Combinatorial single-cell CRISPR screens by direct guide RNA capture and targeted sequencing JM Replogle, TM Norman, A Xu, JA Hussmann, J Chen, JZ Cogan, ... Nature biotechnology 38 (8), 954-961, 2020 | 343 | 2020 |
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis RP Kristjansson, S Benonisdottir, OB Davidsson, A Oddsson, V Tragante, ... Nature genetics 51 (2), 267-276, 2019 | 118 | 2019 |
Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562 B Zhou, SS Ho, SU Greer, X Zhu, JM Bell, JG Arthur, N Spies, X Zhang, ... Genome research 29 (3), 472-484, 2019 | 112 | 2019 |
Haplotype-resolved and integrated genome analysis of the cancer cell line HepG2 B Zhou, SS Ho, SU Greer, N Spies, JM Bell, X Zhang, X Zhu, JG Arthur, ... Nucleic acids research 47 (8), 3846-3861, 2019 | 64 | 2019 |
Sequence variants associating with urinary biomarkers S Benonisdottir, RP Kristjansson, A Oddsson, V Steinthorsdottir, ... Human molecular genetics 28 (7), 1199-1211, 2019 | 34 | 2019 |
Sc-compReg enables the comparison of gene regulatory networks between conditions using single-cell data Z Duren, WS Lu, JG Arthur, P Shah, J Xin, F Meschi, ML Li, CM Nemec, ... Nature Communications 12 (1), 4763, 2021 | 28 | 2021 |
On the relationship of steady states of continuous and discrete models arising from biology A Veliz-Cuba, J Arthur, L Hochstetler, V Klomps, E Korpi Bulletin of mathematical biology 74, 2779-2792, 2012 | 20 | 2012 |
Nonlinear Kalman filtering for censored observations J Arthur, A Attarian, F Hamilton, H Tran Applied Mathematics and Computation 316, 155-166, 2018 | 17 | 2018 |
Feasibility of parameter estimation in hepatitis C viral dynamics models JG Arthur, HT Tran, P Aston Journal of Inverse and Ill-Posed Problems 25 (1), 69-80, 2017 | 15 | 2017 |
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin GR Oskarsson, RP Kristjansson, AL Lee, G Sveinbjornsson, ... Communications Biology 1 (1), 49, 2018 | 14 | 2018 |
Extensive and deep sequencing of the Venter/HuRef genome for developing and benchmarking genome analysis tools B Zhou, JG Arthur, SS Ho, R Pattni, Y Huang, WH Wong, AE Urban Scientific data 5 (1), 1-12, 2018 | 12 | 2018 |
Detection of complex structural variation from paired-end sequencing data JG Arthur, X Chen, B Zhou, AE Urban, WH Wong bioRxiv, 200170, 2018 | 7 | 2018 |
Stimulus features, resetting curves, and the dependence on adaptation JG Arthur, SD Burton, GB Ermentrout Journal of computational neuroscience 34 (3), 505-520, 2013 | 6 | 2013 |
Automatic detection of complex structural genome variation across world populations B Zhou, JG Arthur, H Guo, CR Hughes, T Kim, Y Huang, R Pattni, HJ Lee, ... bioRxiv, 200170, 2017 | 4 | 2017 |
Detection and Validation of Genomic Structural Variation from DNA Sequencing Data JG Arthur Stanford University, 2018 | 2 | 2018 |
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders B Zhou, JG Arthur, H Guo, T Kim, Y Huang, R Pattni, T Wang, S Kundu, ... Cell 187 (23), 6687-6706. e25, 2024 | 1 | 2024 |
Sequence variants associated with resistant hypertension implicate mechanisms affecting potassium levels V Tragante, P Sulem, G Thorleifsson, ML Frigge, JG Arthur, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1108-1109, 2019 | 1 | 2019 |
80. IMPLICATION OF COMPLEX STRUCTURAL GENOME VARIATION IN THE GENETIC ARCHITECTURE OF NEUROPSYCHIATRIC DISORDERS: INSIGHTS FROM HUMAN POPULATION ANALYSIS AND FROM POSTMORTEM … B Zhou, J Arthur, H Guo, T Kim, Y Huang, R Pattni, G Song, D Palejev, ... European Neuropsychopharmacology 87, 93, 2024 | | 2024 |
Reference free spot deconvolution in spatial transcriptomics SR Williams, GM Kamath, JG Arthur US Patent App. 18/587,627, 2024 | | 2024 |
Systems and methods for detection of low-abundance molecular barcodes from a sequencing library DP Riordan, M Alexis, JG Arthur, AJ Hill US Patent App. 18/090,903, 2023 | | 2023 |