| Structural and functional characterization of G protein–coupled receptors with deep mutational scanning EM Jones, NB Lubock, AJ Venkatakrishnan, J Wang, AM Tseng, JM Paggi, ... Elife 9, e54895, 2020 | 108 | 2020 |
| Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism N Matoba, D Liang, H Sun, N Aygün, JC McAfee, JE Davis, LM Raffield, ... Translational Psychiatry 10 (1), 265, 2020 | 68 | 2020 |
| Functional regulatory variants implicate distinct transcriptional networks in dementia YA Cooper, N Teyssier, NM Dräger, Q Guo, JE Davis, SM Sattler, Z Yang, ... Science 377 (6608), eabi8654, 2022 | 58 | 2022 |
| Efficient synthesis of 4-hydroxycyclopentenones: dysprosium (III) triflate catalyzed Piancatelli rearrangement D Fisher, LI Palmer, JE Cook, JE Davis, JR de Alaniz Tetrahedron 70 (27-28), 4105-4110, 2014 | 54 | 2014 |
| Multiplexed characterization of rationally designed promoter architectures deconstructs combinatorial logic for IPTG-inducible systems TC Yu, WL Liu, MS Brinck, JE Davis, J Shek, G Bower, T Einav, ... Nature communications 12 (1), 325, 2021 | 36 | 2021 |
| Dissection of c-AMP response element architecture by using genomic and episomal massively parallel reporter assays JE Davis, KD Insigne, EM Jones, QA Hastings, WC Boldridge, S Kosuri Cell Systems 11 (1), 75-85. e7, 2020 | 29 | 2020 |
| Catalytic Enantioselective Aza-Piancatelli Rearrangement AB Gade, NT Patil Synlett 28 (09), 1096-1100, 2017 | 28 | 2017 |
| Boronic acid catalysis for aza-piancatelli rearrangement WB Tang, KS Cao, SS Meng, WH Zheng Synthesis 49 (16), 3670-3675, 2017 | 24 | 2017 |
| Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants JC McAfee, S Lee, J Lee, JL Bell, O Krupa, J Davis, K Insigne, ML Bond, ... Cell Genomics 3 (10), 2023 | 7 | 2023 |
| Multiplexed dissection of a model human transcription factor binding site architecture JE Davis, KD Insigne, EM Jones, QB Hastings, S Kosuri bioRxiv, 625434, 2019 | 6 | 2019 |
| Common genetic risk variants identified in the SPARK cohort implicate DDHD2 as a novel autism risk gene N Matoba, D Liang, H Sun, N Aygün, JC McAfee, JE Davis, LM Raffield, ... medRxiv, 2020.01. 13.20017319, 2020 | 4 | 2020 |
| A Multiplexed Approach to Defining Sequence-Function Relationships in Gene Expression Using a Model Human Transcription Factor Binding Site JE Davis University of California, Los Angeles, 2019 | | 2019 |
