jardetzky grad student 1989 Stanford (Chemistry Tree)

Children

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Liping Wei grad student 2000 Stanford
Ramon M. Felciano grad student 2001 Stanford
Soumya Raychaudhuri grad student 2002 Stanford
Michael Bada grad student 2003 Stanford
Michelle W. Carrillo grad student 2003 Stanford
Olga G. Troyanskaya grad student 2003 Stanford (Cell Biology Tree)
Jonathan Dugan grad student 1999-2003 Stanford
Jeffrey T. Chang grad student 2004 Stanford
Mike H. Liang grad student 2005 Stanford
Zhen Lin grad student 2005 Stanford
Iwei Yeh grad student 2006 Stanford
Michael N. Cantor grad student 2009 Stanford
Shirley Wu grad student 2009 Stanford
Nicholas Tatonetti grad student 2012 Stanford
Mor Peleg post-doc 2003 (Chemistry Tree)
Kai J Kohlhoff post-doc 2009-2010 Stanford Medical School (Computational Biology Tree)
Irene S. Gabashvili research scientist 2003 Stanford (Chemistry Tree)

Collaborators

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Joshua C. Denny collaborator (Computational Biology Tree)
BETA: Related publications

Publications

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McInnes G, Sharo AG, Koleske ML, et al. (2021) Opportunities and challenges for the computational interpretation of rare variation in clinically important genes. American Journal of Human Genetics. 108: 535-548
Wang S, Flynn ER, Altman RB. (2020) Gaussian Embedding for Large-scale Gene Set Analysis. Nature Machine Intelligence. 2: 387-395
Lever J, Altman R, Kim JD. (2020) Extending TextAE for annotation of non-contiguous entities. Genomics & Informatics. 18: e15
Altman RB. (2017) Artificial Intelligence (AI) Systems for Interpreting Complex Medical Data Sets. Clinical Pharmacology and Therapeutics
Daneshjou R, Cavallari LH, Weeke PE, et al. (2016) Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans. Molecular Genetics & Genomic Medicine. 4: 513-520
Kohlhoff KJ, Shukla D, Lawrenz M, et al. (2015) Corrigendum: Cloud-based simulations on Google Exacycle reveal ligand modulation of GPCR activation pathways. Nature Chemistry. 7: 759
Mugzach O, Peleg M, Bagley SC, et al. (2015) An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview-Revised data. Journal of Biomedical Informatics. 56: 333-47
Mugzach O, Peleg M, Bagley SC, et al. (2015) An ontology for Autism Spectrum Disorder (ASD) to infer ASD phenotypes from Autism Diagnostic Interview-Revised data Journal of Biomedical Informatics. 56: 333-347
MacArthur DG, Manolio TA, Dimmock DP, et al. (2014) Guidelines for investigating causality of sequence variants in human disease. Nature. 508: 469-76
Karczewski KJ, Snyder M, Altman RB, et al. (2014) Coherent Functional Modules Improve Transcription Factor Target Identification, Cooperativity Prediction, and Disease Association Plos Genetics. 10
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