Integrative analysis of 111 reference human epigenomes A Kundaje, W Meuleman, J Ernst, M Bilenky, A Yen, A Heravi-Moussavi, ... Nature 518 (7539), 317-330, 2015 | 3688 | 2015 |
An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues MR Corces, AE Trevino, EG Hamilton, PG Greenside, ... Nature methods 14 (10), 959-962, 2017 | 452 | 2017 |
Super-resolution chromatin tracing reveals domains and cooperative interactions in single cells B Bintu, LJ Mateo, JH Su, NA Sinnott-Armstrong, M Parker, S Kinrot, ... Science 362 (6413), 2018 | 304 | 2018 |
Opportunities and challenges for transcriptome-wide association studies M Wainberg, N Sinnott-Armstrong, N Mancuso, AN Barbeira, DA Knowles, ... Nature genetics 51 (4), 592-599, 2019 | 166* | 2019 |
GAMETES: a fast, direct algorithm for generating pure, strict, epistatic models with random architectures RJ Urbanowicz, J Kiralis, NA Sinnott-Armstrong, T Heberling, JM Fisher, ... BioData mining 5 (1), 1-14, 2012 | 152 | 2012 |
Reduced signal for polygenic adaptation of height in UK Biobank JJ Berg, A Harpak, N Sinnott-Armstrong, AM Joergensen, H Mostafavi, ... eLife 8, e39725, 2019 | 143 | 2019 |
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes E Rheinbay, MM Nielsen, F Abascal, JA Wala, O Shapira, G Tiao, ... Nature 578 (7793), 102-111, 2020 | 141* | 2020 |
Characterizing genetic interactions in human disease association studies using statistical epistasis networks T Hu, NA Sinnott-Armstrong, JW Kiralis, AS Andrew, MR Karagas, ... BMC bioinformatics 12 (1), 1-13, 2011 | 115 | 2011 |
Discovery of common and rare genetic risk variants for colorectal cancer JR Huyghe, SA Bien, TA Harrison, HM Kang, S Chen, SL Schmit, ... Nature genetics 51 (1), 76-87, 2019 | 114 | 2019 |
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 AM Dunning, K Michailidou, KB Kuchenbaecker, D Thompson, JD French, ... Nature genetics 48 (4), 374-386, 2016 | 91 | 2016 |
Multifactor dimensionality reduction for graphics processing units enables genome-wide testing of epistasis in sporadic ALS CS Greene, NA Sinnott-Armstrong, DS Himmelstein, PJ Park, JH Moore, ... Bioinformatics 26 (5), 694-695, 2010 | 87 | 2010 |
Noncoding somatic and inherited single-nucleotide variants converge to promote ESR1 expression in breast cancer SD Bailey, K Desai, KJ Kron, P Mazrooei, NA Sinnott-Armstrong, ... Nature genetics 48 (10), 1260, 2016 | 61 | 2016 |
Accelerating epistasis analysis in human genetics with consumer graphics hardware NA Sinnott-Armstrong, CS Greene, F Cancare, JH Moore BMC Research Notes 2 (1), 149, 2009 | 53 | 2009 |
High-resolution genome-wide functional dissection of transcriptional regulatory regions and nucleotides in human X Wang, L He, SM Goggin, A Saadat, L Wang, N Sinnott-Armstrong, ... Nature communications 9 (1), 1-15, 2018 | 49 | 2018 |
Wording effects in moral judgments RE O’Hara, NA Sinnott-Armstrong, W Sinnott-Armstrong Judgment and Decision Making 5 (7), 547-554, 2010 | 37 | 2010 |
Evaluation of Group Testing for SARS-CoV-2 RNA N Sinnott-Armstrong, D Klein, B Hickey medRxiv, 2020 | 33 | 2020 |
Chromatin accessibility dynamics in a model of human forebrain development AE Trevino, N Sinnott-Armstrong, J Andersen, SJ Yoon, N Huber, ... Science 367 (6476), 2020 | 28 | 2020 |
Reports from CAGI: The critical assessment of genome interpretation RA Hoskins, S Repo, D Barsky, G Andreoletti, J Moult, SE Brenner Human mutation 38 (9), 1039, 2017 | 28 | 2017 |
Predicting gene expression in massively parallel reporter assays: A comparative study A Kreimer, H Zeng, MD Edwards, Y Guo, K Tian, S Shin, R Welch, ... Human mutation 38 (9), 1240-1250, 2017 | 27 | 2017 |
Pan-cancer screen for mutations in non-coding elements with conservation and cancer specificity reveals correlations with expression and survival H Hornshøj, MM Nielsen, NA Sinnott-Armstrong, MP Świtnicki, M Juul, ... npj Genomic Medicine 3 (1), 1, 2018 | 25 | 2018 |