Alan F Rubin
Titre
Citée par
Citée par
Année
BET inhibitor resistance emerges from leukaemia stem cells
CY Fong, O Gilan, EYN Lam, AF Rubin, S Ftouni, D Tyler, K Stanley, ...
Nature 525 (7570), 538-542, 2015
3622015
Comment on "The consensus coding sequences of human breast and colorectal cancers"
AF Rubin, P Green
Science 317 (5844), 1500, 2007
1572007
A statistical framework for analyzing deep mutational scanning data
AF Rubin, H Gelman, N Lucas, SM Bajjalieh, AT Papenfuss, TP Speed, ...
Genome biology 18 (1), 1-15, 2017
812017
Mutation patterns in cancer genomes
AF Rubin, P Green
Proceedings of the National Academy of Sciences 106 (51), 21766-21770, 2009
812009
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effect
D Esposito, J Weile, J Shendure, LM Starita, AT Papenfuss, FP Roth, ...
Genome biology 20 (1), 1-11, 2019
292019
Comprehensive Analysis of the SUL1 Promoter of Saccharomyces cerevisiae
MS Rich, C Payen, AF Rubin, GT Ong, MR Sanchez, N Yachie, ...
Genetics 203 (1), 191-202, 2016
202016
Two of a kind: transmissible Schwann cell cancers in the endangered Tasmanian devil (Sarcophilus harrisii)
AL Patchett, THH Coorens, J Darby, R Wilson, MJ McKay, KS Kamath, ...
Cellular and Molecular Life Sciences 77 (9), 1847-1858, 2020
192020
A combined approach reveals a regulatory mechanism coupling Src’s kinase activity, localization, and phosphotransferase-independent functions
E Ahler, AC Register, S Chakraborty, L Fang, EM Dieter, KA Sitko, ...
Molecular cell 74 (2), 393-408. e20, 2019
162019
Recommendations for the collection and use of multiplexed functional data for clinical variant interpretation
H Gelman, JN Dines, J Berg, AH Berger, S Brnich, FM Hisama, RG James, ...
Genome medicine 11 (1), 1-11, 2019
122019
Collateral fitness effects of mutations
JD Mehlhoff, FW Stearns, D Rohm, B Wang, EY Tsou, N Dutta, MH Hsiao, ...
Proceedings of the National Academy of Sciences 117 (21), 11597-11607, 2020
112020
Novel drivers and modifiers of MPL-dependent oncogenic transformation identified by deep mutational scanning
JL Bridgford, SM Lee, CMM Lee, P Guglielmelli, E Rumi, D Pietra, ...
Blood, The Journal of the American Society of Hematology 135 (4), 287-292, 2020
92020
Enrich2: a statistical framework for analyzing deep mutational scanning data
AF Rubin, N Lucas, SM Bajjalieh, AT Papenfuss, TP Speed, DM Fowler
BioRxiv, 075150, 2016
42016
Expression-based segmentation of the Drosophila genome
AF Rubin, P Green
BMC genomics 14 (1), 1-8, 2013
42013
An open-source platform to distribute and interpret data from multiplexed assays of variant effect
D Esposito, J Weile, J Shendure, LM Starita, AT Papenfuss, FP Roth, ...
BioRxiv, 555797, 2019
32019
Correction to: A statistical framework for analyzing deep mutational scanning data
AF Rubin, H Gelman, N Lucas, SM Bajjalieh, AT Papenfuss, TP Speed, ...
Genome biology 19 (1), 1-4, 2018
12018
The Effects of Cis-Regulatory Mutations in the SUL1 Gene on Sulfate-Limited Fitness in Yeast
MS Rich, C Payen, AF Rubin, GT Ong, MR Sanchez, N Yachie, ...
Genetics, 2016
12016
Identifying New Hybrid Insulin Peptides (HIPs) in Type 1 Diabetes
SI Mannering, AF Rubin, R Wang, P Bhattacharjee
Frontiers in Immunology 12, 1542, 2021
2021
MaveRegistry: a collaboration platform for multiplexed assays of variant effect
D Kuang, J Weile, N Kishore, AF Rubin, S Fields, DM Fowler, FP Roth
bioRxiv, 2020
2020
Computational Tools for Deep Mutational Scanning
AF Rubin, D Esposito, J Weile, FP Roth, DM Fowler, AT Papenfuss
PROTEIN SCIENCE 27, 51-51, 2018
2018
A statistical framework for analyzing deep mutational scanning data (vol 18, 150, 2017)
AF Rubin, H Gelman, N Lucas, SM Bajjalieh, AT Papenfuss, TP Speed, ...
BIOMED CENTRAL LTD, 2018
2018
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20